NM_012431.3(SEMA3E):c.447T>A (p.Tyr149Ter) AND CHARGE association

Clinical significance:Uncertain significance (Last evaluated: Feb 13, 2019)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV001054029.2

Allele description [Variation Report for NM_012431.3(SEMA3E):c.447T>A (p.Tyr149Ter)]

NM_012431.3(SEMA3E):c.447T>A (p.Tyr149Ter)

Gene:
SEMA3E:semaphorin 3E [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
7q21.11
Genomic location:
Preferred name:
NM_012431.3(SEMA3E):c.447T>A (p.Tyr149Ter)
HGVS:
  • NC_000007.14:g.83466491A>T
  • NG_021242.2:g.187673T>A
  • NM_001178129.2:c.267T>A
  • NM_012431.3:c.447T>AMANE SELECT
  • NP_001171600.1:p.Tyr89Ter
  • NP_036563.1:p.Tyr149Ter
  • LRG_1287t1:c.447T>A
  • LRG_1287:g.187673T>A
  • LRG_1287p1:p.Tyr149Ter
  • NC_000007.13:g.83095807A>T
  • NM_012431.2:c.447T>A
Protein change:
Y149*
Links:
dbSNP: rs1789759019
NCBI 1000 Genomes Browser:
rs1789759019
Molecular consequence:
  • NM_001178129.2:c.267T>A - nonsense - [Sequence Ontology: SO:0001587]
  • NM_012431.3:c.447T>A - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

Name:
CHARGE association (CHARGE)
Synonyms:
CHARGE ASSOCIATION--COLOBOMA, HEART ANOMALY, CHOANAL ATRESIA, RETARDATION, GENITAL AND EAR ANOMALIES; CHARGE syndrome; Coloboma, heart anomaly, choanal atresia, retardation, genital and ear anomalies; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0008965; MedGen: C0265354; Orphanet: 138; OMIM: 214800

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001218322Invitaecriteria provided, single submitter
Uncertain significance
(Feb 13, 2019)
germlineclinical testing

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

Summary from all submissions

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240-242.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Invitae, SCV001218322.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

This sequence change creates a premature translational stop signal (p.Tyr149*) in the SEMA3E gene. It is expected to result in an absent or disrupted protein product. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with SEMA3E-related conditions. The current clinical and genetic evidence is not sufficient to establish whether loss-of-function variants in SEMA3E cause disease. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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

Last Updated: Nov 27, 2021

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