Primary Site >> Pancreatic Cancer

Gene >> PTPRD

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8340450:8340450(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200354236
CDS Mutation c.5146G>A
AA Mutation p.Ala1716Thr(p.A1716T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8376626:8376626(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772303653
CDS Mutation c.4487G>A
AA Mutation p.Arg1496Gln(p.R1496Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8636839:8636839(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.70C>T
AA Mutation p.Pro24Ser(p.P24S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8636735:8636735(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.174C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8492935:8492935(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2394C>T
Mutation Classification Silent
Feature Type Transcript