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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ANK3
(S1612C +3 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome
GUncertain significance
ANK3
(R3719C)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome
GUncertain significance
ANK3
(S3322F)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+2 more
GUncertain significance
ANK3
(A3312V)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome
+2 more
GConflicting classifications of pathogenicity
ANK3
(S2858L)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GUncertain significance
ANK3
(I2041T)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome
GUncertain significance
ANK3
(R1636K)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome
+2 more
GConflicting classifications of pathogenicity
ANK3
(P1589L)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome
GUncertain significance
ANK3
(S1569A)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome
+1 more
GUncertain significance
ANK3
(K1074R +3 more)
Single nucleotide variant
(missense variant)
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome
+1 more
GUncertain significance
ANK3
(K24R +3 more)
Single nucleotide variant
(missense variant)
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome
GUncertain significance
ANK3
(M806V +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
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