Primary Site >> Pancreatic Cancer

Gene >> SLC6A2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379906
Start 55699615:55699615(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1551G>T
AA Mutation p.Trp517Cys(p.W517C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000379906
Start 55656962:55656962(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.268G>A
AA Mutation p.Gly90Ser(p.G90S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000379906
Start 55672144:55672144(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.613T>C
AA Mutation p.Tyr205His(p.Y205H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000379906
Start 55696304:55696304(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149035289
CDS Mutation c.1227C>T
Mutation Classification Silent
Feature Type Transcript