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NM_022726.4(ELOVL4):c.351T>A (p.Asn117Lys) AND Inborn genetic diseases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 14, 2022
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:
RCV002524509.3

Allele description [Variation Report for NM_022726.4(ELOVL4):c.351T>A (p.Asn117Lys)]

NM_022726.4(ELOVL4):c.351T>A (p.Asn117Lys)

Gene:
ELOVL4:ELOVL fatty acid elongase 4 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
6q14.1
Genomic location:
Preferred name:
NM_022726.4(ELOVL4):c.351T>A (p.Asn117Lys)
HGVS:
  • NC_000006.12:g.79924970A>T
  • NG_009108.2:g.27629T>A
  • NM_022726.4:c.351T>AMANE SELECT
  • NP_073563.1:p.Asn117Lys
  • NC_000006.11:g.80634687A>T
  • NG_009108.1:g.27629T>A
  • NM_022726.3:c.351T>A
Protein change:
N117K
Links:
dbSNP: rs148018494
NCBI 1000 Genomes Browser:
rs148018494
Molecular consequence:
  • NM_022726.4:c.351T>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Inborn genetic diseases
Identifiers:
MeSH: D030342; MedGen: C0950123

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV003652932Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)
Uncertain significance
(Mar 14, 2022)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV003652932.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

Unlikely to be causative of ELOVL4-related spinocerebellar ataxia (AD) and ELOVL4-related Stargardt macular dystrophy (AD) Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 8, 2024