Primary Site >> Pancreatic Cancer

Gene >> GPR182

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000300098
Start 56995375:56995375(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.166C>A
AA Mutation p.Leu56Ile(p.L56I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000300098
Start 56995735:56995735(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.526G>T
AA Mutation p.Gly176Cys(p.G176C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000300098
Start 56995632:56995632(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.423C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000300098
Start 56996140:56996140(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.931C>T
Mutation Classification Silent
Feature Type Transcript