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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASXL3
(F353L)
Single nucleotide variant
(missense variant)
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome
GUncertain significance
ASXL3
(P618L)
Single nucleotide variant
(missense variant)
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome
GUncertain significance
ASXL3
(L934*)
Single nucleotide variant
(nonsense)
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome
GLikely pathogenic
ASXL3
(G1094fs)
Duplication
(frameshift variant)
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome
GPathogenic
ASXL3
(T1404fs)
Microsatellite
(frameshift variant)
not provided
+1 more
GPathogenic
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