Gene: TraesCS5D02G365500

Location

Chromosome 5D: 442,694,824-442,697,321 forward strand.

About this gene

This gene has 1 transcript (splice variant), 217 orthologues and 79 paralogues.

Transcripts

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Name	Transcript ID	bp	Protein	Biotype	UniProt	Flags
-	TraesCS5D02G365500.1	2235	744aa	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3B6MX47	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical,

Variant table

This table shows known variants for this gene. Use the 'Consequence Type' filter to view a subset of these.

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PTV
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PTV = Protein Truncating Variant
(0)

transcript ablation
(0)

splice acceptor variant
(0)

splice donor variant
(0)

stop gained
(0)

frameshift variant
(0)

stop lost
(0)

start lost
(0)

transcript amplification
(0)

inframe insertion
(0)

inframe deletion
(31)

missense variant
(0)

protein altering variant
(0)

splice donor 5th base variant
(0)

splice region variant
(0)

splice donor region variant
(0)

splice polypyrimidine tract variant
(0)

incomplete terminal codon variant
(0)

start retained variant
(0)

stop retained variant
(30)

synonymous variant
(0)

coding sequence variant
(0)

mature miRNA variant
(0)

5 prime UTR variant
(0)

3 prime UTR variant
(0)

non coding transcript exon variant
(0)

intron variant
(0)

NMD transcript variant
(0)

non coding transcript variant
(0)

coding transcript variant
(9)

upstream gene variant
(395)

downstream gene variant
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LocationAll
Location

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5D:442689824 - 5D:442702321
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ClassAll
Class

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(458)
SNP
(0)
deletion
(0)
genetic marker
(0)
indel
(0)
insertion
(0)
sequence alteration
(7)
substitution
(0)
tandem repeat
(0)
somatic SNV
(0)
somatic deletion
(0)
somatic genetic marker
(0)
somatic indel
(0)
somatic insertion
(0)
somatic sequence alteration
(0)
somatic substitution
(0)
somatic tandem repeat
(0)
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SourceAll
Source

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(10)
CerealsDB
(247)
EMS-induced mutation
(11)
Exome_Capture_Diversity
(142)
Inter-homoeologous
(8)
Watkins_collection
(47)
Watkins-exome-capture
(0)
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EvidenceAll
Evidence

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1000Genomes
(0)
HapMap
(0)
Cited
(0)
ESP
(0)
ExAC
(0)
Frequency
(0)
gnomAD
(0)
Multiple_observations
(0)
Phenotype_or_Disease
(0)
TOPMed
(465)
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Clinical Significance

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(0)
uncertain significance
(0)
not provided
(0)
other
(0)
benign
(0)
likely benign
(0)
association
(0)
histocompatibility
(0)
confers sensitivity
(0)
drug response
(0)
risk factor
(0)
likely pathogenic
(0)
protective
(0)
pathogenic
(465)
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TranscriptAll
Transcript

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TraesCS5D02G365500.1
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- Location
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- Clinical Significance
- AA coord
- Transcript

Variant ID	Chr: bp	Alleles	Class	Source	Evidence	Clin. Sig.	Conseq. Type	AA	AA coord	SIFT	Transcript

