Primary Site >> Pancreatic Cancer

Gene >> CLIP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000540338
Start 122341493:122341493(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1711A>C
AA Mutation p.Thr571Pro(p.T571P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000540338
Start 122364037:122364037(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.728G>A
AA Mutation p.Gly243Asp(p.G243D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000540338
Start 122377700:122377700(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.346G>A
AA Mutation p.Gly116Ser(p.G116S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000540338
Start 122341398:122341398(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757595848
CDS Mutation c.1806C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000540338
Start 122341278:122341278(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1926G>A
Mutation Classification Silent
Feature Type Transcript