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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC117125587, MAST1
(C231R)
Single nucleotide variant
(missense variant)
Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
GPathogenic
MAST1
(K1042N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MAST1
(N1115T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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