Variant #0001090007 (NC_000022.10:g.43011384A>G, NR_029422.1:c.135A>G (RNU12))

Chromosome 22
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.43011384A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr22_003373
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs369601453
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-09-28 15:10:02 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNU12 NR_029422.1 ?/. - c.135A>G r.(?) p.(None)


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