Variant #0001074723 (NC_000023.10:g.49837127T>G, NC_000023.10(NM_001127898.3):c.316-17T>G (CLCN5))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.49837127T>G
DNA change (hg38) g.50072472T>G
Published as -
ISCN -
DB-ID CLCN5_000107 See all 3 reported entries
Variant remarks effect on RNA studied using mini-gene splicing assay
Reference PubMed: Inoue 2020
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0063 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 2026-04-24 19:32:09 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN5 NM_001127898.3 -?/. 2i c.316-17T>G r.315_316= p.=


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