View genomic variant #0000000492

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.121174901G>A
Published as -
GERP 3.950
Segregation -
DB-ID ACADS_000009 See all 2 reported entries
MSCV MSCV_0000492
dbSNP ID rs387906951
Frequency -
Sources ; clinvar;
Reference 20376488
Variant remarks -
Genetic origin -
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.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
ACADS 00000386 NM_000017.2 0000000492 +/+ - 3/10 c.323G>A p.(Gly108Asp) probably_damaging(0.999) missense_variant - tolerated(0.2)
ACADS 00000385 XM_005253878.1 0000000492 +/+ - 3/10 c.323G>A p.(Gly108Asp) probably_damaging(0.999) missense_variant - tolerated(0.2)
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ClinVar @ MSeqDR

RCVaccession RCV000023587;
Chromosome 12:121174901..121174901
ClinVar Allele ID 39570
Disease database name and identifier MedGen:C0342783, OMIM:201470, Orphanet:ORPHA26792, SNOMED CT:124166007
ClinVar preferred disease name Deficiency of butyryl-CoA dehydrogenase
HGVS variant names NC 000012.11:g.121174901G>A
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 OMIM Allelic Variant:606885.0016
Gene symbol:Gene id. ACADS:35
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 387906951
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