ClinVar Miner

List of variants in gene TNNC1 reported as uncertain significance by Ambry Genetics

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_003280.3(TNNC1):c.435C>A (p.Asp145Glu) rs267607124 0.00010
NM_003280.3(TNNC1):c.195C>T (p.Asp65=) rs370426309 0.00006
NM_003280.3(TNNC1):c.243G>C (p.Met81Ile) rs545564444 0.00002
NM_003280.3(TNNC1):c.180G>A (p.Met60Ile) rs1471808574 0.00001
NM_003280.3(TNNC1):c.202+5G>C rs759472560 0.00001
NM_003280.3(TNNC1):c.208G>A (p.Gly70Ser) rs772752716 0.00001
NM_003280.3(TNNC1):c.242T>C (p.Met81Thr) rs771216638 0.00001
NM_003280.3(TNNC1):c.304C>T (p.Arg102Cys) rs370103102 0.00001
NM_003280.3(TNNC1):c.305G>A (p.Arg102His) rs143020831 0.00001
NM_003280.3(TNNC1):c.386C>T (p.Thr129Met) rs749367654 0.00001
NM_003280.3(TNNC1):c.402G>T (p.Glu134Asp) rs397516847 0.00001
NM_003280.3(TNNC1):c.418G>A (p.Gly140Arg) rs752100917 0.00001
NM_003280.3(TNNC1):c.419G>A (p.Gly140Glu) rs764835690 0.00001
NM_003280.3(TNNC1):c.430A>G (p.Asn144Asp) rs730881061 0.00001
NM_003280.3(TNNC1):c.436G>A (p.Gly146Ser) rs567327895 0.00001
NM_003280.3(TNNC1):c.469A>C (p.Met157Leu) rs730880230 0.00001
NM_003280.3(TNNC1):c.116A>G (p.Lys39Arg)
NM_003280.3(TNNC1):c.154C>T (p.Pro52Ser)
NM_003280.3(TNNC1):c.155C>G (p.Pro52Arg) rs730881065
NM_003280.3(TNNC1):c.158C>A (p.Thr53Asn)
NM_003280.3(TNNC1):c.17A>G (p.Lys6Arg) rs2153230085
NM_003280.3(TNNC1):c.184G>A (p.Asp62Asn) rs1040079072
NM_003280.3(TNNC1):c.212C>T (p.Thr71Met) rs1706331809
NM_003280.3(TNNC1):c.225T>G (p.Asp75Glu)
NM_003280.3(TNNC1):c.230del (p.Phe77fs)
NM_003280.3(TNNC1):c.241A>T (p.Met81Leu)
NM_003280.3(TNNC1):c.25G>A (p.Val9Ile) rs1578264552
NM_003280.3(TNNC1):c.341T>G (p.Leu114Arg) rs2153229918
NM_003280.3(TNNC1):c.400G>A (p.Glu134Lys) rs1553651640
NM_003280.3(TNNC1):c.412A>G (p.Lys138Glu)
NM_003280.3(TNNC1):c.416A>G (p.Asp139Gly)
NM_003280.3(TNNC1):c.424_425del (p.Lys142fs)
NM_003280.3(TNNC1):c.440G>A (p.Arg147His) rs769919235
NM_003280.3(TNNC1):c.456G>C (p.Glu152Asp) rs568828576
NM_003280.3(TNNC1):c.53A>C (p.Asn18Thr)
NM_003280.3(TNNC1):c.57G>T (p.Glu19Asp)
NM_003280.3(TNNC1):c.5A>G (p.Asp2Gly) rs397516850
NM_003280.3(TNNC1):c.65C>T (p.Ala22Val)
NM_003280.3(TNNC1):c.94G>A (p.Glu32Lys) rs1553651750

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