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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEP135
Deletion
not provided
GLikely pathogenic
CEP135
(K608N)
Single nucleotide variant
(missense variant)
Microcephaly 8, primary, autosomal recessive
GUncertain significance
CEP135
(H661fs)
Microsatellite
(frameshift variant)
Microcephaly 8, primary, autosomal recessive
GLikely pathogenic
CEP135
(E1034fs)
Deletion
(frameshift variant)
Microcephaly 8, primary, autosomal recessive
GLikely pathogenic
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