Primary Site >> Stomach Cancer

Gene >> AGGF1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000312916
Start 77063071:77063071(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747964895
CDS Mutation c.1964G>A
AA Mutation p.Arg655Gln(p.R655Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000312916
Start 77048949:77048949(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747968547
CDS Mutation c.1327G>C
AA Mutation p.Glu443Gln(p.E443Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000312916
Start 77054104:77054104(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776049702
CDS Mutation c.1607G>A
AA Mutation p.Arg536His(p.R536H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000312916
Start 77035569:77035569(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.342C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000312916
Start 77063142:77063142(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2042delA
AA Mutation p.Asn681ThrfsTer29(p.N681Tfs*29)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000312916
Start 77048177:77048177(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1218G>A
AA Mutation p.Trp406Ter(p.W406*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript