Variant #0000711823 (NC_000019.9:g.48337728C>T, NM_000554.4:c.28C>T (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.48337728C>T
DNA change (hg38) -
Published as AF024711:28C>T (CAC?GAC) His10Asp
ISCN -
DB-ID CRX_000039
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) Retrieve
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.28C>T r.(?) p.(His10Tyr)


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