HACD3[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2373260	NM_016395.4(HACD3):c.215A>G (p.Lys72Arg)	HACD3 (K72R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331289	NM_016395.4(HACD3):c.354G>A (p.Met118Ile)	HACD3 (M118I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3104098	NM_016395.4(HACD3):c.380G>A (p.Arg127His)	HACD3 (R127H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475569	NM_016395.4(HACD3):c.410G>T (p.Gly137Val)	HACD3 (G137V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481996	NM_016395.4(HACD3):c.489G>C (p.Trp163Cys)	HACD3 (W163C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3104099	NM_016395.4(HACD3):c.605C>T (p.Thr202Ile)	HACD3 (T202I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3104100	NM_016395.4(HACD3):c.716A>G (p.Gln239Arg)	HACD3 (Q239R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463746	NM_016395.4(HACD3):c.730G>T (p.Val244Phe)	HACD3 (V244F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2624411	NM_016395.4(HACD3):c.751T>C (p.Trp251Arg)	HACD3 (W251R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3104101	NM_016395.4(HACD3):c.887C>T (p.Ser296Leu)	HACD3 (S179L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620325	NM_016395.4(HACD3):c.901A>C (p.Ile301Leu)	HACD3 (I184L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590990	NM_016395.4(HACD3):c.914A>G (p.Asn305Ser)	HACD3 (N188S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297275	NM_016395.4(HACD3):c.998T>C (p.Ile333Thr)	HACD3 (I216T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3104095	NM_016395.4(HACD3):c.1001T>A (p.Met334Lys)	HACD3 (M217K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3104096	NM_016395.4(HACD3):c.1030C>T (p.Arg344Cys)	HACD3 (R227C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292067	NM_016395.4(HACD3):c.1040A>G (p.Tyr347Cys)	HACD3 (Y230C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251576	NM_016395.4(HACD3):c.1052G>A (p.Arg351Lys)	HACD3 (R351K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300735	NM_016395.4(HACD3):c.1055G>A (p.Arg352Gln)	HACD3 (R352Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance