Primary Site >> Stomach Cancer

Gene >> HOXA5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000222726
Start 27143220:27143220(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.388G>A
AA Mutation p.Ala130Thr(p.A130T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000222726
Start 27142038:27142038(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.610C>T
AA Mutation p.Arg204Cys(p.R204C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000222726
Start 27142053:27142053(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.595C>T
AA Mutation p.Arg199Trp(p.R199W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000222726
Start 27143330:27143330(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.278C>T
AA Mutation p.Thr93Met(p.T93M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000222726
Start 27143473:27143473(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.135C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000222726
Start 27143209:27143209(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.399C>T
Mutation Classification Silent
Feature Type Transcript