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Items: 77

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADO, ANK3
+227 more
Copy number gain
See cases
GPathogenic
LOC129390190, LOC129390191
+610 more
Copy number loss
See cases
GPathogenic
ANK3
(H1854L +4 more)
Single nucleotide variant
(missense variant)
ANK3-related condition
+2 more
GConflicting classifications of pathogenicity
ANK3
(T1703S +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(R1701G +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
Single nucleotide variant
(splice acceptor variant)
not provided
GUncertain significance
ANK3
(I1555V +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(G1527R +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(A1490S +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(S4033L)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(I3997T)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
ANK3
(T3976N)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(T3809I)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(D3623N)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(D3581N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ANK3
(R3560Q)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(R3457C)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(N3388K)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(Y3324C)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(A3312V)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GConflicting classifications of pathogenicity
ANK3
(D2892N)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(K2711fs)
Deletion
(frameshift variant +1 more)
not provided
GUncertain significance
ANK3
(D2655N)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(S2642C)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(M2555T)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
ANK3
(P2490L)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GConflicting classifications of pathogenicity
ANK3
(D2369Y)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(R2328C)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(A2313S)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3, LOC130003862
(A2299T)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3, LOC130003862
(P2286fs)
Deletion
(frameshift variant +1 more)
not provided
GUncertain significance
ANK3, LOC130003862
(M2271R)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(V2233F)
Single nucleotide variant
(intron variant +1 more)
not provided
GUncertain significance
ANK3
(R2232Q)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
ANK3
(A2223T)
Single nucleotide variant
(intron variant +1 more)
not provided
GUncertain significance
ANK3
(V2170I)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(T2107S)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(A2006V)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(D1980G)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(P1884T)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(S1803Y)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(V1713I)
Single nucleotide variant
(missense variant +1 more)
not provided
GConflicting classifications of pathogenicity
ANK3
(S1527Y)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(P1502S)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK3
(P1489S)
Single nucleotide variant
(missense variant +1 more)
ANK3-related condition
+3 more
GConflicting classifications of pathogenicity
ANK3
(K1452R +4 more)
Single nucleotide variant
(missense variant)
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome
+2 more
GUncertain significance
ANK3
Deletion
(intron variant)
not provided
GBenign
ANK3
(K1435N +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(V1345A +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(I1300R +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(D1265fs +3 more)
Deletion
(frameshift variant)
not provided
GLikely pathogenic
ANK3
(G1188E +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ANK3
(I1186N +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(R1170Q +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(I1120V +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
Duplication
(intron variant)
not specified
GLikely benign
ANK3
Single nucleotide variant
(synonymous variant)
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome
+1 more
GBenign
ANK3
(G129fs +3 more)
Deletion
(frameshift variant)
not provided
GUncertain significance
ANK3
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
ANK3
(S910T +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(G27C +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(R846H +2 more)
Single nucleotide variant
(missense variant)
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome
+2 more
GUncertain significance
ANK3
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
ANK3
(V709I +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
Single nucleotide variant
(synonymous variant)
not provided
GBenign/Likely benign
ANK3
(A622T +2 more)
Single nucleotide variant
(missense variant)
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome
+1 more
GUncertain significance
ANK3
(P245S +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(G592R +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(R162* +3 more)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
ANK3
(A473G +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(E425K +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(D382N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANK3
(Q337P +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(G295D +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(A241V +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK3
(R44* +2 more)
Single nucleotide variant
(nonsense)
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome
+1 more
GConflicting classifications of pathogenicity
ANK3
(S29N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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