Primary Site >> Stomach Cancer
Gene >> SPG11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261866 |
| Start | 44596337:44596337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4180T>G |
| AA Mutation | p.Tyr1394Asp(p.Y1394D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261866 |
| Start | 44659247:44659247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.499T>C |
| AA Mutation | p.Phe167Leu(p.F167L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261866 |
| Start | 44651805:44651805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1142T>C |
| AA Mutation | p.Val381Ala(p.V381A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261866 |
| Start | 44565901:44565901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377341108 |
| CDS Mutation | c.6952C>T |
| AA Mutation | p.Arg2318Cys(p.R2318C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261866 |
| Start | 44584365:44584365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150823040 |
| CDS Mutation | c.5315G>A |
| AA Mutation | p.Arg1772His(p.R1772H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261866 |
| Start | 44564644:44564644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149711747 |
| CDS Mutation | c.7054T>C |
| AA Mutation | p.Tyr2352His(p.Y2352H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261866 |
| Start | 44585772:44585772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4985C>T |
| AA Mutation | p.Thr1662Ile(p.T1662I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261866 |
| Start | 44598771:44598771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3752G>T |
| AA Mutation | p.Gly1251Val(p.G1251V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261866 |
| Start | 44663581:44663581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.67G>A |
| AA Mutation | p.Gly23Arg(p.G23R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261866 |
| Start | 44574924:44574924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5984T>C |
| AA Mutation | p.Leu1995Pro(p.L1995P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261866 |
| Start | 44584030:44584030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752889027 |
| CDS Mutation | c.5650C>T |
| AA Mutation | p.Arg1884Cys(p.R1884C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261866 |
| Start | 44615520:44615520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2881C>T |
| AA Mutation | p.Leu961Phe(p.L961F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261866 |
| Start | 44651894:44651894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1053C>G |
| AA Mutation | p.Asn351Lys(p.N351K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261866 |
| Start | 44652140:44652140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.996C>A |
| AA Mutation | p.Phe332Leu(p.F332L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261866 |
| Start | 44615532:44615532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2869T>G |
| AA Mutation | p.Phe957Val(p.F957V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261866 |
| Start | 44652197:44652197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.939A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261866 |
| Start | 44651897:44651897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1050G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261866 |
| Start | 44585750:44585750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5007T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261866 |
| Start | 44659251:44659251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.495A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261866 |
| Start | 44583995:44583995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5685T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261866 |
| Start | 44608515:44608515(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3382delA |
| AA Mutation | p.Thr1128LeufsTer43(p.T1128Lfs*43) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261866 |
| Start | 44615552:44615552(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2849delT |
| AA Mutation | p.Leu950TrpfsTer13(p.L950Wfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261866 |
| Start | 44613500:44613500(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs769721386 |
| CDS Mutation | c.3075delA |
| AA Mutation | p.Glu1026SerfsTer12(p.E1026Sfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |