Variant #0000535579 (NC_000009.11:g.100840478G>T, NM_018946.3:c.452G>T (NANS))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.100840478G>T
DNA change (hg38) g.98078196G>T
Published as NANS(NM_018946.3):c.452G>T (p.(Arg151Leu))
ISCN -
DB-ID NANS_000003
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) 0.00012 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM14 NM_014788.2 +/. - c.*9274C>A r.(=) p.(=)
NANS NM_018946.3 +/. - c.452G>T r.(?) p.(Arg151Leu)


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