Primary Site >> Pancreatic Cancer

Gene >> PTPRG

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000474889
Start 62282817:62282817(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4003G>A
AA Mutation p.Val1335Ile(p.V1335I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000474889
Start 62168139:62168139(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1009C>T
AA Mutation p.Pro337Ser(p.P337S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000474889
Start 62273803:62273803(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3424C>T
AA Mutation p.Pro1142Ser(p.P1142S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000474889
Start 62271421:62271421(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3048G>T
AA Mutation p.Arg1016Ser(p.R1016S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000474889
Start 62003401:62003401(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.423C>T
Mutation Classification Silent
Feature Type Transcript