Variant #0000060837 (NC_000021.8:g.44590650C>A, NM_000394.2:c.213C>A (CRYAA))

Chromosome 21
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.44590650C>A
DNA change (hg38) g.43170540C>A
Published as -
ISCN -
DB-ID CRYAA_000015 See all 3 reported entries
Variant remarks tested in vitro in several assays
Reference PubMed: Bhagyalaxmi 2009
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2010-11-28 15:08:46 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRYAA NM_000394.2 +/. 2 c.213C>A r.(?) p.Phe71Leu


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