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NM_006766.5(KAT6A):c.4971_4994dup (p.Gln1665_Pro1666insGlnProGlnProProProProGln) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 17, 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:
RCV003841472.2

Allele description [Variation Report for NM_006766.5(KAT6A):c.4971_4994dup (p.Gln1665_Pro1666insGlnProGlnProProProProGln)]

NM_006766.5(KAT6A):c.4971_4994dup (p.Gln1665_Pro1666insGlnProGlnProProProProGln)

Gene:
KAT6A:lysine acetyltransferase 6A [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
8p11.21
Genomic location:
Preferred name:
NM_006766.5(KAT6A):c.4971_4994dup (p.Gln1665_Pro1666insGlnProGlnProProProProGln)
HGVS:
  • NC_000008.11:g.41933231_41933254dup
  • NG_042093.1:g.123778_123801dup
  • NM_006766.5:c.4971_4994dupMANE SELECT
  • NP_006757.2:p.Gln1665_Pro1666insGlnProGlnProProProProGln
  • NC_000008.10:g.41790743_41790744insTGTGGCGGCGGCGGCTGTGGCTGC
  • NC_000008.10:g.41790749_41790772dup
Molecular consequence:
  • NM_006766.5:c.4971_4994dup - inframe_insertion - [Sequence Ontology: SO:0001821]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004692925Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Mar 17, 2023) 		germlineclinical testing

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

Help

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 Labcorp Genetics (formerly Invitae), Labcorp, SCV004692925.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. This variant has not been reported in the literature in individuals affected with KAT6A-related conditions. This variant is not present in population databases (gnomAD no frequency). This variant, c.4971_4994dup, results in the insertion of 8 amino acid(s) of the KAT6A protein (p.Gln1658_Gln1665dup), but otherwise preserves the integrity of the reading frame.

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

Last Updated: Sep 29, 2024