Variant #0000016618 (NC_000017.10:g.56283916_56283944del, NC_000017.10(NM_017777.3):c.1408-34_1408-6del (MKS1))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.56283916_56283944del |
| DNA change (hg38) |
g.58206555_58206583del |
| Published as |
Finmajor: IVS15-7_35 del: Exon 16 skipping: P470fsX562; c.1408-35_1408-7del29: p.G470GfsX93 |
| ISCN |
- |
| DB-ID |
MKS1_000004 See all 63 reported entries |
| Variant remarks |
Finmajor, RNA exon 16 skipping; 70% of the Finnish MKS patients (most hom). Also common in non-Finnish MKS patients: observed in Afrikan-American, American, Dutch, English, French, German, Italian, Irish |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-12-04 16:05:24 +01:00 (CET) |
| Date last edited |
2023-11-29 15:13:17 +01:00 (CET) |

Variant on transcripts
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