Variant #0001057338 (NC_000023.10:g.53458547_53458550dup, NC_000023.10(NM_004493.2):c.596-6_596-3dup (HSD17B10))

Chromosome X
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.53458547_53458550dup
DNA change (hg38) -
Published as HSD17B10(NM_004493.3):c.596-6_596-3dup
ISCN -
DB-ID HSD17B10_000032
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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     
RIBC1 NM_001031745.3 ?/. - c.*611_*614dup r.(=) p.(=)
HSD17B10 NM_004493.2 ?/. - c.596-6_596-3dup r.spl? p.?


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