Variant #0000016457 (NC_000004.11:g.(15569410_15570915)_(15581795_15587779)del, NC_000004.11(NM_001080522.2):c.(3398+1_3399-1)_(3975+1_3976-1)del (CC2D2A))
| Chromosome |
4 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(15569410_15570915)_(15581795_15587779)del |
| DNA change (hg38) |
- |
| Published as |
deletion ex28-31 |
| ISCN |
- |
| DB-ID |
CC2D2A_000015 See all 5 reported entries |
| Variant remarks |
1 Algerian MKS6 family (hom) |
| Reference |
PubMed: Mougou-Zerelli et al. 2009 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| 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 |
2012-11-15 14:05:58 +01:00 (CET) |
| Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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