Primary Site >> Esophagus Cancer

Gene >> NCOR1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16091952:16091952(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2927A>C
AA Mutation p.Gln976Pro(p.Q976P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16040446:16040446(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6728C>A
AA Mutation p.Thr2243Lys(p.T2243K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16101284:16101284(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2656G>A
AA Mutation p.Asp886Asn(p.D886N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000268712
Start 16047004:16047004(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6626A>T
AA Mutation p.Lys2209Met(p.K2209M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000268712
Start 16139013:16139013(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1347G>A
Mutation Classification Silent
Feature Type Transcript