ClinVar Miner

List of variants reported as pathogenic for Bailey-Bloch congenital myopathy

Included ClinVar conditions (1):
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Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_145064.3(STAC3):c.851G>C (p.Trp284Ser) rs140291094 0.00039
NM_145064.3(STAC3):c.862A>T (p.Lys288Ter) rs371720347 0.00022
NM_145064.3(STAC3):c.739C>T (p.Gln247Ter) rs1202215410 0.00001
NM_145064.3(STAC3):c.297_301del (p.Pro100fs)
NM_145064.3(STAC3):c.383_399del (p.His128fs) rs1555194630
NM_145064.3(STAC3):c.432+4A>T rs751033943
NM_145064.3(STAC3):c.468_469del (p.Tyr157fs)
NM_145064.3(STAC3):c.694del (p.Ala232fs) rs774555559
NM_145064.3(STAC3):c.763_766del (p.Leu255fs) rs773050511
NM_145064.3(STAC3):c.816_817del (p.Lys273fs)
NM_145064.3(STAC3):c.997-1G>T rs779483367

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