Primary Site >> Stomach Cancer
Gene >> TAF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71378272:71378272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.968A>T |
| AA Mutation | p.Gln323Leu(p.Q323L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71408148:71408148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4378A>G |
| AA Mutation | p.Asn1460Asp(p.N1460D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71408134:71408134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4364A>C |
| AA Mutation | p.Asn1455Thr(p.N1455T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71463949:71463949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763664628 |
| CDS Mutation | c.5522C>T |
| AA Mutation | p.Pro1841Leu(p.P1841L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71398610:71398610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3656A>G |
| AA Mutation | p.Glu1219Gly(p.E1219G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71377181:71377181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.701G>A |
| AA Mutation | p.Arg234Gln(p.R234Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71381901:71381901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1516G>A |
| AA Mutation | p.Asp506Asn(p.D506N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71388776:71388776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2605C>T |
| AA Mutation | p.Arg869Cys(p.R869C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71392624:71392624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2834A>T |
| AA Mutation | p.Lys945Met(p.K945M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71383070:71383070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143439292 |
| CDS Mutation | c.1850G>A |
| AA Mutation | p.Arg617His(p.R617H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71366324:71366324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10G>A |
| AA Mutation | p.Gly4Ser(p.G4S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71378933:71378933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1259A>T |
| AA Mutation | p.Asp420Val(p.D420V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71378962:71378962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1288C>T |
| AA Mutation | p.Arg430Cys(p.R430C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71398616:71398616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3662G>A |
| AA Mutation | p.Arg1221Gln(p.R1221Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71366483:71366483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.169G>A |
| AA Mutation | p.Val57Ile(p.V57I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71385015:71385015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2189T>A |
| AA Mutation | p.Phe730Tyr(p.F730Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71454197:71454197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4778C>T |
| AA Mutation | p.Ala1593Val(p.A1593V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71398624:71398624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3670C>T |
| AA Mutation | p.Arg1224Trp(p.R1224W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71379008:71379008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766246603 |
| CDS Mutation | c.1334C>T |
| AA Mutation | p.Ala445Val(p.A445V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373790 |
| Start | 71384013:71384013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1996C>T |
| AA Mutation | p.Arg666Cys(p.R666C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373790 |
| Start | 71401662:71401662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3918A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373790 |
| Start | 71388359:71388359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2547C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373790 |
| Start | 71388302:71388302(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2496delA |
| AA Mutation | p.Ala833ProfsTer14(p.A833Pfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373790 |
| Start | 71460728:71460728(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5324delA |
| AA Mutation | p.Asn1775MetfsTer5(p.N1775Mfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373790 |
| Start | 71383150:71383150(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs745516519 |
| CDS Mutation | c.1937delA |
| AA Mutation | p.Lys646ArgfsTer4(p.K646Rfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373790 |
| Start | 71377622:71377622(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.735delT |
| AA Mutation | p.Phe245LeufsTer25(p.F245Lfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |