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NM_181675.4(PPP2R2B):c.447+1G>A AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Feb 17, 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:
RCV002278870.2

Allele description [Variation Report for NM_181675.4(PPP2R2B):c.447+1G>A]

NM_181675.4(PPP2R2B):c.447+1G>A

Gene:
PPP2R2B:protein phosphatase 2 regulatory subunit Bbeta [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
5q32
Genomic location:
Preferred name:
NM_181675.4(PPP2R2B):c.447+1G>A
HGVS:
  • NC_000005.10:g.146691127C>T
  • NG_011570.2:g.395344G>A
  • NG_011570.3:g.395393G>A
  • NM_001271899.1:c.465+1G>A
  • NM_001271900.2:c.621+1G>A
  • NM_001271948.2:c.414+1G>A
  • NM_181674.3:c.645+1G>A
  • NM_181675.4:c.447+1G>AMANE SELECT
  • NM_181676.3:c.456+1G>A
  • NM_181677.2:c.387+1G>A
  • NM_181678.2:c.414+1G>A
  • NC_000005.9:g.146070690C>T
Links:
dbSNP: rs2151152854
NCBI 1000 Genomes Browser:
rs2151152854
Molecular consequence:
  • NM_001271899.1:c.465+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001271900.2:c.621+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001271948.2:c.414+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_181674.3:c.645+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_181675.4:c.447+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_181676.3:c.456+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_181677.2:c.387+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_181678.2:c.414+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]

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
SCV002567245GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Uncertain significance
(Feb 17, 2022) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From GeneDx, SCV002567245.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

Not observed at significant frequency in large population cohorts (gnomAD); Canonical splice site variant in a gene for which loss-of-function is not a known mechanism of disease; Has not been previously published as pathogenic or benign to our knowledge

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

Last Updated: Dec 24, 2023