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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DOCK7
(N1939S +5 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 23
+1 more
GUncertain significance
DOCK7
(V1716I +3 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 23
+1 more
GUncertain significance
DOCK7
(M1663V +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
DOCK7
(I1583V +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
DOCK7
(S1523N +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DOCK7
(V1485I +3 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
DOCK7
(E1367K +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DOCK7
(T1281M +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
DOCK7
(R978C +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
DOCK7
(N835D)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 23
+1 more
GConflicting classifications of pathogenicity
DOCK7
(I511V)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 23
+2 more
GUncertain significance
DOCK7
(A283S)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 23
+1 more
GUncertain significance
DOCK7
(I281V)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 23
+1 more
GUncertain significance
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