ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.10009A>C (p.Ile3337Leu)

dbSNP: rs145645790
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000155999 SCV000205711 uncertain significance not specified 2013-10-11 criteria provided, single submitter clinical testing Variant classified as Uncertain Significance - Favor Benign. The Ile3337Leu vari ant in DNAH11 has not been previously identified in individuals with pulmonary d isease or in large population studies. Isoleucine (Ile) at position 3337 is poor ly conserved in evolution and at least 1 mammal (armadillo) carries the variant amino acid, raising the possibility that this change may be tolerated. Additiona l computational analyses (biochemical amino acid properties, AlignGVGD, PolyPhen 2, and SIFT) also suggest that this variant may not impact the protein, though t his information is not predictive enough to rule out pathogenicity. In summary, the lack of evolutionary conservation suggests that this variant may be more lik ely benign, but additional information is needed to fully assess its clinical si gnificance.

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