List of variants in gene TNNI3 reported as pathogenic by OMIM

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.433C>T (p.Arg145Trp)	rs104894724	0.00001
NM_000363.5(TNNI3):c.586G>A (p.Asp196Asn)	rs104894727	0.00001
NM_000363.5(TNNI3):c.106A>C (p.Lys36Gln)	rs267607130
NM_000363.5(TNNI3):c.431T>A (p.Leu144Gln)	rs121917760
NM_000363.5(TNNI3):c.433C>G (p.Arg145Gly)	rs104894724
NM_000363.5(TNNI3):c.511G>A (p.Ala171Thr)	rs121917761
NM_000363.5(TNNI3):c.532A>G (p.Lys178Glu)	rs104894730
NM_000363.5(TNNI3):c.547_549del (p.Lys183del)	rs2147283135
NM_000363.5(TNNI3):c.555C>G (p.Asn185Lys)	rs267607129
NM_000363.5(TNNI3):c.569A>G (p.Asp190Gly)	rs104894728
NM_000363.5(TNNI3):c.575G>A (p.Arg192His)	rs104894729
NM_000363.5(TNNI3):c.5C>T (p.Ala2Val)	rs397516359
NM_000363.5(TNNI3):c.607G>A (p.Gly203Ser)	rs267607127
NM_000363.5(TNNI3):c.616A>C (p.Lys206Gln)	rs104894725
NM_000363.5(TNNI3):c.61C>T (p.Arg21Cys)	rs267607128

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