Primary Site >> Stomach Cancer

Gene >> PAF1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000221265
Start 39389336:39389336(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.407A>G
AA Mutation p.Tyr136Cys(p.Y136C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000221265
Start 39390265:39390265(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.72T>C
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000221265
Start 39386234:39386234(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1353G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000221265
Start 39390286:39390286(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.51C>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000221265
Start 39388791:39388791(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs547127898
CDS Mutation c.711G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000221265
Start 39388677:39388677(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.741-1G>A
Mutation Classification Splice_Site
Feature Type Transcript
ID 7
Mutation Consequence inframe_deletion;splice_region_variant
Transcription ID ENST00000221265
Start 39388762:39388764(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.738_740delTAG
AA Mutation p.Ile246_Arg247delinsMet(p.I246_R247delinsM)
Mutation Classification In_Frame_Del
Feature Type Transcript