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NM_002225.5(IVD):c.784+9C>T AND Isovaleryl-CoA dehydrogenase deficiency

Germline classification:
Likely benign (2 submissions)
Last evaluated:
Aug 29, 2023
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV001277690.2

Allele description [Variation Report for NM_002225.5(IVD):c.784+9C>T]

NM_002225.5(IVD):c.784+9C>T

Gene:
IVD:isovaleryl-CoA dehydrogenase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
15q15.1
Genomic location:
Preferred name:
NM_002225.5(IVD):c.784+9C>T
HGVS:
  • NC_000015.10:g.40413096C>T
  • NG_011986.2:g.12612C>T
  • NM_001159508.3:c.694+9C>T
  • NM_001354597.3:c.736+9C>T
  • NM_001354598.3:c.784+9C>T
  • NM_001354599.3:c.871+9C>T
  • NM_001354600.3:c.871+9C>T
  • NM_001354601.3:c.784+9C>T
  • NM_002225.5:c.784+9C>TMANE SELECT
  • NC_000015.9:g.40705295C>T
Links:
dbSNP: rs1891254953
NCBI 1000 Genomes Browser:
rs1891254953
Molecular consequence:
  • NM_001159508.3:c.694+9C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354597.3:c.736+9C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354598.3:c.784+9C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354599.3:c.871+9C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354600.3:c.871+9C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354601.3:c.784+9C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_002225.5:c.784+9C>T - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Isovaleryl-CoA dehydrogenase deficiency (IVA)
Synonyms:
Isovaleric acid CoA dehydrogenase deficiency; Isovaleric acidemia; Isovaleryl CoA carboxylase deficiency; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0009475; MedGen: C0268575; Orphanet: 33; OMIM: 243500

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001464655Natera, Inc.
no assertion criteria provided
Uncertain significance
(Apr 16, 2020)
germlineclinical testing

SCV004512343Invitae
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))
Likely benign
(Aug 29, 2023)
germlineclinical testing

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Natera, Inc., SCV001464655.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

From Invitae, SCV004512343.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Feb 28, 2024