Variant #0001012547 (NC_000022.10:g.43023631C>A, NM_000398.6:c.527G>T (CYB5R3))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.43023631C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID CYB5R3_000083
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs377689936
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-10-25 12:34:02 +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.527G>T - r.(?) p.(Gly176Val)


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