Variant #0000572243 (NC_000022.10:g.43032729C>G, NM_000398.6:c.145G>C (CYB5R3))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.43032729C>G
DNA change (hg38) g.42636723C>G
Published as CYB5R3(NM_001129819.2):c.76G>C (p.D26H)
ISCN -
DB-ID ATP5L2_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) 0.00062 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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
CYB5R3 NM_000398.6 ?/. - c.145G>C - r.(?) p.(Asp49His)
ATP5L2 NM_001165877.1 ?/. - c.*3249G>C - r.(=) p.(=)


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