Variant #0001075645 (NC_000001.10:g.35250419C>T, NM_024009.2:c.56C>T (GJB3))

Chromosome 1
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.35250419C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr1_018331
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs748403541
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-28 12:03:03 +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     
GJB3 NM_024009.2 ?/. - c.56C>T r.(?) p.(Ala19Val)


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