Primary Site >> Esophagus Cancer

Gene >> MYH9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36289290:36289290(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759107183
CDS Mutation c.4352C>T
AA Mutation p.Ala1451Val(p.A1451V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36289149:36289149(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4493T>G
AA Mutation p.Leu1498Arg(p.L1498R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000216181
Start 36288384:36288384(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201223994
CDS Mutation c.4800C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000216181
Start 36304090:36304090(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2295C>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000216181
Start 36294128:36294128(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3801G>A
Mutation Classification Silent
Feature Type Transcript