Variant #0001006856 (NC_000023.10:g.53457915G>C, NM_004493.2:c.*437C>G (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.53457915G>C
DNA change (hg38) -
Published as RIBC1(NM_001031745.3):c.1119G>C (p.(Gln373His))
ISCN -
DB-ID HSD17B10_000029
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 2024-08-28 13:16:32 +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     
RIBC1 NM_001031745.3 -?/. - c.1119G>C r.(?) p.(Gln373His)
HSD17B10 NM_004493.2 -?/. - c.*437C>G r.(=) p.(=)


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