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NM_018136.5(ASPM):c.5148A>T (p.Lys1716Asn) AND Inborn genetic diseases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Feb 27, 2024
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:
RCV004420898.1

Allele description [Variation Report for NM_018136.5(ASPM):c.5148A>T (p.Lys1716Asn)]

NM_018136.5(ASPM):c.5148A>T (p.Lys1716Asn)

Gene:
ASPM:assembly factor for spindle microtubules [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1q31.3
Genomic location:
Preferred name:
NM_018136.5(ASPM):c.5148A>T (p.Lys1716Asn)
HGVS:
  • NC_000001.11:g.197104103T>A
  • NG_015867.1:g.47592A>T
  • NM_001206846.2:c.4066-7939A>T
  • NM_018136.5:c.5148A>TMANE SELECT
  • NP_060606.3:p.Lys1716Asn
  • NC_000001.10:g.197073233T>A
  • NM_018136.4:c.5148A>T
Protein change:
K1716N
Molecular consequence:
  • NM_001206846.2:c.4066-7939A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_018136.5:c.5148A>T - 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

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004909753Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Feb 27, 2024) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV004909753.1

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

Description

The c.5148A>T (p.K1716N) alteration is located in exon 18 (coding exon 18) of the ASPM gene. This alteration results from a A to T substitution at nucleotide position 5148, causing the lysine (K) at amino acid position 1716 to be replaced by an asparagine (N). 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: May 7, 2024