View genomic variant #0000002662

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.7128292G>A
Published as -
GERP 0.885
Segregation -
DB-ID ACADVL_000034 See all 2 reported entries
MSCV MSCV_0002662
dbSNP ID rs148584617
Frequency -
Sources ; Ensembl;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00254 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 0000002662 ?/? - 20/20 c.1844G>A p.? benign(0.001) missense_variant - tolerated(0.68)
ACADVL 00000391 NM_001033859.2 0000002662 ?/? - 19/19 c.1778G>A p.(Arg593Gln) benign(0.001) missense_variant - tolerated(0.67)
ACADVL 00000388 NM_001270447.1 0000002662 ?/? - 21/21 c.1913G>A p.(Arg638Gln) benign(0.002) missense_variant - tolerated(0.61)
ACADVL 00000389 NM_001270448.1 0000002662 ?/? - 19/19 c.1616G>A p.(Arg539Gln) - missense_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000176020; RCV000193309; RCV002307434;
Chromosome 17:7128292..7128292
Allele frequencies from ESP 0.00254
Allele frequencies from ExAC 0.00285
Allele frequencies from TGP 0.00080
ClinVar Allele ID 192609
Disease database name and identifier MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0008723, MedGen:C3887523, OMIM:201475, Orphanet:26793
ClinVar preferred disease name not specified|not provided|Very long chain acyl-CoA dehydrogenase deficiency
HGVS variant names NC 000017.10:g.7128292G>A
ClinVar review status reviewed by expert panel
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA090895|UniProtKB:P49748#VAR 010106
Gene symbol:Gene id. ACADVL:37
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 148584617
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