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Items: 1 to 100 of 487

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNA5
Single nucleotide variant
not provided
GLikely benign
KCNA5
Single nucleotide variant
not provided
GBenign
KCNA5
Single nucleotide variant
not provided
GBenign
KCNA5
Single nucleotide variant
not provided
GBenign
KCNA5
Microsatellite
(5 prime UTR variant)
not provided
GLikely benign
KCNA5
Insertion
(5 prime UTR variant)
not provided
GLikely benign
KCNA5
Single nucleotide variant
(5 prime UTR variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(5 prime UTR variant)
not provided
+1 more
GBenign
KCNA5
Single nucleotide variant
(5 prime UTR variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(5 prime UTR variant)
not provided
+1 more
GUncertain significance
KCNA5
Single nucleotide variant
(5 prime UTR variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(M1V)
Single nucleotide variant
(missense variant +1 more)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(M1T)
Single nucleotide variant
(missense variant +1 more)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(A4S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(L5P)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(P7R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(N10D)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Microsatellite
(inframe_insertion)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(G12fs)
Deletion
(frameshift variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(G12D)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GConflicting classifications of pathogenicity
KCNA5
(M14R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
+1 more
GUncertain significance
KCNA5
(T15A)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(T15I)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(G19D)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(E21K)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(A22T)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(R23W)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(R23Q)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(A24S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(G27S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
KCNA5
(A29D)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(E33fs)
Duplication
(frameshift variant)
not provided
GUncertain significance
KCNA5
(G31R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(G31A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KCNA5
(G31V)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
KCNA5
(G32E)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(E33Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
KCNA5
(E33V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
+1 more
GUncertain significance
KCNA5
(C36S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(P37L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
+1 more
GUncertain significance
KCNA5
(T39P)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(T39K)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(K47R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(E48K)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(E48G)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GPathogenic
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(A50T)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(K52N)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(G53V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
KCNA5
(G53E)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(R54C)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(A56S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(A56V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(R58I)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(A60S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(A60G)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GBenign/Likely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Duplication
(inframe_insertion)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Deletion
(inframe_deletion)
Atrial fibrillation, familial, 7
+2 more
GConflicting classifications of pathogenicity
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GConflicting classifications of pathogenicity
KCNA5
(G63V)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
KCNA5
(V64M)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(R65W)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KCNA5
(R65P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
KCNA5
(P66S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
+1 more
GUncertain significance
KCNA5
(P69L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GBenign
KCNA5
(D72H)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
+2 more
GUncertain significance
KCNA5
(P73S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(G74E)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(R76L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(P77A)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(P77S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
+1 more
GBenign/Likely benign
KCNA5
(P77R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(L78F)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(P82S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(P82T)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(E84A)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
+1 more
GConflicting classifications of pathogenicity
KCNA5
(L85R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(R87Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KCNA5
(R90W)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(R90L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(P92R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(E99del)
Microsatellite
(inframe_deletion)
Atrial fibrillation, familial, 7
GUncertain significance
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