View genomic variant #0000002648

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.7126471G>C
Published as -
GERP 4.660
Segregation -
DB-ID ACADVL_000038
MSCV MSCV_0002648
dbSNP ID rs112406105
Frequency -
Sources ; Ensembl;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
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 0000002648 ?/? - 11/20 c.1097G>C p.? probably_damaging(1) missense_variant - deleterious(0)
ACADVL 00000391 NM_001033859.2 0000002648 ?/? - 10/19 c.1031G>C p.(Arg344Pro) probably_damaging(1) missense_variant - deleterious(0)
ACADVL 00000388 NM_001270447.1 0000002648 ?/? - 12/21 c.1166G>C p.(Arg389Pro) probably_damaging(1) missense_variant - deleterious(0)
ACADVL 00000389 NM_001270448.1 0000002648 ?/? - 10/19 c.869G>C p.(Arg290Pro) - missense_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000185720; RCV000411732;
Chromosome 17:7126471..7126471
Allele frequencies from TGP 0.00020
ClinVar Allele ID 200333
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0008723, MedGen:C3887523, OMIM:201475, Orphanet:26793
ClinVar preferred disease name not provided|Very long chain acyl-CoA dehydrogenase deficiency
HGVS variant names NC 000017.10:g.7126471G>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:CA312265|UniProtKB:P49748#VAR 000350
Gene symbol:Gene id. ACADVL:37
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 112406105
For included Variant: Tag-value pairs of disease database name and identifier, e.g. OMIM:NNNNNN MONDO:MONDO:0008723, MedGen:C3887523, OMIM:201475, Orphanet:26793
For included Variant : ClinVar preferred disease name for the concept specified by disease identifiers in CLNDISDB Very long chain acyl-CoA dehydrogenase deficiency
Clinical significance for a haplotype or genotype that includes this variant. Reported as pairs of VariationID:clinical significance. 867229:Likely pathogenic
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