"Simons Lab, The University of Queensland"[submitter] AND "TMEM63A"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 689461	NM_014698.3(TMEM63A):c.1699G>A (p.Gly567Ser)	TMEM63A (G567S)	Single nucleotide variant (missense variant)	Leukodystrophy	GPathogenic
Select item 689460	NM_014698.3(TMEM63A):c.1385T>A (p.Ile462Asn)	TMEM63A (I462N)	Single nucleotide variant (missense variant)	Leukodystrophy	GPathogenic
Select item 689459	NM_014698.3(TMEM63A):c.503G>A (p.Gly168Glu)	TMEM63A (G168E)	Single nucleotide variant (missense variant)	Leukodystrophy	GPathogenic

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