Variant #0000016819 (NC_000012.11:g.91445245G>A, NM_007035.3:c.937C>T (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.91445245G>A
DNA change (hg38) g.91051468G>A
Published as 937C>T: R313X; 945C>T: R313X
ISCN -
DB-ID KERA_000006 See all 2 reported entries
Variant remarks 8 Arabian CNA2 families (hom)
Reference PubMed: Khan et al. 2004, PubMed: Khan et al. 2006
ClinVar ID -
dbSNP ID rs121917863
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-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 +/+ 3 c.937C>T r.(937c>u) p.(Arg313*)


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