Primary Site >> Pancreatic Cancer
Gene >> RP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54626977:54626977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3095A>G |
| AA Mutation | p.Asn1032Ser(p.N1032S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54626605:54626605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2723C>G |
| AA Mutation | p.Ala908Gly(p.A908G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621096:54621096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.130G>A |
| AA Mutation | p.Gly44Arg(p.G44R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54626731:54626731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2849A>C |
| AA Mutation | p.Asn950Thr(p.N950T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54628264:54628264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4382A>C |
| AA Mutation | p.Asn1461Thr(p.N1461T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54629231:54629231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5349A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621371:54621371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200402161 |
| CDS Mutation | c.405G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621290:54621290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141074157 |
| CDS Mutation | c.324C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |