Primary Site >> Pancreatic Cancer

Gene >> ARHGAP17

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000289968
Start 24920145:24920145(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2631G>T
AA Mutation p.Glu877Asp(p.E877D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000289968
Start 24935565:24935565(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1799G>A
AA Mutation p.Gly600Asp(p.G600D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000289968
Start 24931002:24931002(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2297T>C
AA Mutation p.Leu766Pro(p.L766P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000289968
Start 24947490:24947490(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1233A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000289968
Start 24931405:24931405(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1895-1G>T
Mutation Classification Splice_Site
Feature Type Transcript