CD34[gene] and "single gene"[properties] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3264821	NM_001025109.2(CD34):c.1138G>A (p.Val380Met)	CD34 (V380M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140559	NM_001025109.2(CD34):c.1135G>C (p.Val379Leu)	CD34 (V379L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2226700	NM_001025109.2(CD34):c.1094G>A (p.Gly365Asp)	CD34 (G365D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2309528	NM_001025109.2(CD34):c.1086C>A (p.Asn362Lys)	CD34 (N362K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140558	NM_001025109.2(CD34):c.1028C>A (p.Pro343His)	CD34 (P343H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2332136	NM_001025109.2(CD34):c.974G>A (p.Gly325Asp)	CD34 (G325D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140563	NM_001025109.2(CD34):c.958A>T (p.Thr320Ser)	CD34 (T320S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222431	NM_001025109.2(CD34):c.944G>A (p.Arg315His)	CD34 (R315H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386805	NM_001025109.2(CD34):c.941G>A (p.Arg314His)	CD34 (R314H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590906	NM_001025109.2(CD34):c.793T>C (p.Ser265Pro)	CD34 (S265P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558829	NM_001025109.2(CD34):c.779T>G (p.Met260Arg)	CD34 (M260R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309960	NM_001025109.2(CD34):c.665C>T (p.Ala222Val)	CD34 (A222V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230559	NM_001025109.2(CD34):c.654G>C (p.Glu218Asp)	CD34 (E218D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385816	NM_001025109.2(CD34):c.478C>T (p.Pro160Ser)	CD34 (P160S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379871	NM_001025109.2(CD34):c.405G>T (p.Lys135Asn)	CD34 (K135N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 725461	NM_001025109.2(CD34):c.379G>A (p.Val127Ile)	CD34 (V127I)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2274001	NM_001025109.2(CD34):c.258C>G (p.Ile86Met)	CD34 (I86M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605428	NM_001025109.2(CD34):c.254A>G (p.Asn85Ser)	CD34 (N85S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264822	NM_001025109.2(CD34):c.244G>A (p.Ala82Thr)	CD34 (A82T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3140561	NM_001025109.2(CD34):c.239A>G (p.Asn80Ser)	CD34 (N80S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3140560	NM_001025109.2(CD34):c.206G>A (p.Ser69Asn)	CD34 (S69N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617540	NM_001025109.2(CD34):c.139G>C (p.Gly47Arg)	CD34 (G47R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207158	NM_001025109.2(CD34):c.109G>A (p.Gly37Ser)	CD34 (G37S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3264823	NM_001025109.2(CD34):c.74T>C (p.Leu25Ser)	CD34 (L25S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589328	NM_001025109.2(CD34):c.52A>C (p.Thr18Pro)	CD34 (T18P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25