Variant #0000016633 (NC_000017.10:g.56293641_56293783del, NC_000017.10(NM_017777.3):c.262-179_262-37del (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.56293641_56293783del |
| DNA change (hg38) |
g.58216280_58216422del |
| Published as |
262-37_179del |
| ISCN |
- |
| DB-ID |
MKS1_000019 See all 6 reported entries |
| Variant remarks |
- |
| 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 13:49:23 +01:00 (CET) |

Variant on transcripts
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