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 InternationalCreative Commons License
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KERA NM_007035.3 +?/+? 2 c.740A>G r.(740a>g) p.(Asn247Ser)


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