ClinVar Miner

Submissions for variant NM_014921.5(ADGRL1):c.671G>A (p.Arg224His)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Molecular Pathology, SA Pathology RCV003447790 SCV004175548 uncertain significance Developmental delay, behavioral abnormalities, and neuropsychiatric disorders 2022-11-21 criteria provided, single submitter clinical testing The ADGRL1 c.686G>A variant is classified as VUS (PP3) The ADGRL1 c.686G>A variant is a single nucleotide change in exon 6/24 of the ADGRL1 gene, which is predicted to change the amino acid arginine at position 229 in the protein to histidine. This variant is present at low frequency in population databases (gnomAD allele frequency = 0.00065%; 1 het and 0 hom in 152190 sequenced alleles; highest frequency = 0.0014%, Non-Finnish European population) (PM2 not applied). Computational predictions support a deleterious effect on the gene or gene product (PP3). The variant has been reported in dbSNP (rs1251422301). It has not been reported in ClinVar or HGMD.

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