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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EFTUD2
(I618L +2 more)
Single nucleotide variant
(missense variant)
Mandibulofacial dysostosis-microcephaly syndrome
GUncertain significance
EFTUD2
(M440I +2 more)
Single nucleotide variant
(missense variant)
Mandibulofacial dysostosis-microcephaly syndrome
GUncertain significance
EFTUD2
(R354* +2 more)
Single nucleotide variant
(nonsense)
not provided
+2 more
GPathogenic
EFTUD2
Deletion
Mandibulofacial dysostosis-microcephaly syndrome
GLikely pathogenic
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