Primary Site >> Stomach Cancer
Gene >> AFF3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 99593830:99593830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770557623 |
| CDS Mutation | c.1831G>A |
| AA Mutation | p.Ala611Thr(p.A611T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 99649642:99649642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762261479 |
| CDS Mutation | c.1168C>T |
| AA Mutation | p.Arg390Cys(p.R390C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 100008904:100008904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780991519 |
| CDS Mutation | c.82C>T |
| AA Mutation | p.Arg28Trp(p.R28W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 99594090:99594090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1571A>G |
| AA Mutation | p.Lys524Arg(p.K524R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 99568878:99568878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2956C>G |
| AA Mutation | p.Arg986Gly(p.R986G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 100007000:100007000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.505A>G |
| AA Mutation | p.Arg169Gly(p.R169G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 99565526:99565526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3080C>A |
| AA Mutation | p.Ser1027Tyr(p.S1027Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 99593437:99593437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2224T>G |
| AA Mutation | p.Phe742Val(p.F742V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 99554386:99554386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776241053 |
| CDS Mutation | c.3484G>A |
| AA Mutation | p.Val1162Ile(p.V1162I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 99554413:99554413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3457C>T |
| AA Mutation | p.Arg1153Cys(p.R1153C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 100007453:100007453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.182A>T |
| AA Mutation | p.Lys61Met(p.K61M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 99601449:99601449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1357T>G |
| AA Mutation | p.Phe453Val(p.F453V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 99565517:99565517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs530073150 |
| CDS Mutation | c.3089C>T |
| AA Mutation | p.Thr1030Met(p.T1030M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 99593938:99593938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1723G>T |
| AA Mutation | p.Ala575Ser(p.A575S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 99594006:99594006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1655C>T |
| AA Mutation | p.Ala552Val(p.A552V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 100006811:100006811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.694A>G |
| AA Mutation | p.Thr232Ala(p.T232A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000409236 |
| Start | 99558966:99558966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3194A>G |
| AA Mutation | p.Tyr1065Cys(p.Y1065C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409236 |
| Start | 100007003:100007003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.502C>T |
| AA Mutation | p.Leu168Phe(p.L168F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000409236 |
| Start | 99587264:99587264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2481C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000409236 |
| Start | 99551489:99551489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3666C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000409236 |
| Start | 99554354:99554354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757906287 |
| CDS Mutation | c.3516C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000409236 |
| Start | 99672585:99672585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755545087 |
| CDS Mutation | c.1096C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000409236 |
| Start | 99554438:99554438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200904404 |
| CDS Mutation | c.3432G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000409236 |
| Start | 100006782:100006782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.723A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000409236 |
| Start | 100007387:100007387(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.248delT |
| AA Mutation | p.Leu83Ter(p.L83*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000409236 |
| Start | 99582844:99582844(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2747delA |
| AA Mutation | p.Lys916SerfsTer72(p.K916Sfs*72) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000409236 |
| Start | 99582862:99582862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2729C>G |
| AA Mutation | p.Ser910Ter(p.S910*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000409236 |
| Start | 99752268:99752268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.955C>T |
| AA Mutation | p.Gln319Ter(p.Q319*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000409236 |
| Start | 99601451:99601452(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs759949420 |
| CDS Mutation | c.1354dupC |
| AA Mutation | p.His452ProfsTer8(p.H452Pfs*8) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |