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NM_001034853.2(RPGR):c.2633G>T (p.Gly878Val) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 16, 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:
RCV001885432.2

Allele description [Variation Report for NM_001034853.2(RPGR):c.2633G>T (p.Gly878Val)]

NM_001034853.2(RPGR):c.2633G>T (p.Gly878Val)

Gene:
RPGR:retinitis pigmentosa GTPase regulator [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
Xp11.4
Genomic location:
Preferred name:
NM_001034853.2(RPGR):c.2633G>T (p.Gly878Val)
HGVS:
  • NC_000023.11:g.38286366C>A
  • NG_009553.1:g.46170G>T
  • NM_000328.3:c.1905+728G>T
  • NM_001034853.2:c.2633G>TMANE SELECT
  • NM_001367245.1:c.1902+728G>T
  • NM_001367246.1:c.1719+728G>T
  • NM_001367247.1:c.1572+4593G>T
  • NM_001367248.1:c.1602+4593G>T
  • NM_001367249.1:c.1569+4593G>T
  • NM_001367250.1:c.1569+4593G>T
  • NM_001367251.1:c.1386+4593G>T
  • NP_001030025.1:p.Gly878Val
  • NC_000023.10:g.38145619C>A
  • NM_001034853.1:c.2633G>T
Protein change:
G878V
Links:
dbSNP: rs1218098015
NCBI 1000 Genomes Browser:
rs1218098015
Molecular consequence:
  • NM_000328.3:c.1905+728G>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001367245.1:c.1902+728G>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001367246.1:c.1719+728G>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001367247.1:c.1572+4593G>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001367248.1:c.1602+4593G>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001367249.1:c.1569+4593G>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001367250.1:c.1569+4593G>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001367251.1:c.1386+4593G>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001034853.2:c.2633G>T - missense variant - [Sequence Ontology: SO:0001583]

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
SCV002107256GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Uncertain significance
(Mar 16, 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, SCV002107256.2

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

Description

Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge; This variant is associated with the following publications: (PMID: 27535533)

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

Last Updated: Dec 24, 2023