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NM_052852.4(ZNF486):c.1085C>T (p.Ser362Phe) AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
May 30, 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:
RCV004288306.1

Allele description [Variation Report for NM_052852.4(ZNF486):c.1085C>T (p.Ser362Phe)]

NM_052852.4(ZNF486):c.1085C>T (p.Ser362Phe)

Gene:
ZNF486:zinc finger protein 486 [Gene - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
19p12
Genomic location:
Preferred name:
NM_052852.4(ZNF486):c.1085C>T (p.Ser362Phe)
HGVS:
  • NC_000019.10:g.20197795C>T
  • NM_052852.4:c.1085C>TMANE SELECT
  • NP_443084.2:p.Ser362Phe
  • NC_000019.9:g.20308604C>T
  • NM_052852.2:c.1085C>T
Protein change:
S362F
Molecular consequence:
  • NM_052852.4:c.1085C>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
SCV003942693Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(May 30, 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, SCV003942693.2

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

Description

The c.1085C>T (p.S362F) alteration is located in exon 4 (coding exon 4) of the ZNF486 gene. This alteration results from a C to T substitution at nucleotide position 1085, causing the serine (S) at amino acid position 362 to be replaced by a phenylalanine (F). 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 10, 2024