Variant #0001003704 (NC_000017.10:g.74524651T>G, NM_001077620.2:c.-11573T>G (PRCD))

Chromosome 17
Allele Unknown
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.74524651T>G
DNA change (hg38) -
Published as CYGB(NM_134268.4):c.*9A>C (p.?)
ISCN -
DB-ID CYGB_000003
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.44695 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRCD NM_001077620.2 -?/. - c.-11573T>G r.(?) p.(=)
CYGB NM_134268.4 -?/. - c.*9A>C r.(=) p.(=)


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