Variant #0000965432 (NC_000009.11:g.35808587C>T, NM_003995.3:c.2794C>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.35808587C>T
DNA change (hg38) -
Published as NPR2(NM_003995.3):c.2794C>T (p.(Arg932Cys))
ISCN -
DB-ID HINT2_000010 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 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPAG8 NM_001039592.1 ?/. - c.*1348G>A r.(=) p.(=)
NPR2 NM_003995.3 ?/. - c.2794C>T r.(?) p.(Arg932Cys)
HINT2 NM_032593.2 ?/. - c.*4464G>A r.(=) p.(=)


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