Variant #0000978700 (NC_000009.11:g.35792495G>A, NM_003995.3:c.90G>A (NPR2))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.35792495G>A
DNA change (hg38) -
Published as NPR2(NM_003995.3):c.90G>A (p.(Val30=)), NPR2(NM_003995.4):c.90G>A (p.V30=)
ISCN -
DB-ID NPR2_000080 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) 0.00041 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-04-19 20:27:30 +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     
NPR2 NM_003995.3 -?/. - c.90G>A r.(?) p.(Val30=)


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