Variant #0000880000 (NC_000009.11:g.99060700C>T, NM_000197.1:c.199G>A (HSD17B3))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.99060700C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID HSD17B3_000030
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1017003712
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-09-30 09:53:01 +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     
HSD17B3 NM_000197.1 +?/. - c.199G>A r.(?) p.(Glu67Lys)


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