Variant #0001035262 (NC_000005.9:g.60448763del, NM_174889.4:c.491del (NDUFAF2))

Chromosome 5
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.60448763del
DNA change (hg38) -
Published as NDUFAF2(NM_174889.5):c.491del (p.(Gly164AlafsTer25))
ISCN -
DB-ID NDUFAF2_000008
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 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     
SMIM15 NM_001048249.3 ?/. - c.*7012del r.(?) p.(=)
NDUFAF2 NM_174889.4 ?/. - c.491del r.(?) p.(Gly164Alafs*25)


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