Primary Site >> Stomach Cancer
Gene >> NTSR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370501 |
| Start | 62709649:62709649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764154462 |
| CDS Mutation | c.442C>T |
| AA Mutation | p.Arg148Cys(p.R148C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370501 |
| Start | 62754877:62754877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769550075 |
| CDS Mutation | c.907C>T |
| AA Mutation | p.Arg303Cys(p.R303C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370501 |
| Start | 62760153:62760153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1143C>G |
| AA Mutation | p.Cys381Trp(p.C381W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370501 |
| Start | 62709622:62709622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.415G>A |
| AA Mutation | p.Ala139Thr(p.A139T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370501 |
| Start | 62709655:62709655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753717597 |
| CDS Mutation | c.448G>A |
| AA Mutation | p.Ala150Thr(p.A150T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370501 |
| Start | 62754878:62754878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772996912 |
| CDS Mutation | c.908G>A |
| AA Mutation | p.Arg303His(p.R303H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370501 |
| Start | 62709832:62709832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.625G>A |
| AA Mutation | p.Glu209Lys(p.E209K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370501 |
| Start | 62709866:62709866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.659G>A |
| AA Mutation | p.Gly220Asp(p.G220D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370501 |
| Start | 62709306:62709306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.99G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370501 |
| Start | 62709363:62709363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150733474 |
| CDS Mutation | c.156C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370501 |
| Start | 62760252:62760252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1242C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370501 |
| Start | 62760060:62760060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199992458 |
| CDS Mutation | c.1050C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |