Primary Site >> Stomach Cancer

Gene >> TNFRSF25

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000356876
Start 6461633:6461633(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1055G>A
AA Mutation p.Arg352His(p.R352H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000356876
Start 6465189:6465189(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.194G>A
AA Mutation p.Cys65Tyr(p.C65Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000356876
Start 6461504:6461504(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs567034403
CDS Mutation c.1184C>T
AA Mutation p.Ala395Val(p.A395V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000356876
Start 6462142:6462142(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.777C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000356876
Start 6461605:6461605(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763359221
CDS Mutation c.1083C>A
Mutation Classification Silent
Feature Type Transcript