chr5D_442690503	5D:442690503	G/A	SNP	Watkins_collection	-	-	A sequence variant located 5' of a geneupstream gene variant	-	-	-	TraesCS5D02G365500.1
chr5D_442691423	5D:442691423	G/A	SNP	Watkins_collection	-	-	A sequence variant located 5' of a geneupstream gene variant	-	-	-	TraesCS5D02G365500.1
chr5D_442691811	5D:442691811	G/A	SNP	Watkins_collection	-	-	A sequence variant located 5' of a geneupstream gene variant	-	-	-	TraesCS5D02G365500.1
chr5D_442691875	5D:442691875	C/T	SNP	Watkins_collection	-	-	A sequence variant located 5' of a geneupstream gene variant	-	-	-	TraesCS5D02G365500.1
chr5D_scaffold65372_4181569	5D:442691875	C/T	SNP	Exome_Capture_Diversity	-	-	A sequence variant located 5' of a geneupstream gene variant	-	-	-	TraesCS5D02G365500.1
chr5D_scaffold65372_4181183	5D:442692261	G/A	SNP	Exome_Capture_Diversity	-	-	A sequence variant located 5' of a geneupstream gene variant	-	-	-	TraesCS5D02G365500.1
chr5D_442692261	5D:442692261	G/A	SNP	Watkins_collection	-	-	A sequence variant located 5' of a geneupstream gene variant	-	-	-	TraesCS5D02G365500.1
chr5D_442692824	5D:442692824	G/T	SNP	Watkins_collection	-	-	A sequence variant located 5' of a geneupstream gene variant	-	-	-	TraesCS5D02G365500.1
chr5D_442693694	5D:442693694	T/C	SNP	Watkins_collection	-	-	A sequence variant located 5' of a geneupstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0643.chr5D.442696321	5D:442696321	A/G	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	H/R	412	0.11	TraesCS5D02G365500.1
Cadenza1665.chr5D.442696344	5D:442696344	A/G	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	S/G	420	0.2	TraesCS5D02G365500.1
Cadenza0268.chr5D.442696344	5D:442696344	A/G	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	S/G	420	0.2	TraesCS5D02G365500.1
Cadenza1685.chr5D.442696344	5D:442696344	A/G	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	S/G	420	0.2	TraesCS5D02G365500.1
Cadenza0268.chr5D.442696345	5D:442696345	G/A	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	S/N	420	0.52	TraesCS5D02G365500.1
Cadenza1685.chr5D.442696345	5D:442696345	G/A	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	S/N	420	0.52	TraesCS5D02G365500.1
Cadenza1665.chr5D.442696345	5D:442696345	G/A	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	S/N	420	0.52	TraesCS5D02G365500.1
Cadenza1653.chr5D.442696348	5D:442696348	G/A	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	R/K	421	0.29	TraesCS5D02G365500.1
Cadenza1517.chr5D.442696426	5D:442696426	C/T	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	A/V	447	0.26	TraesCS5D02G365500.1
Cadenza1783.chr5D.442696426	5D:442696426	C/T	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	A/V	447	0.26	TraesCS5D02G365500.1
Cadenza0212.chr5D.442696426	5D:442696426	C/T	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	A/V	447	0.26	TraesCS5D02G365500.1
Cadenza1491.chr5D.442696426	5D:442696426	C/T	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	A/V	447	0.26	TraesCS5D02G365500.1
Cadenza0373.chr5D.442696426	5D:442696426	C/T	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	A/V	447	0.26	TraesCS5D02G365500.1
Cadenza0336.chr5D.442696426	5D:442696426	C/T	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	A/V	447	0.26	TraesCS5D02G365500.1
Cadenza1411.chr5D.442696426	5D:442696426	C/T	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	A/V	447	0.26	TraesCS5D02G365500.1
5D_442696526	5D:442696526	T/C	SNP	Watkins-exome-capture	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	L	480	-	TraesCS5D02G365500.1
5D_442696558	5D:442696558	T/A	SNP	Watkins-exome-capture	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	F/Y	491	0.14	TraesCS5D02G365500.1
Cadenza1257.chr5D.442696563	5D:442696563	C/T	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	P/S	493	0.17	TraesCS5D02G365500.1
Cadenza1783.chr5D.442696563	5D:442696563	C/T	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	P/S	493	0.17	TraesCS5D02G365500.1
5D_442696563	5D:442696563	C/T	SNP	Watkins-exome-capture	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	P/S	493	0.17	TraesCS5D02G365500.1
Cadenza0056.chr5D.442696563	5D:442696563	C/T	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	P/S	493	0.17	TraesCS5D02G365500.1
Cadenza0282.chr5D.442696563	5D:442696563	C/T	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	P/S	493	0.17	TraesCS5D02G365500.1
Cadenza0465.chr5D.442696563	5D:442696563	C/T	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	P/S	493	0.17	TraesCS5D02G365500.1
Cadenza0108.chr5D.442696563	5D:442696563	C/T	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	P/S	493	0.17	TraesCS5D02G365500.1
Cadenza1721.chr5D.442696563	5D:442696563	C/T	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	P/S	493	0.17	TraesCS5D02G365500.1
Cadenza2086.chr5D.442696563	5D:442696563	C/T	SNP	EMS-induced mutation	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	P/S	493	0.17	TraesCS5D02G365500.1
Cadenza0667.chr5D.442696568	5D:442696568	T/C	SNP	EMS-induced mutation	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	H	494	-	TraesCS5D02G365500.1
Cadenza0108.chr5D.442696568	5D:442696568	T/C	SNP	EMS-induced mutation	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	H	494	-	TraesCS5D02G365500.1
5D_442696568	5D:442696568	T/C	SNP	Watkins-exome-capture	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	H	494	-	TraesCS5D02G365500.1
Cadenza1721.chr5D.442696568	5D:442696568	T/C	SNP	EMS-induced mutation	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	H	494	-	TraesCS5D02G365500.1
Cadenza0282.chr5D.442696568	5D:442696568	T/C	SNP	EMS-induced mutation	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	H	494	-	TraesCS5D02G365500.1
Cadenza1783.chr5D.442696568	5D:442696568	T/C	SNP	EMS-induced mutation	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	H	494	-	TraesCS5D02G365500.1
Cadenza1257.chr5D.442696568	5D:442696568	T/C	SNP	EMS-induced mutation	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	H	494	-	TraesCS5D02G365500.1
5D_442696604	5D:442696604-442696608	CGCAT/TGCAT	substitution	Watkins-exome-capture	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	HAL	506-508	-	TraesCS5D02G365500.1
Cadenza1701.chr5D.442696610	5D:442696610	G/A	SNP	EMS-induced mutation	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	L	508	-	TraesCS5D02G365500.1
5D_442696703	5D:442696703	T/C	SNP	Watkins-exome-capture	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	H	539	-	TraesCS5D02G365500.1
5D_442696757	5D:442696757	G/C	SNP	Watkins-exome-capture	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	V	557	-	TraesCS5D02G365500.1
Cadenza1942.chr5D.442696757	5D:442696757	G/C	SNP	EMS-induced mutation	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	V	557	-	TraesCS5D02G365500.1
Cadenza0587.chr5D.442696757	5D:442696757	G/C	SNP	EMS-induced mutation	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	V	557	-	TraesCS5D02G365500.1
Cadenza1357.chr5D.442696757	5D:442696757	G/C	SNP	EMS-induced mutation	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	V	557	-	TraesCS5D02G365500.1
Cadenza1667.chr5D.442696760	5D:442696760	G/A	SNP	EMS-induced mutation	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	S	558	-	TraesCS5D02G365500.1
Cadenza2071.chr5D.442696760	5D:442696760	G/A	SNP	EMS-induced mutation	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	S	558	-	TraesCS5D02G365500.1
Cadenza0256.chr5D.442696760	5D:442696760	G/A	SNP	EMS-induced mutation	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	S	558	-	TraesCS5D02G365500.1
5D_442696760	5D:442696760	G/A	SNP	Watkins-exome-capture	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	S	558	-	TraesCS5D02G365500.1
5D_442696871	5D:442696871	A/T	SNP	Watkins-exome-capture	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	T	595	-	TraesCS5D02G365500.1
5D_442696886	5D:442696886	G/A	SNP	Watkins-exome-capture	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	V	600	-	TraesCS5D02G365500.1
5D_442696908	5D:442696908	C/T	SNP	Watkins-exome-capture	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	L	608	-	TraesCS5D02G365500.1
chr5D_scaffold65372_4176519	5D:442696925	T/C	SNP	Exome_Capture_Diversity	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	G	613	-	TraesCS5D02G365500.1
5D_442696925	5D:442696925	T/C	SNP	Watkins-exome-capture	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	G	613	-	TraesCS5D02G365500.1
5D_442696934	5D:442696934	A/G	SNP	Watkins-exome-capture	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	P	616	-	TraesCS5D02G365500.1
5D_442696944	5D:442696944	A/G	SNP	Watkins-exome-capture	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	K/E	620	1	TraesCS5D02G365500.1
5D_442696952	5D:442696952	C/T	SNP	Watkins-exome-capture	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	S	622	-	TraesCS5D02G365500.1
5D_442696964	5D:442696964	G/A	SNP	Watkins-exome-capture	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	R	626	-	TraesCS5D02G365500.1
5D_442696977	5D:442696977	A/G	SNP	Watkins-exome-capture	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	I/V	631	0.53	TraesCS5D02G365500.1
5D_442697003	5D:442697003	T/C	SNP	Watkins-exome-capture	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	N	639	-	TraesCS5D02G365500.1
chr5D_scaffold65372_4176414	5D:442697030	T/C	SNP	Exome_Capture_Diversity	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	H	648	-	TraesCS5D02G365500.1
5D_442697039	5D:442697039-442697042	TGAA/GAAA/CGAG	substitution	Watkins-exome-capture	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	GE/GK	651-652	-	TraesCS5D02G365500.1
5D_442697039	5D:442697039-442697042	TGAA/GAAA/CGAG	substitution	Watkins-exome-capture	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	GE	651-652	-	TraesCS5D02G365500.1
5D_442697118	5D:442697118	T/C	SNP	Watkins-exome-capture	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	F/L	678	0.04	TraesCS5D02G365500.1
5D_442697129	5D:442697129	G/T	SNP	Watkins-exome-capture	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	E/D	681	0.21	TraesCS5D02G365500.1
5D_442697136	5D:442697136	G/A	SNP	Watkins-exome-capture	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	D/N	684	0.07	TraesCS5D02G365500.1
