Primary Site >> Stomach Cancer

Gene >> SMC1A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000322213
Start 53409481:53409481(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1277G>A
AA Mutation p.Arg426Gln(p.R426Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000322213
Start 53409121:53409121(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1486C>T
AA Mutation p.Arg496Cys(p.R496C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000322213
Start 53413104:53413104(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.650T>A
AA Mutation p.Val217Glu(p.V217E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000322213
Start 53411804:53411804(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1211A>G
AA Mutation p.Gln404Arg(p.Q404R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000322213
Start 53405953:53405953(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1549G>A
AA Mutation p.Gly517Ser(p.G517S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000322213
Start 53383172:53383172(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3055C>T
AA Mutation p.Arg1019Cys(p.R1019C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000322213
Start 53409177:53409177(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1430T>C
AA Mutation p.Leu477Pro(p.L477P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000322213
Start 53405526:53405526(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1878C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000322213
Start 53413388:53413388(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.459T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000322213
Start 53405655:53405655(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1749G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000322213
Start 53399634:53399634(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2517G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000322213
Start 53411838:53411838(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1177C>T
Mutation Classification Silent
Feature Type Transcript