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NM_019032.6(ADAMTSL4):c.356G>A (p.Arg119Gln) AND Inborn genetic diseases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jan 23, 2024
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:
RCV004370609.1

Allele description [Variation Report for NM_019032.6(ADAMTSL4):c.356G>A (p.Arg119Gln)]

NM_019032.6(ADAMTSL4):c.356G>A (p.Arg119Gln)

Genes:
ADAMTSL4:ADAMTS like 4 [Gene - OMIM - HGNC]
ADAMTSL4-AS2:ADAMTSL4 antisense RNA 2 [Gene - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1q21.2
Genomic location:
Preferred name:
NM_019032.6(ADAMTSL4):c.356G>A (p.Arg119Gln)
HGVS:
  • NC_000001.11:g.150553175G>A
  • NG_012172.1:g.8754G>A
  • NM_001288607.2:c.356G>A
  • NM_001288608.2:c.356G>A
  • NM_001378596.1:c.356G>A
  • NM_019032.6:c.356G>AMANE SELECT
  • NM_025008.5:c.356G>A
  • NP_001275536.1:p.Arg119Gln
  • NP_001275537.1:p.Arg119Gln
  • NP_001365525.1:p.Arg119Gln
  • NP_061905.2:p.Arg119Gln
  • NP_079284.2:p.Arg119Gln
  • NC_000001.10:g.150525651G>A
  • NM_019032.4:c.356G>A
Protein change:
R119Q
Molecular consequence:
  • NM_001288607.2:c.356G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001288608.2:c.356G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001378596.1:c.356G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_019032.6:c.356G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_025008.5:c.356G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Inborn genetic diseases
Identifiers:
MeSH: D030342; MedGen: C0950123

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004854517Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Jan 23, 2024) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV004854517.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The c.356G>A (p.R119Q) alteration is located in exon 5 (coding exon 3) of the ADAMTSL4 gene. This alteration results from a G to A substitution at nucleotide position 356, causing the arginine (R) at amino acid position 119 to be replaced by a glutamine (Q). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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

Last Updated: May 7, 2024