"GeneDx"[submitter] AND "PRDM9"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59605	GRCh38/hg38 5p14.3-14.1(chr5:23279693-26849830)x1	CDH10, LINC02211 +13 more	Copy number loss	See cases	GPathogenic
Select item 1295150	NM_020227.4(PRDM9):c.301+43_301+44del	PRDM9	Deletion (intron variant)	not provided	GBenign
Select item 1249566	NM_020227.4(PRDM9):c.301+44del	PRDM9	Deletion (intron variant)	not provided	GBenign
Select item 1252878	NM_020227.4(PRDM9):c.301+67A>G	PRDM9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242393	NM_020227.4(PRDM9):c.301+185G>T	PRDM9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1226826	NM_020227.4(PRDM9):c.509-41C>T	PRDM9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1278507	NM_020227.4(PRDM9):c.883-52C>T	PRDM9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239553	NM_020227.4(PRDM9):c.1145-188T>A	PRDM9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 436411	NM_020227.4(PRDM9):c.2042C>G (p.Thr681Ser)	PRDM9 (T681S)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign/Likely benign
Select item 1250528	NM_020227.4(PRDM9):c.*37A>G	PRDM9	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1246202	NM_020227.4(PRDM9):c.*125G>A	PRDM9	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1180241	NC_000005.10:g.23528117C>T	PRDM9	Single nucleotide variant	not provided	GBenign
Select item 253597	GRCh37/hg19 5p15.2-12(chr5:13461664-46098927)x3	RXFP3, GDNF +89 more	Copy number gain	See cases	GPathogenic
Select item 253537	GRCh37/hg19 5p15.33-13.2(chr5:22149-34041255)x3	AHRR, ADAMTS12 +82 more	Copy number gain	See cases	GPathogenic