Variant #0001043914 (NC_000022.10:g.43023369G>A, NM_000398.6:c.574C>T (CYB5R3))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.43023369G>A
DNA change (hg38) -
Published as CYB5R3(NM_000398.7):c.574C>T (p.(Arg192Cys))
ISCN -
DB-ID ATP5L2_000013
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) 4.0E-5 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
CYB5R3 NM_000398.6 +?/. - c.574C>T - r.(?) p.(Arg192Cys)
ATP5L2 NM_001165877.1 +?/. - c.*12609C>T - r.(=) p.(=)


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