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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KIF11
(R53*)
Single nucleotide variant
(nonsense)
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
+1 more
GPathogenic
KIF11
(H141L)
Single nucleotide variant
(missense variant)
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
GLikely pathogenic
KIF11
(V158fs)
Deletion
(frameshift variant)
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
GLikely pathogenic
KIF11
(E505fs)
Deletion
(frameshift variant)
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
GLikely pathogenic
KIF11
(H768fs)
Microsatellite
(frameshift variant)
not provided
+1 more
GPathogenic
KIF11
Deletion
(nonsense)
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
GPathogenic
KIF11
(N838fs)
Deletion
(frameshift variant)
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
GPathogenic
KIF11
(Q928*)
Single nucleotide variant
(nonsense)
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
GPathogenic
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