Primary Site >> Stomach Cancer
Gene >> PLOD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000196061 |
| Start | 11965564:11965564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750991056 |
| CDS Mutation | c.1555G>A |
| AA Mutation | p.Asp519Asn(p.D519N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000196061 |
| Start | 11958612:11958612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.940C>T |
| AA Mutation | p.Pro314Ser(p.P314S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000196061 |
| Start | 11964234:11964234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1262C>T |
| AA Mutation | p.Ala421Val(p.A421V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000196061 |
| Start | 11950364:11950364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141809154 |
| CDS Mutation | c.310G>A |
| AA Mutation | p.Val104Met(p.V104M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000196061 |
| Start | 11964753:11964753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1438G>A |
| AA Mutation | p.Asp480Asn(p.D480N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000196061 |
| Start | 11958556:11958556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.884A>G |
| AA Mutation | p.Glu295Gly(p.E295G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000196061 |
| Start | 11974668:11974668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2044T>C |
| AA Mutation | p.Phe682Leu(p.F682L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000196061 |
| Start | 11948026:11948026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778603432 |
| CDS Mutation | c.127C>T |
| AA Mutation | p.Arg43Cys(p.R43C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000196061 |
| Start | 11964293:11964293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs11553676 |
| CDS Mutation | c.1321C>T |
| AA Mutation | p.Arg441Trp(p.R441W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000196061 |
| Start | 11970693:11970693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758425988 |
| CDS Mutation | c.1779C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000196061 |
| Start | 11970801:11970801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1887C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000196061 |
| Start | 11965569:11965589(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1561_1581delTGGGAGGTGTTCAGCAACCCC |
| AA Mutation | p.Trp521_Pro527del(p.W521_P527del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |