Variant #0000997879 (NC_000009.11:g.35805514G>A, NM_003995.3:c.1894G>A (NPR2))

Chromosome 9
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.35805514G>A
DNA change (hg38) -
Published as NPR2(NM_003995.3):c.1894G>A (p.(Ala632Thr))
ISCN -
DB-ID NPR2_000177
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPAG8 NM_001039592.1 ?/. - c.*4421C>T r.(=) p.(=)
NPR2 NM_003995.3 ?/. - c.1894G>A r.(?) p.(Ala632Thr)


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