Related gene-specific medical variations for Gene (Select 79711) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3286312	NM_024658.4(IPO4):c.3161A>T (p.Gln1054Leu)	IPO4, REC8 (Q1054L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3110330	NM_024658.4(IPO4):c.3149T>C (p.Phe1050Ser)	IPO4, REC8 (F1050S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3110327	NM_024658.4(IPO4):c.209G>A (p.Arg70Gln)	IPO4, LOC130055399 (R70Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2606783	NM_024658.4(IPO4):c.227A>C (p.Gln76Pro)	IPO4, LOC130055399 (Q76P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2606081	NM_024658.4(IPO4):c.3208A>G (p.Lys1070Glu)	IPO4, REC8 (K1070E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370302	NM_024658.4(IPO4):c.3229G>A (p.Val1077Ile)	IPO4, REC8 (V1077I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2270578	NM_024658.4(IPO4):c.221C>T (p.Ala74Val)	IPO4, LOC130055399 (A74V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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