Primary Site >> Pancreatic Cancer

Gene >> ARHGAP6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000337414
Start 11169560:11169560(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376590462
CDS Mutation c.1754C>T
AA Mutation p.Thr585Met(p.T585M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000337414
Start 11139213:11139213(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2575C>A
AA Mutation p.Leu859Met(p.L859M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000337414
Start 11188957:11188957(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.848C>T
AA Mutation p.Pro283Leu(p.P283L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000337414
Start 11138893:11138893(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2895C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000337414
Start 11142258:11142258(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759367604
CDS Mutation c.2232C>T
Mutation Classification Silent
Feature Type Transcript