Primary Site >> Stomach Cancer
Gene >> SLFN12L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260908 |
| Start | 35479806:35479806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763566782 |
| CDS Mutation | c.404C>T |
| AA Mutation | p.Pro135Leu(p.P135L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260908 |
| Start | 35475092:35475092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766547706 |
| CDS Mutation | c.1598C>T |
| AA Mutation | p.Ser533Leu(p.S533L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260908 |
| Start | 35475035:35475035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1655T>C |
| AA Mutation | p.Leu552Ser(p.L552S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260908 |
| Start | 35479486:35479486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.724C>G |
| AA Mutation | p.Gln242Glu(p.Q242E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260908 |
| Start | 35475274:35475274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1416A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260908 |
| Start | 35479345:35479345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.865C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260908 |
| Start | 35475163:35475163(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1527delA |
| AA Mutation | p.Val510CysfsTer4(p.V510Cfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260908 |
| Start | 35479600:35479601(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs774797739 |
| CDS Mutation | c.609dupT |
| AA Mutation | p.Asn204Ter(p.N204*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000260908 |
| Start | 35479864:35479926(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.284_346delTAGATTTGGAAAATTCTTTTAGTAACATGCTGCCATTTGTTCCTAATTTCCTGGACTTCATGC |
| AA Mutation | p.Leu95_Met115del(p.L95_M115del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |