Primary Site >> Stomach Cancer

Gene >> GPSM2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264126
Start 108904236:108904236(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1174A>G
AA Mutation p.Ile392Val(p.I392V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264126
Start 108924197:108924197(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1798A>C
AA Mutation p.Ile600Leu(p.I600L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264126
Start 108922439:108922439(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1463G>C
AA Mutation p.Gly488Ala(p.G488A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264126
Start 108898086:108898086(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.542C>T
AA Mutation p.Ala181Val(p.A181V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264126
Start 108898074:108898074(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.530C>T
AA Mutation p.Ala177Val(p.A177V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264126
Start 108901835:108901835(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.843A>C
AA Mutation p.Glu281Asp(p.E281D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000264126
Start 108918662:108918662(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1313C>T
AA Mutation p.Ala438Val(p.A438V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000264126
Start 108897519:108897519(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.306G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000264126
Start 108897041:108897042(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.234_235insACAGGACA
AA Mutation p.Ala79ThrfsTer7(p.A79Tfs*7)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 10
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000264126
Start 108903125:108903125(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.954-1G>T
Mutation Classification Splice_Site
Feature Type Transcript