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Links from Gene

Items: 1 to 100 of 133

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC114827827, NPPA
+1 more
(L43S)
Single nucleotide variant
(non-coding transcript variant +1 more)
Inborn genetic diseases
GUncertain significance
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
(F149L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
NPPA-AS1, LOC114827827
+1 more
(R123W)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 6
GLikely benign
NPPA, NPPA-AS1
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
NPPA, LOC114827827
+1 more
(P89Q)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(A25T)
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(R137K)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(L37P)
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
(L47W)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GLikely benign
NPPA-AS1, LOC114827827
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
NPPA, NPPA-AS1
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Deletion
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
(P60R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
(P66T)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Deletion
(intron variant)
Atrial fibrillation, familial, 6
GBenign
LOC114827827, NPPA
+1 more
(L77fs)
Deletion
(frameshift variant)
Atrial fibrillation, familial, 6
+1 more
GUncertain significance
LOC114827827, NPPA
+1 more
(W102*)
Single nucleotide variant
(nonsense)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(L110P)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
(R107P)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(D55E)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(R107L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(E54del)
Microsatellite
(inframe_deletion)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(M38I)
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(G94V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(T84P)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
(A73T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC114827827, NPPA
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
(T120A)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(S75N)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
NPPA, NPPA-AS1
+1 more
(L63I)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
NPPA, NPPA-AS1
Inversion
(stop lost)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(S124R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(F131L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(K41N)
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(S75R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(R126W)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
(A70V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(M38R)
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(R107Q)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(A70G)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(R116K)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(D45G)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(I138T)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(P81R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(R150W)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
Deletion
(intron variant)
not provided
GBenign
NPPA, NPPA-AS1
Single nucleotide variant
(3 prime UTR variant)
not provided
GBenign
NPPA, NPPA-AS1
Single nucleotide variant
(3 prime UTR variant)
not provided
GBenign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(intron variant)
not provided
GBenign
NPPA, NPPA-AS1
Duplication
(intron variant)
not provided
GBenign
NPPA, NPPA-AS1
Deletion
(non-coding transcript variant +1 more)
not provided
GBenign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GBenign
NPPA, NPPA-AS1
Single nucleotide variant
(3 prime UTR variant)
not provided
GBenign
LOC114827827, NPPA
+1 more
Duplication
(intron variant)
not provided
GBenign
NPPA, NPPA-AS1
Single nucleotide variant
(3 prime UTR variant)
not provided
GBenign
NPPA, NPPA-AS1
+1 more
Single nucleotide variant
(intron variant)
not provided
GBenign
NPPA-AS1, NPPA
+1 more
Single nucleotide variant
(intron variant)
not provided
GBenign
LOC114827827, NPPA
+1 more
Deletion
(intron variant)
not provided
GBenign
LOC114827827, NPPA
+1 more
(V32M)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
+1 more
GBenign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
NPPA, NPPA-AS1
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GLikely benign
NPPA, NPPA-AS1
Single nucleotide variant
(intron variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
+2 more
GLikely benign
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
GLikely benign
LOC114827827, NPPA
+1 more
(K50M)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(S113T)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(P52S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(D106H)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(S113G)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
(R107*)
Single nucleotide variant
(nonsense)
Atrial fibrillation, familial, 6
+1 more
GUncertain significance
LOC114827827, NPPA
+1 more
(A35T)
Single nucleotide variant
(non-coding transcript variant +1 more)
NPPA-related disorder
+1 more
GUncertain significance
LOC114827827, NPPA
+1 more
(R123Q)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
GUncertain significance
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GLikely benign
LOC114827827, NPPA
+1 more
(R126Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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