Variant #0001084321 (NC_000016.9:g.78142364A>G, NM_016373.2:c.152A>G (WWOX))

Chromosome 16
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.78142364A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr16_007737
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2032292763
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 2026-09-04 16:30:02 +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     
WWOX NM_016373.2 ?/. - c.152A>G r.(?) p.(Lys51Arg)


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