Primary Site >> Pancreatic Cancer

Gene >> DAAM2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39883965:39883965(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749423164
CDS Mutation c.1849C>T
AA Mutation p.Arg617Cys(p.R617C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39896968:39896968(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2498C>A
AA Mutation p.Ser833Tyr(p.S833Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39901312:39901312(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2822C>T
AA Mutation p.Ala941Val(p.A941V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000274867
Start 39878212:39878212(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376008956
CDS Mutation c.1311C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000274867
Start 39887545:39887545(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2013G>A
Mutation Classification Silent
Feature Type Transcript