Primary Site >> Pancreatic Cancer

Gene >> NUP153

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262077
Start 17688522:17688522(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138192099
CDS Mutation c.208A>G
AA Mutation p.Thr70Ala(p.T70A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262077
Start 17626137:17626137(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3572G>C
AA Mutation p.Ser1191Thr(p.S1191T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262077
Start 17661745:17661745(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1303G>T
AA Mutation p.Ala435Ser(p.A435S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262077
Start 17688454:17688454(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.276G>T
AA Mutation p.Glu92Asp(p.E92D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000262077
Start 17669299:17669299(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1008G>A
Mutation Classification Silent
Feature Type Transcript