Variant #0000925050 (NC_000009.11:g.35806217C>T, NM_003995.3:c.2359C>T (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.35806217C>T
DNA change (hg38) -
Published as NPR2(NM_003995.3):c.2359C>T (p.(Arg787Trp))
ISCN -
DB-ID NPR2_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) 0.00028 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 2023-04-16 21:50:28 +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     
SPAG8 NM_001039592.1 ?/. - c.*3718G>A r.(=) p.(=)
NPR2 NM_003995.3 ?/. - c.2359C>T r.(?) p.(Arg787Trp)


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