Primary Site >> Pancreatic Cancer

Gene >> PHLPP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262719
Start 62895930:62895930(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2363T>G
AA Mutation p.Leu788Arg(p.L788R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262719
Start 62975429:62975429(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3788G>A
AA Mutation p.Gly1263Asp(p.G1263D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000262719
Start 62978354:62978354(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376314377
CDS Mutation c.4077C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000262719
Start 62978921:62978921(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748230117
CDS Mutation c.4644C>T
Mutation Classification Silent
Feature Type Transcript