Variant #0001068189 (NC_000016.9:g.30997024_30997025del, NM_025193.3:c.45_46del (HSD3B7))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.30997024_30997025del
DNA change (hg38) -
Published as -
ISCN -
DB-ID HSD3B7_000002 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs786200876
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 2026-02-10 15:56:01 +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     
HSD3B7 NM_025193.3 +/. - c.45_46del r.(?) p.(Gly17LeufsTer26)


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