Gene: AT2G07360

Description

SH3 domain-containing protein [Source:NCBI gene (formerly Entrezgene);Acc:815305]

Gene Synonyms

T13E11.13, T13E11_13

Location

Chromosome 2: 3,047,252-3,057,214 reverse strand.

About this gene

This gene has 2 transcripts (splice variants) and 142 orthologues.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Biotype	UniProt	RefSeq	Flags
AT2G07360-201	AT2G07360.2	4065	1198aa	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F4IL68	-	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,
AT2G07360-202	AT2G07360.1	4023	1196aa	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q84R15	-	-

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
(124)

missense variant
(0)

protein altering variant
(0)

splice donor 5th base variant
(70)

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
(254)

synonymous variant
(0)

coding sequence variant
(0)

mature miRNA variant
(24)

5 prime UTR variant
(104)

3 prime UTR variant
(0)

non coding transcript exon variant
(1696)

intron variant
(0)

NMD transcript variant
(0)

non coding transcript variant
(0)

coding transcript variant
(126)

upstream gene variant
(78)

downstream gene variant
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LocationAll
Location

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2:3042252 - 2:3062214
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ClassAll
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(2036)
SNP
(116)
deletion
(0)
genetic marker
(118)
indel
(106)
insertion
(30)
sequence alteration
(0)
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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(2406)
The 1001 Genomes Project
(0)
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(0)
1000Genomes
(0)
HapMap
(0)
Cited
(0)
ESP
(0)
ExAC
(0)
Frequency
(0)
gnomAD
(0)
Multiple_observations
(0)
Phenotype_or_Disease
(0)
TOPMed
(2406)
No data
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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
(2406)
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TranscriptAll
Transcript

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(1201)
AT2G07360.1
(1205)
AT2G07360.2
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- Transcript

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

tmp_2_3047109_T_C	2:3047109	T/C	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH00215227	2:3047116	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH01689222	2:3047120	C/A	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH09426681	2:3047127	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH01689223	2:3047128	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH11956074	2:3047130	C/G	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH01689224	2:3047131	A/G	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047154_C_T	2:3047154	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047157_T_C	2:3047157	T/C	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH01689225	2:3047160	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH09861395	2: between 3047164 & 3047165	-/GTTTAGG/GTTTAAG	insertion	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH09861395	2: between 3047164 & 3047165	-/GTTTAGG/GTTTAAG	insertion	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH01689226	2:3047166	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047190_T_C	2:3047190	T/C	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047194_T_C	2:3047194	T/C	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047196_TG_T	2:3047197	G/-	deletion	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047202_C_T	2:3047202	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH01689227	2:3047203	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047210_T_A	2:3047210	T/A	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH05317884	2:3047218	G/A	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047228_G_T	2:3047228	G/T	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH05317885	2:3047230	C/A	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH01689228	2:3047231	A/C	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047232_T_C	2:3047232	T/C	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH11956288	2:3047233	G/A/GA	indel	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH11956288	2:3047233	G/A/GA	indel	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047254_A_AAT	2: between 3047254 & 3047255	-/AT	insertion	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047257_T_A	2:3047257	T/A	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047266_C_T	2:3047266	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047273_CAA_CA,C	2:3047274-3047275	AA/A/-	sequence alteration	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047273_CAA_CA,C	2:3047274-3047275	AA/A/-	sequence alteration	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH01689229	2:3047281	A/G/AG	indel	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH01689229	2:3047281	A/G/AG	indel	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047280_A_AT	2: between 3047280 & 3047281	-/T	insertion	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047282_A_G	2:3047282	A/G	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH01689230	2:3047285	A/G/T/AAG	indel	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH01689230	2:3047285	A/G/T/AAG	indel	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH01689230	2:3047285	A/G/T/AAG	indel	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047286_A_G	2:3047286	A/G	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH11956290	2:3047289	A/T	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH01689231	2:3047293	G/A	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
ENSVATH14115679	2:3047303	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant located 3' of a genedownstream gene variant	-	-	-	AT2G07360.1
tmp_2_3047310_G_A	2:3047310	G/A	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH05317886	2:3047311	C/T	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047315_T_A	2:3047315	T/A	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH11956292	2:3047315	T/-	deletion	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH11956293	2:3047330	A/T	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047333_T_A	2:3047333	T/A	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH01689232	2:3047337	T/A	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH04109571	2: between 3047344 & 3047345	-/CA	insertion	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047353_A_G	2:3047353	A/G	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047354_A_AC	2: between 3047354 & 3047355	-/C	insertion	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH04109572	2:3047357-3047359	ACA/-	deletion	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH05317887	2:3047360	A/C	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047373_T_G	2:3047373	T/G	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH05317888	2:3047388	G/C	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH01689233	2:3047390	G/A	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047408_C_A	2:3047408	C/A	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047421_C_T	2:3047421	C/T	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH01689234	2:3047432	T/A	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047438_C_T	2:3047438	C/T	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH05317890	2:3047444	G/A	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047447_T_A	2:3047447	T/A	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH11956346	2:3047461	C/A	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH01689235	2:3047476	C/G	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH04109573	2: between 3047477 & 3047478	-/AACAA	insertion	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047502_C_G	2:3047502	C/G	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH14868819	2:3047511	C/-	deletion	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH01689236	2:3047514	T/A	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047519_CTT_GTT,C	2:3047519-3047521	CTT/GTT/C	indel	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047519_CTT_GTT,C	2:3047519-3047521	CTT/GTT/C	indel	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047525_G_A	2:3047525	G/A	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH00215228	2:3047550	T/C	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047563_AGTC_A	2:3047564-3047566	GTC/-	deletion	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047566_CCA_C	2:3047567-3047568	CA/-	deletion	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047575_A_C	2:3047575	A/C	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH05317892	2:3047576	T/C	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH01689237	2:3047577	A/G	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047580_C_G	2:3047580	C/G	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH11956347	2:3047582	T/A	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH05317893	2:3047593	C/G	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH00215229	2:3047601	T/A	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH11956348	2:3047610	G/A/T	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH11956348	2:3047610	G/A/T	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH05317894	2:3047615	C/T	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
tmp_2_3047620_A_T	2:3047620	A/T	SNP	The 1001 Genomes Project	-	-	A UTR variant of the 3' UTR3 prime UTR variant	-	-	-	AT2G07360.1
ENSVATH05317895	2:3047644	A/G	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	V	1190	-	AT2G07360.1
ENSVATH05317896	2:3047680	A/T	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	P	1178	-	AT2G07360.1
