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NM_181659.3(NCOA3):c.1056C>G (p.Phe352Leu) AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
May 28, 2024
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:
RCV004654518.1

Allele description [Variation Report for NM_181659.3(NCOA3):c.1056C>G (p.Phe352Leu)]

NM_181659.3(NCOA3):c.1056C>G (p.Phe352Leu)

Gene:
NCOA3:nuclear receptor coactivator 3 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
20q13.12
Genomic location:
Preferred name:
NM_181659.3(NCOA3):c.1056C>G (p.Phe352Leu)
HGVS:
  • NC_000020.11:g.47634139C>G
  • NG_016810.1:g.137283C>G
  • NG_016810.2:g.137254C>G
  • NM_001174087.2:c.1056C>G
  • NM_001174088.2:c.1086C>G
  • NM_006534.4:c.1056C>G
  • NM_181659.3:c.1056C>GMANE SELECT
  • NP_001167558.1:p.Phe352Leu
  • NP_001167559.1:p.Phe362Leu
  • NP_006525.2:p.Phe352Leu
  • NP_858045.1:p.Phe352Leu
  • NC_000020.10:g.46262883C>G
  • NM_181659.2:c.1056C>G
Protein change:
F352L
Molecular consequence:
  • NM_001174087.2:c.1056C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001174088.2:c.1086C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_006534.4:c.1056C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_181659.3:c.1056C>G - 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
SCV005142702Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(May 28, 2024) 		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, SCV005142702.1

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

Description

The c.1056C>G (p.F352L) alteration is located in exon 10 (coding exon 8) of the NCOA3 gene. This alteration results from a C to G substitution at nucleotide position 1056, causing the phenylalanine (F) at amino acid position 352 to be replaced by a leucine (L). 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: Aug 11, 2024