Primary Site >> Stomach Cancer

Gene >> TIMP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000218388
Start 47585308:47585308(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.305G>T
AA Mutation p.Arg102Leu(p.R102L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000218388
Start 47585628:47585628(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.414C>A
Mutation Classification Silent
Feature Type Transcript