Primary Site >> Stomach Cancer
Gene >> PCSK7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320934 |
| Start | 117206329:117206329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559962536 |
| CDS Mutation | c.2026G>A |
| AA Mutation | p.Val676Ile(p.V676I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320934 |
| Start | 117208940:117208940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1648A>G |
| AA Mutation | p.Ser550Gly(p.S550G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320934 |
| Start | 117228280:117228280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.539G>T |
| AA Mutation | p.Gly180Val(p.G180V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320934 |
| Start | 117218509:117218509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1491G>T |
| AA Mutation | p.Lys497Asn(p.K497N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320934 |
| Start | 117227192:117227192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753800942 |
| CDS Mutation | c.734G>A |
| AA Mutation | p.Cys245Tyr(p.C245Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320934 |
| Start | 117227216:117227216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143167780 |
| CDS Mutation | c.710C>T |
| AA Mutation | p.Ala237Val(p.A237V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320934 |
| Start | 117207109:117207109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1838A>C |
| AA Mutation | p.Tyr613Ser(p.Y613S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320934 |
| Start | 117219666:117219666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1248A>G |
| AA Mutation | p.Ile416Met(p.I416M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320934 |
| Start | 117228242:117228242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.577A>G |
| AA Mutation | p.Thr193Ala(p.T193A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320934 |
| Start | 117229577:117229577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.268G>A |
| AA Mutation | p.Gly90Arg(p.G90R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320934 |
| Start | 117229528:117229528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs75310602 |
| CDS Mutation | c.317C>T |
| AA Mutation | p.Pro106Leu(p.P106L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320934 |
| Start | 117229653:117229653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs182787931 |
| CDS Mutation | c.192C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |