Related gene-specific medical variations for Gene (Select 9088) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3213892	NM_004203.5(PKMYT1):c.1457G>A (p.Arg486Gln)	PAQR4, PKMYT1 (R417Q +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2350546	NM_004203.5(PKMYT1):c.1369C>T (p.Arg457Trp)	PAQR4, PKMYT1 (R457W +2 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance