ClinVar Miner

List of variants in gene TNNI3 reported as likely benign for Cardiovascular phenotype

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Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_000363.5(TNNI3):c.273G>A (p.Ala91=) rs75491697 0.00198
NM_000363.5(TNNI3):c.25-4C>T rs202086705 0.00069
NM_000363.5(TNNI3):c.132G>C (p.Ser44=) rs727504941 0.00012
NM_000363.5(TNNI3):c.207C>G (p.Arg69=) rs201422579 0.00012
NM_000363.5(TNNI3):c.246G>T (p.Pro82=) rs397516343 0.00007
NM_000363.5(TNNI3):c.139T>C (p.Leu47=) rs587780967 0.00006
NM_000363.5(TNNI3):c.363C>T (p.Asn121=) rs371490136 0.00006
NM_000363.5(TNNI3):c.39C>G (p.Arg13=) rs397516346 0.00005
NM_000363.5(TNNI3):c.303C>T (p.His101=) rs199539066 0.00004
NM_000363.5(TNNI3):c.6G>A (p.Ala2=) rs397516361 0.00004
NM_000363.5(TNNI3):c.93G>C (p.Thr31=) rs765719980 0.00003
NM_000363.5(TNNI3):c.471G>A (p.Ala157=) rs747756509 0.00002
NM_000363.5(TNNI3):c.213G>A (p.Glu71=) rs770487905 0.00001
NM_000363.5(TNNI3):c.277C>T (p.Leu93=) rs1221536494 0.00001
NM_000363.5(TNNI3):c.300C>G (p.Leu100=) rs772145171 0.00001
NM_000363.5(TNNI3):c.340A>G (p.Ile114Val) rs730881070 0.00001
NM_000363.5(TNNI3):c.34C>T (p.Pro12Ser) rs553214254 0.00001
NM_000363.5(TNNI3):c.417T>C (p.Phe139=) rs1371643118 0.00001
NM_000363.5(TNNI3):c.426C>T (p.Pro142=) rs532949659 0.00001
NM_000363.5(TNNI3):c.474G>C (p.Leu158=) rs749880457 0.00001
NM_000363.5(TNNI3):c.585C>T (p.Ile195=) rs200085986 0.00001
NM_000363.5(TNNI3):c.11G>A (p.Gly4Glu) rs1351385449
NM_000363.5(TNNI3):c.16A>G (p.Ser6Gly)
NM_000363.5(TNNI3):c.201G>A (p.Glu67=)
NM_000363.5(TNNI3):c.207C>T (p.Arg69=) rs201422579
NM_000363.5(TNNI3):c.339C>T (p.Asp113=) rs786204400
NM_000363.5(TNNI3):c.444G>A (p.Arg148=)
NM_000363.5(TNNI3):c.519C>T (p.Leu173=)
NM_000363.5(TNNI3):c.525G>A (p.Gln175=)
NM_000363.5(TNNI3):c.63C>G (p.Arg21=) rs1555864377
NM_000363.5(TNNI3):c.93G>A (p.Thr31=)

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