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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
INPP5E
(Q633E +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
INPP5E
(T580M +1 more)
Single nucleotide variant
(missense variant)
Familial aplasia of the vermis
+1 more
GUncertain significance
INPP5E
(G538R +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
INPP5E
(R435Q +1 more)
Single nucleotide variant
(missense variant)
Familial aplasia of the vermis
+3 more
GPathogenic/Likely pathogenic
INPP5E
(C342R)
Single nucleotide variant
(missense variant)
not provided
GLikely pathogenic
INPP5E
(S198T)
Single nucleotide variant
(missense variant)
Familial aplasia of the vermis
+2 more
GUncertain significance
INPP5E
(P154S)
Single nucleotide variant
(missense variant)
Familial aplasia of the vermis
+2 more
GUncertain significance
INPP5E
Deletion
(inframe_deletion +1 more)
Familial aplasia of the vermis
+1 more
GPathogenic/Likely pathogenic
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