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NM_032444.4(SLX4):c.761-32T>G AND not provided

Germline classification:
Likely benign (1 submission)
Last evaluated:
Mar 6, 2019
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:
RCV001527751.1

Allele description [Variation Report for NM_032444.4(SLX4):c.761-32T>G]

NM_032444.4(SLX4):c.761-32T>G

Gene:
SLX4:SLX4 structure-specific endonuclease subunit [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
16p13.3
Genomic location:
Preferred name:
NM_032444.4(SLX4):c.761-32T>G
HGVS:
  • NC_000016.10:g.3602339A>C
  • NG_028123.1:g.14246T>G
  • NM_032444.4:c.761-32T>GMANE SELECT
  • LRG_503t1:c.761-32T>G
  • LRG_503:g.14246T>G
  • NC_000016.9:g.3652340A>C
  • NM_032444.2:c.761-32T>G
Links:
dbSNP: rs118098382
NCBI 1000 Genomes Browser:
rs118098382
Molecular consequence:
  • NM_032444.4:c.761-32T>G - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001738881GeneDx
criteria provided, single submitter

(GeneDx Variant Classification (06012015))
Likely benign
(Mar 6, 2019)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From GeneDx, SCV001738881.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Dec 24, 2023