Variant #0001006857 (NC_000023.10:g.53459223G>A, NM_004493.2:c.329C>T (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.53459223G>A
DNA change (hg38) -
Published as HSD17B10(NM_004493.3):c.329C>T (p.T110I)
ISCN -
DB-ID HSD17B10_000030
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RIBC1 NM_001031745.3 ?/. - c.*1287G>A r.(=) p.(=)
HSD17B10 NM_004493.2 ?/. - c.329C>T r.(?) p.(Thr110Ile)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.