Primary Site >> Stomach Cancer
Gene >> SCEL
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000349847 |
| Start | 77602066:77602066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.919A>G |
| AA Mutation | p.Ile307Val(p.I307V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349847 |
| Start | 77604363:77604363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1105G>T |
| AA Mutation | p.Asp369Tyr(p.D369Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349847 |
| Start | 77613906:77613906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1402C>A |
| AA Mutation | p.Leu468Ile(p.L468I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349847 |
| Start | 77569381:77569381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143114727 |
| CDS Mutation | c.409G>A |
| AA Mutation | p.Gly137Ser(p.G137S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349847 |
| Start | 77555879:77555879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4T>C |
| AA Mutation | p.Ser2Pro(p.S2P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349847 |
| Start | 77617815:77617815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762819731 |
| CDS Mutation | c.1524T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349847 |
| Start | 77559819:77559819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.177T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000349847 |
| Start | 77604356:77604356(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs752946345 |
| CDS Mutation | c.1104delA |
| AA Mutation | p.Asp369ThrfsTer28(p.D369Tfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000349847 |
| Start | 77640784:77640785(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1947_1947+1insT |
| AA Mutation | p.Cys650LeufsTer2(p.C650Lfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000349847 |
| Start | 77591462:77591462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.692+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000349847 |
| Start | 77556594:77556594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.44-2A>G |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | inframe_insertion;splice_region_variant |
| Transcription ID | ENST00000349847 |
| Start | 77555918:77555919(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.43_43+1insAGATGAAGAGCACCACTCAGGGAACCACAC |
| AA Mutation | p.Thr24_Arg25insGlnMetLysSerThrThrGlnGlyThrThr(p.T24_R25insQMKSTTQGTT) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | inframe_insertion;splice_region_variant |
| Transcription ID | ENST00000349847 |
| Start | 77634450:77634451(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1763_1763+1insTAAATCACCCAAGGATGGATATCAGGA |
| AA Mutation | p.Gln596_Glu597insAspLysSerProLysAspGlyTyrGln(p.Q596_E597insDKSPKDGYQ) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |