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NM_012310.5(KIF4A):c.3167A>T (p.Glu1056Val) AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Apr 20, 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:
RCV004313615.1

Allele description [Variation Report for NM_012310.5(KIF4A):c.3167A>T (p.Glu1056Val)]

NM_012310.5(KIF4A):c.3167A>T (p.Glu1056Val)

Gene:
KIF4A:kinesin family member 4A [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
Xq13.1
Genomic location:
Preferred name:
NM_012310.5(KIF4A):c.3167A>T (p.Glu1056Val)
HGVS:
  • NC_000023.11:g.70406987A>T
  • NG_016799.1:g.121959A>T
  • NG_016799.2:g.121885A>T
  • NM_012310.5:c.3167A>TMANE SELECT
  • NP_036442.3:p.Glu1056Val
  • NC_000023.10:g.69626837A>T
  • NM_012310.4:c.3167A>T
Protein change:
E1056V
Molecular consequence:
  • NM_012310.5:c.3167A>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003976722Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Apr 20, 2023) 		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, SCV003976722.2

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

Description

The c.3167A>T (p.E1056V) alteration is located in exon 28 (coding exon 27) of the KIF4A gene. This alteration results from a A to T substitution at nucleotide position 3167, causing the glutamic acid (E) at amino acid position 1056 to be replaced by a valine (V). 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 26, 2024