Primary Site >> Stomach Cancer

Gene >> VIPR2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262178
Start 159035976:159035976(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.785C>T
AA Mutation p.Ala262Val(p.A262V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262178
Start 159034222:159034222(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.962C>T
AA Mutation p.Ser321Phe(p.S321F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262178
Start 159103777:159103777(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149519347
CDS Mutation c.337G>A
AA Mutation p.Asp113Asn(p.D113N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262178
Start 159035967:159035967(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.794A>G
AA Mutation p.Tyr265Cys(p.Y265C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000262178
Start 159142460:159142460(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.137C>T
AA Mutation p.Thr46Ile(p.T46I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000262178
Start 159036755:159036755(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.745T>G
AA Mutation p.Trp249Gly(p.W249G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000262178
Start 159032052:159032052(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.987C>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000262178
Start 159043075:159043105(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.527_557delTGCTGGTCAAGGACGACGTTCTCTACTCCAG
AA Mutation p.Val176AlafsTer19(p.V176Afs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript