Primary Site >> Stomach Cancer

Gene >> HAND1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000231121
Start 154475825:154475825(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.629C>T
AA Mutation p.Ala210Val(p.A210V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000231121
Start 154477921:154477921(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753450334
CDS Mutation c.88G>A
AA Mutation p.Gly30Ser(p.G30S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000231121
Start 154477728:154477728(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.281G>A
AA Mutation p.Arg94Gln(p.R94Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000231121
Start 154477692:154477692(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.317G>A
AA Mutation p.Arg106His(p.R106H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000231121
Start 154477502:154477502(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774078948
CDS Mutation c.507G>A
Mutation Classification Silent
Feature Type Transcript