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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MOB1A
(R215K +2 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
MOB1A
(T119S +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MOB1A
(M45I +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MOB1A
(M88T +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MOB1A
(H31R +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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