ClinVar Miner

List of variants reported as uncertain significance for Hypertrophic cardiomyopathy 7

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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_000363.5(TNNI3):c.373-15C>G rs192630178 0.00141
NM_000363.5(TNNI3):c.373-4C>G rs2288530 0.00007
NM_001281740.3(FHOD3):c.1943T>C (p.Ile648Thr) rs144993045 0.00007
NM_000363.5(TNNI3):c.139T>C (p.Leu47=) rs587780967 0.00006
NM_000363.5(TNNI3):c.356C>A (p.Thr119Asn) rs184709702 0.00006
NM_000363.5(TNNI3):c.*44A>G rs1182120462 0.00004
NM_000363.5(TNNI3):c.372+7C>T rs367809676 0.00004
NM_000363.5(TNNI3):c.484C>T (p.Arg162Trp) rs368861241 0.00004
NM_000363.5(TNNI3):c.151-6C>G rs377258542 0.00002
NM_000363.5(TNNI3):c.236G>T (p.Arg79Leu) rs397516342 0.00002
NM_000363.5(TNNI3):c.439G>C (p.Val147Leu) rs777782551 0.00002
NM_000363.5(TNNI3):c.-45C>T rs1242688089 0.00001
NM_000363.5(TNNI3):c.217G>C (p.Gly73Arg) rs1170054667 0.00001
NM_000363.5(TNNI3):c.283-9C>T rs759922995 0.00001
NM_000363.5(TNNI3):c.347C>G (p.Ala116Gly) rs777177571 0.00001
NM_000363.5(TNNI3):c.550-11C>T rs886054635 0.00001
NM_000363.5(TNNI3):c.5C>T (p.Ala2Val) rs397516359 0.00001
NM_001256715.2(DNAAF3):c.484C>A (p.Arg162Ser) rs760391305 0.00001
NM_000363.5(TNNI3):c.104C>A (p.Ala35Asp) rs1190447904
NM_000363.5(TNNI3):c.109-15A>G rs779144176
NM_000363.5(TNNI3):c.124T>C (p.Ser42Pro) rs2515502440
NM_000363.5(TNNI3):c.185A>G (p.Glu62Gly)
NM_000363.5(TNNI3):c.206G>A (p.Arg69His) rs1401968020
NM_000363.5(TNNI3):c.370G>C (p.Glu124Gln) rs727503506
NM_000363.5(TNNI3):c.440T>C (p.Val147Ala) rs2085712229
NM_000363.5(TNNI3):c.466C>G (p.Gln156Glu) rs2085712011
NM_000363.5(TNNI3):c.550-1G>A rs1555863017
NM_000363.5(TNNI3):c.596G>A (p.Ser199Asn) rs730881091
NM_001256715.2(DNAAF3):c.990C>T (p.Thr330=) rs371092262
NM_001276345.2(TNNT2):c.852-3C>T rs749454768

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