Primary Site >> Stomach Cancer

Gene >> RAD21

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000297338
Start 116848960:116848960(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1690C>T
AA Mutation p.Leu564Phe(p.L564F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000297338
Start 116854285:116854285(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1121C>T
AA Mutation p.Ser374Phe(p.S374F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000297338
Start 116856742:116856742(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs575505257
CDS Mutation c.718G>A
AA Mutation p.Gly240Ser(p.G240S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000297338
Start 116854341:116854341(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202233096
CDS Mutation c.1065G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000297338
Start 116858365:116858365(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs530697556
CDS Mutation c.468A>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000297338
Start 116847640:116847640(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1756C>T
AA Mutation p.Arg586Ter(p.R586*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript