Primary Site >> Pancreatic Cancer

Gene >> CCKAR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000295589
Start 26489452:26489452(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.145T>G
AA Mutation p.Ser49Ala(p.S49A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000295589
Start 26481694:26481694(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1231G>T
AA Mutation p.Ala411Ser(p.A411S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000295589
Start 26482140:26482140(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.785A>C
AA Mutation p.Lys262Thr(p.K262T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000295589
Start 26490201:26490201(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.67G>A
AA Mutation p.Glu23Lys(p.E23K)
Mutation Classification Missense_Mutation
Feature Type Transcript