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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MECOM
(K288* +5 more)
Single nucleotide variant
(nonsense)
Radioulnar synostosis with amegakaryocytic thrombocytopenia 2
GLikely pathogenic
MECOM
(P260L +5 more)
Single nucleotide variant
(missense variant)
Radioulnar synostosis with amegakaryocytic thrombocytopenia 2
GUncertain significance
MECOM
(S231F +3 more)
Single nucleotide variant
(missense variant +1 more)
Radioulnar synostosis with amegakaryocytic thrombocytopenia 2
GUncertain significance
MECOM
(Q123* +2 more)
Single nucleotide variant
(nonsense)
Radioulnar synostosis with amegakaryocytic thrombocytopenia 2
GLikely pathogenic
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