NM_144573.4(NEXN):c.-10T>C AND not specified

Clinical significance:Uncertain significance (Last evaluated: Jul 24, 2014)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000156717.1

Allele description [Variation Report for NM_144573.4(NEXN):c.-10T>C]

NM_144573.4(NEXN):c.-10T>C

Gene:
NEXN:nexilin F-actin binding protein [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1p31.1
Genomic location:
Preferred name:
NM_144573.4(NEXN):c.-10T>C
HGVS:
  • NC_000001.11:g.77916097T>C
  • NG_016625.1:g.32583T>C
  • NM_001172309.1:c.-10T>C
  • NM_144573.3:c.-10T>C
  • NM_144573.4:c.-10T>CMANE SELECT
  • LRG_442t1:c.-10T>C
  • LRG_442:g.32583T>C
  • NC_000001.10:g.78381782T>C
Links:
dbSNP: rs727505219
NCBI 1000 Genomes Browser:
rs727505219
Molecular consequence:
  • NM_001172309.1:c.-10T>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_144573.3:c.-10T>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_144573.4:c.-10T>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
Observations:
1

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000206438Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicinecriteria provided, single submitter
Uncertain significance
(Jul 24, 2014)
germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenot provided11not providednot providednot providedclinical testing

Citations

PubMed

A systematic approach to assessing the clinical significance of genetic variants.

Duzkale H, Shen J, McLaughlin H, Alfares A, Kelly MA, Pugh TJ, Funke BH, Rehm HL, Lebo MS.

Clin Genet. 2013 Nov;84(5):453-63. doi: 10.1111/cge.12257.

PubMed [citation]
PMID:
24033266
PMCID:
PMC3995020

Details of each submission

From Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine, SCV000206438.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlinenot providednot providednot providednot provided1not provided1not provided

Last Updated: Jul 7, 2021

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