ClinVar Miner

Submissions for variant NM_152263.4(TPM3):c.855del (p.Ter286AsnextTer?)

dbSNP: rs199474719
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000013266 SCV000033513 pathogenic Congenital myopathy 4B, autosomal recessive 2008-09-01 no assertion criteria provided literature only
TPM3 homepage - Leiden Muscular Dystrophy pages RCV000128707 SCV000172347 not provided not provided no assertion provided not provided

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