NM_000018.4(ACADVL):c.1349G>A (p.Arg450His) AND multiple conditions

Clinical significance:Pathogenic

Review status:(0/4) 0 stars out of maximum of 4 stars

no assertion criteria provided

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV001003625.1

Allele description [Variation Report for NM_000018.4(ACADVL):c.1349G>A (p.Arg450His)]

NM_000018.4(ACADVL):c.1349G>A (p.Arg450His)

Gene:
ACADVL:acyl-CoA dehydrogenase very long chain [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
17p13.1
Genomic location:
Preferred name:
NM_000018.4(ACADVL):c.1349G>A (p.Arg450His)
Other names:
R410H
HGVS:
  • NC_000017.11:g.7223984G>A
  • NG_007975.1:g.9151G>A
  • NG_008391.2:g.1067C>T
  • NG_033038.1:g.15561C>T
  • NM_000018.4:c.1349G>AMANE SELECT
  • NM_001033859.2:c.1283G>A
  • NM_001270447.1:c.1418G>A
  • NM_001270448.1:c.1121G>A
  • NP_000009.1:p.Arg450His
  • NP_001029031.1:p.Arg428His
  • NP_001257376.1:p.Arg473His
  • NP_001257377.1:p.Arg374His
  • NC_000017.10:g.7127303G>A
  • NM_000018.2:c.1349G>A
  • NM_000018.3:c.1349G>A
  • P49748:p.Arg450His
Protein change:
R374H; ARG410HIS
Links:
UniProtKB: P49748#VAR_000355; OMIM: 609575.0010; OMIM: 609575.0014; dbSNP: rs118204016
NCBI 1000 Genomes Browser:
rs118204016
Molecular consequence:
  • NM_000018.4:c.1349G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001033859.2:c.1283G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001270447.1:c.1418G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001270448.1:c.1121G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Abnormality of circulating enzyme level
Identifiers:
MedGen: C4023591; Human Phenotype Ontology: HP:0011021
Name:
Rhabdomyolysis
Synonyms:
Rhabdomyolysis (disease)
Identifiers:
MONDO: MONDO:0005290; MedGen: C0035410; Human Phenotype Ontology: HP:0003201

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001162036NIHR Bioresource Rare Diseases, University of Cambridgeno assertion criteria providedPathogenicunknownresearch

PubMed (1)
[See all records that cite this PMID]

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownyes1not providednot provided1not providedresearch

Citations

PubMed

Whole-genome sequencing of patients with rare diseases in a national health system.

Turro E, Astle WJ, Megy K, Gräf S, Greene D, Shamardina O, Allen HL, Sanchis-Juan A, Frontini M, Thys C, Stephens J, Mapeta R, Burren OS, Downes K, Haimel M, Tuna S, Deevi SVV, Aitman TJ, Bennett DL, Calleja P, Carss K, Caulfield MJ, et al.

Nature. 2020 Jul;583(7814):96-102. doi: 10.1038/s41586-020-2434-2. Epub 2020 Jun 24.

PubMed [citation]
PMID:
32581362
PMCID:
PMC7610553

Details of each submission

From NIHR Bioresource Rare Diseases, University of Cambridge, SCV001162036.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedresearch PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownyes1not providednot provided1not providednot providednot provided

Last Updated: Sep 7, 2021

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