Primary Site >> Pancreatic Cancer

Gene >> ARHGAP20

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000260283
Start 110580307:110580307(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2639G>T
AA Mutation p.Gly880Val(p.G880V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000260283
Start 110583604:110583604(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1549A>G
AA Mutation p.Ile517Val(p.I517V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000260283
Start 110624194:110624194(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.471C>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000260283
Start 110580351:110580351(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2595A>G
Mutation Classification Silent
Feature Type Transcript