Primary Site >> Stomach Cancer

Gene >> HOXC9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000303450
Start 54000355:54000355(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.167C>T
AA Mutation p.Ala56Val(p.A56V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000303450
Start 54002438:54002438(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767515230
CDS Mutation c.547G>A
AA Mutation p.Val183Met(p.V183M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000303450
Start 54002456:54002456(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.565G>A
AA Mutation p.Ala189Thr(p.A189T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000303450
Start 54000257:54000257(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.69C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000303450
Start 54002656:54002656(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.765C>T
Mutation Classification Silent
Feature Type Transcript