Primary Site >> Stomach Cancer
Gene >> PPFIA3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334186 |
| Start | 49134682:49134682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1421A>G |
| AA Mutation | p.Asp474Gly(p.D474G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334186 |
| Start | 49148685:49148685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3031A>C |
| AA Mutation | p.Ile1011Leu(p.I1011L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334186 |
| Start | 49139716:49139716(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2125G>A |
| AA Mutation | p.Ala709Thr(p.A709T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334186 |
| Start | 49130537:49130537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.817G>A |
| AA Mutation | p.Ala273Thr(p.A273T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334186 |
| Start | 49142831:49142831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2572G>A |
| AA Mutation | p.Val858Met(p.V858M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334186 |
| Start | 49138300:49138300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756648044 |
| CDS Mutation | c.1949G>A |
| AA Mutation | p.Arg650His(p.R650H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334186 |
| Start | 49149665:49149665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3473C>T |
| AA Mutation | p.Ala1158Val(p.A1158V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334186 |
| Start | 49142963:49142963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2704G>T |
| AA Mutation | p.Val902Phe(p.V902F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334186 |
| Start | 49133346:49133346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1136C>T |
| AA Mutation | p.Ala379Val(p.A379V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334186 |
| Start | 49142843:49142843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2584C>T |
| AA Mutation | p.Arg862Trp(p.R862W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334186 |
| Start | 49138368:49138368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2017G>A |
| AA Mutation | p.Gly673Ser(p.G673S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334186 |
| Start | 49130484:49130484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.764G>A |
| AA Mutation | p.Arg255His(p.R255H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334186 |
| Start | 49148204:49148204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2957A>G |
| AA Mutation | p.His986Arg(p.H986R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334186 |
| Start | 49140005:49140005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2285G>A |
| AA Mutation | p.Ser762Asn(p.S762N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334186 |
| Start | 49134081:49134081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755095884 |
| CDS Mutation | c.1293C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334186 |
| Start | 49128051:49128051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.178C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334186 |
| Start | 49139796:49139796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376973066 |
| CDS Mutation | c.2205G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000334186 |
| Start | 49135779:49135780(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1524_1527dupTCTC |
| AA Mutation | p.Pro510SerfsTer71(p.P510Sfs*71) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | splice_donor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000334186 |
| Start | 49149297:49149382(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3327_3354+58delCTTAGGCACAGACAGGCGGCTGGACGAGGTGGGCGCGGCAACAGCTCAGAGGGCTCTGCTCCCAGCGGCTCCTCGAGAGGCTGAGC |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000334186 |
| Start | 49128070:49128072(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.199_201delAAG |
| AA Mutation | p.Lys67del(p.K67del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |