Primary Site >> Stomach Cancer
Gene >> SLFN5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299977 |
| Start | 35265356:35265356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2144C>T |
| AA Mutation | p.Ala715Val(p.A715V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299977 |
| Start | 35258923:35258923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.233T>C |
| AA Mutation | p.Val78Ala(p.V78A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299977 |
| Start | 35259601:35259601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149363506 |
| CDS Mutation | c.911C>T |
| AA Mutation | p.Ala304Val(p.A304V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299977 |
| Start | 35264277:35264277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1233G>A |
| AA Mutation | p.Met411Ile(p.M411I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299977 |
| Start | 35259158:35259158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.468G>T |
| AA Mutation | p.Gln156His(p.Q156H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299977 |
| Start | 35259157:35259157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.467A>C |
| AA Mutation | p.Gln156Pro(p.Q156P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299977 |
| Start | 35258979:35258979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.289A>T |
| AA Mutation | p.Ile97Phe(p.I97F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299977 |
| Start | 35264797:35264797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1753A>C |
| AA Mutation | p.Thr585Pro(p.T585P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299977 |
| Start | 35259252:35259252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.562A>G |
| AA Mutation | p.Asn188Asp(p.N188D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299977 |
| Start | 35264873:35264873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1829G>A |
| AA Mutation | p.Cys610Tyr(p.C610Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299977 |
| Start | 35259010:35259010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.320G>A |
| AA Mutation | p.Gly107Asp(p.G107D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299977 |
| Start | 35259228:35259228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139273106 |
| CDS Mutation | c.538C>T |
| AA Mutation | p.Arg180Trp(p.R180W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000299977 |
| Start | 35261094:35261094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1136C>T |
| AA Mutation | p.Pro379Leu(p.P379L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299977 |
| Start | 35259573:35259573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766152812 |
| CDS Mutation | c.883G>A |
| AA Mutation | p.Ala295Thr(p.A295T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299977 |
| Start | 35264279:35264279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs568188480 |
| CDS Mutation | c.1235G>A |
| AA Mutation | p.Arg412His(p.R412H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299977 |
| Start | 35259482:35259482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.792C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299977 |
| Start | 35265723:35265723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148974561 |
| CDS Mutation | c.2511C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000299977 |
| Start | 35264516:35264516(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1476delC |
| AA Mutation | p.Leu493TrpfsTer5(p.L493Wfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000299977 |
| Start | 35265300:35265300(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2093delC |
| AA Mutation | p.Pro698LeufsTer21(p.P698Lfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000299977 |
| Start | 35265082:35265082(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1874delA |
| AA Mutation | p.Asn625ThrfsTer6(p.N625Tfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000299977 |
| Start | 35265299:35265300(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs745817019 |
| CDS Mutation | c.2093dupC |
| AA Mutation | p.Pro699SerfsTer22(p.P699Sfs*22) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |