ClinVar Miner

Submissions for variant NM_001089.3(ABCA3):c.1595T>C (p.Ile532Thr)

dbSNP: rs2093686483
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Johns Hopkins Genomics, Johns Hopkins University RCV001200888 SCV001371800 uncertain significance Interstitial lung disease due to ABCA3 deficiency 2020-01-16 criteria provided, single submitter clinical testing This ABCA3 variant is absent from a large population dataset and has not been reported in the literature, to our knowledge. Three bioinformatic tools queried predict that this substitution would be probably damaging, and the isoleucine residue at this position is evolutionarily conserved across all species assessed. Bioinformatic analysis predicts that this missense variant would not affect normal exon 13 splicing, although this has not been confirmed experimentally to our knowledge. We consider the clinical significance of c.1595T>C to be uncertain at this time.

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