Primary Site >> Stomach Cancer

Gene >> HOXD1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000331462
Start 176189436:176189436(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.635G>T
AA Mutation p.Arg212Met(p.R212M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000331462
Start 176189835:176189835(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.680G>A
AA Mutation p.Ser227Asn(p.S227N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000331462
Start 176189223:176189223(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.422C>T
AA Mutation p.Ser141Leu(p.S141L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000331462
Start 176189315:176189315(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.514G>A
AA Mutation p.Asp172Asn(p.D172N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000331462
Start 176188840:176188840(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779498756
CDS Mutation c.39C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000331462
Start 176189215:176189215(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.414C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000331462
Start 176190020:176190020(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.865C>T
AA Mutation p.Arg289Ter(p.R289*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript