Variant #0000535580 (NC_000009.11:g.100840588T>C, NM_018946.3:c.562T>C (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.100840588T>C
DNA change (hg38) g.98078306T>C
Published as NANS(NM_018946.4):c.562T>C (p.(Tyr188His))
ISCN -
DB-ID NANS_000004 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) 0 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM14 NM_014788.2 +/. - c.*9164A>G r.(=) p.(=)
NANS NM_018946.3 +/. - c.562T>C r.(?) p.(Tyr188His)


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