Primary Site >> Pancreatic Cancer

Gene >> LCP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000323076
Start 46144460:46144460(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772323138
CDS Mutation c.1235G>A
AA Mutation p.Arg412Gln(p.R412Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000323076
Start 46127703:46127703(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1772G>A
AA Mutation p.Arg591Gln(p.R591Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000323076
Start 46142407:46142407(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs541702713
CDS Mutation c.1387G>A
AA Mutation p.Ala463Thr(p.A463T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000323076
Start 46156480:46156480(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.449C>T
AA Mutation p.Thr150Met(p.T150M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000323076
Start 46159658:46159658(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5C>T
AA Mutation p.Ala2Val(p.A2V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000323076
Start 46130831:46130831(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1734G>A
Mutation Classification Silent
Feature Type Transcript