Primary Site >> Esophagus Cancer

Gene >> NOS3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000297494
Start 150998444:150998444(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.670C>T
AA Mutation p.Leu224Phe(p.L224F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000297494
Start 150996777:150996777(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.434C>T
AA Mutation p.Ala145Val(p.A145V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000297494
Start 150998372:150998372(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.598G>A
AA Mutation p.Asp200Asn(p.D200N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000297494
Start 151010735:151010735(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2824G>T
AA Mutation p.Val942Phe(p.V942F)
Mutation Classification Missense_Mutation
Feature Type Transcript