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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EFTUD2
(C745R +2 more)
Single nucleotide variant
(missense variant)
Mandibulofacial dysostosis-microcephaly syndrome
GUncertain significance
EFTUD2
(S614* +2 more)
Single nucleotide variant
(nonsense)
Mandibulofacial dysostosis-microcephaly syndrome
GLikely pathogenic
EFTUD2
(R610W +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
EFTUD2
(I517T +2 more)
Single nucleotide variant
(missense variant)
Mandibulofacial dysostosis-microcephaly syndrome
GUncertain significance
EFTUD2
(R508C +2 more)
Single nucleotide variant
(missense variant)
Mandibulofacial dysostosis-microcephaly syndrome
GUncertain significance
EFTUD2
(Y514* +2 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic/Likely pathogenic
EFTUD2
Single nucleotide variant
(splice acceptor variant)
Mandibulofacial dysostosis-microcephaly syndrome
GLikely pathogenic
EFTUD2
(R206Q +2 more)
Single nucleotide variant
(missense variant)
Mandibulofacial dysostosis-microcephaly syndrome
+1 more
GUncertain significance
EFTUD2
Indel
(intron variant)
Mandibulofacial dysostosis-microcephaly syndrome
GUncertain significance
EFTUD2
(D41Y +1 more)
Single nucleotide variant
(missense variant)
Mandibulofacial dysostosis-microcephaly syndrome
GUncertain significance
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