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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MEGF8
(R107Q)
Single nucleotide variant
(missense variant)
MEGF8-related Carpenter syndrome
+1 more
GUncertain significance
MEGF8
(R419*)
Single nucleotide variant
(nonsense)
MEGF8-related Carpenter syndrome
GConflicting classifications of pathogenicity
MEGF8
(G1133D +1 more)
Single nucleotide variant
(missense variant)
MEGF8-related Carpenter syndrome
GUncertain significance
MEGF8
(P1255S +1 more)
Single nucleotide variant
(missense variant)
MEGF8-related Carpenter syndrome
GUncertain significance
MEGF8
(A1657T +1 more)
Single nucleotide variant
(missense variant)
MEGF8-related Carpenter syndrome
GUncertain significance
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