U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 24

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNC1
Single nucleotide variant
(stop lost)
Cardiomyopathy
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+3 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+2 more
GConflicting classifications of pathogenicity
TNNC1
(R147C)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
TNNC1
(D145E)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GUncertain significance
TNNC1
(D145H)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
TNNC1
(N144D)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+6 more
GConflicting classifications of pathogenicity
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+4 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+2 more
GLikely benign
TNNC1
(E126K)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
TNNC1
Single nucleotide variant
(intron variant)
Cardiomyopathy
GUncertain significance
TNNC1
(R102L)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+4 more
GConflicting classifications of pathogenicity
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+5 more
GConflicting classifications of pathogenicity
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+3 more
GConflicting classifications of pathogenicity
TNNC1
Single nucleotide variant
(intron variant)
Cardiomyopathy
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+6 more
GBenign/Likely benign
TNNC1
Single nucleotide variant
(synonymous variant)
not specified
+5 more
GConflicting classifications of pathogenicity
TNNC1
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GLikely benign
TNNC1
(D25N)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+3 more
GUncertain significance
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+2 more
GConflicting classifications of pathogenicity
TNNC1
(A8V)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GPathogenic/Likely pathogenic
Format
Items per page
Sort by
Choose Destination