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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GEMIN5
(A1048G +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction
GUncertain significance
GEMIN5
(W961* +1 more)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction
GLikely pathogenic
GEMIN5
(A639V +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction
GUncertain significance
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