Primary Site >> Liver Cancer

Gene >> VAV3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107704971:107704971(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1593G>C
AA Mutation p.Gln531His(p.Q531H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107964793:107964793(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.77A>G
AA Mutation p.Asp26Gly(p.D26G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107596289:107596289(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2273T>C
AA Mutation p.Leu758Ser(p.L758S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107609947:107609947(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1999T>A
AA Mutation p.Tyr667Asn(p.Y667N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107772772:107772772(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.518A>C
AA Mutation p.Tyr173Ser(p.Y173S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107779487:107779487(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.327A>G
AA Mutation p.Ile109Met(p.I109M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000370056
Start 107779457:107779457(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.357T>A
Mutation Classification Silent
Feature Type Transcript