NM_001079668.3(NKX2-1):c.816C>T (p.Thr272=) AND Benign hereditary chorea

Clinical significance:Uncertain significance (Last evaluated: Jan 12, 2018)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000300343.2

Allele description [Variation Report for NM_001079668.3(NKX2-1):c.816C>T (p.Thr272=)]

NM_001079668.3(NKX2-1):c.816C>T (p.Thr272=)

Genes:
NKX2-1:NK2 homeobox 1 [Gene - OMIM - HGNC]
SFTA3:surfactant associated 3 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
14q13.3
Genomic location:
Preferred name:
NM_001079668.3(NKX2-1):c.816C>T (p.Thr272=)
HGVS:
  • NC_000014.9:g.36517668G>A
  • NG_013365.1:g.7558C>T
  • NM_001079668.3:c.816C>TMANE SELECT
  • NM_003317.4:c.726C>T
  • NP_001073136.1:p.Thr272=
  • NP_003308.1:p.Thr242=
  • NC_000014.8:g.36986873G>A
  • NM_001079668.2:c.816C>T
Links:
dbSNP: rs886050483
NCBI 1000 Genomes Browser:
rs886050483
Molecular consequence:
  • NM_001079668.3:c.816C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_003317.4:c.726C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:
Benign hereditary chorea (BHC)
Synonyms:
HEREDITARY PROGRESSIVE CHOREA WITHOUT DEMENTIA
Identifiers:
MONDO: MONDO:0021011; MedGen: C0393584; Orphanet: 1429; OMIM: 118700

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000386678Illumina Clinical Services Laboratory,Illuminacriteria provided, single submitter
Uncertain significance
(Jan 12, 2018)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Illumina Clinical Services Laboratory,Illumina, SCV000386678.3

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

Description

This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score, this variant could not be ruled out of causing disease and therefore its association with disease required further investigation. A literature search was performed for the gene, cDNA change, and amino acid change (if applicable). No publications were found based on this search. This variant was therefore classified as a variant of unknown significance for this disease.

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

Last Updated: May 31, 2020

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