Cadenza0897.chr5D.442699250	5D:442699250	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0897.chr5D.442699253	5D:442699253	C/G	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1653.chr5D.442699253	5D:442699253	C/G	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0897.chr5D.442699254	5D:442699254	A/G	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1653.chr5D.442699254	5D:442699254	A/G	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0393.chr5D.442699254	5D:442699254	A/G	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0897.chr5D.442699258	5D:442699258	A/G	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0393.chr5D.442699258	5D:442699258	A/G	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1653.chr5D.442699258	5D:442699258	A/G	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1019.chr5D.442699283	5D:442699283	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1463.chr5D.442699283	5D:442699283	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1260.chr5D.442699283	5D:442699283	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1357.chr5D.442699283	5D:442699283	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0393.chr5D.442699283	5D:442699283	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1722.chr5D.442699283	5D:442699283	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1257.chr5D.442699283	5D:442699283	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0720.chr5D.442699283	5D:442699283	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1019.chr5D.442699284	5D:442699284	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1463.chr5D.442699284	5D:442699284	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1357.chr5D.442699284	5D:442699284	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1722.chr5D.442699284	5D:442699284	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0393.chr5D.442699284	5D:442699284	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0720.chr5D.442699284	5D:442699284	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1257.chr5D.442699284	5D:442699284	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1260.chr5D.442699284	5D:442699284	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1559.chr5D.442699291	5D:442699291	T/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0926.chr5D.442699291	5D:442699291	T/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0522.chr5D.442699291	5D:442699291	T/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1697.chr5D.442699291	5D:442699291	T/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0818.chr5D.442699291	5D:442699291	T/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1057.chr5D.442699291	5D:442699291	T/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0393.chr5D.442699296	5D:442699296	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1722.chr5D.442699296	5D:442699296	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1463.chr5D.442699296	5D:442699296	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza2050.chr5D.442699296	5D:442699296	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1019.chr5D.442699296	5D:442699296	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1257.chr5D.442699296	5D:442699296	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0393.chr5D.442699302	5D:442699302	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1722.chr5D.442699302	5D:442699302	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza2050.chr5D.442699302	5D:442699302	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza2050.chr5D.442699323	5D:442699323	A/G	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0942.chr5D.442699341	5D:442699341	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1646.chr5D.442699344	5D:442699344	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0369.chr5D.442699378	5D:442699378	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0909.chr5D.442699455	5D:442699455	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1442.chr5D.442699460	5D:442699460	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0713.chr5D.442699462	5D:442699462	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1487.chr5D.442699490	5D:442699490	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1409.chr5D.442699502	5D:442699502	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0860.chr5D.442699504	5D:442699504	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza2104.chr5D.442699506	5D:442699506	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1789.chr5D.442699518	5D:442699518	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0710.chr5D.442699532	5D:442699532	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1800.chr5D.442699542	5D:442699542	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
BA00629108	5D:442699542	C/T	SNP	CerealsDB	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1008.chr5D.442699545	5D:442699545	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1190.chr5D.442699551	5D:442699551	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0049.chr5D.442699555	5D:442699555	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
