Primary Site >> Esophagus Cancer

Gene >> KRT1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000252244
Start 52675434:52675434(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1694G>A
AA Mutation p.Ser565Asn(p.S565N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000252244
Start 52675320:52675320(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1808G>A
AA Mutation p.Gly603Asp(p.G603D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000252244
Start 52675266:52675266(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1862G>A
AA Mutation p.Gly621Glu(p.G621E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000252244
Start 52679980:52679980(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.369C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000252244
Start 52675388:52675388(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771998586
CDS Mutation c.1740C>T
Mutation Classification Silent
Feature Type Transcript