Variant #0000895783 (NC_000022.10:g.43015795C>T, NM_000398.6:c.890G>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.43015795C>T
DNA change (hg38) -
Published as CYB5R3(NM_000398.6):c.890G>A (p.(Arg297His)), CYB5R3(NM_000398.7):c.890G>A (p.R297H)
ISCN -
DB-ID ATP5L2_000007 See all 2 reported entries
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) 0.00211 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
CYB5R3 NM_000398.6 -?/. - c.890G>A - r.(?) p.(Arg297His)
ATP5L2 NM_001165877.1 -?/. - c.*20183G>A - r.(=) p.(=)
POLDIP3 NM_032311.3 -?/. - c.-4932G>A - r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.