Variant #0000915740 (NC_000023.10:g.53459267C>T, NM_004493.2:c.285G>A (HSD17B10))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.53459267C>T
DNA change (hg38) -
Published as HSD17B10(NM_004493.2):c.285G>A (p.A95=)
ISCN -
DB-ID HSD17B10_000027
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) 2.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +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.*1331C>T r.(=) p.(=)
HSD17B10 NM_004493.2 -?/. - c.285G>A r.(?) p.(Ala95=)


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