View genomic variant #0000005192

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.7125591T>C
Published as -
GERP 5.220
Segregation -
DB-ID ACADVL_000016 See all 3 reported entries
MSCV MSCV_0005192
dbSNP ID rs113994167
Frequency -
Sources ; ensembl;
Reference 20301763;17374501;23757202;8845838
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00092 View details
Owner LOVD




Variant on transcripts

4 entries on 1 page. Showing entries 1 - 4.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
ACADVL 00000390 NM_000018.3 0000005192 ./. - 9/20 c.848T>C p.(Val283Ala) benign(0.371) missense_variant - deleterious(0)
ACADVL 00000391 NM_001033859.2 0000005192 ./. - 8/19 c.782T>C p.(Val261Ala) possibly_damaging(0.569) missense_variant - deleterious(0)
ACADVL 00000388 NM_001270447.1 0000005192 ./. - 10/21 c.917T>C p.(Val306Ala) possibly_damaging(0.652) missense_variant - deleterious(0)
ACADVL 00000389 NM_001270448.1 0000005192 ./. - 8/19 c.620T>C p.(Val207Ala) - missense_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000020081; RCV000077925; RCV001807006; RCV002513135;
Chromosome 17:7125591..7125591
Allele frequencies from ESP 0.00092
Allele frequencies from ExAC 0.00143
ClinVar Allele ID 33877
Disease database name and identifier MeSH:D030342, MedGen:C0950123|Human Phenotype Ontology:HP:0008167, MedGen:C3279397|MedGen:C3661900|MONDO:MONDO:0008723, MedGen:C3887523, OMIM:201475, Orphanet:26793
ClinVar preferred disease name Inborn genetic diseases|Very long chain fatty acid accumulation|not provided|Very long chain acyl-CoA dehydrogenase deficiency
HGVS variant names NC 000017.10:g.7125591T>C
ClinVar review status reviewed by expert panel
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA285294|UniProtKB:P49748#VAR 000342
Gene symbol:Gene id. ACADVL:37
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 113994167
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