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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KIF11
(I101fs)
Deletion
(frameshift variant)
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
GLikely pathogenic
KIF11
Single nucleotide variant
(splice acceptor variant)
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
GLikely pathogenic
KIF11
(S235C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
KIF11
Single nucleotide variant
(splice donor variant)
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
GLikely pathogenic
KIF11
Deletion
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
GPathogenic
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