Primary Site >> Stomach Cancer
Gene >> RECQL4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144512874:144512874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374225917 |
| CDS Mutation | c.2728G>A |
| AA Mutation | p.Val910Ile(p.V910I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144511540:144511540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3518C>T |
| AA Mutation | p.Pro1173Leu(p.P1173L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144512236:144512236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3144G>T |
| AA Mutation | p.Lys1048Asn(p.K1048N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144514977:144514977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760080894 |
| CDS Mutation | c.1579A>G |
| AA Mutation | p.Thr527Ala(p.T527A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144513002:144513002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2600C>T |
| AA Mutation | p.Ala867Val(p.A867V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144512315:144512315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs560476442 |
| CDS Mutation | c.3065G>A |
| AA Mutation | p.Arg1022His(p.R1022H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144512484:144512484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760325940 |
| CDS Mutation | c.2963A>G |
| AA Mutation | p.Asp988Gly(p.D988G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144512518:144512518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780492921 |
| CDS Mutation | c.2929G>A |
| AA Mutation | p.Asp977Asn(p.D977N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144512490:144512490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2957A>G |
| AA Mutation | p.Glu986Gly(p.E986G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144515803:144515803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs117670586 |
| CDS Mutation | c.1219G>A |
| AA Mutation | p.Glu407Lys(p.E407K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144512319:144512319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137853232 |
| CDS Mutation | c.3061C>T |
| AA Mutation | p.Arg1021Trp(p.R1021W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144512234:144512234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3146A>G |
| AA Mutation | p.Asp1049Gly(p.D1049G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144513343:144513343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372741479 |
| CDS Mutation | c.2338C>T |
| AA Mutation | p.Arg780Trp(p.R780W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144515871:144515871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376045624 |
| CDS Mutation | c.1151G>A |
| AA Mutation | p.Arg384Gln(p.R384Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144513670:144513670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2101G>A |
| AA Mutation | p.Asp701Asn(p.D701N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617875 |
| Start | 144516681:144516681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764797288 |
| CDS Mutation | c.438G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617875 |
| Start | 144515038:144515038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757280460 |
| CDS Mutation | c.1518C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000617875 |
| Start | 144512672:144512672(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2855delG |
| AA Mutation | p.Gly952AlafsTer92(p.G952Afs*92) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000617875 |
| Start | 144515847:144515847(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs754177646 |
| CDS Mutation | c.1175delG |
| AA Mutation | p.Gly392ValfsTer14(p.G392Vfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000617875 |
| Start | 144516129:144516134(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.985_990delAGGGCT |
| AA Mutation | p.Arg329_Ala330del(p.R329_A330del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |