Variant #0000978709 (NC_000009.11:g.35809510C>G, NM_003995.3:c.*68C>G (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.35809510C>G
DNA change (hg38) -
Published as NPR2(NM_003995.3):c.*68C>G (p.(=))
ISCN -
DB-ID HINT2_000029
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 2024-04-19 20:27:30 +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.*425G>C r.(=) p.(=)
NPR2 NM_003995.3 -?/. - c.*68C>G r.(=) p.(=)
HINT2 NM_032593.2 -?/. - c.*3541G>C r.(=) p.(=)


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