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NM_005410.4(SELENOP):c.290G>A (p.Arg97Gln) AND not specified

Germline classification:
Likely benign (1 submission)
Last evaluated:
Jun 3, 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:
RCV004450441.1

Allele description [Variation Report for NM_005410.4(SELENOP):c.290G>A (p.Arg97Gln)]

NM_005410.4(SELENOP):c.290G>A (p.Arg97Gln)

Gene:
SELENOP:selenoprotein P [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
5p12
Genomic location:
Preferred name:
NM_005410.4(SELENOP):c.290G>A (p.Arg97Gln)
HGVS:
  • NC_000005.10:g.42807022C>T
  • NM_001085486.3:c.290G>A
  • NM_001093726.3:c.380G>A
  • NM_005410.4:c.290G>AMANE SELECT
  • NP_001078955.1:p.Arg97Gln
  • NP_001087195.1:p.Arg127Gln
  • NP_005401.3:p.Arg97Gln
  • NC_000005.9:g.42807124C>T
  • NM_005410.2:c.290G>A
Protein change:
R127Q
Molecular consequence:
  • NM_001085486.3:c.290G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001093726.3:c.380G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_005410.4:c.290G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004945933Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(Jun 3, 2022) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV004945933.1

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

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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

Last Updated: May 7, 2024