List of variants in gene TNNI3 reported as benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 35

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.12-129A>G	rs11671293	0.36524
NM_000363.5(TNNI3):c.11+128T>C	rs11667847	0.21853
NM_000363.5(TNNI3):c.11+99C>G	rs3729708	0.09027
NM_000363.5(TNNI3):c.151-106A>G	rs3729709	0.07534
NM_000363.5(TNNI3):c.109-132A>G	rs73617693	0.07431
NM_000363.5(TNNI3):c.549+211A>G	rs10414493	0.06837
NM_000363.5(TNNI3):c.109-185A>C	rs2278281	0.06191
NM_000363.5(TNNI3):c.108+21G>A	rs3729837	0.04872
NC_000019.10:g.55151563T>G	rs73935312	0.03615
NM_000363.5(TNNI3):c.198G>A (p.Glu66=)	rs3729710	0.03372
NM_000363.5(TNNI3):c.549+128A>C	rs10414696	0.03166
NM_000363.5(TNNI3):c.108+182C>G	rs28526132	0.02827
NM_000363.5(TNNI3):c.244C>T (p.Pro82Ser)	rs77615401	0.00699
NM_000363.5(TNNI3):c.-47C>T	rs202159627	0.00625
NM_000363.5(TNNI3):c.273G>A (p.Ala91=)	rs75491697	0.00198
NM_000363.5(TNNI3):c.550-10C>T	rs201240150	0.00190
NM_000363.5(TNNI3):c.109-17C>A	rs139150276	0.00147
NM_000363.5(TNNI3):c.-85A>C	rs186540595	0.00142
NM_000363.5(TNNI3):c.373-15C>G	rs192630178	0.00141
NM_000363.5(TNNI3):c.-103C>T	rs557391836	0.00102
NM_000363.5(TNNI3):c.207C>G (p.Arg69=)	rs201422579	0.00012
NM_000363.5(TNNI3):c.*35C>T	rs375447438	0.00004
NM_000363.5(TNNI3):c.-17C>A	rs1439592517	0.00003
NM_000363.5(TNNI3):c.-8G>A	rs773513015	0.00003
NM_000363.5(TNNI3):c.*16G>A	rs778220410	0.00002
NM_000363.5(TNNI3):c.550-14T>C	rs758992431	0.00001
NC_000019.10:g.55151632C>A	rs2147281499
NM_000363.5(TNNI3):c.-60G>A	rs2147286810
NM_000363.5(TNNI3):c.-98C>A	rs12973773
NM_000363.5(TNNI3):c.108+108G>C	rs3729838
NM_000363.5(TNNI3):c.12-50_12-47dup	rs377373012
NM_000363.5(TNNI3):c.173A>G (p.Lys58Arg)	rs878853955
NM_000363.5(TNNI3):c.373-115G>C	rs2288529
NM_000363.5(TNNI3):c.549+68_549+69insGGCCTA	rs139158921
NM_000363.5(TNNI3):c.550-256_550-255del	rs56007758

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