Variant #0000067168 (NC_000017.10:g.40706273C>A, NC_000017.10(NM_000413.2):c.540-150C>A (HSD17B1))

Chromosome 17
Allele Both (homozygous)
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.40706273C>A
DNA change (hg38) g.42554255C>A
Published as -
ISCN -
DB-ID HSD17B1_000002 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs676387
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Carolina Lemos
Database submission license No license selected
Created by Carolina Lemos
Date created 2015-06-11 18:52:46 +02:00 (CEST)
Date last edited 2025-06-08 02:05:33 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSD17B1 NM_000413.2 ?/? 4i c.540-150C>A r.(=) p.(=)


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