Primary Site >> Stomach Cancer

Gene >> SAMD4A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000392067
Start 54737180:54737180(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.872T>C
AA Mutation p.Leu291Pro(p.L291P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000392067
Start 54702283:54702283(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.418C>T
AA Mutation p.Arg140Cys(p.R140C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000392067
Start 54774998:54774998(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201673766
CDS Mutation c.1780C>T
AA Mutation p.Arg594Trp(p.R594W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000392067
Start 54702430:54702430(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.565G>T
AA Mutation p.Gly189Trp(p.G189W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000392067
Start 54784585:54784585(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2093C>T
AA Mutation p.Ser698Leu(p.S698L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000392067
Start 54702170:54702170(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.305T>C
AA Mutation p.Met102Thr(p.M102T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000392067
Start 54702327:54702327(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748177073
CDS Mutation c.462G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000392067
Start 54702243:54702243(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.378G>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000392067
Start 54760172:54760172(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1193delG
AA Mutation p.Gly398AlafsTer13(p.G398Afs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000392067
Start 54737137:54737137(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.829C>T
AA Mutation p.Arg277Ter(p.R277*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000392067
Start 54770121:54770122(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1621dupA
AA Mutation p.Arg541LysfsTer111(p.R541Kfs*111)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript