C4225210[trait identifier] AND "SNPedia"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 221269	NM_177987.3(TUBB8):c.1249G>A (p.Asp417Asn)	TUBB8 (D417N +1 more)	Single nucleotide variant (missense variant)	Oocyte maturation defect 2	GPathogenic
Select item 223145	NM_177987.3(TUBB8):c.1088T>C (p.Met363Thr)	TUBB8 (M363T +1 more)	Single nucleotide variant (missense variant)	Oocyte maturation defect 2	GPathogenic
Select item 223146	NM_177987.3(TUBB8):c.900G>A (p.Met300Ile)	TUBB8 (M300I +1 more)	Single nucleotide variant (missense variant)	Oocyte maturation defect 2	GPathogenic
Select item 223144	NM_177987.3(TUBB8):c.785G>A (p.Arg262Gln)	TUBB8 (R262Q +1 more)	Single nucleotide variant (missense variant)	Oocyte maturation defect 2	GPathogenic
Select item 221268	NM_177987.3(TUBB8):c.686T>C (p.Val229Ala)	TUBB8 (V229A +1 more)	Single nucleotide variant (missense variant)	Oocyte maturation defect 2	GPathogenic
Select item 223143	NM_177987.3(TUBB8):c.527C>T (p.Ser176Leu)	TUBB8 (S176L +1 more)	Single nucleotide variant (missense variant)	Oocyte maturation defect 2	GPathogenic
Select item 221270	NM_177987.3(TUBB8):c.5G>A (p.Arg2Lys)	TUBB8 (R2K)	Single nucleotide variant (missense variant +1 more)	Oocyte maturation defect 2	GPathogenic

ClinVar