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Items: 1 to 100 of 255

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNC1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+2 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+2 more
GLikely benign
TNNC1
(K158R)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(K158T)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(M157R)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(M157L)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
TNNC1
(M157L)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+3 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
not provided
+2 more
GConflicting classifications of pathogenicity
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
not provided
+2 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
Duplication
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Cardiomyopathy
+2 more
GConflicting classifications of pathogenicity
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+2 more
GConflicting classifications of pathogenicity
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+2 more
GUncertain significance
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(D151V)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(D149N)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+2 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+2 more
GConflicting classifications of pathogenicity
TNNC1
(I148V)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+3 more
GUncertain significance
TNNC1
(R147H)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GUncertain significance
TNNC1
(G146R)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(G146C)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(G146S)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+2 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GLikely benign
TNNC1
(D145E)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GUncertain significance
TNNC1
(D145V)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(D145N)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 13
+3 more
GLikely benign
TNNC1
(N144del)
Microsatellite
(inframe_deletion)
not specified
+2 more
GUncertain significance
TNNC1
(N144D)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
TNNC1
(N143K)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(K142N)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(G140E)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GUncertain significance
TNNC1
(G140R)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GLikely benign
TNNC1
(D139A)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
(E135A)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(E134D)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GUncertain significance
TNNC1
(E134K)
Single nucleotide variant
(missense variant)
TNNC1-related disorder
+4 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
(I133V)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
(D132del)
Microsatellite
(inframe_deletion)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(D131E)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
not provided
+4 more
GLikely benign
TNNC1
(D131fs)
Deletion
(frameshift variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
TNNC1
(T129R)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(T129M)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+2 more
GLikely benign
TNNC1
(I128T)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(E126K)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+2 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+2 more
GLikely benign
TNNC1
(T124P)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Indel
(nonsense)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(Q122fs)
Duplication
(frameshift variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+2 more
GLikely benign
TNNC1
(I119T)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(I119V)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(K118N)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
(E116D)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(L114R)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+2 more
GUncertain significance
TNNC1
(D113E)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(A108fs)
Deletion
(frameshift variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(D113fs)
Deletion
(frameshift variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(D113N)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+2 more
GUncertain significance
TNNC1
(I112M)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+2 more
GLikely benign
TNNC1
(I112V)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+2 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
(G110C)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+2 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+3 more
GBenign/Likely benign
TNNC1
(N107K)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Duplication
(splice acceptor variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+2 more
GBenign/Likely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+2 more
GBenign/Likely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
not specified
+2 more
GUncertain significance
TNNC1
(D105G)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
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