Variant #0000856192 (NC_000022.10:g.43027385G>A, NM_000398.6:c.225C>T (CYB5R3))

Chromosome 22
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.43027385G>A
DNA change (hg38) -
Published as CYB5R3(NM_001129819.2):c.156C>T (p.V52=)
ISCN -
DB-ID ATP5L2_000010
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +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.225C>T - r.(?) p.(Val75=)
ATP5L2 NM_001165877.1 -?/. - c.*8593C>T - r.(=) p.(=)


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