"PreventionGenetics, part of Exact Sciences"[submitter] AND "PRDM9"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3052715	NM_020227.4(PRDM9):c.696G>C (p.Lys232Asn)	PRDM9 (K232N)	Single nucleotide variant (missense variant)	PRDM9-related disorder	GLikely benign
Select item 3052780	NM_020227.4(PRDM9):c.968G>A (p.Arg323Gln)	PRDM9 (R323Q)	Single nucleotide variant (missense variant)	PRDM9-related disorder	GLikely benign
Select item 3038618	NM_020227.4(PRDM9):c.1016T>A (p.Ile339Asn)	PRDM9 (I339N)	Single nucleotide variant (missense variant)	PRDM9-related disorder	GLikely benign
Select item 3055641	NM_020227.4(PRDM9):c.1024A>G (p.Arg342Gly)	PRDM9 (R342G)	Single nucleotide variant (missense variant)	PRDM9-related disorder	GLikely benign
Select item 3039250	NM_020227.4(PRDM9):c.2126C>G (p.Thr709Ser)	PRDM9 (T709S)	Single nucleotide variant (missense variant)	PRDM9-related disorder	GLikely benign
Select item 3039403	NM_020227.4(PRDM9):c.2127T>A (p.Thr709=)	PRDM9	Single nucleotide variant (synonymous variant)	PRDM9-related disorder	GLikely benign

ClinVar