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NM_213598.4(ZNF543):c.1064C>T (p.Thr355Met) AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Nov 1, 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:
RCV004201249.1

Allele description [Variation Report for NM_213598.4(ZNF543):c.1064C>T (p.Thr355Met)]

NM_213598.4(ZNF543):c.1064C>T (p.Thr355Met)

Gene:
ZNF543:zinc finger protein 543 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
19q13.43
Genomic location:
Preferred name:
NM_213598.4(ZNF543):c.1064C>T (p.Thr355Met)
HGVS:
  • NC_000019.10:g.57328526C>T
  • NM_213598.4:c.1064C>TMANE SELECT
  • NP_998763.2:p.Thr355Met
  • NC_000019.9:g.57839894C>T
  • NM_213598.3:c.1064C>T
Protein change:
T355M
Molecular consequence:
  • NM_213598.4:c.1064C>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
SCV003702416Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Nov 1, 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, SCV003702416.2

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

Description

The c.1064C>T (p.T355M) alteration is located in exon 4 (coding exon 4) of the ZNF543 gene. This alteration results from a C to T substitution at nucleotide position 1064, causing the threonine (T) at amino acid position 355 to be replaced by a methionine (M). 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: Nov 3, 2024