Variant #0000711824 (NC_000019.9:g.48339595G>A, NM_000554.4:c.196G>A (CRX))

Chromosome 19
Allele Parent #1
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48339595G>A
DNA change (hg38) -
Published as AF024711:196G>A (GTC?ATC) Val66Ile
ISCN -
DB-ID CRX_000001 See all 12 reported entries
Variant remarks -
Reference PubMed: Sohocki 2001
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00327 View details
Owner Julia Lopez
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2021-01-14 12:40:33 +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     
CRX NM_000554.4 -?/. 1 c.196G>A r.(?) p.(Val66Ile)


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