Primary Site >> Stomach Cancer
Gene >> NT5C1A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235628 |
| Start | 39665584:39665584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.370G>A |
| AA Mutation | p.Val124Ile(p.V124I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235628 |
| Start | 39665626:39665626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.328C>A |
| AA Mutation | p.Leu110Met(p.L110M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235628 |
| Start | 39665623:39665623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144180251 |
| CDS Mutation | c.331C>T |
| AA Mutation | p.Arg111Trp(p.R111W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235628 |
| Start | 39671969:39671969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.70G>T |
| AA Mutation | p.Ala24Ser(p.A24S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235628 |
| Start | 39665629:39665629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557786217 |
| CDS Mutation | c.325C>T |
| AA Mutation | p.Arg109Trp(p.R109W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235628 |
| Start | 39663341:39663341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763507322 |
| CDS Mutation | c.527C>T |
| AA Mutation | p.Ala176Val(p.A176V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235628 |
| Start | 39659419:39659419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752949958 |
| CDS Mutation | c.809G>A |
| AA Mutation | p.Arg270Gln(p.R270Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000235628 |
| Start | 39659178:39659178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1050T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000235628 |
| Start | 39659316:39659316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.912T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000235628 |
| Start | 39663373:39663373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.495C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000235628 |
| Start | 39671967:39671967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.72C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000235628 |
| Start | 39672009:39672009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763839002 |
| CDS Mutation | c.30G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |