"SIB Swiss Institute of Bioinformatics"[submitter] AND "RAB11B"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 453254	NM_004218.4(RAB11B):c.64G>A (p.Val22Met)	RAB11B (V22M)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter	GPathogenic/Likely pathogenic
Select item 453255	NM_004218.4(RAB11B):c.202G>A (p.Ala68Thr)	RAB11B (A68T)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter +1 more	GPathogenic/Likely pathogenic

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