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NM_005732.3(RAD50):c.-352G>A AND not provided

Germline classification:
not provided (1 submission)
Review status:
no classification provided
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:
RCV000114857.1

Allele description [Variation Report for NM_005732.3(RAD50):c.-352G>A]

NM_005732.3(RAD50):c.-352G>A

Variant type:
single nucleotide variant
Cytogenetic location:
5q31.1
Genomic location:
Preferred name:
NM_005732.3(RAD50):c.-352G>A
HGVS:
  • NC_000005.10:g.132556973G>A
  • NG_021151.2:g.4997G>A
  • LRG_312:g.4997G>A
  • NC_000005.8:g.131920564G>A
  • NC_000005.9:g.131892665G>A
  • NG_021151.1:g.5050G>A
Links:
dbSNP: rs104895040
NCBI 1000 Genomes Browser:
rs104895040

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000148752Harris Lab, University of Minnesota
no classification provided
not providedunknownnot provided

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownnot providednot providednot providednot provided1not providedliterature only

Details of each submission

From Harris Lab, University of Minnesota, SCV000148752.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providednot providednot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownnot provided1not providednot providednot providednot providednot providednot provided

Last Updated: Dec 24, 2023