Variant #0000658973 (NC_000022.10:g.43019891C>T, NM_000398.6:c.637G>A (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.43019891C>T
DNA change (hg38) g.42623885C>T
Published as CYB5R3(NM_001129819.2):c.568G>A (p.E190K)
ISCN -
DB-ID CYB5R3_000044 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) 0.00025 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 2020-03-23 16:13:27 +01:00 (CET)
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.637G>A - r.(?) p.(Glu213Lys)
ATP5L2 NM_001165877.1 ?/. - c.*16087G>A - r.(=) p.(=)


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