Primary Site >> Pancreatic Cancer

Gene >> MEN1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000337652
Start 64805095:64805095(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1304C>T
AA Mutation p.Pro435Leu(p.P435L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000337652
Start 64806286:64806286(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1010G>A
AA Mutation p.Arg337His(p.R337H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000337652
Start 64807100:64807100(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.840-2A>G
Mutation Classification Splice_Site
Feature Type Transcript
ID 4
Mutation Consequence inframe_deletion
Transcription ID ENST00000337652
Start 64805731:64805733(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1102_1104delGAG
AA Mutation p.Glu368del(p.E368del)
Mutation Classification In_Frame_Del
Feature Type Transcript