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Items: 1 to 100 of 213

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
(K4R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(K5R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(E7K)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(P8A)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
+1 more
GUncertain significance
MYL4
(P8L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(K9E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYL4
(K10N)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(E11K)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GPathogenic
MYL4
(A13V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Microsatellite
(inframe_insertion)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Microsatellite
(inframe_deletion)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Microsatellite
(inframe_deletion)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
Deletion
(inframe_deletion)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
(P23L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(A24S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
Duplication
(inframe_insertion)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
(A28T)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Duplication
(inframe_insertion)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
(K35E)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(A38G)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(A38D)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(K42R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(S43N)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(S43R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYL4
(V44A)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Single nucleotide variant
(splice donor variant)
Atrial fibrillation, familial, 18
GLikely pathogenic
MYL4
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
Single nucleotide variant
(intron variant)
not provided
GBenign
MYL4
Single nucleotide variant
(intron variant)
not provided
GBenign
MYL4
Single nucleotide variant
(intron variant)
not provided
GBenign
MYL4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
MYL4
Deletion
(intron variant)
not provided
GBenign
MYL4
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(I46L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(I46V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
+1 more
GUncertain significance
MYL4
(I46R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
+1 more
GUncertain significance
MYL4
(I46T)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
+1 more
GUncertain significance
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
+1 more
GBenign/Likely benign
MYL4
(D51E)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(I53M)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
Microsatellite
(intron variant)
not provided
GBenign
MYL4
Single nucleotide variant
(intron variant)
not provided
GBenign
MYL4
Single nucleotide variant
(intron variant)
not provided
GBenign
MYL4
Single nucleotide variant
(intron variant)
not provided
GBenign
MYL4
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 18
+1 more
GBenign
MYL4
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
Single nucleotide variant
(splice acceptor variant)
Atrial fibrillation, familial, 18
GLikely pathogenic
MYL4
(F56S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
+1 more
GConflicting classifications of pathogenicity
MYL4
(A59S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
(R65W)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(R65Q)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(T66P)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(P67S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(P67L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
MYL4
(T68I)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
(E70D)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(M71V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(M71R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(Y75N)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
(Q77R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(Q77H)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(C78R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
+1 more
GUncertain significance
MYL4
(C78Y)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(C78*)
Single nucleotide variant
(nonsense)
Atrial fibrillation, familial, 18
GLikely pathogenic
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
(C78fs)
Deletion
(frameshift variant)
Atrial fibrillation, familial, 18
GPathogenic
MYL4
(G79R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(G79E)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(R83Q)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(R83L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(A84V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
(L85V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
(E93K)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
MYL4
(L95P)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(R96C)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 18
GUncertain significance
MYL4
(R96H)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GLikely benign
MYL4
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 18
GLikely benign
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