Primary Site >> Stomach Cancer
Gene >> PPM1F
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263212 |
| Start | 21931245:21931245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.794C>T |
| AA Mutation | p.Ala265Val(p.A265V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263212 |
| Start | 21933545:21933545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.593A>G |
| AA Mutation | p.Asp198Gly(p.D198G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263212 |
| Start | 21925649:21925649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs549205418 |
| CDS Mutation | c.905G>A |
| AA Mutation | p.Arg302His(p.R302H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263212 |
| Start | 21931170:21931170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.869A>C |
| AA Mutation | p.Glu290Ala(p.E290A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000263212 |
| Start | 21933391:21933391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.747G>T |
| AA Mutation | p.Glu249Asp(p.E249D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263212 |
| Start | 21923265:21923265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745310134 |
| CDS Mutation | c.1192C>T |
| AA Mutation | p.Arg398Trp(p.R398W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263212 |
| Start | 21923362:21923362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769089726 |
| CDS Mutation | c.1095C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263212 |
| Start | 21933571:21933571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.567G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263212 |
| Start | 21923236:21923236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199787665 |
| CDS Mutation | c.1221G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000263212 |
| Start | 21931198:21931198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759818451 |
| CDS Mutation | c.841C>T |
| AA Mutation | p.Gln281Ter(p.Q281*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | splice_acceptor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000263212 |
| Start | 21931269:21931303(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.748-12_770delCTCTCCCTGCAGCGGCTGCAGAGCGGCACCACAGG |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |