Primary Site >> Pancreatic Cancer

Gene >> XPC

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000285021
Start 14146092:14146092(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2672G>T
AA Mutation p.Ser891Ile(p.S891I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000285021
Start 14148724:14148724(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2258G>T
AA Mutation p.Arg753Leu(p.R753L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000285021
Start 14165564:14165564(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.643G>T
AA Mutation p.Ala215Ser(p.A215S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000285021
Start 14168334:14168334(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.459C>T
Mutation Classification Silent
Feature Type Transcript