Primary Site >> Stomach Cancer
Gene >> AFAP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358461 |
| Start | 7819098:7819098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.800T>C |
| AA Mutation | p.Val267Ala(p.V267A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358461 |
| Start | 7843191:7843191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.494G>A |
| AA Mutation | p.Arg165Gln(p.R165Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358461 |
| Start | 7800473:7800473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1235T>C |
| AA Mutation | p.Leu412Pro(p.L412P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358461 |
| Start | 7786249:7786249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1475C>T |
| AA Mutation | p.Ala492Val(p.A492V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358461 |
| Start | 7800464:7800464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1244G>A |
| AA Mutation | p.Gly415Asp(p.G415D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358461 |
| Start | 7843200:7843200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.485G>A |
| AA Mutation | p.Arg162Gln(p.R162Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358461 |
| Start | 7793757:7793757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1336C>T |
| AA Mutation | p.Pro446Ser(p.P446S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358461 |
| Start | 7786244:7786244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768741809 |
| CDS Mutation | c.1480C>T |
| AA Mutation | p.Pro494Ser(p.P494S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358461 |
| Start | 7793781:7793781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1312G>A |
| AA Mutation | p.Ala438Thr(p.A438T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358461 |
| Start | 7800572:7800572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1136A>G |
| AA Mutation | p.Asp379Gly(p.D379G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358461 |
| Start | 7768912:7768912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776677074 |
| CDS Mutation | c.2098G>A |
| AA Mutation | p.Val700Ile(p.V700I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358461 |
| Start | 7793700:7793700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1393A>G |
| AA Mutation | p.Thr465Ala(p.T465A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358461 |
| Start | 7800480:7800480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769468121 |
| CDS Mutation | c.1228C>T |
| AA Mutation | p.Arg410Trp(p.R410W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358461 |
| Start | 7774805:7774805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766985200 |
| CDS Mutation | c.1744C>T |
| AA Mutation | p.Arg582Trp(p.R582W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358461 |
| Start | 7786293:7786293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1431T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358461 |
| Start | 7838629:7838629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144556165 |
| CDS Mutation | c.621G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358461 |
| Start | 7800643:7800643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752923590 |
| CDS Mutation | c.1065C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358461 |
| Start | 7786233:7786233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370469870 |
| CDS Mutation | c.1491G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358461 |
| Start | 7868682:7868682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374798435 |
| CDS Mutation | c.165C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |