ClinVar Miner

List of variants in gene TNNI3 reported as uncertain significance by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_000363.5(TNNI3):c.356C>A (p.Thr119Asn) rs184709702 0.00006
NM_000363.5(TNNI3):c.236G>T (p.Arg79Leu) rs397516342 0.00004
NM_000363.5(TNNI3):c.282+5C>G rs770260866 0.00004
NM_000363.5(TNNI3):c.292C>T (p.Arg98Ter) rs730881068 0.00004
NM_000363.5(TNNI3):c.-8G>A rs773513015 0.00003
NM_000363.5(TNNI3):c.304G>A (p.Ala102Thr) rs374618872 0.00003
NM_000363.5(TNNI3):c.143A>C (p.Gln48Pro) rs200720341 0.00002
NM_000363.5(TNNI3):c.151-6C>G rs377258542 0.00002
NM_000363.5(TNNI3):c.347C>G (p.Ala116Gly) rs777177571 0.00002
NM_000363.5(TNNI3):c.439G>C (p.Val147Leu) rs777782551 0.00002
NM_000363.5(TNNI3):c.331A>G (p.Arg111Gly) rs730881088 0.00001
NM_000363.5(TNNI3):c.34C>T (p.Pro12Ser) rs553214254 0.00001
NM_000363.5(TNNI3):c.370G>C (p.Glu124Gln) rs727503506 0.00001
NM_000363.5(TNNI3):c.421C>T (p.Arg141Trp) rs730881071 0.00001
NM_000363.5(TNNI3):c.114A>T (p.Lys38Asn) rs730881066
NM_000363.5(TNNI3):c.125C>T (p.Ser42Phe) rs2085732640
NM_000363.5(TNNI3):c.150+8C>T rs1568859373
NM_000363.5(TNNI3):c.15C>A (p.Ser5Arg) rs989588363
NM_000363.5(TNNI3):c.204del (p.Arg69fs) rs727504872
NM_000363.5(TNNI3):c.208G>A (p.Gly70Arg) rs730881067
NM_000363.5(TNNI3):c.245C>G (p.Pro82Arg) rs752503819
NM_000363.5(TNNI3):c.25-10_25-8del rs2147286052
NM_000363.5(TNNI3):c.586G>T (p.Asp196Tyr) rs104894727
NM_000363.5(TNNI3):c.5C>T (p.Ala2Val) rs397516359
NM_000363.5(TNNI3):c.64C>G (p.Arg22Gly) rs2085738602

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