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NM_030787.4(CFHR5):c.617G>A (p.Arg206Gln) AND CFHR5 deficiency

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Apr 9, 2024
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:
RCV004560424.1

Allele description [Variation Report for NM_030787.4(CFHR5):c.617G>A (p.Arg206Gln)]

NM_030787.4(CFHR5):c.617G>A (p.Arg206Gln)

Gene:
CFHR5:complement factor H related 5 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1q31.3
Genomic location:
Preferred name:
NM_030787.4(CFHR5):c.617G>A (p.Arg206Gln)
HGVS:
  • NC_000001.11:g.196995726G>A
  • NG_016365.1:g.23190G>A
  • NM_030787.4:c.617G>AMANE SELECT
  • NP_110414.1:p.Arg206Gln
  • NP_110414.1:p.Arg206Gln
  • LRG_227t1:c.617G>A
  • LRG_227:g.23190G>A
  • LRG_227p1:p.Arg206Gln
  • NC_000001.10:g.196964856G>A
  • NM_030787.3:c.617G>A
Protein change:
R206Q
Molecular consequence:
  • NM_030787.4:c.617G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
CFHR5 deficiency
Identifiers:
MedGen: C3553720

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV005047161Clinical Genomics Laboratory, Washington University in St. Louis
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Apr 9, 2024) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Clinical Genomics Laboratory, Washington University in St. Louis, SCV005047161.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

The CFHR5 c.617G>A (p.Arg206Gln) variant, to our knowledge, has not been reported in association with renal disease in the medical literature. This variant is only observed on 2/251,100 alleles in the general population (gnomAD v2.1.1), indicating it is not a common variant. Computational predictors suggest that the variant does not impact CFHR5 function. Due to limited information, and based on ACMG/AMP guidelines for variant interpretation (Richards S et al., PMID: 25741868), the clinical significance of the CFHR5 c.617G>A (p.Arg206Gln) variant is uncertain at this time.

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

Last Updated: Jun 17, 2024