Variant #0000082508 (NC_000015.9:g.34635029G>T, NC_000015.9(NM_018648.3):c.54+192C>A (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.34635029G>T
DNA change (hg38) g.34342828G>T
Published as IVS1+192C>A
ISCN -
DB-ID NOP10_000008
Variant remarks -
Reference PubMed: Walne 2007, Journal: Walne 2007
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 0.31
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 19:39:03 +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 -/. 1i c.54+192C>A r.(?) p.(=)


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