IPO5[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2381520	NM_002271.6(IPO5):c.24G>T (p.Gln8His)	IPO5 (Q8H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 771466	NM_002271.6(IPO5):c.573G>A (p.Thr191=)	IPO5	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2240150	NM_002271.6(IPO5):c.1517A>G (p.Lys506Arg)	IPO5 (K506R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2643883	NM_002271.6(IPO5):c.1716+39_1716+44dup	IPO5	Duplication (intron variant)	not provided	GLikely benign
Select item 2643882	NM_002271.6(IPO5):c.1716+40_1716+44dup	IPO5	Duplication (intron variant)	not provided	GLikely benign
Select item 773274	NM_002271.6(IPO5):c.2766G>A (p.Arg922=)	IPO5	Single nucleotide variant (synonymous variant)	not provided	GBenign

ClinVar