Primary Site >> Stomach Cancer

Gene >> RFWD3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361070
Start 74632562:74632562(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1538T>C
AA Mutation p.Leu513Pro(p.L513P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361070
Start 74623950:74623950(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2303T>C
AA Mutation p.Val768Ala(p.V768A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361070
Start 74637950:74637950(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs187844792
CDS Mutation c.1100T>C
AA Mutation p.Met367Thr(p.M367T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000361070
Start 74660974:74660974(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.476G>A
AA Mutation p.Arg159Gln(p.R159Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000361070
Start 74636479:74636479(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1293G>A
Mutation Classification Silent
Feature Type Transcript