Variant #0001037105 (NC_000009.11:g.100823187C>T, NM_018946.3:c.256C>T (NANS))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.100823187C>T
DNA change (hg38) -
Published as NANS(NM_018946.4):c.256C>T (p.(Arg86*))
ISCN -
DB-ID NANS_000029
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_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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM14 NM_014788.2 +?/. - c.*26565G>A r.(=) p.(=)
NANS NM_018946.3 +?/. - c.256C>T r.(?) p.(Arg86*)


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