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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC112543452, MAST1
(E772D)
Single nucleotide variant
(missense variant)
Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
GUncertain significance
MAST1
(E854Q)
Single nucleotide variant
(missense variant)
Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
GUncertain significance
MAST1
(A887V)
Single nucleotide variant
(missense variant)
Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
GUncertain significance
MAST1
(G1151S)
Single nucleotide variant
(missense variant)
Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
GUncertain significance
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