Variant #0000082502 (NC_000015.9:g.34635241C>G, NM_018648.3:c.34G>C (NOP10))

Chromosome 15
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.34635241C>G
DNA change (hg38) g.34343040C>G
Published as -
ISCN -
DB-ID NOP10_000002 See all 2 reported entries
Variant remarks -
Reference PubMed: Walne 2007, Journal: Walne 2007
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 1/171 families
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01001 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2015-10-26 19:29:19 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NOP10 NM_018648.3 -/. 1 c.34G>C r.(?) p.(Asp12His)


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