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NM_016373.4(WWOX):c.107+18G>A AND Autosomal recessive spinocerebellar ataxia 12

Germline classification:
Benign (1 submission)
Last evaluated:
Dec 5, 2021
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:
RCV002244900.1

Allele description [Variation Report for NM_016373.4(WWOX):c.107+18G>A]

NM_016373.4(WWOX):c.107+18G>A

Gene:
WWOX:WW domain containing oxidoreductase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
16q23.1
Genomic location:
Preferred name:
NM_016373.4(WWOX):c.107+18G>A
HGVS:
  • NC_000016.10:g.78099903G>A
  • NG_011698.1:g.5250G>A
  • NM_001291997.2:c.-168+18G>A
  • NM_016373.4:c.107+18G>AMANE SELECT
  • NM_130791.5:c.107+18G>A
  • NC_000016.9:g.78133800G>A
  • NM_016373.2:c.107+18G>A
  • NR_120435.2:n.250G>A
  • NR_120436.3:n.250G>A
Links:
dbSNP: rs146301453
NCBI 1000 Genomes Browser:
rs146301453
Molecular consequence:
  • NM_001291997.2:c.-168+18G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_016373.4:c.107+18G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_130791.5:c.107+18G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NR_120435.2:n.250G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_120436.3:n.250G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

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
SCV002515105Genome-Nilou Lab
criteria provided, single submitter

(ACMG Guidelines, 2015)		Benign
(Dec 5, 2021) 		germlineclinical testing

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

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Genome-Nilou Lab, SCV002515105.1

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

Last Updated: Sep 29, 2024