NM_004260.4(RECQL4):c.1093C>G (p.Arg365Gly) AND Baller-Gerold syndrome

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Sep 29, 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:: RCV003072707.3

Allele description [Variation Report for NM_004260.4(RECQL4):c.1093C>G (p.Arg365Gly)]

NM_004260.4(RECQL4):c.1093C>G (p.Arg365Gly)

Gene:

RECQL4:RecQ like helicase 4 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

8q24.3

Genomic location:

Preferred name:

NM_004260.4(RECQL4):c.1093C>G (p.Arg365Gly)

HGVS:

NC_000008.11:g.144516026G>C
NG_016430.2:g.6801C>G
NG_033083.2:g.3036G>C
NM_001413017.1:c.997C>G
NM_001413018.1:c.1093C>G
NM_001413019.1:c.1093C>G
NM_001413020.1:c.997C>G
NM_001413021.1:c.22C>G
NM_001413022.1:c.22C>G
NM_001413023.1:c.22C>G
NM_001413024.1:c.22C>G
NM_001413025.1:c.964C>G
NM_001413027.1:c.-41C>G
NM_001413028.1:c.22C>G
NM_001413029.1:c.742C>G
NM_001413030.1:c.-41C>G
NM_001413031.1:c.-41C>G
NM_001413032.1:c.-41C>G
NM_001413033.1:c.1093C>G
NM_001413034.1:c.22C>G
NM_001413035.1:c.22C>G
NM_001413036.1:c.1093C>G
NM_001413037.1:c.22C>G
NM_001413038.1:c.22C>G
NM_001413039.1:c.1093C>G
NM_001413040.1:c.22C>G
NM_001413041.1:c.-41C>G
NM_001413042.1:c.22C>G
NM_001413043.1:c.-248C>G
NM_004260.4:c.1093C>GMANE SELECT
NP_001399946.1:p.Arg333Gly
NP_001399947.1:p.Arg365Gly
NP_001399948.1:p.Arg365Gly
NP_001399949.1:p.Arg333Gly
NP_001399950.1:p.Arg8Gly
NP_001399951.1:p.Arg8Gly
NP_001399952.1:p.Arg8Gly
NP_001399953.1:p.Arg8Gly
NP_001399954.1:p.Arg322Gly
NP_001399957.1:p.Arg8Gly
NP_001399958.1:p.Arg248Gly
NP_001399962.1:p.Arg365Gly
NP_001399963.1:p.Arg8Gly
NP_001399964.1:p.Arg8Gly
NP_001399965.1:p.Arg365Gly
NP_001399966.1:p.Arg8Gly
NP_001399967.1:p.Arg8Gly
NP_001399968.1:p.Arg365Gly
NP_001399969.1:p.Arg8Gly
NP_001399971.1:p.Arg8Gly
NP_004251.4:p.Arg365Gly
LRG_277t1:c.1093C>G
LRG_277:g.6801C>G
LRG_277p1:p.Arg365Gly
NC_000008.10:g.145741410G>C
NG_033083.1:g.3062G>C
NR_182090.1:n.1142C>G
NR_182091.1:n.1142C>G
NR_182092.1:n.1142C>G

Protein change:

R248G

Molecular consequence:

NM_001413017.1:c.997C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413018.1:c.1093C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413019.1:c.1093C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413020.1:c.997C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413021.1:c.22C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413022.1:c.22C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413023.1:c.22C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413024.1:c.22C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413025.1:c.964C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413028.1:c.22C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413029.1:c.742C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413033.1:c.1093C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413034.1:c.22C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413035.1:c.22C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413036.1:c.1093C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413037.1:c.22C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413038.1:c.22C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413039.1:c.1093C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413040.1:c.22C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001413042.1:c.22C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_004260.4:c.1093C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Baller-Gerold syndrome (BGS)
Synonyms:: Craniosynostosis radial aplasia syndrome; Craniosynostosis with radial defects
Identifiers:: MONDO: MONDO:0009039; MedGen: C0265308; Orphanet: 1225; OMIM: 218600

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003471541	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Sep 29, 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

SCV003471541

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Sep 29, 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 Labcorp Genetics (formerly Invitae), Labcorp, SCV003471541.2

#	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. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has not been reported in the literature in individuals affected with RECQL4-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces arginine, which is basic and polar, with glycine, which is neutral and non-polar, at codon 365 of the RECQL4 protein (p.Arg365Gly).

#	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: Sep 29, 2024

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