Variant #0000861653 (NC_000009.11:g.35793924C>T, NM_003995.3:c.697C>T (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.35793924C>T
DNA change (hg38) -
Published as NPR2(NM_003995.3):c.697C>T (p.(Leu233=)), NPR2(NM_003995.4):c.697C>T (p.L233=)
ISCN -
DB-ID NPR2_000103 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) 0.00038 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPR2 NM_003995.3 -?/. - c.697C>T r.(?) p.(Leu233=)


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