Primary Site >> Stomach Cancer

Gene >> COMT

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361682
Start 19968672:19968672(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.752G>T
AA Mutation p.Arg251Met(p.R251M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361682
Start 19968620:19968620(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139449932
CDS Mutation c.700C>T
AA Mutation p.Arg234Cys(p.R234C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361682
Start 19964270:19964270(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374506541
CDS Mutation c.586C>T
AA Mutation p.Arg196Trp(p.R196W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000361682
Start 19962771:19962771(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.245A>G
AA Mutation p.Tyr82Cys(p.Y82C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000361682
Start 19968616:19968616(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs567830018
CDS Mutation c.696C>T
Mutation Classification Silent
Feature Type Transcript