Variant #0000016820 (NC_000012.11:g.91445157del, NM_007035.3:c.1026del (KERA))
| Chromosome |
12 |
| 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.91445157del |
| DNA change (hg38) |
g.91051380del |
| Published as |
1634delC/ 1033delC (at 342): adds 15 amino acids before premature truncation |
| ISCN |
- |
| DB-ID |
KERA_000007 |
| Variant remarks |
5 Arabian CNA2 families (hom) |
| Reference |
PubMed: Khan et al. 2006 |
| 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 |
2012-12-10 17:19:49 +01:00 (CET) |
| Date last edited |
2020-07-02 17:41:51 +02:00 (CEST) |

Variant on transcripts
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