Primary Site >> Pancreatic Cancer

Gene >> GLI2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361492
Start 120982840:120982840(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1643C>T
AA Mutation p.Ser548Leu(p.S548L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361492
Start 120984531:120984531(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1744C>T
AA Mutation p.Arg582Trp(p.R582W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000361492
Start 120984611:120984611(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776509889
CDS Mutation c.1824G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000361492
Start 120990192:120990192(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143388073
CDS Mutation c.4278G>A
Mutation Classification Silent
Feature Type Transcript