Variant #0001055692 (NC_000016.9:g.84188352C>G, NM_178452.4:c.523C>G (DNAAF1))

Chromosome 16
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.84188352C>G
DNA change (hg38) -
Published as DNAAF1(NM_178452.6):c.523C>G (p.(Leu175Val))
ISCN -
DB-ID DNAAF1_000074
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) 3.0E-5 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAF1C NM_005679.3 ?/. - c.*24195G>C r.(=) p.(=)
DNAAF1 NM_178452.4 ?/. - c.523C>G r.(?) p.(Leu175Val)


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