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NM_001142800.2(EYS):c.8689T>C (p.Phe2897Leu) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Aug 23, 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:
RCV001914439.6

Allele description [Variation Report for NM_001142800.2(EYS):c.8689T>C (p.Phe2897Leu)]

NM_001142800.2(EYS):c.8689T>C (p.Phe2897Leu)

Genes:
PHF3:PHD finger protein 3 [Gene - OMIM - HGNC]
EYS:eyes shut homolog [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
6q12
Genomic location:
Preferred name:
NM_001142800.2(EYS):c.8689T>C (p.Phe2897Leu)
HGVS:
  • NC_000006.12:g.63721342A>G
  • NG_023443.2:g.1990884T>C
  • NG_034034.2:g.90542A>G
  • NM_001142800.2:c.8689T>CMANE SELECT
  • NM_001290259.2:c.*7634A>G
  • NM_001292009.2:c.8752T>C
  • NM_001370348.2:c.*7634A>GMANE SELECT
  • NM_001370349.2:c.*7634A>G
  • NM_001370350.2:c.*7634A>G
  • NM_015153.4:c.*7634A>G
  • NP_001136272.1:p.Phe2897Leu
  • NP_001278938.1:p.Phe2918Leu
  • NC_000006.11:g.64431238A>G
Protein change:
F2897L
Links:
dbSNP: rs1207064455
NCBI 1000 Genomes Browser:
rs1207064455
Molecular consequence:
  • NM_001290259.2:c.*7634A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001370348.2:c.*7634A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001370349.2:c.*7634A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001370350.2:c.*7634A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_015153.4:c.*7634A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001142800.2:c.8689T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001292009.2:c.8752T>C - 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
SCV002192056Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Aug 23, 2022) 		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

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, SCV002192056.3

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

Description

This sequence change replaces phenylalanine, which is neutral and non-polar, with leucine, which is neutral and non-polar, at codon 2897 of the EYS protein (p.Phe2897Leu). 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. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). ClinVar contains an entry for this variant (Variation ID: 1420662). This variant has not been reported in the literature in individuals affected with EYS-related conditions. This variant is not present in population databases (gnomAD no frequency).

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

Last Updated: Sep 29, 2024