"Color Diagnostics, LLC DBA Color Health"[submitter] AND "TNNT2"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1171777	NM_001276345.2(TNNT2):c.*3C>G	TNNT2	Single nucleotide variant (3 prime UTR variant)	Cardiomyopathy	GUncertain significance
Select item 921153	NM_001276345.2(TNNT2):c.*3C>A	TNNT2	Single nucleotide variant (3 prime UTR variant)	Cardiomyopathy +1 more	GConflicting classifications of pathogenicity
Select item 927992	NM_001276345.2(TNNT2):c.*2G>A	TNNT2	Single nucleotide variant (3 prime UTR variant)	Cardiomyopathy	GUncertain significance
Select item 43677	NM_001276345.2(TNNT2):c.887G>A (p.Arg296His)	TNNT2 (R286H +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +6 more	GUncertain significance
Select item 43676	NM_001276345.2(TNNT2):c.886C>T (p.Arg296Cys)	TNNT2 (R286C +5 more)	Single nucleotide variant (missense variant)	Cardiomyopathy, familial restrictive, 3 +7 more	GConflicting classifications of pathogenicity
Select item 180555	NM_001276345.2(TNNT2):c.883G>A (p.Gly295Arg)	TNNT2 (G285R +5 more)	Single nucleotide variant (missense variant)	not provided +5 more	GUncertain significance
Select item 388233	NM_001276345.2(TNNT2):c.882C>T (p.Thr294=)	TNNT2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +6 more	GLikely benign
Select item 629597	NM_001276345.2(TNNT2):c.864C>T (p.Arg288=)	TNNT2	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 2 +4 more	GLikely benign
Select item 43674	NM_001276345.2(TNNT2):c.863G>A (p.Arg288His)	TNNT2 (R278H +5 more)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 2 +6 more	GConflicting classifications of pathogenicity
Select item 12411	NM_001276345.2(TNNT2):c.862C>T (p.Arg288Cys)	TNNT2 (R278C +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +9 more	GConflicting classifications of pathogenicity
Select item 537266	NM_001276345.2(TNNT2):c.861C>A (p.Thr287=)	TNNT2	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 2 +5 more	GLikely benign
Select item 807896	NM_001276345.2(TNNT2):c.852-3C>T	TNNT2	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 2 +5 more	GConflicting classifications of pathogenicity
Select item 1172179	NM_001276345.2(TNNT2):c.849A>G (p.Lys283=)	TNNT2	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 2 +3 more	GConflicting classifications of pathogenicity
Select item 43672	NM_001276345.2(TNNT2):c.837C>T (p.Asn279=)	TNNT2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +6 more	GConflicting classifications of pathogenicity
Select item 181647	NM_001276345.2(TNNT2):c.835A>G (p.Asn279Asp)	TNNT2 (N269D +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1D +4 more	GUncertain significance
Select item 1332673	NM_001276345.2(TNNT2):c.834C>T (p.Ile278=)	TNNT2	Single nucleotide variant (synonymous variant)	Cardiomyopathy +3 more	GLikely benign
Select item 181646	NM_001276345.2(TNNT2):c.824G>A (p.Arg275Gln)	TNNT2 (R265Q +5 more)	Single nucleotide variant (missense variant)	Cardiomyopathy +4 more	GUncertain significance
Select item 43671	NM_001276345.2(TNNT2):c.815A>G (p.Asn272Ser)	TNNT2 (N262S +5 more)	Single nucleotide variant (missense variant)	Cardiomyopathy, familial restrictive, 3 +4 more	GUncertain significance
Select item 922494	NM_001276345.2(TNNT2):c.812T>G (p.Ile271Ser)	TNNT2 (I228S +5 more)	Single nucleotide variant (missense variant)	Cardiomyopathy, familial restrictive, 3 +3 more	GUncertain significance
Select item 926911	NM_001276345.2(TNNT2):c.811-1G>T	TNNT2	Single nucleotide variant (splice acceptor variant)	Cardiomyopathy	GUncertain significance
Select item 2774626	NM_001276345.2(TNNT2):c.811-13A>C	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy	GUncertain significance
Select item 181633	NM_001276345.2(TNNT2):c.810+5G>A	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy +4 more	GUncertain significance
Select item 43670	NM_001276345.2(TNNT2):c.803A>T (p.Lys268Ile)	TNNT2 (K258I +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +8 more	GConflicting classifications of pathogenicity
