Variant #0000925051 (NC_000009.11:g.35809239A>G, NM_003995.3:c.3073A>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.35809239A>G
DNA change (hg38) -
Published as NPR2(NM_003995.3):c.3073A>G (p.(Met1025Val))
ISCN -
DB-ID HINT2_000023
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_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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPAG8 NM_001039592.1 ?/. - c.*696T>C r.(=) p.(=)
NPR2 NM_003995.3 ?/. - c.3073A>G r.(?) p.(Met1025Val)
HINT2 NM_032593.2 ?/. - c.*3812T>C r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.