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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EFTUD2
(A816fs +2 more)
Deletion
(frameshift variant)
Mandibulofacial dysostosis-microcephaly syndrome
GLikely pathogenic
EFTUD2
Single nucleotide variant
(splice acceptor variant)
Mandibulofacial dysostosis-microcephaly syndrome
GLikely pathogenic
EFTUD2
(R494C +2 more)
Single nucleotide variant
(missense variant)
Mandibulofacial dysostosis-microcephaly syndrome
+1 more
GUncertain significance
EFTUD2
(G310S +2 more)
Single nucleotide variant
(missense variant)
Mandibulofacial dysostosis-microcephaly syndrome
GUncertain significance
EFTUD2
(I135fs +2 more)
Deletion
(frameshift variant)
Mandibulofacial dysostosis-microcephaly syndrome
GPathogenic
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