"Ambry Genetics"[submitter] AND "PSMD9"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2266824	NM_002813.7(PSMD9):c.38C>T (p.Ser13Leu)	PSMD9 (S13L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2514023	NM_002813.7(PSMD9):c.43G>A (p.Ala15Thr)	PSMD9 (A15T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2365774	NM_002813.7(PSMD9):c.148A>G (p.Ile50Val)	PSMD9 (I50V)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3220466	NM_002813.7(PSMD9):c.149T>C (p.Ile50Thr)	PSMD9 (I50T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2245353	NM_002813.7(PSMD9):c.199G>A (p.Val67Met)	PSMD9 (V67M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3220468	NM_002813.7(PSMD9):c.302A>G (p.His101Arg)	PSMD9 (H101R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220469	NM_002813.7(PSMD9):c.310G>A (p.Asp104Asn)	PSMD9 (D104N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530300	NM_002813.7(PSMD9):c.326C>T (p.Ala109Val)	PSMD9 (A109V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2539187	NM_002813.7(PSMD9):c.365G>T (p.Arg122Leu)	PSMD9 (R122L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3311020	NM_002813.7(PSMD9):c.433G>A (p.Gly145Ser)	PSMD9 (G145S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3311016	NM_002813.7(PSMD9):c.443C>T (p.Ala148Val)	PSMD9 (A148V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609111	NM_002813.7(PSMD9):c.512A>C (p.Gln171Pro)	PSMD9 (Q171P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491569	NM_002813.7(PSMD9):c.558G>T (p.Lys186Asn)	PSMD9 (K186N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491570	NM_002813.7(PSMD9):c.559C>T (p.Pro187Ser)	PSMD9 (P187S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3311019	NM_002813.7(PSMD9):c.581G>A (p.Arg194His)	PSMD9 (R194H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544699	NM_002813.7(PSMD9):c.585G>C (p.Arg195Ser)	PSMD9 (R195S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2524633	NM_002813.7(PSMD9):c.629G>C (p.Gly210Ala)	PSMD9 (G210A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance