Primary Site >> Stomach Cancer

Gene >> PHF10

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000339209
Start 169718841:169718841(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.272A>G
AA Mutation p.Gln91Arg(p.Q91R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000339209
Start 169710279:169710279(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1070G>A
AA Mutation p.Gly357Asp(p.G357D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence frameshift_variant
Transcription ID ENST00000339209
Start 169704019:169704019(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1481delA
AA Mutation p.Asn494ThrfsTer?(p.N494Tfs*?)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000339209
Start 169704052:169704052(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1448delC
AA Mutation p.Pro483GlnfsTer?(p.P483Qfs*?)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000339209
Start 169705172:169705172(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1372delT
AA Mutation p.Tyr458IlefsTer?(p.Y458Ifs*?)
Mutation Classification Frame_Shift_Del
Feature Type Transcript