Select item 921661	NM_001276345.2(TNNT2):c.795G>A (p.Lys265=)	TNNT2	Single nucleotide variant (synonymous variant)	Cardiomyopathy	GLikely benign
Select item 1332351	NM_001276345.2(TNNT2):c.789G>A (p.Lys263=)	TNNT2	Single nucleotide variant (synonymous variant)	Cardiomyopathy	GLikely benign
Select item 43669	NM_001276345.2(TNNT2):c.788A>G (p.Lys263Arg)	TNNT2 (K253R +5 more)	Single nucleotide variant (missense variant)	Dilated Cardiomyopathy, Dominant +11 more	GBenign/Likely benign
Select item 404398	NM_001276345.2(TNNT2):c.779T>C (p.Leu260Pro)	TNNT2 (L250P +5 more)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 2 +5 more	GUncertain significance
Select item 2774627	NM_001276345.2(TNNT2):c.776A>T (p.Asp259Val)	TNNT2 (D243V +7 more)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance
Select item 2774628	NM_001276345.2(TNNT2):c.775G>T (p.Asp259Tyr)	TNNT2 (D216Y +7 more)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance
Select item 181630	NM_001276345.2(TNNT2):c.775G>A (p.Asp259Asn)	TNNT2 (D249N +5 more)	Single nucleotide variant (missense variant)	not provided +5 more	GUncertain significance
Select item 43668	NM_001276345.2(TNNT2):c.774C>T (p.Phe258=)	TNNT2	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 2 +6 more	GLikely benign
Select item 181645	NM_001276345.2(TNNT2):c.772T>G (p.Phe258Val)	TNNT2 (F248V +5 more)	Single nucleotide variant (missense variant)	Cardiomyopathy +4 more	GUncertain significance
Select item 181629	NM_001276345.2(TNNT2):c.772T>C (p.Phe258Leu)	TNNT2 (F248L +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1D +5 more	GUncertain significance
Select item 177873	NM_001276345.2(TNNT2):c.764C>T (p.Ala255Val)	TNNT2 (A245V +5 more)	Single nucleotide variant (missense variant)	not specified +7 more	GUncertain significance
Select item 43667	NM_001276345.2(TNNT2):c.762G>T (p.Glu254Asp)	TNNT2 (E244D +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +8 more	GConflicting classifications of pathogenicity
Select item 191800	NM_001276345.2(TNNT2):c.752A>G (p.Tyr251Cys)	TNNT2 (Y241C +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +5 more	GUncertain significance
Select item 1332481	NM_001276345.2(TNNT2):c.751T>C (p.Tyr251His)	TNNT2 (Y208H +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1172232	NM_001276345.2(TNNT2):c.747C>T (p.Ser249=)	TNNT2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2774629	NM_001276345.2(TNNT2):c.744G>A (p.Gln248=)	TNNT2	Single nucleotide variant (synonymous variant)	Cardiomyopathy	GLikely benign
Select item 1332218	NM_001276345.2(TNNT2):c.727G>A (p.Ala243Thr)	TNNT2 (A200T +5 more)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance
Select item 43664	NM_001276345.2(TNNT2):c.720-4G>T	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy, familial restrictive, 3 +7 more	GConflicting classifications of pathogenicity
Select item 181605	NM_001276345.2(TNNT2):c.720-5T>G	TNNT2	Single nucleotide variant (intron variant)	Cardiovascular phenotype +9 more	GConflicting classifications of pathogenicity
Select item 755790	NM_001276345.2(TNNT2):c.720-6G>T	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy +3 more	GLikely benign
Select item 43665	NM_001276345.2(TNNT2):c.720-6G>A	TNNT2	Single nucleotide variant (intron variant)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 43666	NM_001276345.2(TNNT2):c.720-7C>T	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy +4 more	GConflicting classifications of pathogenicity
Select item 294894	NM_001276345.2(TNNT2):c.720-9C>A	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy +4 more	GConflicting classifications of pathogenicity
Select item 1171991	NM_001276345.2(TNNT2):c.720-10G>A	TNNT2	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 2 +3 more	GLikely benign
Select item 43663	NM_001276345.2(TNNT2):c.720-13_720-11del	TNNT2	Deletion (intron variant)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 2774630	NM_001276345.2(TNNT2):c.720-32_720-14dup	TNNT2	Duplication (intron variant)	Cardiomyopathy +3 more	GConflicting classifications of pathogenicity
