Variant #0000329077 (NC_000022.10:g.43040474G>A, NC_000022.10(NM_000398.6):c.21+4827C>T (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.43040474G>A
DNA change (hg38) g.42644468G>A
Published as CYB5R3(NM_000398.6):c.21+4827C>T (p.(=))
ISCN -
DB-ID CYB5R3_000077
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) 0.0023 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.21+4827C>T - r.(=) p.(=)
ATP5L2 NM_001165877.1 ?/. - c.-4194C>T - r.(?) p.(=)


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