ENSVATH05317897	2:3047701	T/A	SNP	The 1001 Genomes Project	-	-	A sequence variant in which a change has occurred within the region of the splice site, either within 1-3 bases of the exon or 3-8 bases of the intronsplice region variant A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH11956349	2:3047702	C/A	SNP	The 1001 Genomes Project	-	-	A sequence variant in which a change has occurred within the region of the splice site, either within 1-3 bases of the exon or 3-8 bases of the intronsplice region variant A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH00215230	2:3047712	C/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689238	2:3047713	A/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3047743_A_T	2:3047743	A/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH11956350	2:3047745	G/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH11956351	2:3047760	A/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689239	2:3047767	A/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH11956352	2:3047773	C/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317898	2:3047817	C/T/A	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	E	1162	-	AT2G07360.1
ENSVATH05317898	2:3047817	C/T/A	SNP	The 1001 Genomes Project	-	-	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	1162	0.16	AT2G07360.1
tmp_2_3047830_T_C	2:3047830	T/C	SNP	The 1001 Genomes Project	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	E/G	1158	1	AT2G07360.1
tmp_2_3047861_T_TA	2: between 3047861 & 3047862	-/A	insertion	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689240	2:3047863	C/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317899	2:3047865	T/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317900	2:3047867	T/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3047866_G_GT	2: between 3047866 & 3047867	-/T	insertion	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3047871_A_G	2:3047871	A/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH11956353	2:3047874	G/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH04109575	2:3047882	A/-	deletion	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3047883_A_G	2:3047883	A/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317901	2:3047886	T/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689241	2:3047890	A/T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689241	2:3047890	A/T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3047909_A_T	2:3047909	A/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH14868822	2:3047921	A/-	deletion	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317902	2:3047927	C/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317904	2:3047929	A/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3047932_G_C	2:3047932	G/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317905	2:3047938	T/A	SNP	The 1001 Genomes Project	-	-	A sequence variant in which a change has occurred within the region of the splice site, either within 1-3 bases of the exon or 3-8 bases of the intronsplice region variant A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689242	2:3047960	T/A	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	T	1146	-	AT2G07360.1
ENSVATH05317906	2:3047974	G/A	SNP	The 1001 Genomes Project	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	L/F	1142	0	AT2G07360.1
tmp_2_3048072_T_A	2:3048072	T/A	SNP	The 1001 Genomes Project	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	E/V	1109	0	AT2G07360.1
ENSVATH01689243	2:3048073	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	E/K	1109	0.01	AT2G07360.1
ENSVATH01689244	2:3048104	C/A/T	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	P	1098	-	AT2G07360.1
ENSVATH01689244	2:3048104	C/A/T	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	P	1098	-	AT2G07360.1
tmp_2_3048112_G_A	2:3048112	G/A	SNP	The 1001 Genomes Project	-	-	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	1096	0.16	AT2G07360.1
tmp_2_3048113_C_T	2:3048113	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	E	1095	-	AT2G07360.1
ENSVATH01689245	2:3048132	G/A	SNP	The 1001 Genomes Project	-	-	A sequence variant in which a change has occurred within the region of the splice site, either within 1-3 bases of the exon or 3-8 bases of the intronsplice region variant A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689246	2:3048138	G/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689247	2:3048153	G/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048161_C_A	2:3048161	C/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689248	2:3048169	C/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048178_A_T	2:3048178	A/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689249	2:3048184	A/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048191_C_T	2:3048191	C/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH04109576	2:3048195-3048196	AA/-	deletion	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689250	2:3048210	T/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048216_C_T	2:3048216	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant in which a change has occurred within the region of the splice site, either within 1-3 bases of the exon or 3-8 bases of the intronsplice region variant A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689251	2:3048259	A/G	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	S	1079	-	AT2G07360.1
tmp_2_3048289_C_A	2:3048289	C/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048290_C_T	2:3048290	C/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH04109577	2:3048302	A/-	deletion	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH11956516	2:3048315	T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH04109578	2:3048322-3048323	AA/-	deletion	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH14868895	2:3048322	A/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317908	2:3048345	A/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048346_A_G	2:3048346	A/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH04109579	2: between 3048351 & 3048352	-/T	insertion	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317909	2:3048354	G/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317910	2:3048356	G/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH00215231	2:3048368	G/A	SNP	The 1001 Genomes Project	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant A sequence variant in which a change has occurred within the region of the splice site, either within 1-3 bases of the exon or 3-8 bases of the intronsplice region variant	T/M	1073	0.02	AT2G07360.1
ENSVATH11956517	2:3048370	T/A	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	A	1072	-	AT2G07360.1
tmp_2_3048432_A_T	2:3048432	A/T	SNP	The 1001 Genomes Project	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	S/T	1052	0.05	AT2G07360.1
ENSVATH01689252	2:3048436	T/A	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	S	1050	-	AT2G07360.1
tmp_2_3048445_C_T	2:3048445	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	V	1047	-	AT2G07360.1
ENSVATH01689253	2:3048476	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	G/D	1037	0	AT2G07360.1
ENSVATH01689254	2:3048484	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	A	1034	-	AT2G07360.1
ENSVATH01689255	2:3048521	C/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317911	2:3048524	A/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH11956518	2:3048536	T/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689256	2:3048542	T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689257	2:3048555	G/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048560_G_A	2:3048560	G/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH11956519	2:3048569	T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048577_G_C	2:3048577	G/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH11956520	2:3048589	C/A	SNP	The 1001 Genomes Project	-	-	A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preservedmissense variant	L/F	1029	0.2	AT2G07360.1
ENSVATH00215232	2:3048592	T/C	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	E	1028	-	AT2G07360.1
ENSVATH00215233	2:3048613	T/C	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	K	1021	-	AT2G07360.1
ENSVATH05317912	2:3048640	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	S	1012	-	AT2G07360.1
ENSVATH01689258	2:3048655	G/C	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	V	1007	-	AT2G07360.1
ENSVATH00215234	2:3048676	C/T	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	P	1000	-	AT2G07360.1
tmp_2_3048691_G_A	2:3048691	G/A	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	V	995	-	AT2G07360.1
ENSVATH00215235	2:3048697	A/G	SNP	The 1001 Genomes Project	-	-	A sequence variant where there is no resulting change to the encoded amino acidsynonymous variant	A	993	-	AT2G07360.1
tmp_2_3048720_A_G	2:3048720	A/G	SNP	The 1001 Genomes Project	-	-	A sequence variant in which a change has occurred within the region of the splice site, either within 1-3 bases of the exon or 3-8 bases of the intronsplice region variant A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689259	2:3048726	T/G/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689259	2:3048726	T/G/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317913	2:3048734	T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048735_C_T	2:3048735	C/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH11956521	2:3048736	T/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689260	2:3048742	C/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689261	2:3048745	T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689262	2:3048748	C/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689263	2:3048749	T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048750_AG_A	2:3048751	G/-	deletion	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048755_T_C	2:3048755	T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689264	2:3048760	C/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317914	2:3048761	A/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689265	2:3048768	A/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH04109580	2:3048772	T/-	deletion	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689266	2:3048779	T/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689267	2:3048785	C/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048792_G_A	2:3048792	G/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689268	2:3048806	G/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048821_T_G	2:3048821	T/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048822_T_A	2:3048822	T/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048831_C_G	2:3048831	C/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689269	2:3048832	T/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048842_T_G	2:3048842	T/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689270	2:3048858	T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689271	2:3048861	C/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689272	2:3048865	T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689273	2:3048866	T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689274	2:3048869	A/T/AT	indel	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689274	2:3048869	A/T/AT	indel	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689275	2:3048872	G/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048873_G_T	2:3048873	G/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048874_C_CT,T	2:3048874	C/CT/T	indel	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048874_C_CT,T	2:3048874	C/CT/T	indel	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689276	2:3048876	C/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048877_C_G	2:3048877	C/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH11956523	2:3048884	T/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH04109582	2:3048908	C/-	deletion	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689277	2:3048911	C/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689278	2:3048943	C/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689279	2:3048946	G/T/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689279	2:3048946	G/T/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689280	2:3048960	T/C/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689280	2:3048960	T/C/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689281	2:3048965	G/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048969_G_A	2:3048969	G/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689282	2:3048982	A/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689283	2:3048983	T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048991_A_T	2:3048991	A/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3048995_G_A	2:3048995	G/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317915	2:3049017	A/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317916	2:3049031	T/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317917	2:3049043	T/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH11956727	2:3049048	G/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH11956728	2:3049055	T/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3049060_T_C	2:3049060	T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3049068_T_C	2:3049068	T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH04109583	2: between 3049079 & 3049080	-/AC	insertion	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3049087_A_C	2:3049087	A/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3049096_A_C	2:3049096	A/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3049097_A_T	2:3049097	A/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317918	2:3049099	T/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689284	2:3049106	A/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689285	2:3049109	A/T/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689285	2:3049109	A/T/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689286	2:3049113	C/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689287	2:3049134	C/T	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3049137_T_A	2:3049137	T/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3049138_T_A	2:3049138	T/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH05317919	2:3049139	T/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3049144_TAA_T	2:3049145-3049146	AA/-	deletion	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3049147_A_C	2:3049147	A/C	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689288	2:3049149	G/A	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH01689289	2:3049157	A/G	SNP	The 1001 Genomes Project	-	-	A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH11956815	2:3049170	G/T/A	SNP	The 1001 Genomes Project	-	-	A sequence variant in which a change has occurred within the region of the splice site, either within 1-3 bases of the exon or 3-8 bases of the intronsplice region variant A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
ENSVATH11956815	2:3049170	G/T/A	SNP	The 1001 Genomes Project	-	-	A sequence variant in which a change has occurred within the region of the splice site, either within 1-3 bases of the exon or 3-8 bases of the intronsplice region variant A transcript variant occurring within an intronintron variant	-	-	-	AT2G07360.1
tmp_2_3049187_G_A	2:3049187	G/A	SNP	The 1001 Genomes Project	-	-	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	983	0.02	AT2G07360.1

Gene: AT2G07360

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Variant table

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Gene: AT2G07360

Variant table

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