"ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 995710	NM_017553.3(INO80):c.4162G>C (p.Ala1388Pro)	INO80 (A1388P)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 777246	NM_017553.3(INO80):c.3906A>G (p.Glu1302=)	INO80	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2428538	NM_017553.3(INO80):c.3323T>G (p.Val1108Gly)	INO80 (V1108G)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 71887	NM_017553.3(INO80):c.2998C>T (p.Arg1000Cys)	INO80, INO80-AS1 (R1000C)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2428545	NM_017553.3(INO80):c.2644A>G (p.Ile882Val)	INO80 (I882V)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1330753	NM_017553.3(INO80):c.2577-17A>T	INO80	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 993389	NM_017553.3(INO80):c.2070+12T>A	INO80	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 994175	NM_017553.3(INO80):c.432C>T (p.Asp144=)	INO80	Single nucleotide variant (synonymous variant +1 more)	INO80-related condition +1 more	GBenign/Likely benign

ClinVar