ClinVar Miner

Submissions for variant NM_000037.4(ANK1):c.4538G>A (p.Gly1513Asp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neuberg Centre For Genomic Medicine, NCGM RCV003448774 SCV004176481 uncertain significance Hereditary spherocytosis type 1 2023-03-01 criteria provided, single submitter clinical testing The missense c.4538G>A (p.Gly1513Asp) variant in ANK1 gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. The p.Gly1513Asp variant is novel (not in any individuals) in both gnomAD Exomes and 1000 Genomes databases. This variant has not been reported to the ClinVar database. The amino acid change p.Gly1513Asp in ANK1 is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. The amino acid Gly at position 1513 is changed to a Asp changing protein sequence and it might alter its composition and physico-chemical properties. For these reasons, this variant has been classified as a Variant of Uncertain Significance (VUS).

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