"Ambry Genetics"[submitter] AND "BRD7"[gene] - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2310123	NM_013263.5(BRD7):c.1792C>G (p.Gln598Glu)	BRD7, LOC126862343 (Q598E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261728	NM_013263.5(BRD7):c.1771A>G (p.Asn591Asp)	BRD7, LOC126862343 (N591D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261727	NM_013263.5(BRD7):c.1762C>G (p.Gln588Glu)	BRD7, LOC126862343 (Q589E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540308	NM_013263.5(BRD7):c.1748T>A (p.Met583Lys)	BRD7, LOC126862343 (M584K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261724	NM_013263.5(BRD7):c.1730G>A (p.Gly577Asp)	BRD7, LOC126862343 (G578D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261729	NM_013263.5(BRD7):c.1675G>A (p.Ala559Thr)	BRD7 (A559T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612607	NM_013263.5(BRD7):c.1559C>T (p.Ala520Val)	BRD7 (A520V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592375	NM_013263.5(BRD7):c.1528T>G (p.Leu510Val)	BRD7 (L511V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346164	NM_013263.5(BRD7):c.1510G>A (p.Val504Ile)	BRD7 (V505I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3261730	NM_013263.5(BRD7):c.1484C>A (p.Thr495Lys)	BRD7 (T495K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134978	NM_013263.5(BRD7):c.1477C>G (p.Leu493Val)	BRD7 (L493V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281652	NM_013263.5(BRD7):c.1415A>T (p.His472Leu)	BRD7 (H472L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329239	NM_013263.5(BRD7):c.1385G>C (p.Ser462Thr)	BRD7 (S462T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375735	NM_013263.5(BRD7):c.1246T>A (p.Ser416Thr)	BRD7 (S416T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134977	NM_013263.5(BRD7):c.1186G>A (p.Val396Ile)	BRD7 (V396I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134976	NM_013263.5(BRD7):c.1102C>T (p.Pro368Ser)	BRD7 (P368S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134982	NM_013263.5(BRD7):c.983A>G (p.Lys328Arg)	BRD7 (K328R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528957	NM_013263.5(BRD7):c.827G>T (p.Arg276Ile)	BRD7 (R276I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588348	NM_013263.5(BRD7):c.513C>G (p.Ile171Met)	BRD7 (I171M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292048	NM_013263.5(BRD7):c.423T>A (p.Asn141Lys)	BRD7 (N141K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249817	NM_013263.5(BRD7):c.406C>G (p.Leu136Val)	BRD7 (L136V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379665	NM_013263.5(BRD7):c.391G>A (p.Val131Ile)	BRD7 (V131I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338416	NM_013263.5(BRD7):c.373T>A (p.Leu125Ile)	BRD7 (L125I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261723	NM_013263.5(BRD7):c.347C>T (p.Pro116Leu)	BRD7 (P116L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402662	NM_013263.5(BRD7):c.319T>C (p.Cys107Arg)	BRD7 (C107R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256818	NM_013263.5(BRD7):c.305A>G (p.Glu102Gly)	BRD7 (E102G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134981	NM_013263.5(BRD7):c.296A>G (p.Asn99Ser)	BRD7 (N99S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377197	NM_013263.5(BRD7):c.287G>A (p.Arg96Gln)	BRD7 (R96Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134980	NM_013263.5(BRD7):c.215A>G (p.Gln72Arg)	BRD7 (Q72R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223381	NM_013263.5(BRD7):c.162T>A (p.Asp54Glu)	BRD7 (D54E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261726	NM_013263.5(BRD7):c.158A>T (p.Asn53Ile)	BRD7 (N53I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522638	NM_013263.5(BRD7):c.136T>C (p.Ser46Pro)	BRD7 (S46P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134979	NM_013263.5(BRD7):c.15C>A (p.His5Gln)	BRD7, LOC130058995 (H5Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541379	NM_013263.5(BRD7):c.5G>A (p.Gly2Asp)	BRD7, LOC130058995 (G2D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 34