Primary Site >> Stomach Cancer
Gene >> PIKFYVE
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208342633:208342633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5011A>G |
| AA Mutation | p.Ile1671Val(p.I1671V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208352748:208352748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5810T>C |
| AA Mutation | p.Met1937Thr(p.M1937T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208330566:208330566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3835G>A |
| AA Mutation | p.Val1279Ile(p.V1279I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208304282:208304282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1432G>A |
| AA Mutation | p.Glu478Lys(p.E478K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208300958:208300958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1072C>A |
| AA Mutation | p.Leu358Met(p.L358M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208285849:208285849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.737T>A |
| AA Mutation | p.Leu246His(p.L246H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208335848:208335848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4312A>G |
| AA Mutation | p.Thr1438Ala(p.T1438A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208353973:208353973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5920C>A |
| AA Mutation | p.Leu1974Met(p.L1974M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208345152:208345152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375710914 |
| CDS Mutation | c.5069C>T |
| AA Mutation | p.Ala1690Val(p.A1690V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000264380 |
| Start | 208320358:208320358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2189A>C |
| AA Mutation | p.Gln730Pro(p.Q730P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208335370:208335370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4207G>A |
| AA Mutation | p.Ala1403Thr(p.A1403T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000264380 |
| Start | 208345194:208345194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5111G>A |
| AA Mutation | p.Ser1704Asn(p.S1704N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264380 |
| Start | 208273600:208273600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.189C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264380 |
| Start | 208325715:208325715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2904T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264380 |
| Start | 208329857:208329857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3735A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264380 |
| Start | 208277671:208277671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.576T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264380 |
| Start | 208314352:208314352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1755G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264380 |
| Start | 208339551:208339551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143759936 |
| CDS Mutation | c.4806C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264380 |
| Start | 208333485:208333485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760133678 |
| CDS Mutation | c.4134G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264380 |
| Start | 208333389:208333389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4038T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264380 |
| Start | 208285751:208285751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.639T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264380 |
| Start | 208347998:208347998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369369378 |
| CDS Mutation | c.5349C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264380 |
| Start | 208326192:208326192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3381C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264380 |
| Start | 208305008:208305008(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1635delA |
| AA Mutation | p.Glu546SerfsTer3(p.E546Sfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |