Variant #0000929611 (NC_000009.11:g.35805562T>G, NM_003995.3:c.1942T>G (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.35805562T>G
DNA change (hg38) -
Published as NPR2(NM_003995.4):c.1942T>G (p.S648A)
ISCN -
DB-ID NPR2_000150 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +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.*4373A>C r.(=) p.(=)
NPR2 NM_003995.3 ?/. - c.1942T>G r.(?) p.(Ser648Ala)


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