Primary Site >> Stomach Cancer
Gene >> PRDM5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264808 |
| Start | 120853520:120853520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.198A>C |
| AA Mutation | p.Glu66Asp(p.E66D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264808 |
| Start | 120816880:120816880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.695G>A |
| AA Mutation | p.Arg232Gln(p.R232Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264808 |
| Start | 120922580:120922580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.29T>C |
| AA Mutation | p.Phe10Ser(p.F10S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264808 |
| Start | 120781207:120781207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1379A>C |
| AA Mutation | p.Lys460Thr(p.K460T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264808 |
| Start | 120853501:120853501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.217G>T |
| AA Mutation | p.Ala73Ser(p.A73S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264808 |
| Start | 120798286:120798286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1169T>A |
| AA Mutation | p.Val390Asp(p.V390D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264808 |
| Start | 120821294:120821294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.352G>C |
| AA Mutation | p.Glu118Gln(p.E118Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264808 |
| Start | 120818518:120818518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.485G>C |
| AA Mutation | p.Gly162Ala(p.G162A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264808 |
| Start | 120922530:120922530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373822101 |
| CDS Mutation | c.79C>T |
| AA Mutation | p.Arg27Cys(p.R27C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264808 |
| Start | 120798316:120798316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1139T>G |
| AA Mutation | p.Leu380Arg(p.L380R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264808 |
| Start | 120853487:120853487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765603481 |
| CDS Mutation | c.231G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |