ClinVar Miner

List of variants in gene MYOZ2 reported as likely benign for not specified

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Gene type:
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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_016599.5(MYOZ2):c.738A>G (p.Ile246Met) rs140126678 0.00220
NM_016599.5(MYOZ2):c.39G>A (p.Gln13=) rs145688699 0.00024
NM_016599.5(MYOZ2):c.76+10A>G rs372006344 0.00012
NM_016599.5(MYOZ2):c.303G>A (p.Ser101=) rs527258961 0.00009
NM_016599.5(MYOZ2):c.245A>C (p.Asn82Thr) rs149125238 0.00007
NM_016599.5(MYOZ2):c.-41G>A rs532582620 0.00006
NM_016599.5(MYOZ2):c.-14-20T>C rs765760107 0.00003
NM_016599.5(MYOZ2):c.423C>T (p.Thr141=) rs148220911 0.00003
NM_016599.5(MYOZ2):c.768C>A (p.Thr256=) rs727503333 0.00003
NM_016599.5(MYOZ2):c.504T>C (p.Pro168=) rs769668877 0.00002
NM_016599.5(MYOZ2):c.561-13T>A rs774606671 0.00002
NM_016599.5(MYOZ2):c.190A>C (p.Arg64=) rs727505324 0.00001
NM_016599.5(MYOZ2):c.247-3C>T rs774202003 0.00001
NM_016599.5(MYOZ2):c.330C>T (p.Asn110=) rs370237979 0.00001
NM_016599.5(MYOZ2):c.560+9A>G rs397517290 0.00001
NM_016599.5(MYOZ2):c.17C>G (p.Thr6Ser) rs397517289
NM_016599.5(MYOZ2):c.84T>C (p.Asp28=) rs397517292

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