BA00148979	5D:442699562	G/A	SNP	CerealsDB	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442699571	5D:442699571	T/C	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1498.chr5D.442699602	5D:442699602	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0982.chr5D.442699606	5D:442699606	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1529.chr5D.442699606	5D:442699606	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1222.chr5D.442699606	5D:442699606	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442699613	5D:442699613	A/G	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1447.chr5D.442699614	5D:442699614	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1081.chr5D.442699647	5D:442699647	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1535.chr5D.442699657	5D:442699657	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1668.chr5D.442699657	5D:442699657	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442699662	5D:442699662-442699664	GAG/AAA/GAA	substitution	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442699662	5D:442699662-442699664	GAG/AAA/GAA	substitution	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1727.chr5D.442699666	5D:442699666	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0778.chr5D.442699671	5D:442699671	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1305.chr5D.442699680	5D:442699680	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1392.chr5D.442699686	5D:442699686	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442699704	5D:442699704	T/C	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442699710	5D:442699710	G/A	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
BA00132318	5D:442699725	T/C	SNP	CerealsDB	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1616.chr5D.442699745	5D:442699745	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442699755	5D:442699755	G/C	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1750.chr5D.442699761	5D:442699761	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza2007.chr5D.442699772	5D:442699772	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442699773	5D:442699773	A/G	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442699814	5D:442699814	G/A	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0728.chr5D.442699815	5D:442699815	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442699821	5D:442699821	C/G	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza2061.chr5D.442699822	5D:442699822	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0610.chr5D.442699828	5D:442699828	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1201.chr5D.442699828	5D:442699828	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442699837	5D:442699837	C/G	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0670.chr5D.442699869	5D:442699869	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0548.chr5D.442699888	5D:442699888	C/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza2048.chr5D.442699945	5D:442699945	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1477.chr5D.442699948	5D:442699948	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1478.chr5D.442699955	5D:442699955	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
BA00270380	5D:442699964	A/G	SNP	CerealsDB	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1267.chr5D.442699968	5D:442699968	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0251.chr5D.442700003	5D:442700003	G/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442700013	5D:442700013-442700014	CA/TG	substitution	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0259.chr5D.442700056	5D:442700056	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0761.chr5D.442700066	5D:442700066	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0548.chr5D.442700076	5D:442700076	C/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1698.chr5D.442700086	5D:442700086	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1023.chr5D.442700107	5D:442700107	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1070.chr5D.442700112	5D:442700112	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
BA00452579	5D:442700122	C/T	SNP	CerealsDB	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0669.chr5D.442700123	5D:442700123	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
BA00109069	5D:442700144	A/G	SNP	CerealsDB	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1061.chr5D.442700154	5D:442700154	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
BA00597092	5D:442700183	T/A	SNP	CerealsDB	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0368.chr5D.442700201	5D:442700201	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1555.chr5D.442700243	5D:442700243	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1672.chr5D.442700316	5D:442700316	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0500.chr5D.442700321	5D:442700321	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0303.chr5D.442700358	5D:442700358	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0431.chr5D.442700358	5D:442700358	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0629.chr5D.442700358	5D:442700358	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116893	5D:442700378	A/G	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0849.chr5D.442700394	5D:442700394	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0763.chr5D.442700395	5D:442700395	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116894	5D:442700398	A/T	