"Women's Health and Genetics/Laboratory Corporation of America, LabCor - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1704521	NM_181552.4(CUX1):c.97C>T (p.Arg33Trp)	CUX1 (R33W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1696179	NM_181552.4(CUX1):c.358G>A (p.Glu120Lys)	CUX1, LOC126860126 (E115K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2682211	NM_181552.4(CUX1):c.1632C>G (p.Ser544Arg)	CUX1 (S544R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1722371	NM_181552.4(CUX1):c.2753C>A (p.Pro918His)	CUX1 (P918H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1705151	NM_181552.4(CUX1):c.2907+5G>A	CUX1	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2581371	NM_181552.4(CUX1):c.4224G>T (p.Ala1408=)	CUX1	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 2506255	NC_000007.13:g.(101559506_101671377)_(101671426_101713618)dup	CUX1	Duplication	not specified	GUncertain significance

ClinVar