U.S. flag

An official website of the United States government

NM_014049.5(ACAD9):c.1641_1659dup (p.Ile554fs) AND Acyl-CoA dehydrogenase 9 deficiency

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Sep 26, 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:
RCV003469657.1

Allele description [Variation Report for NM_014049.5(ACAD9):c.1641_1659dup (p.Ile554fs)]

NM_014049.5(ACAD9):c.1641_1659dup (p.Ile554fs)

Genes:
ACAD9:acyl-CoA dehydrogenase family member 9 [Gene - OMIM - HGNC]
CFAP92:cilia and flagella associated protein 92 (putative) [Gene - HGNC]
Variant type:
Duplication
Cytogenetic location:
3q21.3
Genomic location:
Preferred name:
NM_014049.5(ACAD9):c.1641_1659dup (p.Ile554fs)
HGVS:
  • NC_000003.12:g.128910098_128910116dup
  • NG_017064.1:g.35609_35627dup
  • NM_001348520.2:c.*183_*201dup
  • NM_001348521.2:c.*183_*201dup
  • NM_001394090.1:c.*183_*201dupMANE SELECT
  • NM_014049.4:c.1641_1659dupGTCGCGGGCCAGCCGCTCC
  • NM_014049.5:c.1641_1659dupMANE SELECT
  • NP_054768.2:p.Ile554fs
  • NC_000003.11:g.128628940_128628941insGTCGCGGGCCAGCCGCTCC
  • NC_000003.11:g.128628941_128628959dup
  • NM_014049.5:c.1641_1659dup
  • NR_033426.2:n.1889_1907dup
Protein change:
I554fs
Links:
dbSNP: rs755346624
NCBI 1000 Genomes Browser:
rs755346624
Molecular consequence:
  • NM_001348520.2:c.*183_*201dup - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001348521.2:c.*183_*201dup - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001394090.1:c.*183_*201dup - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_014049.5:c.1641_1659dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NR_033426.2:n.1889_1907dup - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Acyl-CoA dehydrogenase 9 deficiency
Synonyms:
Acyl-CoA dehydrogenase family, member 9, deficiency of; MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
Identifiers:
MONDO: MONDO:0012624; MedGen: C4747517; Orphanet: 99901; OMIM: 611126

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004209448Baylor Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely pathogenic
(Sep 26, 2023) 		unknownclinical testing

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

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Baylor Genetics, SCV004209448.1

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

Last Updated: May 1, 2024