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0844.chr5D.442700399	5D:442700399	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1118.chr5D.442700410	5D:442700410	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116895	5D:442700420	T/G	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116896	5D:442700427	T/G	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116897	5D:442700433	T/A	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116898	5D:442700435	T/C	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116899	5D:442700441	A/T	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116900	5D:442700445	T/A	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116901	5D:442700448	C/T	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116902	5D:442700455	C/A	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116903	5D:442700457	A/C	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116904	5D:442700459	T/G	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116905	5D:442700464	G/T	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116906	5D:442700477	C/T	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116907	5D:442700485	G/C	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116908	5D:442700500	G/A	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116909	5D:442700513	C/T	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0543.chr5D.442700515	5D:442700515	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0628.chr5D.442700519	5D:442700519	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1150.chr5D.442700519	5D:442700519	T/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116910	5D:442700520	A/G	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0628.chr5D.442700520	5D:442700520	A/C	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0628.chr5D.442700533	5D:442700533	A/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116911	5D:442700533	A/T	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442700550	5D:442700550	A/C	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0628.chr5D.442700564	5D:442700564	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1308.chr5D.442700573	5D:442700573	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0267.chr5D.442700573	5D:442700573	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0462.chr5D.442700574	5D:442700574	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1442.chr5D.442700584	5D:442700584	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1931.chr5D.442700584	5D:442700584	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1735.chr5D.442700586	5D:442700586	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0119.chr5D.442700612	5D:442700612	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442700622	5D:442700622	C/A	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116912	5D:442700630	G/A	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
chr5D_scaffold65372_4172806	5D:442700638	C/T	SNP	Exome_Capture_Diversity	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442700638	5D:442700638	C/T	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza0985.chr5D.442700646	5D:442700646	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442700651	5D:442700651	C/T	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116913	5D:442700651	C/A	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116914	5D:442700659	C/T	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442700662	5D:442700662	A/G	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116915	5D:442700664	G/A	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
chr5D_scaffold65372_4172761	5D:442700683	G/A	SNP	Exome_Capture_Diversity	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116916	5D:442700686	G/A	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442700686	5D:442700686	G/A	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116917	5D:442700704	A/G	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116918	5D:442700709	C/G	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442700734	5D:442700734	C/T	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116919	5D:442700749	A/C	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1067.chr5D.442700753	5D:442700753	G/A	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
5D_442700768	5D:442700768	C/T	SNP	Watkins-exome-capture	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116920	5D:442700768	C/T	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116921	5D:442700770	G/A	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116922	5D:442700772	C/T	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116923	5D:442700777	A/G	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116924	5D:442700788	C/T	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
Cadenza1616.chr5D.442700788	5D:442700788	C/T	SNP	EMS-induced mutation	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1
EPlTAEV_COMPDB_02116925	5D:442700790	T/G	SNP	Inter-homoeologous	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	TraesCS5D02G365500.1

Gene: TraesCS5D02G365500

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Gene: TraesCS5D02G365500

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