Primary Site >> Stomach Cancer

Gene >> VWA1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000476993
Start 1436948:1436948(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376449591
CDS Mutation c.95G>A
AA Mutation p.Arg32Gln(p.R32Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000476993
Start 1437307:1437307(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774823840
CDS Mutation c.454G>A
AA Mutation p.Gly152Ser(p.G152S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000476993
Start 1439284:1439284(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.835T>C
AA Mutation p.Tyr279His(p.Y279H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000476993
Start 1437297:1437297(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375729899
CDS Mutation c.444C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000476993
Start 1437309:1437309(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs760281341
CDS Mutation c.462delC
AA Mutation p.Met155CysfsTer51(p.M155Cfs*51)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000476993
Start 1436941:1436942(version: GRCh38)
Mutation Type INS
dbSNP_RS rs761604051
CDS Mutation c.94dupC
AA Mutation p.Arg32ProfsTer64(p.R32Pfs*64)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000476993
Start 1437308:1437309(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.462dupC
AA Mutation p.Met155HisfsTer43(p.M155Hfs*43)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript