Primary Site >> Stomach Cancer
Gene >> ZFYVE16
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338008 |
| Start | 80443234:80443234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2531C>A |
| AA Mutation | p.Pro844His(p.P844H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338008 |
| Start | 80440005:80440005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769797533 |
| CDS Mutation | c.2392G>A |
| AA Mutation | p.Val798Ile(p.V798I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338008 |
| Start | 80438249:80438249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367799631 |
| CDS Mutation | c.1564G>A |
| AA Mutation | p.Ala522Thr(p.A522T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338008 |
| Start | 80436935:80436935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145932207 |
| CDS Mutation | c.250A>G |
| AA Mutation | p.Thr84Ala(p.T84A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338008 |
| Start | 80437209:80437209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.524T>C |
| AA Mutation | p.Val175Ala(p.V175A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338008 |
| Start | 80456491:80456491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3721A>C |
| AA Mutation | p.Asn1241His(p.N1241H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338008 |
| Start | 80437130:80437130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.445T>A |
| AA Mutation | p.Leu149Ile(p.L149I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338008 |
| Start | 80448297:80448297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2996G>T |
| AA Mutation | p.Arg999Met(p.R999M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338008 |
| Start | 80437644:80437644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.959G>A |
| AA Mutation | p.Arg320Lys(p.R320K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338008 |
| Start | 80437599:80437599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.914G>A |
| AA Mutation | p.Ser305Asn(p.S305N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338008 |
| Start | 80437430:80437430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.745A>G |
| AA Mutation | p.Thr249Ala(p.T249A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338008 |
| Start | 80474706:80474706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4337C>G |
| AA Mutation | p.Thr1446Ser(p.T1446S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338008 |
| Start | 80445344:80445344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2663T>C |
| AA Mutation | p.Leu888Ser(p.L888S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338008 |
| Start | 80437220:80437220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.535G>A |
| AA Mutation | p.Asp179Asn(p.D179N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338008 |
| Start | 80437915:80437915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1230A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338008 |
| Start | 80450570:80450570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3366T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338008 |
| Start | 80450478:80450478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3274T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338008 |
| Start | 80477370:80477370(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs747539668 |
| CDS Mutation | c.4618delT |
| AA Mutation | p.Ter1540Ser(p.*1540S) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338008 |
| Start | 80437120:80437121(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.435_436insCAAGTCCTGTTACATTTTTTTC |
| AA Mutation | p.Ile146GlnfsTer9(p.I146Qfs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338008 |
| Start | 80437872:80437873(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1193dupT |
| AA Mutation | p.Leu398PhefsTer5(p.L398Ffs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |