Primary Site >> Pancreatic Cancer

Gene >> ENPP2

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000075322
Start 119557689:119557689(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780642132
CDS Mutation c.2424C>A
AA Mutation p.Ser808Arg(p.S808R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000075322
Start 119562889:119562889(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2389C>T
AA Mutation p.Pro797Ser(p.P797S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000075322
Start 119569328:119569328(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138793770
CDS Mutation c.1960C>T
AA Mutation p.Arg654Trp(p.R654W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000075322
Start 119621404:119621404(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.408G>A
Mutation Classification Silent
Feature Type Transcript