Select item 628663	NM_001276345.2(TNNT2):c.720-13C>G	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy +3 more	GLikely benign
Select item 923487	NM_001276345.2(TNNT2):c.720-14C>A	TNNT2	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 2 +3 more	GLikely benign
Select item 925704	NM_001276345.2(TNNT2):c.719+3G>T	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy +1 more	GUncertain significance
Select item 918895	NM_001276345.2(TNNT2):c.719+3G>A	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy	GLikely benign
Select item 1172229	NM_001276345.2(TNNT2):c.719G>A (p.Arg240Lys)	TNNT2 (R197K +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GUncertain significance
Select item 1171967	NM_001276345.2(TNNT2):c.709G>C (p.Asp237His)	TNNT2 (D194H +5 more)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance
Select item 181626	NM_001276345.2(TNNT2):c.706G>A (p.Glu236Lys)	TNNT2 (E226K +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1D +5 more	GUncertain significance
Select item 2774631	NM_001276345.2(TNNT2):c.693T>C (p.Ile231=)	TNNT2	Single nucleotide variant (synonymous variant)	Cardiomyopathy	GLikely benign
Select item 181604	NM_001276345.2(TNNT2):c.692T>C (p.Ile231Thr)	TNNT2 (I221T +5 more)	Single nucleotide variant (missense variant)	Cardiomyopathy +8 more	GConflicting classifications of pathogenicity
Select item 294895	NM_001276345.2(TNNT2):c.691A>G (p.Ile231Val)	TNNT2 (I228V +5 more)	Single nucleotide variant (missense variant)	Left ventricular noncompaction cardiomyopathy +8 more	GUncertain significance
Select item 967621	NM_001276345.2(TNNT2):c.682G>C (p.Val228Leu)	TNNT2 (V228L +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1D +3 more	GUncertain significance
Select item 927370	NM_001276345.2(TNNT2):c.679A>T (p.Lys227Ter)	TNNT2 (K184* +5 more)	Single nucleotide variant (nonsense)	Cardiomyopathy	GUncertain significance
Select item 518816	NM_001276345.2(TNNT2):c.677G>A (p.Arg226Lys)	TNNT2 (R216K +5 more)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 2 +4 more	GUncertain significance
Select item 1332049	NM_001276345.2(TNNT2):c.664C>T (p.Leu222=)	TNNT2	Single nucleotide variant (synonymous variant)	Cardiomyopathy	GLikely benign
Select item 2774632	NM_001276345.2(TNNT2):c.662T>G (p.Ile221Ser)	TNNT2 (I206S +7 more)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance
Select item 836380	NM_001276345.2(TNNT2):c.659A>T (p.Lys220Met)	TNNT2 (K210M +5 more)	Single nucleotide variant (missense variant)	Cardiomyopathy +4 more	GUncertain significance
Select item 2774633	NM_001276345.2(TNNT2):c.634C>T (p.Gln212Ter)	TNNT2 (Q197* +7 more)	Single nucleotide variant (nonsense)	Cardiomyopathy	GUncertain significance
Select item 918896	NM_001276345.2(TNNT2):c.627G>C (p.Gly209=)	TNNT2	Single nucleotide variant (synonymous variant)	Cardiomyopathy	GLikely benign
Select item 537255	NM_001276345.2(TNNT2):c.617G>A (p.Arg206Gln)	TNNT2 (R203Q +5 more)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 2 +5 more	GUncertain significance
Select item 181624	NM_001276345.2(TNNT2):c.613G>A (p.Glu205Lys)	TNNT2 (E195K +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1D +4 more	GUncertain significance
Select item 2774634	NM_001276345.2(TNNT2):c.612A>G (p.Thr204=)	TNNT2	Single nucleotide variant (synonymous variant)	Cardiomyopathy	GLikely benign
Select item 1332160	NM_001276345.2(TNNT2):c.611C>T (p.Thr204Ile)	TNNT2 (T161I +5 more)	Single nucleotide variant (missense variant)	Cardiomyopathy, familial restrictive, 3 +4 more	GUncertain significance
Select item 496078	NM_001276345.2(TNNT2):c.610-6C>T	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy +4 more	GConflicting classifications of pathogenicity
Select item 920190	NM_001276345.2(TNNT2):c.610-7C>A	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy	GUncertain significance
Select item 924391	NM_001276345.2(TNNT2):c.610-9A>G	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy	GLikely benign
Select item 537263	NM_001276345.2(TNNT2):c.610-10C>T	TNNT2	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 2 +3 more	GConflicting classifications of pathogenicity
