View genomic variant #0000023499

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.53459295T>C
Published as -
GERP -
Segregation -
DB-ID HSD17B10_000007
MSCV MSCV_0023499
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
HSD17B10 00000821 NM_001037811.2 0000023499 ./. - - c.257A>G p.(Asp86Gly) - - - -
HSD17B10 00000822 NM_004493.2 0000023499 ./. - - c.257A>G p.(Asp86Gly) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000133540;
Chromosome X:53459295..53459295
ClinVar Allele ID 153772
Disease database name and identifier MONDO:MONDO:0010327, MedGen:C3266731, OMIM:300438, Orphanet:391417, Orphanet:85295
ClinVar preferred disease name HSD10 mitochondrial disease
HGVS variant names NC 000023.10:g.53459295T>C
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA170593|OMIM:300256.0006
Gene symbol:Gene id. HSD17B10:3028
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 587777651
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None