Primary Site >> Stomach Cancer
Gene >> UHRF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612630 |
| Start | 4929279:4929279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.211C>A |
| AA Mutation | p.Leu71Ile(p.L71I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612630 |
| Start | 4950908:4950908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1730G>A |
| AA Mutation | p.Arg577His(p.R577H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612630 |
| Start | 4944437:4944437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1292G>A |
| AA Mutation | p.Arg431Gln(p.R431Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612630 |
| Start | 4930845:4930845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.538G>C |
| AA Mutation | p.Glu180Gln(p.E180Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612630 |
| Start | 4954806:4954806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2114C>T |
| AA Mutation | p.Pro705Leu(p.P705L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612630 |
| Start | 4932923:4932923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.752C>A |
| AA Mutation | p.Thr251Lys(p.T251K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612630 |
| Start | 4947108:4947108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1414C>G |
| AA Mutation | p.His472Asp(p.H472D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612630 |
| Start | 4929411:4929411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.343G>A |
| AA Mutation | p.Ala115Thr(p.A115T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612630 |
| Start | 4947145:4947145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1451G>A |
| AA Mutation | p.Arg484Gln(p.R484Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612630 |
| Start | 4932892:4932892(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.721G>A |
| AA Mutation | p.Ala241Thr(p.A241T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612630 |
| Start | 4954668:4954668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1976C>T |
| AA Mutation | p.Ala659Val(p.A659V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612630 |
| Start | 4930719:4930719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.412A>G |
| AA Mutation | p.Asn138Asp(p.N138D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000612630 |
| Start | 4932930:4932930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.759G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000612630 |
| Start | 4954789:4954789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2097G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000612630 |
| Start | 4945872:4945872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369224803 |
| CDS Mutation | c.1317G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000612630 |
| Start | 4941585:4941585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.843G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000612630 |
| Start | 4929347:4929347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760355998 |
| CDS Mutation | c.279C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000612630 |
| Start | 4954678:4954678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376205188 |
| CDS Mutation | c.1986G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000612630 |
| Start | 4932868:4932872(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.697_701delAAGGA |
| AA Mutation | p.Lys233AlafsTer30(p.K233Afs*30) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |