List of variants in gene TNNT3 reported as uncertain significance for congenital limb malformation

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_006757.3(TNNT3):c.-182C>G	rs574250591	0.00207
NM_006757.4(TNNT3):c.107-6G>A	rs200739738	0.00202
NM_006757.4(TNNT3):c.759C>T (p.Val253=)	rs140388684	0.00112
NM_006757.4(TNNT3):c.68-14C>T	rs202175253	0.00084
NM_006757.4(TNNT3):c.480+9C>T	rs374137056	0.00016
NM_006757.4(TNNT3):c.429G>A (p.Lys143=)	rs184687090	0.00011
NM_006757.4(TNNT3):c.101C>T (p.Ala34Val)	rs757234740	0.00008
NM_006757.4(TNNT3):c.515G>A (p.Arg172Gln)	rs200937415	0.00006
NM_006757.4(TNNT3):c.417C>T (p.Asp139=)	rs367932695	0.00004
NM_006757.4(TNNT3):c.*151G>A	rs544425439	0.00003
NM_006757.4(TNNT3):c.*86C>T	rs200540491	0.00003
NM_006757.4(TNNT3):c.*57C>T	rs772512169	0.00001
NM_006757.4(TNNT3):c.257A>G (p.Glu86Gly)	rs755143093	0.00001
NM_006757.4(TNNT3):c.504G>A (p.Lys168=)	rs1367784766	0.00001
NM_006757.4(TNNT3):c.690G>A (p.Thr230=)	rs753756081	0.00001
NM_006757.3(TNNT3):c.-177dup	rs886048104
NM_006757.4(TNNT3):c.*62G>T	rs886048105
NM_006757.4(TNNT3):c.-22G>T	rs879755445
NM_006757.4(TNNT3):c.176T>C (p.Ile59Thr)	rs2133451032
NM_006757.4(TNNT3):c.187C>T (p.Arg63Cys)	rs199474721
NM_006757.4(TNNT3):c.299G>A (p.Arg100His)
NM_006757.4(TNNT3):c.464G>A (p.Ser155Asn)	rs1854343743
NM_006757.4(TNNT3):c.480+8C>T	rs370243709
NM_006757.4(TNNT3):c.491A>G (p.Lys164Arg)	rs1161353535
NM_006757.4(TNNT3):c.496G>A (p.Gly166Ser)	rs775584381
NM_006757.4(TNNT3):c.524AGA[2] (p.Lys177del)	rs765275660
NM_006757.4(TNNT3):c.591-12C>T	rs1854492172
NM_006757.4(TNNT3):c.668G>C (p.Arg223Pro)	rs766691409
NM_006757.4(TNNT3):c.722+15C>T	rs201336939
NM_006757.4(TNNT3):c.757G>C (p.Val253Leu)	rs1855793483

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