Primary Site >> Pancreatic Cancer

Gene >> RPTOR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000306801
Start 80707908:80707908(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767783333
CDS Mutation c.416G>A
AA Mutation p.Arg139His(p.R139H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000306801
Start 80949509:80949509(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3332C>T
AA Mutation p.Ala1111Val(p.A1111V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000306801
Start 80949528:80949528(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760760990
CDS Mutation c.3351C>G
AA Mutation p.Asp1117Glu(p.D1117E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000306801
Start 80822255:80822255(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.945C>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000306801
Start 80960143:80960143(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138030342
CDS Mutation c.3543C>T
Mutation Classification Silent
Feature Type Transcript