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NM_000092.5(COL4A4):c.4550T>G (p.Phe1517Cys) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jul 20, 2023
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:
RCV003727083.2

Allele description [Variation Report for NM_000092.5(COL4A4):c.4550T>G (p.Phe1517Cys)]

NM_000092.5(COL4A4):c.4550T>G (p.Phe1517Cys)

Gene:
COL4A4:collagen type IV alpha 4 chain [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2q36.3
Genomic location:
Preferred name:
NM_000092.5(COL4A4):c.4550T>G (p.Phe1517Cys)
HGVS:
  • NC_000002.12:g.227008277A>C
  • NG_011592.1:g.161283T>G
  • NM_000092.5:c.4550T>GMANE SELECT
  • NP_000083.3:p.Phe1517Cys
  • NP_000083.3:p.Phe1517Cys
  • LRG_231t1:c.4550T>G
  • LRG_231:g.161283T>G
  • LRG_231p1:p.Phe1517Cys
  • NC_000002.11:g.227872993A>C
  • NM_000092.4:c.4550T>G
Protein change:
F1517C
Molecular consequence:
  • NM_000092.5:c.4550T>G - 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
SCV004535307Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Jul 20, 2023) 		germlineclinical testing

PubMed (2)
[See all records that cite these PMIDs]

Help

Summary from all submissions

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

Citations

PubMed

[Clinical and genetic diagnosis of a pedigree affected with autosomal recessive Alport syndrome].

Ge L, Chen C, Liu L, Song Y.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Sep 10;36(9):914-917. doi: 10.3760/cma.j.issn.1003-9406.2019.09.015. Chinese.

PubMed [citation]
PMID:
31515789

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV004535307.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (2)

Description

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt COL4A4 protein function. This missense change has been observed in individuals with Alport syndrome (PMID: 31515789; Invitae). This variant is not present in population databases (gnomAD no frequency). This sequence change replaces phenylalanine, which is neutral and non-polar, with cysteine, which is neutral and slightly polar, at codon 1517 of the COL4A4 protein (p.Phe1517Cys).

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

Last Updated: Sep 29, 2024