Primary Site >> Esophagus Cancer

Gene >> KRT9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000246662
Start 41567454:41567454(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1691C>T
AA Mutation p.Ser564Phe(p.S564F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000246662
Start 41567400:41567400(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775942442
CDS Mutation c.1745G>A
AA Mutation p.Ser582Asn(p.S582N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000246662
Start 41571920:41571920(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762726903
CDS Mutation c.73G>A
AA Mutation p.Gly25Arg(p.G25R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000246662
Start 41571399:41571399(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.594G>A
Mutation Classification Silent
Feature Type Transcript