Primary Site >> Stomach Cancer

Gene >> C1GALT1C1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000304661
Start 120627157:120627157(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10G>A
AA Mutation p.Glu4Lys(p.E4K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000304661
Start 120626244:120626244(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.923T>C
AA Mutation p.Val308Ala(p.V308A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000304661
Start 120626952:120626952(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.215T>C
AA Mutation p.Ile72Thr(p.I72T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000304661
Start 120626357:120626357(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.810T>G
AA Mutation p.Cys270Trp(p.C270W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000304661
Start 120626782:120626782(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752497228
CDS Mutation c.385G>A
AA Mutation p.Ala129Thr(p.A129T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000304661
Start 120626738:120626738(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.429A>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000304661
Start 120626867:120626867(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.300C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence stop_gained;frameshift_variant
Transcription ID ENST00000304661
Start 120626699:120626700(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.467_468insG
AA Mutation p.Tyr156Ter(p.Y156*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript