Variant #0000572244 (NC_000022.10:g.43032737C>T, NM_000398.6:c.137G>A (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.43032737C>T
DNA change (hg38) g.42636731C>T
Published as CYB5R3(NM_001129819.2):c.68G>A (p.R23Q)
ISCN -
DB-ID ATP5L2_000004
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
CYB5R3 NM_000398.6 -?/. - c.137G>A - r.(?) p.(Arg46Gln)
ATP5L2 NM_001165877.1 -?/. - c.*3241G>A - r.(=) p.(=)


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