Variant #0001035759 (NC_000006.11:g.41037832G>A, NM_002505.4:c.-3053G>A (NFYA))

Chromosome 6
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.41037832G>A
DNA change (hg38) -
Published as OARD1(NM_001329686.2):c.226C>T (p.(Arg76*))
ISCN -
DB-ID NFYA_000001
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) 0.00289 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NFYA NM_002505.4 ?/. - c.-3053G>A r.(?) p.(=)
OARD1 NM_145063.2 ?/. - c.226C>T r.(?) p.(Arg76*)


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