Primary Site >> Stomach Cancer
Gene >> NKX3-2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382438 |
| Start | 13544297:13544297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.118G>A |
| AA Mutation | p.Ala40Thr(p.A40T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382438 |
| Start | 13542226:13542226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.769C>T |
| AA Mutation | p.Arg257Cys(p.R257C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382438 |
| Start | 13542286:13542286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778533056 |
| CDS Mutation | c.709G>A |
| AA Mutation | p.Ala237Thr(p.A237T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382438 |
| Start | 13542254:13542254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.741G>C |
| AA Mutation | p.Glu247Asp(p.E247D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382438 |
| Start | 13542196:13542196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.799G>A |
| AA Mutation | p.Ala267Thr(p.A267T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382438 |
| Start | 13544173:13544173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.242C>T |
| AA Mutation | p.Ala81Val(p.A81V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382438 |
| Start | 13542469:13542469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.526G>A |
| AA Mutation | p.Ala176Thr(p.A176T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382438 |
| Start | 13542063:13542063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.932A>G |
| AA Mutation | p.Tyr311Cys(p.Y311C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382438 |
| Start | 13544083:13544083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760235144 |
| CDS Mutation | c.332G>A |
| AA Mutation | p.Arg111Gln(p.R111Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |