Primary_assembly 3H: 621,516,506-621,516,506

Variant table

Filter

ClassAll
Class

more rows pending
(17/17 on)
Turn All Off
Only Somatic
Not Somatic
Turn All On
(0)
SNP
(0)
deletion
(0)
genetic marker
(0)
indel
(0)
insertion
(0)
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)
No data
Apply »
Cancel
ConsequencesAll
Consequences

more rows pending
(41/41 on)
Turn All Off
PTV
PTV & Missense
Only Exonic
Turn All On
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)

feature elongation
(0)

feature truncation
(0)

inframe insertion
(0)

inframe deletion
(0)

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
(0)

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
(0)

upstream gene variant
(0)

downstream gene variant
(0)

TFBS ablation
(0)

TFBS amplification
(0)

TF binding site
(0)

regulatory region ablation
(0)

regulatory region amplification
(0)

regulatory region variant
(0)

intergenic variant
(0)

sequence variant
Apply »
Cancel
LocationAll
Location

more rows pending

3H:621516506 - 3H:621516506
Apply »
Cancel
SourceAll
Source

more rows pending
(1/1 on)
Turn All Off
Turn All On
(0)
No data
Apply »
Cancel
EvidenceAll
Evidence

more rows pending
(11/11 on)
Turn All Off
Turn All On
(0)
1000Genomes
(0)
HapMap
(0)
Cited
(0)
ESP
(0)
ExAC
(0)
Frequency
(0)
gnomAD
(0)
Multiple_observations
(0)
Phenotype_or_Disease
(0)
TOPMed
(0)
No data
Apply »
Cancel
ClinVar IDAll
ClinVar ID

more rows pending

None present
PhenotypesAll
Phenotypes

more rows pending
(1/1 on)
Turn All Off
Turn All On
(0)
No data
Apply »
Cancel
Filter Other ColumnsAll
- Location
- Source
- Evidence
- ClinVar ID
- Phenotypes