Primary Site >> Stomach Cancer
Gene >> PRKD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291281 |
| Start | 46675073:46675073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751808641 |
| CDS Mutation | c.2384G>A |
| AA Mutation | p.Arg795His(p.R795H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291281 |
| Start | 46689545:46689545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1963A>G |
| AA Mutation | p.Ile655Val(p.I655V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291281 |
| Start | 46674563:46674563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2597A>G |
| AA Mutation | p.His866Arg(p.H866R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291281 |
| Start | 46697795:46697795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201153892 |
| CDS Mutation | c.1177C>T |
| AA Mutation | p.Arg393Trp(p.R393W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291281 |
| Start | 46678573:46678573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2161G>A |
| AA Mutation | p.Glu721Lys(p.E721K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291281 |
| Start | 46693905:46693905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774048512 |
| CDS Mutation | c.1546G>A |
| AA Mutation | p.Ala516Thr(p.A516T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291281 |
| Start | 46694012:46694012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1439A>G |
| AA Mutation | p.Glu480Gly(p.E480G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291281 |
| Start | 46704529:46704529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.632C>A |
| AA Mutation | p.Thr211Asn(p.T211N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291281 |
| Start | 46700905:46700905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs10402397 |
| CDS Mutation | c.1015G>A |
| AA Mutation | p.Ala339Thr(p.A339T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291281 |
| Start | 46697827:46697827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1145T>C |
| AA Mutation | p.Met382Thr(p.M382T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291281 |
| Start | 46704387:46704387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752855161 |
| CDS Mutation | c.671G>A |
| AA Mutation | p.Arg224His(p.R224H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291281 |
| Start | 46674544:46674544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754132860 |
| CDS Mutation | c.2616G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291281 |
| Start | 46674673:46674673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2487G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291281 |
| Start | 46678445:46678445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766259352 |
| CDS Mutation | c.2289C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |