Variant #0000953764 (NC_000002.11:g.208994281A>C, NM_020989.3:c.136T>G (CRYGC))

Chromosome 2
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.208994281A>C
DNA change (hg38) g.208129557A>C
Published as -
ISCN -
DB-ID CRYGC_000031 See all 2 reported entries
Variant remarks functional analysis shows aggregate formation at physiological temperature, altered thermal unfolding, less thermal stability with increasing concentrations and a concentration-dependent rescue by αA-crystallin
Reference PubMed: Fu 2021
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 2023-12-18 16:55:14 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRYGC NM_020989.3 +/. - c.136T>G - p.Tyr46Asp


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