Primary Site >> Stomach Cancer
Gene >> CDC5L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371477 |
| Start | 44408513:44408513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748222402 |
| CDS Mutation | c.973G>A |
| AA Mutation | p.Glu325Lys(p.E325K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371477 |
| Start | 44392795:44392795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.278C>T |
| AA Mutation | p.Ala93Val(p.A93V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371477 |
| Start | 44403972:44403972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.703C>G |
| AA Mutation | p.Leu235Val(p.L235V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371477 |
| Start | 44424432:44424432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773109480 |
| CDS Mutation | c.1418G>A |
| AA Mutation | p.Arg473Gln(p.R473Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371477 |
| Start | 44408565:44408565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376004864 |
| CDS Mutation | c.1025A>G |
| AA Mutation | p.Asn342Ser(p.N342S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371477 |
| Start | 44392819:44392819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.302A>C |
| AA Mutation | p.Glu101Ala(p.E101A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371477 |
| Start | 44403850:44403850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.581C>T |
| AA Mutation | p.Ala194Val(p.A194V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371477 |
| Start | 44408582:44408582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1042G>A |
| AA Mutation | p.Val348Ile(p.V348I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371477 |
| Start | 44408509:44408509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.969T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371477 |
| Start | 44424478:44424478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1464T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371477 |
| Start | 44445853:44445853(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2293delC |
| AA Mutation | p.Arg765GlyfsTer3(p.R765Gfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371477 |
| Start | 44403919:44403919(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.656delA |
| AA Mutation | p.Lys219SerfsTer24(p.K219Sfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371477 |
| Start | 44403826:44403826(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.562delA |
| AA Mutation | p.Arg188GlufsTer9(p.R188Efs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000371477 |
| Start | 44408600:44408600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148664123 |
| CDS Mutation | c.1060C>T |
| AA Mutation | p.Arg354Ter(p.R354*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371477 |
| Start | 44406343:44406344(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.786dupA |
| AA Mutation | p.Asp263ArgfsTer12(p.D263Rfs*12) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371477 |
| Start | 44406365:44406366(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.805dupA |
| AA Mutation | p.Arg269LysfsTer6(p.R269Kfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |