Primary Site >> Stomach Cancer

Gene >> XPC

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000285021
Start 14156356:14156356(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs3731140
CDS Mutation c.2012G>A
AA Mutation p.Arg671His(p.R671H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000285021
Start 14168275:14168275(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770955020
CDS Mutation c.518C>T
AA Mutation p.Ala173Val(p.A173V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000285021
Start 14158686:14158686(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747977181
CDS Mutation c.1197C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000285021
Start 14158695:14158695(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1188C>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000285021
Start 14158641:14158641(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1242G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000285021
Start 14148663:14148663(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2319G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000285021
Start 14156385:14156385(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1983C>T
Mutation Classification Silent
Feature Type Transcript