Primary Site >> Stomach Cancer
Gene >> LONP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360614 |
| Start | 5705836:5705836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1303A>G |
| AA Mutation | p.Met435Val(p.M435V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360614 |
| Start | 5699099:5699099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115968490 |
| CDS Mutation | c.1613G>A |
| AA Mutation | p.Arg538His(p.R538H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360614 |
| Start | 5699193:5699193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143983421 |
| CDS Mutation | c.1519G>A |
| AA Mutation | p.Val507Ile(p.V507I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360614 |
| Start | 5713209:5713209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147052599 |
| CDS Mutation | c.563C>T |
| AA Mutation | p.Thr188Met(p.T188M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360614 |
| Start | 5692111:5692111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2801A>G |
| AA Mutation | p.His934Arg(p.H934R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360614 |
| Start | 5705897:5705897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1242G>T |
| AA Mutation | p.Lys414Asn(p.K414N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360614 |
| Start | 5708372:5708372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.902G>A |
| AA Mutation | p.Arg301Gln(p.R301Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360614 |
| Start | 5693661:5693661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2429T>C |
| AA Mutation | p.Met810Thr(p.M810T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360614 |
| Start | 5692148:5692148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139476430 |
| CDS Mutation | c.2764G>A |
| AA Mutation | p.Asp922Asn(p.D922N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360614 |
| Start | 5700797:5700797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377243139 |
| CDS Mutation | c.1498C>T |
| AA Mutation | p.Arg500Cys(p.R500C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360614 |
| Start | 5700813:5700813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1482G>A |
| AA Mutation | p.Met494Ile(p.M494I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360614 |
| Start | 5694781:5694781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2134C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360614 |
| Start | 5711810:5711810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776204640 |
| CDS Mutation | c.831C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360614 |
| Start | 5696682:5696682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1761C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360614 |
| Start | 5700852:5700852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146759309 |
| CDS Mutation | c.1443G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360614 |
| Start | 5693343:5693343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142397293 |
| CDS Mutation | c.2658G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360614 |
| Start | 5699200:5699200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763432896 |
| CDS Mutation | c.1512C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |