Primary Site >> Stomach Cancer
Gene >> PHF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359246 |
| Start | 93654440:93654440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.817C>A |
| AA Mutation | p.Pro273Thr(p.P273T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359246 |
| Start | 93665847:93665847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745947229 |
| CDS Mutation | c.2099C>T |
| AA Mutation | p.Pro700Leu(p.P700L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359246 |
| Start | 93665765:93665765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750048636 |
| CDS Mutation | c.2017G>A |
| AA Mutation | p.Val673Met(p.V673M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359246 |
| Start | 93674987:93674987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2687G>T |
| AA Mutation | p.Arg896Met(p.R896M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359246 |
| Start | 93677593:93677593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs530932207 |
| CDS Mutation | c.3208C>T |
| AA Mutation | p.Arg1070Cys(p.R1070C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359246 |
| Start | 93665786:93665786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2038G>A |
| AA Mutation | p.Val680Met(p.V680M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359246 |
| Start | 93673638:93673638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2402T>C |
| AA Mutation | p.Met801Thr(p.M801T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359246 |
| Start | 93675761:93675761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761181154 |
| CDS Mutation | c.2804C>T |
| AA Mutation | p.Ala935Val(p.A935V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359246 |
| Start | 93660225:93660225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1363A>G |
| AA Mutation | p.Thr455Ala(p.T455A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359246 |
| Start | 93663573:93663573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142130095 |
| CDS Mutation | c.1875G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359246 |
| Start | 93675747:93675747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148663364 |
| CDS Mutation | c.2790C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359246 |
| Start | 93675000:93675000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2700C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359246 |
| Start | 93645773:93645773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769570807 |
| CDS Mutation | c.444C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359246 |
| Start | 93665773:93665773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2025T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359246 |
| Start | 93653191:93653191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750708120 |
| CDS Mutation | c.615C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359246 |
| Start | 93660330:93660330(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs775621348 |
| CDS Mutation | c.1475delA |
| AA Mutation | p.Lys492ArgfsTer6(p.K492Rfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |