Primary Site >> Stomach Cancer
Gene >> NCOA6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34776305:34776305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.379G>A |
| AA Mutation | p.Val127Ile(p.V127I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34750153:34750153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2042A>G |
| AA Mutation | p.Lys681Arg(p.K681R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34742075:34742075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4181G>A |
| AA Mutation | p.Ser1394Asn(p.S1394N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34742760:34742760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3496C>T |
| AA Mutation | p.Pro1166Ser(p.P1166S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34741089:34741089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750413656 |
| CDS Mutation | c.5167G>C |
| AA Mutation | p.Ala1723Pro(p.A1723P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34754864:34754864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1533G>A |
| AA Mutation | p.Met511Ile(p.M511I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34742903:34742903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767151504 |
| CDS Mutation | c.3353C>T |
| AA Mutation | p.Pro1118Leu(p.P1118L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34757735:34757735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1013T>C |
| AA Mutation | p.Met338Thr(p.M338T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34727351:34727351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6056G>C |
| AA Mutation | p.Arg2019Pro(p.R2019P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34736707:34736707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756299397 |
| CDS Mutation | c.5945C>T |
| AA Mutation | p.Ala1982Val(p.A1982V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34754737:34754737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1660A>G |
| AA Mutation | p.Asn554Asp(p.N554D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34741697:34741697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4559T>A |
| AA Mutation | p.Val1520Asp(p.V1520D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359003 |
| Start | 34742707:34742707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780751438 |
| CDS Mutation | c.3549A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359003 |
| Start | 34742710:34742710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3546G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359003 |
| Start | 34757326:34757326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1422G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359003 |
| Start | 34740568:34740568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141863711 |
| CDS Mutation | c.5688G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359003 |
| Start | 34743163:34743163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3093A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359003 |
| Start | 34715352:34715352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144649777 |
| CDS Mutation | c.6162G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359003 |
| Start | 34741276:34741277(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4979_4980delTT |
| AA Mutation | p.Phe1660TyrfsTer56(p.F1660Yfs*56) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359003 |
| Start | 34757417:34757417(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1331delC |
| AA Mutation | p.Pro444GlnfsTer48(p.P444Qfs*48) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359003 |
| Start | 34758891:34758891(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.557delC |
| AA Mutation | p.Pro186ArgfsTer9(p.P186Rfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359003 |
| Start | 34743266:34743266(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2990delC |
| AA Mutation | p.Pro997HisfsTer37(p.P997Hfs*37) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359003 |
| Start | 34749703:34749703(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2492delC |
| AA Mutation | p.Pro831LeufsTer52(p.P831Lfs*52) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359003 |
| Start | 34750198:34750198(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1997delC |
| AA Mutation | p.Pro666ArgfsTer12(p.P666Rfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000359003 |
| Start | 34742508:34742508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3748G>T |
| AA Mutation | p.Gly1250Ter(p.G1250*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000359003 |
| Start | 34757967:34757967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753265917 |
| CDS Mutation | c.781C>T |
| AA Mutation | p.Gln261Ter(p.Q261*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |