Primary Site >> Stomach Cancer
Gene >> SLC19A3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258403 |
| Start | 227699215:227699215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.500T>C |
| AA Mutation | p.Met167Thr(p.M167T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258403 |
| Start | 227688176:227688176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1304T>C |
| AA Mutation | p.Val435Ala(p.V435A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258403 |
| Start | 227698808:227698808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.907T>C |
| AA Mutation | p.Trp303Arg(p.W303R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258403 |
| Start | 227696034:227696034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1027C>T |
| AA Mutation | p.Leu343Phe(p.L343F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258403 |
| Start | 227702251:227702251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121917882 |
| CDS Mutation | c.68G>T |
| AA Mutation | p.Gly23Val(p.G23V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258403 |
| Start | 227699397:227699397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.318G>A |
| AA Mutation | p.Met106Ile(p.M106I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258403 |
| Start | 227688171:227688171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1309A>T |
| AA Mutation | p.Ile437Phe(p.I437F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258403 |
| Start | 227699159:227699159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.556T>C |
| AA Mutation | p.Phe186Leu(p.F186L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258403 |
| Start | 227695988:227695988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1073G>A |
| AA Mutation | p.Gly358Asp(p.G358D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258403 |
| Start | 227699363:227699363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.352G>A |
| AA Mutation | p.Ala118Thr(p.A118T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258403 |
| Start | 227698794:227698794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776544411 |
| CDS Mutation | c.921G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |