View genomic variant #0000002655

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.7127312G>A
Published as -
GERP 5.740
Segregation -
DB-ID ACADVL_000032
MSCV MSCV_0002655
dbSNP ID rs138058572
Frequency -
Sources ; Ensembl;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00015 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 0000002655 ?/? - 14/20 c.1358G>A p.? probably_damaging(0.999) missense_variant - deleterious(0)
ACADVL 00000391 NM_001033859.2 0000002655 ?/? - 13/19 c.1292G>A p.(Arg431Gln) probably_damaging(0.998) missense_variant - deleterious(0)
ACADVL 00000388 NM_001270447.1 0000002655 ?/? - 15/21 c.1427G>A p.(Arg476Gln) probably_damaging(0.998) missense_variant - deleterious(0)
ACADVL 00000389 NM_001270448.1 0000002655 ?/? - 13/19 c.1130G>A p.(Arg377Gln) - missense_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000415274; RCV001091164; RCV001075888;
Chromosome 17:7127312..7127312
Allele frequencies from ESP 0.00015
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 361026
Disease database name and identifier Human Phenotype Ontology:HP:0003198, Human Phenotype Ontology:HP:0003569, Human Phenotype Ontology:HP:0003705, Human Phenotype Ontology:HP:0003742, Human Phenotype Ontology:HP:0003802, MONDO:MONDO:0005336, MeSH:D009135, MedGen:C0026848|Human Phenotype Ontology:HP:0003201, MedGen:C0035410|MedGen:C3661900|MONDO:MONDO:0008723, MedGen:C3887523, OMIM:201475, Orphanet:26793
ClinVar preferred disease name Myopathy|Rhabdomyolysis|not provided|Very long chain acyl-CoA dehydrogenase deficiency
HGVS variant names NC 000017.10:g.7127312G>A
ClinVar review status reviewed by expert panel
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA8338089
Gene symbol:Gene id. ACADVL:37
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 138058572
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV001200708;
Chromosome 17:7127312..7127312
ClinVar Allele ID 921130
Disease database name and identifier MONDO:MONDO:0008723, MedGen:C3887523, OMIM:201475, Orphanet:26793
ClinVar preferred disease name Very long chain acyl-CoA dehydrogenase deficiency
HGVS variant names NC 000017.10:g.7127312G>C
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. ACADVL:37
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 138058572
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