Primary Site >> Stomach Cancer
Gene >> VLDLR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382100 |
| Start | 2635519:2635519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.149G>T |
| AA Mutation | p.Trp50Leu(p.W50L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382100 |
| Start | 2647580:2647580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147695876 |
| CDS Mutation | c.1810G>A |
| AA Mutation | p.Gly604Arg(p.G604R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382100 |
| Start | 2651469:2651469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2306T>C |
| AA Mutation | p.Ile769Thr(p.I769T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382100 |
| Start | 2648781:2648781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745637519 |
| CDS Mutation | c.2075T>C |
| AA Mutation | p.Ile692Thr(p.I692T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000382100 |
| Start | 2650372:2650372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370208560 |
| CDS Mutation | c.2107A>G |
| AA Mutation | p.Lys703Glu(p.K703E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382100 |
| Start | 2645662:2645662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1401G>T |
| AA Mutation | p.Gln467His(p.Q467H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382100 |
| Start | 2644970:2644970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1200C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382100 |
| Start | 2650419:2650419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746506982 |
| CDS Mutation | c.2154A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382100 |
| Start | 2643347:2643347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758704925 |
| CDS Mutation | c.636C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382100 |
| Start | 2635505:2635505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.135T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382100 |
| Start | 2646469:2646469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1620T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382100 |
| Start | 2643350:2643350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779155452 |
| CDS Mutation | c.639C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000382100 |
| Start | 2646515:2646515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141396971 |
| CDS Mutation | c.1666C>T |
| AA Mutation | p.Arg556Ter(p.R556*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000382100 |
| Start | 2651938:2651938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2400G>A |
| AA Mutation | p.Trp800Ter(p.W800*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000382100 |
| Start | 2652951:2652951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2586+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000382100 |
| Start | 2639982:2639982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778298702 |
| CDS Mutation | c.325+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |