U.S. flag

An official website of the United States government

Display optionsSort by LocationDownload
Format
Items per page
Sort by
Choose Destination

Search results

Items: 1 to 100 of 392

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
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
(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
(G31R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
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
(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
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
(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
(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)
not provided
+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
(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
+1 more
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
(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
(R87Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
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
KCNA5
Deletion
(inframe_deletion)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(G105V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(V107G)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Duplication
(inframe_insertion)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(S116F)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
+1 more
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(R121H)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(V122F)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(H123R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(I126T)
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)
not provided
+2 more
GBenign/Likely benign
KCNA5
(G128R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(T133K)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(L135del)
Deletion
(inframe_deletion)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(A139V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(A139E)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(Q140H)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
Display optionsSort by LocationDownload
Format
Items per page
Sort by
Choose Destination