View genomic variant #0000000075

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.120306854T>C
Published as -
GERP 5.040
Segregation -
DB-ID HMGCS2_000005 See all 2 reported entries
MSCV MSCV_0000075
dbSNP ID rs137852640
Frequency -
Sources ; clinVar; Ensembl;
Reference 12647205
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 0000000075 +/+ - 2/10 c.500A>G p.(Tyr167Cys) probably_damaging(1) missense_variant - deleterious(0)
HMGCS2 00000820 NM_005518.3 0000000075 +/+ - 2/10 c.500A>G p.(Tyr167Cys) probably_damaging(1) missense_variant - deleterious(0)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000009844;
Chromosome 1:120306854..120306854
ClinVar Allele ID 24301
Disease database name and identifier MONDO:MONDO:0011614, MedGen:C2751532, OMIM:605911, Orphanet:35701
ClinVar preferred disease name 3-hydroxy-3-methylglutaryl-CoA synthase deficiency
HGVS variant names NC 000001.10:g.120306854T>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:CA120266|OMIM:600234.0006|UniProtKB:P54868#VAR 032758
Gene symbol:Gene id. HMGCS2:3158
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 137852640
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