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NM_016373.4(WWOX):c.77CCA[1] (p.Thr27del) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Apr 28, 2022
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:
RCV001343112.6

Allele description [Variation Report for NM_016373.4(WWOX):c.77CCA[1] (p.Thr27del)]

NM_016373.4(WWOX):c.77CCA[1] (p.Thr27del)

Gene:
WWOX:WW domain containing oxidoreductase [Gene - OMIM - HGNC]
Variant type:
Microsatellite
Cytogenetic location:
16q23.1
Genomic location:
Preferred name:
NM_016373.4(WWOX):c.77CCA[1] (p.Thr27del)
HGVS:
  • NC_000016.10:g.78099855CCA[1]
  • NG_011698.1:g.5202CCA[1]
  • NM_001291997.2:c.-198CCA[1]
  • NM_016373.4:c.77CCA[1]MANE SELECT
  • NM_130791.5:c.77CCA[1]
  • NP_057457.1:p.Thr27del
  • NP_570607.1:p.Thr27del
  • NC_000016.9:g.78133751_78133753del
  • NC_000016.9:g.78133752CCA[1]
  • NR_120435.2:n.202CCA[1]
  • NR_120436.3:n.202CCA[1]
Protein change:
T27del
Links:
dbSNP: rs763124571
NCBI 1000 Genomes Browser:
rs763124571
Molecular consequence:
  • NM_001291997.2:c.-198CCA[1] - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_016373.4:c.77CCA[1] - inframe_deletion - [Sequence Ontology: SO:0001822]
  • NM_130791.5:c.77CCA[1] - inframe_deletion - [Sequence Ontology: SO:0001822]
  • NR_120435.2:n.202CCA[1] - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_120436.3:n.202CCA[1] - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Developmental and epileptic encephalopathy, 1 (DEE1)
Synonyms:
INFANTILE SPASM SYNDROME, X-LINKED 1; X-linked infantile spasms; West's syndrome; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0010632; MedGen: C3463992; OMIM: 308350
Name:
Autosomal recessive spinocerebellar ataxia 12
Synonyms:
SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY
Identifiers:
MONDO: MONDO:0013687; MedGen: C3280452; Orphanet: 284282; OMIM: 614322

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001537075Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Apr 28, 2022) 		germlineclinical testing

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

Help

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. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV001537075.3

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

Description

This variant, c.80_82del, results in the deletion of 1 amino acid(s) of the WWOX protein (p.Thr27del), but otherwise preserves the integrity of the reading frame. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with WWOX-related conditions. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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: Sep 29, 2024