View genomic variant #0000023493

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.53458461C>T
Published as -
GERP -
Segregation -
DB-ID HSD17B10_000001
MSCV MSCV_0023493
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 0000023493 ./. - - c.650G>A p.(Arg217Gln) - - - -
HSD17B10 00000822 NM_004493.2 0000023493 ./. - - c.677G>A p.(Arg226Gln) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000591328; RCV001843531;
Chromosome X:53458461..53458461
ClinVar Allele ID 488318
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0010327, MedGen:C3266731, OMIM:300438, Orphanet:391417, Orphanet:85295
ClinVar preferred disease name not provided|HSD10 mitochondrial disease
HGVS variant names NC 000023.10:g.53458461C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA413150543
Gene symbol:Gene id. HSD17B10:3028
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 1556894502
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