Primary Site >> Stomach Cancer
Gene >> NDST1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261797 |
| Start | 150521642:150521642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746465319 |
| CDS Mutation | c.388C>T |
| AA Mutation | p.Arg130Cys(p.R130C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261797 |
| Start | 150541612:150541612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1792G>A |
| AA Mutation | p.Glu598Lys(p.E598K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000261797 |
| Start | 150553213:150553213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2530T>C |
| AA Mutation | p.Ser844Pro(p.S844P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261797 |
| Start | 150548297:150548297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2225C>T |
| AA Mutation | p.Ser742Leu(p.S742L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261797 |
| Start | 150527913:150527913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.623A>G |
| AA Mutation | p.Tyr208Cys(p.Y208C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261797 |
| Start | 150521288:150521288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753004555 |
| CDS Mutation | c.34C>T |
| AA Mutation | p.Arg12Trp(p.R12W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261797 |
| Start | 150534998:150534998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1228G>A |
| AA Mutation | p.Ala410Thr(p.A410T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261797 |
| Start | 150521654:150521654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757320453 |
| CDS Mutation | c.400G>A |
| AA Mutation | p.Ala134Thr(p.A134T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261797 |
| Start | 150535754:150535754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754419698 |
| CDS Mutation | c.1306G>A |
| AA Mutation | p.Val436Met(p.V436M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261797 |
| Start | 150540254:150540254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1739C>T |
| AA Mutation | p.Pro580Leu(p.P580L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261797 |
| Start | 150521747:150521747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.493G>A |
| AA Mutation | p.Gly165Ser(p.G165S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261797 |
| Start | 150548276:150548276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2204C>A |
| AA Mutation | p.Thr735Asn(p.T735N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261797 |
| Start | 150521487:150521487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.233C>A |
| AA Mutation | p.Pro78His(p.P78H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261797 |
| Start | 150535707:150535707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1259G>A |
| AA Mutation | p.Gly420Asp(p.G420D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261797 |
| Start | 150521401:150521401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376546047 |
| CDS Mutation | c.147G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261797 |
| Start | 150521536:150521536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372526615 |
| CDS Mutation | c.282G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261797 |
| Start | 150548289:150548289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374191724 |
| CDS Mutation | c.2217C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261797 |
| Start | 150521698:150521698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373243938 |
| CDS Mutation | c.444C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261797 |
| Start | 150528124:150528124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376056556 |
| CDS Mutation | c.834C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261797 |
| Start | 150521311:150521311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.57C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261797 |
| Start | 150548298:150548298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766151934 |
| CDS Mutation | c.2226G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261797 |
| Start | 150539256:150539257(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1474_1475dupAC |
| AA Mutation | p.Ile493ProfsTer36(p.I493Pfs*36) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |