ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.4800G>T (p.Gly1600=) (rs397516314)

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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,Partners HealthCare Personalized Medicine RCV000036164 SCV000059816 likely benign not specified 2010-10-07 criteria provided, single submitter clinical testing Gly1600Gly in exon 35 of MYO7A: This variant is not expected to have clinical si gnificance because it does not alter an amino acid residue and is not located ne ar a splice junction.

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