Primary Site >> Pancreatic Cancer
Gene >> PKD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262304 |
| Start | 2106825:2106825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7189A>G |
| AA Mutation | p.Ser2397Gly(p.S2397G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262304 |
| Start | 2110249:2110249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781184044 |
| CDS Mutation | c.4918G>A |
| AA Mutation | p.Gly1640Ser(p.G1640S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262304 |
| Start | 2097771:2097771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10177G>A |
| AA Mutation | p.Val3393Ile(p.V3393I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262304 |
| Start | 2097954:2097954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556305710 |
| CDS Mutation | c.10081G>A |
| AA Mutation | p.Gly3361Arg(p.G3361R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262304 |
| Start | 2103409:2103409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8648C>A |
| AA Mutation | p.Ala2883Asp(p.A2883D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262304 |
| Start | 2103862:2103862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs78185588 |
| CDS Mutation | c.8195G>A |
| AA Mutation | p.Arg2732Gln(p.R2732Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262304 |
| Start | 2110528:2110528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4639C>T |
| AA Mutation | p.Arg1547Cys(p.R1547C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262304 |
| Start | 2112877:2112877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774135682 |
| CDS Mutation | c.3072C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262304 |
| Start | 2111453:2111453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769745056 |
| CDS Mutation | c.3714C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |