View genomic variant #0000015542

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.120311380G>C
Published as -
GERP -
Segregation -
DB-ID HMGCS2_000011
MSCV MSCV_0015542
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     
HMGCS2 00000819 NM_001166107.1 0000015542 ./. - - c.88C>G p.(Pro30Ala) - - - -
HMGCS2 00000820 NM_005518.3 0000015542 ./. - - c.88C>G p.(Pro30Ala) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000381823; RCV002519380;
Chromosome 1:120311380..120311380
Allele frequencies from TGP 0.00020
ClinVar Allele ID 276948
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MONDO:MONDO:0011614, MedGen:C2751532, OMIM:605911, Orphanet:35701
ClinVar preferred disease name Inborn genetic diseases|3-hydroxy-3-methylglutaryl-CoA synthase deficiency
HGVS variant names NC 000001.10:g.120311380G>C
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1037984
Gene symbol:Gene id. HMGCS2:3158|LOC122094910:122094910
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 202069145
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