Primary Site >> Pancreatic Cancer

Gene >> ABCC2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370449
Start 99813045:99813045(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1995A>C
AA Mutation p.Gln665His(p.Q665H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000370449
Start 99844465:99844465(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3987G>T
AA Mutation p.Lys1329Asn(p.K1329N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000370449
Start 99793667:99793667(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.450G>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000370449
Start 99804159:99804159(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1350A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence splice_donor_variant
Transcription ID ENST00000370449
Start 99800565:99800565(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1209+2T>C
Mutation Classification Splice_Site
Feature Type Transcript