NM_001123385.2(BCOR):c.2396A>G (p.Lys799Arg) AND Oculofaciocardiodental syndrome

This record was updated by the submitter. Please see the current version.

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Oct 20, 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:: RCV002994378.2

Allele description

NM_001123385.2(BCOR):c.2396A>G (p.Lys799Arg)

Gene:

BCOR:BCL6 corepressor [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xp11.4

Genomic location:

Preferred name:

NM_001123385.2(BCOR):c.2396A>G (p.Lys799Arg)

HGVS:

NC_000023.11:g.40072950T>C
NG_008880.1:g.109380A>G
NM_001123383.1:c.2396A>G
NM_001123384.2:c.2396A>G
NM_001123385.2:c.2396A>GMANE SELECT
NM_017745.6:c.2396A>G
NP_001116855.1:p.Lys799Arg
NP_001116856.1:p.Lys799Arg
NP_001116857.1:p.Lys799Arg
NP_001116857.1:p.Lys799Arg
NP_060215.4:p.Lys799Arg
LRG_627t1:c.2396A>G
LRG_627t2:c.2396A>G
LRG_627:g.109380A>G
LRG_627p1:p.Lys799Arg
LRG_627p2:p.Lys799Arg
NC_000023.10:g.39932203T>C
NM_001123385.1:c.2396A>G

Protein change:

K799R

Molecular consequence:

NM_001123383.1:c.2396A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001123384.2:c.2396A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001123385.2:c.2396A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_017745.6:c.2396A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Oculofaciocardiodental syndrome (MCOPS2)
Synonyms:: Microphthalmia cataracts radiculomegaly and septal heart defects
Identifiers:: MONDO: MONDO:0010261; MedGen: C1846265; OMIM: 300166

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003298045	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Oct 20, 2022)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003298045

Invitae

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Oct 20, 2022)

germline

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical 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 Invitae, SCV003298045.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

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. 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: "Benign"; Align-GVGD: "Class C25"). This variant has not been reported in the literature in individuals affected with BCOR-related conditions. This variant is present in population databases (rs769227489, gnomAD 0.01%). This sequence change replaces lysine, which is basic and polar, with arginine, which is basic and polar, at codon 799 of the BCOR protein (p.Lys799Arg).

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: May 1, 2024

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