Primary Site >> Pancreatic Cancer

Gene >> PRKD2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000291281
Start 46675076:46675076(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2381A>C
AA Mutation p.Lys794Thr(p.K794T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000291281
Start 46693944:46693944(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1507G>A
AA Mutation p.Ala503Thr(p.A503T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000291281
Start 46704586:46704586(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.575G>A
AA Mutation p.Arg192His(p.R192H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000291281
Start 46690615:46690615(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1794A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000291281
Start 46691742:46691742(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1695C>A
Mutation Classification Silent
Feature Type Transcript