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 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.835C>T r.(835c>u) p.(Arg279*)


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