Variant #0000681561 (NC_000020.10:g.13782223C>T, NM_024120.4:c.611C>T (NDUFAF5))

Chromosome 20
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.13782223C>T
DNA change (hg38) -
Published as NDUFAF5(NM_001352407.1):c.50C>T (p.A17V), NDUFAF5(NM_001352407.2):c.50C>T (p.A17V)
ISCN -
DB-ID NDUFAF5_000012 See all 2 reported entries
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFAF5 NM_024120.4 ?/. - c.611C>T r.(?) p.(Ala204Val)


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