"Ambry Genetics"[submitter] AND "CD93"[gene] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2457153	NM_012072.4(CD93):c.1937C>T (p.Pro646Leu)	CD93 (P646L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456611	NM_012072.4(CD93):c.1901G>A (p.Arg634Gln)	CD93 (R634Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308171	NM_012072.4(CD93):c.1856A>C (p.Lys619Thr)	CD93 (K619T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140714	NM_012072.4(CD93):c.1838G>A (p.Arg613Lys)	CD93 (R613K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250419	NM_012072.4(CD93):c.1832C>G (p.Ala611Gly)	CD93 (A611G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140713	NM_012072.4(CD93):c.1820G>A (p.Arg607His)	CD93 (R607H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323972	NM_012072.4(CD93):c.1777A>G (p.Ile593Val)	CD93 (I593V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598344	NM_012072.4(CD93):c.1751T>A (p.Phe584Tyr)	CD93 (F584Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257446	NM_012072.4(CD93):c.1609C>T (p.Pro537Ser)	CD93 (P537S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544445	NM_012072.4(CD93):c.1547C>G (p.Thr516Arg)	CD93 (T516R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140712	NM_012072.4(CD93):c.1483C>T (p.Pro495Ser)	CD93 (P495S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462733	NM_012072.4(CD93):c.1409G>A (p.Gly470Glu)	CD93 (G470E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140710	NM_012072.4(CD93):c.1390G>A (p.Gly464Arg)	CD93 (G464R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213357	NM_012072.4(CD93):c.1301C>T (p.Pro434Leu)	CD93 (P434L)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2333984	NM_012072.4(CD93):c.1264G>C (p.Gly422Arg)	CD93 (G422R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538599	NM_012072.4(CD93):c.1135G>A (p.Gly379Arg)	CD93 (G379R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391384	NM_012072.4(CD93):c.833G>C (p.Gly278Ala)	CD93 (G278A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389291	NM_012072.4(CD93):c.833G>A (p.Gly278Glu)	CD93 (G278E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470856	NM_012072.4(CD93):c.832G>T (p.Gly278Trp)	CD93 (G278W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388141	NM_012072.4(CD93):c.832G>A (p.Gly278Arg)	CD93 (G278R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140717	NM_012072.4(CD93):c.783G>C (p.Lys261Asn)	CD93 (K261N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266783	NM_012072.4(CD93):c.764C>G (p.Pro255Arg)	CD93 (P255R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522351	NM_012072.4(CD93):c.549C>A (p.Ser183Arg)	CD93 (S183R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140716	NM_012072.4(CD93):c.393G>C (p.Glu131Asp)	CD93 (E131D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355235	NM_012072.4(CD93):c.335A>G (p.Lys112Arg)	CD93 (K112R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213992	NM_012072.4(CD93):c.320C>T (p.Pro107Leu)	CD93 (P107L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140709	NM_012072.4(CD93):c.103G>C (p.Ala35Pro)	CD93 (A35P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289528	NM_012072.4(CD93):c.70G>C (p.Ala24Pro)	CD93 (A24P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527240	NM_012072.4(CD93):c.61G>A (p.Gly21Arg)	CD93 (G21R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494564	NM_012072.4(CD93):c.50A>T (p.Gln17Leu)	CD93 (Q17L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318875	NM_012072.4(CD93):c.23T>C (p.Leu8Pro)	CD93 (L8P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 31