Primary Site >> Stomach Cancer
Gene >> KDM3A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312912 |
| Start | 86449811:86449811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.191G>A |
| AA Mutation | p.Cys64Tyr(p.C64Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312912 |
| Start | 86489594:86489594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3508C>G |
| AA Mutation | p.Pro1170Ala(p.P1170A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312912 |
| Start | 86477895:86477895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1958G>A |
| AA Mutation | p.Arg653Gln(p.R653Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312912 |
| Start | 86464213:86464213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1004A>G |
| AA Mutation | p.Gln335Arg(p.Q335R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312912 |
| Start | 86477948:86477948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2011A>G |
| AA Mutation | p.Asn671Asp(p.N671D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312912 |
| Start | 86449913:86449913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.293A>G |
| AA Mutation | p.Glu98Gly(p.E98G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312912 |
| Start | 86470266:86470266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1582G>A |
| AA Mutation | p.Glu528Lys(p.E528K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312912 |
| Start | 86466697:86466697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1333T>C |
| AA Mutation | p.Ser445Pro(p.S445P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312912 |
| Start | 86490954:86490954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144713807 |
| CDS Mutation | c.3647G>A |
| AA Mutation | p.Arg1216Gln(p.R1216Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312912 |
| Start | 86478719:86478719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2300A>C |
| AA Mutation | p.Lys767Thr(p.K767T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312912 |
| Start | 86489380:86489380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3376G>A |
| AA Mutation | p.Ala1126Thr(p.A1126T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312912 |
| Start | 86470383:86470383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1699T>G |
| AA Mutation | p.Phe567Val(p.F567V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312912 |
| Start | 86482575:86482575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2803A>G |
| AA Mutation | p.Ser935Gly(p.S935G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312912 |
| Start | 86478709:86478709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2290C>T |
| AA Mutation | p.Pro764Ser(p.P764S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312912 |
| Start | 86477998:86477998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2061C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312912 |
| Start | 86442161:86442161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.114C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312912 |
| Start | 86456858:86456858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755089864 |
| CDS Mutation | c.735C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312912 |
| Start | 86442116:86442116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376742455 |
| CDS Mutation | c.69C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312912 |
| Start | 86470274:86470274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762222097 |
| CDS Mutation | c.1590C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312912 |
| Start | 86485855:86485855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3309T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000312912 |
| Start | 86470245:86470245(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1565delA |
| AA Mutation | p.Lys522SerfsTer16(p.K522Sfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000312912 |
| Start | 86489570:86489570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3484C>T |
| AA Mutation | p.Arg1162Ter(p.R1162*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000312912 |
| Start | 86449939:86449939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150111816 |
| CDS Mutation | c.319C>T |
| AA Mutation | p.Arg107Ter(p.R107*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |