NM_004260.4(RECQL4):c.1143G>C (p.Gln381His) AND Baller-Gerold syndrome

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

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jul 1, 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:: RCV002856323.2

Allele description

NM_004260.4(RECQL4):c.1143G>C (p.Gln381His)

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.1143G>C (p.Gln381His)

HGVS:

NC_000008.11:g.144515879C>G
NG_016430.2:g.6948G>C
NG_033083.1:g.2915C>G
NG_033083.2:g.2889C>G
NM_001413017.1:c.1047G>C
NM_001413018.1:c.1143G>C
NM_001413019.1:c.1143G>C
NM_001413020.1:c.1047G>C
NM_001413021.1:c.72G>C
NM_001413022.1:c.72G>C
NM_001413023.1:c.72G>C
NM_001413024.1:c.72G>C
NM_001413025.1:c.1014G>C
NM_001413027.1:c.10G>C
NM_001413028.1:c.72G>C
NM_001413029.1:c.792G>C
NM_001413030.1:c.10G>C
NM_001413031.1:c.10G>C
NM_001413032.1:c.10G>C
NM_001413033.1:c.1143G>C
NM_001413034.1:c.72G>C
NM_001413035.1:c.72G>C
NM_001413036.1:c.1143G>C
NM_001413037.1:c.72G>C
NM_001413038.1:c.72G>C
NM_001413039.1:c.1143G>C
NM_001413040.1:c.72G>C
NM_001413041.1:c.10G>C
NM_001413042.1:c.72G>C
NM_004260.4:c.1143G>CMANE SELECT
NP_001399946.1:p.Gln349His
NP_001399947.1:p.Gln381His
NP_001399948.1:p.Gln381His
NP_001399949.1:p.Gln349His
NP_001399950.1:p.Gln24His
NP_001399951.1:p.Gln24His
NP_001399952.1:p.Gln24His
NP_001399953.1:p.Gln24His
NP_001399954.1:p.Gln338His
NP_001399956.1:p.Glu4Gln
NP_001399957.1:p.Gln24His
NP_001399958.1:p.Gln264His
NP_001399959.1:p.Glu4Gln
NP_001399960.1:p.Glu4Gln
NP_001399961.1:p.Glu4Gln
NP_001399962.1:p.Gln381His
NP_001399963.1:p.Gln24His
NP_001399964.1:p.Gln24His
NP_001399965.1:p.Gln381His
NP_001399966.1:p.Gln24His
NP_001399967.1:p.Gln24His
NP_001399968.1:p.Gln381His
NP_001399969.1:p.Gln24His
NP_001399970.1:p.Glu4Gln
NP_001399971.1:p.Gln24His
NP_004251.4:p.Gln381His
LRG_277t1:c.1143G>C
LRG_277:g.6948G>C
LRG_277p1:p.Gln381His
NC_000008.10:g.145741263C>G
NR_182090.1:n.1192G>C
NR_182091.1:n.1192G>C
NR_182092.1:n.1192G>C

Protein change:

E4Q

Molecular consequence:

NM_001413017.1:c.1047G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413018.1:c.1143G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413019.1:c.1143G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413020.1:c.1047G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413021.1:c.72G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413022.1:c.72G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413023.1:c.72G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413024.1:c.72G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413025.1:c.1014G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413027.1:c.10G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413028.1:c.72G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413029.1:c.792G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413030.1:c.10G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413031.1:c.10G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413032.1:c.10G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413033.1:c.1143G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413034.1:c.72G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413035.1:c.72G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413036.1:c.1143G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413037.1:c.72G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413038.1:c.72G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413039.1:c.1143G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413040.1:c.72G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413041.1:c.10G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001413042.1:c.72G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_004260.4:c.1143G>C - 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
SCV003211657	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Jul 1, 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

SCV003211657

Invitae

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Jul 1, 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, SCV003211657.2

#	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 glutamine, which is neutral and polar, with histidine, which is basic and polar, at codon 381 of the RECQL4 protein (p.Gln381His).

#	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: Feb 20, 2024

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