Variant #0000066398 (NC_000012.11:g.91449739A>C, NM_007035.3:c.320T>G (KERA))

Chromosome 12
Allele Unknown
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.91449739A>C
DNA change (hg38) g.91055962A>C
Published as -
ISCN -
DB-ID KERA_000008
Variant remarks 1 Czech patient (com-het) with CNA2
Reference 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) 0 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2015-05-08 20:42:08 +02:00 (CEST)
Date last edited 2017-05-05 18:33:04 +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.320T>G r.(?) p.(Ile107Arg)


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