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Items: 30

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYL3
Single nucleotide variant
(intron variant)
Cardiomyopathy
+2 more
GLikely benign
MYL3
(N180S)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
MYL3
(D178N)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
MYL3
(E177G)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 8
+5 more
GUncertain significance
MYL3
(A174P)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+2 more
GUncertain significance
MYL3
(V156L)
Single nucleotide variant
(missense variant)
Primary familial hypertrophic cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
MYL3
(V156M)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
MYL3
(R154H)
Single nucleotide variant
(missense variant)
not provided
+4 more
GUncertain significance
MYL3
(E143K)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+6 more
GConflicting classifications of pathogenicity
MYL3
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+5 more
GLikely benign
MYL3
(F140C)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
MYL3
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy
+3 more
GBenign/Likely benign
MYL3
(K123E)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+1 more
GConflicting classifications of pathogenicity
MYL3
(R94H)
Single nucleotide variant
(missense variant)
Primary familial hypertrophic cardiomyopathy
+4 more
GPathogenic/Likely pathogenic
MYL3
(V92M)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
MYL3
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy
+2 more
GBenign/Likely benign
MYL3
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 8
+4 more
GBenign/Likely benign
MYL3
(V79I)
Single nucleotide variant
(missense variant)
not specified
+4 more
GUncertain significance
MYL3
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GLikely benign
MYL3
Single nucleotide variant
(synonymous variant)
not specified
+6 more
GConflicting classifications of pathogenicity
MYL3
(T14A +1 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
MYL3
(R63H)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+1 more
GUncertain significance
MYL3
(D62N)
Single nucleotide variant
(missense variant)
not specified
+3 more
GUncertain significance
MYL3
(A57D)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
MYL3
(A57G)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
MYL3
(R31H)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
MYL3
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
MYL3
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+2 more
GLikely benign
MYL3
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+4 more
GLikely benign
MYL3
(P3H)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
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