View genomic variant #0000023498

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.53459058G>C
Published as -
GERP -
Segregation -
DB-ID HSD17B10_000006
MSCV MSCV_0023498
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 0000023498 ./. - - c.364C>G p.(Leu122Val) - - - -
HSD17B10 00000822 NM_004493.2 0000023498 ./. - - c.364C>G p.(Leu122Val) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000012196; RCV002307362;
Chromosome X:53459058..53459058
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 26482
Disease database name and identifier MedGen:CN169374|MONDO:MONDO:0010327, MedGen:C3266731, OMIM:300438, Orphanet:391417, Orphanet:85295
ClinVar preferred disease name not specified|HSD10 mitochondrial disease
HGVS variant names NC 000023.10:g.53459058G>C
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA121451|OMIM:300256.0002|UniProtKB:Q99714#VAR 015987
Gene symbol:Gene id. HSD17B10:3028
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 28935476
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