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Items: 24

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYPN
(Y20C)
Single nucleotide variant
(missense variant +2 more)
Dilated cardiomyopathy 1KK
+5 more
GConflicting classifications of pathogenicity
MYPN
(R27P)
Single nucleotide variant
(missense variant +2 more)
Cardiovascular phenotype
+2 more
GUncertain significance
MYPN
(P37S)
Single nucleotide variant
(missense variant +2 more)
Primary familial dilated cardiomyopathy
GUncertain significance
MYPN
(G368D +1 more)
Single nucleotide variant
(missense variant +1 more)
Dilated cardiomyopathy 1A
+3 more
GUncertain significance
MYPN
(V393A +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+2 more
GBenign
MYPN
Single nucleotide variant
(synonymous variant +1 more)
Cardiovascular phenotype
+3 more
GBenign
MYPN
(R597H +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
MYPN
(T326S +1 more)
Single nucleotide variant
(missense variant +1 more)
Primary familial dilated cardiomyopathy
GUncertain significance
MYPN
Single nucleotide variant
(synonymous variant +1 more)
Cardiovascular phenotype
+2 more
GBenign
MYPN
(F628L +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+3 more
GBenign/Likely benign
MYPN
(S691N +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+3 more
GBenign/Likely benign
MYPN
(T705I +1 more)
Single nucleotide variant
(missense variant +1 more)
Primary familial hypertrophic cardiomyopathy
+3 more
GUncertain significance
MYPN
(S707N +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+3 more
GBenign/Likely benign
MYPN
Single nucleotide variant
(synonymous variant +1 more)
Cardiovascular phenotype
+2 more
GBenign
MYPN
(S803R +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+2 more
GBenign
MYPN
(G804R +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+3 more
GBenign/Likely benign
MYPN
(R822Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+2 more
GUncertain significance
MYPN
(P532T +1 more)
Single nucleotide variant
(missense variant +1 more)
Dilated cardiomyopathy 1A
GUncertain significance
MYPN
(G847V +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+5 more
GConflicting classifications of pathogenicity
MYPN
(P1112L +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
+6 more
GConflicting classifications of pathogenicity
MYPN
(P1135T +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+3 more
GBenign/Likely benign
MYPN
(L1161I +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
+7 more
GConflicting classifications of pathogenicity
MYPN
(V1255M +1 more)
Single nucleotide variant
(missense variant +1 more)
Dilated cardiomyopathy 1A
+4 more
GUncertain significance
MYPN
(R1312Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Dilated cardiomyopathy 1KK
+2 more
GUncertain significance
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