Variant #0000016817 (NC_000012.11:g.91449319T>C, NM_007035.3:c.740A>G (KERA))
| Chromosome |
12 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.91449319T>C |
| DNA change (hg38) |
g.91055542T>C |
| Published as |
AAC>AGC at codon 247: Asn247Ser |
| ISCN |
- |
| DB-ID |
KERA_000004 See all 4 reported entries |
| Variant remarks |
Finnish major KERA mutation: 46 Finnish CNA2 patients (hom). Also 1 British CNA2 family (hom). |
| Reference |
PubMed: Pellegata et al. 2000, PubMed: Liskova et al. 2007 |
| ClinVar ID |
- |
| dbSNP ID |
rs121917858 |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
2/807 FIN (het) |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00068 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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