Variant #0000984292 (NC_000022.10:g.43027396C>T, NM_000398.6:c.214G>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.43027396C>T
DNA change (hg38) -
Published as CYB5R3(NM_000398.7):c.214G>A (p.(Gly72Ser))
ISCN -
DB-ID ATP5L2_000012
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
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.214G>A - r.(?) p.(Gly72Ser)
ATP5L2 NM_001165877.1 ?/. - c.*8582G>A - r.(=) p.(=)


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