"Victorian Clinical Genetics Services, Murdoch Childrens Research Inst - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1805337	NM_006885.4(ZFHX3):c.9643_9657del (p.Ala3215_Pro3219del)	ZFHX3, ZFHX3-AS1	Deletion (inframe_deletion)	Neurodevelopmental disorder	GUncertain significance
Select item 1805417	NM_006885.4(ZFHX3):c.8002C>T (p.Arg2668Ter)	ZFHX3, ZFHX3-AS1 (R1754* +1 more)	Single nucleotide variant (nonsense)	Neurodevelopmental disorder	GLikely pathogenic
Select item 1805351	NM_006885.4(ZFHX3):c.6040C>T (p.Gln2014Ter)	ZFHX3, ZFHX3-AS1 (Q1100* +1 more)	Single nucleotide variant (nonsense)	Neurodevelopmental disorder	GLikely pathogenic
Select item 1805360	NM_006885.4(ZFHX3):c.5767C>T (p.Pro1923Ser)	ZFHX3, ZFHX3-AS1 (P1009S +1 more)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder	GUncertain significance
Select item 1805363	NM_006885.4(ZFHX3):c.5749G>T (p.Glu1917Ter)	ZFHX3, ZFHX3-AS1 (E1003* +1 more)	Single nucleotide variant (nonsense)	Neurodevelopmental disorder	GLikely pathogenic
Select item 1805305	NM_006885.4(ZFHX3):c.3355C>T (p.Arg1119Ter)	ZFHX3 (R1119* +1 more)	Single nucleotide variant (nonsense)	Neurodevelopmental disorder	GLikely pathogenic

ClinVar