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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AFG2A
(R510* +1 more)
Single nucleotide variant
(nonsense)
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome
+1 more
GPathogenic/Likely pathogenic
AFG2A
(S555T +1 more)
Single nucleotide variant
(missense variant)
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome
GConflicting classifications of pathogenicity
AFG2A
Microsatellite
(frameshift variant)
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome
GUncertain significance
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