Primary Site >> Pancreatic Cancer

Gene >> BCHE

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264381
Start 165830214:165830214(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.820T>G
AA Mutation p.Leu274Val(p.L274V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264381
Start 165773390:165773390(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1801G>A
AA Mutation p.Gly601Ser(p.G601S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264381
Start 165829698:165829698(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1336T>G
AA Mutation p.Phe446Val(p.F446V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264381
Start 165830006:165830006(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1028C>A
AA Mutation p.Thr343Asn(p.T343N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000264381
Start 165786227:165786227(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1602G>A
Mutation Classification Silent
Feature Type Transcript