Primary Site >> Stomach Cancer
Gene >> RIF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151462995:151462995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3475G>A |
| AA Mutation | p.Asp1159Asn(p.D1159N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151463998:151463998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4478C>G |
| AA Mutation | p.Thr1493Ser(p.T1493S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151440122:151440122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1642A>C |
| AA Mutation | p.Thr548Pro(p.T548P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151451625:151451625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2264G>T |
| AA Mutation | p.Arg755Ile(p.R755I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151463898:151463898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4378G>T |
| AA Mutation | p.Asp1460Tyr(p.D1460Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151461205:151461205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3143A>G |
| AA Mutation | p.Asp1048Gly(p.D1048G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151435509:151435509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1124C>T |
| AA Mutation | p.Ala375Val(p.A375V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151465079:151465079(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5559G>T |
| AA Mutation | p.Glu1853Asp(p.E1853D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151465510:151465510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5990G>A |
| AA Mutation | p.Gly1997Glu(p.G1997E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151473989:151473989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7121T>C |
| AA Mutation | p.Ile2374Thr(p.I2374T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151468063:151468063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752900757 |
| CDS Mutation | c.6664C>T |
| AA Mutation | p.Arg2222Trp(p.R2222W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151465034:151465034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5514T>G |
| AA Mutation | p.Ile1838Met(p.I1838M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151468117:151468117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6718G>A |
| AA Mutation | p.Val2240Ile(p.V2240I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151463166:151463166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3646A>T |
| AA Mutation | p.Ser1216Cys(p.S1216C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151416624:151416624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.344T>C |
| AA Mutation | p.Val115Ala(p.V115A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151475009:151475009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7357A>G |
| AA Mutation | p.Asn2453Asp(p.N2453D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151463817:151463817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4297G>T |
| AA Mutation | p.Asp1433Tyr(p.D1433Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243326 |
| Start | 151464704:151464704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5184A>T |
| AA Mutation | p.Arg1728Ser(p.R1728S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243326 |
| Start | 151416857:151416857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149505451 |
| CDS Mutation | c.459G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243326 |
| Start | 151463534:151463534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4014G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243326 |
| Start | 151437314:151437314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1446T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243326 |
| Start | 151428882:151428882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.885T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243326 |
| Start | 151437296:151437296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1428T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243326 |
| Start | 151463777:151463777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4257G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000243326 |
| Start | 151464027:151464027(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.4514delA |
| AA Mutation | p.Lys1505ArgfsTer18(p.K1505Rfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000243326 |
| Start | 151469831:151469831(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.7067delA |
| AA Mutation | p.Lys2356ArgfsTer11(p.K2356Rfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000243326 |
| Start | 151464475:151464475(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4961delA |
| AA Mutation | p.Asn1654MetfsTer21(p.N1654Mfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000243326 |
| Start | 151428865:151428865(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.872delA |
| AA Mutation | p.Lys291ArgfsTer2(p.K291Rfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000243326 |
| Start | 151437276:151437276(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1414delT |
| AA Mutation | p.Ser472ProfsTer34(p.S472Pfs*34) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000243326 |
| Start | 151463039:151463039(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3525delA |
| AA Mutation | p.Ala1176LeufsTer2(p.A1176Lfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000243326 |
| Start | 151466078:151466078(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6562delA |
| AA Mutation | p.Arg2188AspfsTer49(p.R2188Dfs*49) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000243326 |
| Start | 151464730:151464730(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.5214delA |
| AA Mutation | p.Lys1738AsnfsTer12(p.K1738Nfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000243326 |
| Start | 151464748:151464749(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5230_5231delAA |
| AA Mutation | p.Lys1744ValfsTer11(p.K1744Vfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000243326 |
| Start | 151445420:151445420(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2074delT |
| AA Mutation | p.Ser692GlnfsTer10(p.S692Qfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000243326 |
| Start | 151443707:151443707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1984C>T |
| AA Mutation | p.Gln662Ter(p.Q662*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000243326 |
| Start | 151464648:151464649(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.5134dupA |
| AA Mutation | p.Thr1712AsnfsTer6(p.T1712Nfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000243326 |
| Start | 151468127:151468129(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs772018521 |
| CDS Mutation | c.6730_6732delCCT |
| AA Mutation | p.Pro2244del(p.P2244del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |