Primary Site >> Pancreatic Cancer

Gene >> TRPC6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000344327
Start 101504667:101504667(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778491013
CDS Mutation c.302G>A
AA Mutation p.Arg101His(p.R101H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000344327
Start 101471311:101471311(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745349298
CDS Mutation c.2281C>T
AA Mutation p.Pro761Ser(p.P761S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000344327
Start 101472225:101472225(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2117T>C
AA Mutation p.Val706Ala(p.V706A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000344327
Start 101483134:101483134(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1325A>C
AA Mutation p.Lys442Thr(p.K442T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000344327
Start 101504032:101504032(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.937G>A
AA Mutation p.Glu313Lys(p.E313K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000344327
Start 101504643:101504643(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.326G>A
AA Mutation p.Gly109Asp(p.G109D)
Mutation Classification Missense_Mutation
Feature Type Transcript