Variant #0000016818 (NC_000012.11:g.91449224G>A, NM_007035.3:c.835C>T (KERA))
| Chromosome |
12 |
| Allele |
Unknown |
| 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.91449224G>A |
| DNA change (hg38) |
g.91055447G>A |
| Published as |
1454C>T: R279X |
| ISCN |
- |
| DB-ID |
KERA_000005 See all 2 reported entries |
| Variant remarks |
1 Saudi Arabian CNA2 family (hom) and 1 Czech CNA2 patient (com-het) |
| Reference |
PubMed: Khan et al. 2005, PubMed: Dudakova et al 2014 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| 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 |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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