Primary Site >> Esophagus Cancer

Gene >> MMP9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46013309:46013309(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1385C>T
AA Mutation p.Thr462Met(p.T462M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46012450:46012450(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1198G>A
AA Mutation p.Ala400Thr(p.A400T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46013456:46013456(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1532C>T
AA Mutation p.Pro511Leu(p.P511L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000372330
Start 46011165:46011165(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.672C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000372330
Start 46012180:46012180(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770663427
CDS Mutation c.1041C>T
Mutation Classification Silent
Feature Type Transcript