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NM_014830.3(ZBTB39):c.1336G>A (p.Ala446Thr) AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jan 3, 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:
RCV004227312.1

Allele description [Variation Report for NM_014830.3(ZBTB39):c.1336G>A (p.Ala446Thr)]

NM_014830.3(ZBTB39):c.1336G>A (p.Ala446Thr)

Gene:
ZBTB39:zinc finger and BTB domain containing 39 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
12q13.3
Genomic location:
Preferred name:
NM_014830.3(ZBTB39):c.1336G>A (p.Ala446Thr)
HGVS:
  • NC_000012.12:g.57003582C>T
  • NM_014830.3:c.1336G>AMANE SELECT
  • NP_055645.1:p.Ala446Thr
  • NC_000012.11:g.57397366C>T
  • NM_014830.2:c.1336G>A
Protein change:
A446T
Molecular consequence:
  • NM_014830.3:c.1336G>A - 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
SCV003735453Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Jan 3, 2022) 		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, SCV003735453.2

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

Description

The c.1336G>A (p.A446T) alteration is located in exon 2 (coding exon 1) of the ZBTB39 gene. This alteration results from a G to A substitution at nucleotide position 1336, causing the alanine (A) at amino acid position 446 to be replaced by a threonine (T). 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