Variant #0001056234 (NC_000017.10:g.79214895G>A, NM_001086521.1:c.*79G>A (C17orf89))

Chromosome 17
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.79214895G>A
DNA change (hg38) -
Published as NDUFAF8(NM_001353402.1):c.308G>A (p.(Arg103Gln))
ISCN -
DB-ID chr17_010993
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C17orf89 NM_001086521.1 ?/. - c.*79G>A r.(=) p.(=)
SLC38A10 NM_138570.2 ?/. - c.*10120C>T r.(=) p.(=)


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