Select item 1901554	NM_001276345.2(TNNT2):c.610-12C>T	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy +3 more	GLikely benign
Select item 925695	NM_001276345.2(TNNT2):c.610-15T>A	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy +3 more	GConflicting classifications of pathogenicity
Select item 921830	NM_001276345.2(TNNT2):c.610-89C>T	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy	GLikely benign
Select item 627650	NM_001276345.2(TNNT2):c.610-90G>A	TNNT2	Single nucleotide variant (intron variant)	not specified +5 more	GBenign
Select item 925742	NM_001276345.2(TNNT2):c.610-106C>T	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy +1 more	GBenign
Select item 569640	NM_001276345.2(TNNT2):c.609+3G>A	TNNT2	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 2 +4 more	GUncertain significance
Select item 132940	NM_001276345.2(TNNT2):c.601-1G>A	TNNT2	Single nucleotide variant (intron variant +1 more)	Cardiomyopathy +7 more	GConflicting classifications of pathogenicity
Select item 412947	NM_001276345.2(TNNT2):c.601-6G>A	TNNT2	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 2 +4 more	GLikely benign
Select item 43656	NM_001276345.2(TNNT2):c.601-7G>A	TNNT2	Single nucleotide variant (intron variant)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 505238	NM_001276345.2(TNNT2):c.601-8C>A	TNNT2	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1D +4 more	GConflicting classifications of pathogenicity
Select item 43657	NM_001276345.2(TNNT2):c.601-8C>T	TNNT2	Single nucleotide variant (intron variant)	Dilated Cardiomyopathy, Dominant +9 more	GConflicting classifications of pathogenicity
Select item 1171535	NM_001276345.2(TNNT2):c.570C>T (p.Asn190=)	TNNT2	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 2 +3 more	GLikely benign
Select item 2774635	NM_001276345.2(TNNT2):c.569A>G (p.Asn190Ser)	TNNT2 (N179S +4 more)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance
Select item 43655	NM_001276345.2(TNNT2):c.567C>T (p.Ser189=)	TNNT2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +6 more	GBenign/Likely benign
Select item 43654	NM_001276345.2(TNNT2):c.564G>C (p.Leu188Phe)	TNNT2 (L178F +3 more)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 2 +4 more	GUncertain significance
Select item 807897	NM_001276345.2(TNNT2):c.550AAG[2] (p.Lys186del)	TNNT2 (K186del +3 more)	Microsatellite (inframe_deletion)	Hypertrophic cardiomyopathy 2 +3 more	GUncertain significance
Select item 387041	NM_001276345.2(TNNT2):c.552G>A (p.Lys184=)	TNNT2	Single nucleotide variant (synonymous variant)	Cardiomyopathy +4 more	GLikely benign
Select item 181612	NM_001276345.2(TNNT2):c.544G>T (p.Ala182Ser)	TNNT2 (A172S +3 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1D +4 more	GConflicting classifications of pathogenicity
Select item 132941	NM_001276345.2(TNNT2):c.522C>T (p.Asn174=)	TNNT2	Single nucleotide variant (synonymous variant)	Cardiomyopathy +5 more	GBenign/Likely benign
Select item 928421	NM_001276345.2(TNNT2):c.511G>A (p.Glu171Lys)	TNNT2 (E131K +3 more)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance
Select item 181619	NM_001276345.2(TNNT2):c.490-1G>C	TNNT2	Single nucleotide variant (splice acceptor variant)	Primary familial dilated cardiomyopathy +6 more	GConflicting classifications of pathogenicity
Select item 2196513	NM_001276345.2(TNNT2):c.490-14C>G	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy, familial restrictive, 3 +3 more	GConflicting classifications of pathogenicity
Select item 924697	NM_001276345.2(TNNT2):c.489+5G>A	TNNT2	Single nucleotide variant (intron variant)	Cardiomyopathy	GUncertain significance
Select item 961661	NM_001276345.2(TNNT2):c.487G>T (p.Ala163Ser)	TNNT2 (A148S +3 more)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 2 +5 more	GUncertain significance
Select item 537256	NM_001276345.2(TNNT2):c.481C>T (p.Arg161Cys)	TNNT2 (R161C +3 more)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 2 +8 more	GConflicting classifications of pathogenicity

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