Primary Site >> Stomach Cancer

Gene >> HOXC8

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000040584
Start 54009300:54009300(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs557022782
CDS Mutation c.16G>A
AA Mutation p.Val6Ile(p.V6I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000040584
Start 54009531:54009531(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.247G>A
AA Mutation p.Gly83Arg(p.G83R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000040584
Start 54009602:54009602(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.318G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000040584
Start 54009329:54009329(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142847294
CDS Mutation c.45C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000040584
Start 54009530:54009530(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.246C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000040584
Start 54009437:54009437(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.153C>T
Mutation Classification Silent
Feature Type Transcript