Variant #0000850895 (NC_000005.9:g.32784939C>T, NM_001204375.1:c.1464C>T (NPR3))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32784939C>T
DNA change (hg38) -
Published as NPR3(NM_001204375.2):c.1464C>T (p.(Val488=), p.V488=)
ISCN -
DB-ID NPR3_000029 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) 0.00127 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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPR3 NM_001204375.1 -/. - c.1464C>T r.(?) p.(Val488=)


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