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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EFTUD2
(T643M +2 more)
Single nucleotide variant
(missense variant)
Mandibulofacial dysostosis-microcephaly syndrome
GLikely pathogenic
EFTUD2
Single nucleotide variant
(splice donor variant)
Mandibulofacial dysostosis-microcephaly syndrome
GPathogenic
EFTUD2
Single nucleotide variant
(splice donor variant)
Mandibulofacial dysostosis-microcephaly syndrome
GLikely pathogenic
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