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NM_004260.4(RECQL4):c.1073T>G (p.Met358Arg) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Oct 21, 2021
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:
RCV002484591.1

Allele description [Variation Report for NM_004260.4(RECQL4):c.1073T>G (p.Met358Arg)]

NM_004260.4(RECQL4):c.1073T>G (p.Met358Arg)

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.1073T>G (p.Met358Arg)
HGVS:
  • NC_000008.11:g.144516046A>C
  • NG_016430.2:g.6781T>G
  • NG_033083.1:g.3082A>C
  • NM_004260.4:c.1073T>GMANE SELECT
  • NP_004251.4:p.Met358Arg
  • LRG_277t1:c.1073T>G
  • LRG_277:g.6781T>G
  • LRG_277p1:p.Met358Arg
  • NC_000008.10:g.145741430A>C
  • NG_016430.1:g.6781T>G
Protein change:
M358R
Links:
dbSNP: rs376652305
NCBI 1000 Genomes Browser:
rs376652305
Molecular consequence:
  • NM_004260.4:c.1073T>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
Name:
Rapadilino syndrome
Synonyms:
Radial and patellar aplasia; Radial and patellar hypoplasia; Absent thumbs, dislocated joints, long face with narrow palpebral fissures, long slender nose, arched palate
Identifiers:
MONDO: MONDO:0009955; MedGen: C1849453; Orphanet: 3021; OMIM: 266280
Name:
Rothmund-Thomson syndrome type 2 (RTS2)
Identifiers:
MONDO: MONDO:0016369; MedGen: C5203410; OMIM: 268400

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002786771Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Oct 21, 2021) 		unknownclinical testing

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

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Fulgent Genetics, Fulgent Genetics, SCV002786771.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024