NOC3L[gene] and "single gene"[properties] - ClinVar

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Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2226480	NM_022451.11(NOC3L):c.2342G>A (p.Ser781Asn)	NOC3L (S781N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2391508	NM_022451.11(NOC3L):c.2221A>G (p.Met741Val)	NOC3L (M741V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495736	NM_022451.11(NOC3L):c.2207T>C (p.Phe736Ser)	NOC3L (F736S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214666	NM_022451.11(NOC3L):c.2192C>T (p.Ser731Phe)	NOC3L (S731F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387123	NM_022451.11(NOC3L):c.2186G>A (p.Arg729Gln)	NOC3L (R729Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218666	NM_022451.11(NOC3L):c.2068C>A (p.Leu690Met)	NOC3L (L690M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306037	NM_022451.11(NOC3L):c.2023C>A (p.Pro675Thr)	NOC3L (P675T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597486	NM_022451.11(NOC3L):c.1873G>A (p.Ala625Thr)	NOC3L (A625T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300220	NM_022451.11(NOC3L):c.1784C>T (p.Ala595Val)	NOC3L (A595V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304341	NM_022451.11(NOC3L):c.1777G>A (p.Ala593Thr)	NOC3L (A593T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300222	NM_022451.11(NOC3L):c.1603G>A (p.Asp535Asn)	NOC3L (D535N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200959	NM_022451.11(NOC3L):c.1537C>T (p.Pro513Ser)	NOC3L (P513S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319610	NM_022451.11(NOC3L):c.1477G>C (p.Glu493Gln)	NOC3L (E493Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300224	NM_022451.11(NOC3L):c.1427G>T (p.Arg476Leu)	NOC3L (R476L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200958	NM_022451.11(NOC3L):c.1145G>A (p.Cys382Tyr)	NOC3L (C382Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533564	NM_022451.11(NOC3L):c.1038G>C (p.Leu346Phe)	NOC3L (L346F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300221	NM_022451.11(NOC3L):c.1024G>T (p.Ala342Ser)	NOC3L (A342S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405306	NM_022451.11(NOC3L):c.1010G>T (p.Gly337Val)	NOC3L (G337V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461736	NM_022451.11(NOC3L):c.862C>G (p.Arg288Gly)	NOC3L (R288G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200973	NM_022451.11(NOC3L):c.859A>T (p.Thr287Ser)	NOC3L (T287S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590700	NM_022451.11(NOC3L):c.806T>C (p.Ile269Thr)	NOC3L (I269T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200972	NM_022451.11(NOC3L):c.791A>T (p.Glu264Val)	NOC3L (E264V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200971	NM_022451.11(NOC3L):c.733G>A (p.Glu245Lys)	NOC3L (E245K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265437	NM_022451.11(NOC3L):c.729G>C (p.Leu243Phe)	NOC3L (L243F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220542	NM_022451.11(NOC3L):c.724A>G (p.Met242Val)	NOC3L (M242V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200969	NM_022451.11(NOC3L):c.712G>C (p.Glu238Gln)	NOC3L (E238Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200968	NM_022451.11(NOC3L):c.636G>C (p.Gln212His)	NOC3L (Q212H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200967	NM_022451.11(NOC3L):c.623A>G (p.Lys208Arg)	NOC3L (K208R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618919	NM_022451.11(NOC3L):c.530A>T (p.Glu177Val)	NOC3L (E177V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618918	NM_022451.11(NOC3L):c.529G>A (p.Glu177Lys)	NOC3L (E177K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213739	NM_022451.11(NOC3L):c.527A>G (p.Asp176Gly)	NOC3L (D176G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381262	NM_022451.11(NOC3L):c.385C>T (p.Arg129Cys)	NOC3L (R129C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200965	NM_022451.11(NOC3L):c.319G>A (p.Val107Ile)	NOC3L (V107I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200964	NM_022451.11(NOC3L):c.314A>G (p.Gln105Arg)	NOC3L (Q105R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300223	NM_022451.11(NOC3L):c.269A>C (p.Asp90Ala)	NOC3L (D90A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208459	NM_022451.11(NOC3L):c.266T>C (p.Leu89Ser)	NOC3L (L89S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3200963	NM_022451.11(NOC3L):c.257C>G (p.Ala86Gly)	NOC3L (A86G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200961	NM_022451.11(NOC3L):c.212G>A (p.Arg71Gln)	NOC3L (R71Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200960	NM_022451.11(NOC3L):c.205G>C (p.Glu69Gln)	NOC3L (E69Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200966	NM_022451.11(NOC3L):c.52A>C (p.Lys18Gln)	NOC3L (K18Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325469	NM_022451.11(NOC3L):c.41G>T (p.Arg14Leu)	NOC3L (R14L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 41