View genomic variant #0000015532

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.120302538C>T
Published as -
GERP -
Segregation -
DB-ID HMGCS2_000003 See all 2 reported entries
MSCV MSCV_0000073
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00023 View details
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     
HMGCS2 00000819 NM_001166107.1 0000015532 ./. - - c.560-633G>A p.(=) - - - -
HMGCS2 00000820 NM_005518.3 0000015532 ./. - - c.634G>A p.(Gly212Arg) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000009841; RCV000498667;
Chromosome 1:120302538..120302538
Allele frequencies from ExAC 0.00023
ClinVar Allele ID 24298
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0011614, MedGen:C2751532, OMIM:605911, Orphanet:35701
ClinVar preferred disease name not provided|3-hydroxy-3-methylglutaryl-CoA synthase deficiency
HGVS variant names NC 000001.10:g.120302538C>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:CA120256|OMIM:600234.0003|UniProtKB:P54868#VAR 032759
Gene symbol:Gene id. HMGCS2:3158
Molecular consequence SO:0001583|missense variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 137852638
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