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

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Items: 49

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3135003	NM_207189.4(BRDT):c.10C>T (p.Pro4Ser)	BRDT (P4S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361150	NM_207189.4(BRDT):c.212A>C (p.Lys71Thr)	BRDT (K71T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2612474	NM_207189.4(BRDT):c.214A>T (p.Asn72Tyr)	BRDT (N72Y)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2292938	NM_207189.4(BRDT):c.275C>T (p.Ser92Leu)	BRDT (S19L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528363	NM_207189.4(BRDT):c.294C>A (p.Phe98Leu)	BRDT (F25L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2242619	NM_207189.4(BRDT):c.349C>T (p.Leu117Phe)	BRDT (L44F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135015	NM_207189.4(BRDT):c.590T>G (p.Val197Gly)	BRDT (V124G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135016	NM_207189.4(BRDT):c.619G>A (p.Val207Ile)	BRDT (V134I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513479	NM_207189.4(BRDT):c.713A>T (p.Lys238Ile)	BRDT (K238I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295681	NM_207189.4(BRDT):c.733A>T (p.Ile245Leu)	BRDT (I245L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261867	NM_207189.4(BRDT):c.839T>C (p.Leu280Pro)	BRDT (L234P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307302	NM_207189.4(BRDT):c.863A>C (p.His288Pro)	BRDT (H242P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610630	NM_207189.4(BRDT):c.904A>C (p.Asn302His)	BRDT (N229H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287102	NM_207189.4(BRDT):c.955C>A (p.Leu319Ile)	BRDT (L323I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135017	NM_207189.4(BRDT):c.980A>G (p.Asp327Gly)	BRDT (D331G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554036	NM_207189.4(BRDT):c.1003T>A (p.Tyr335Asn)	BRDT (Y335N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280335	NM_207189.4(BRDT):c.1018G>C (p.Asp340His)	BRDT (D340H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135002	NM_207189.4(BRDT):c.1048A>G (p.Lys350Glu)	BRDT (K350E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528229	NM_207189.4(BRDT):c.1129C>A (p.Pro377Thr)	BRDT (P304T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554153	NM_207189.4(BRDT):c.1130C>G (p.Pro377Arg)	BRDT (P381R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264537	NM_207189.4(BRDT):c.1133T>C (p.Ile378Thr)	BRDT (I305T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389086	NM_207189.4(BRDT):c.1166T>C (p.Ile389Thr)	BRDT (I316T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558118	NM_207189.4(BRDT):c.1207A>G (p.Asn403Asp)	BRDT (N330D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135005	NM_207189.4(BRDT):c.1213G>A (p.Ala405Thr)	BRDT (A332T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526518	NM_207189.4(BRDT):c.1240G>T (p.Asp414Tyr)	BRDT (D368Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483060	NM_207189.4(BRDT):c.1264C>T (p.Arg422Cys)	BRDT (R349C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261753	NM_207189.4(BRDT):c.1327G>T (p.Val443Leu)	BRDT (V447L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135006	NM_207189.4(BRDT):c.1336C>T (p.Arg446Cys)	BRDT (R373C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261750	NM_207189.4(BRDT):c.1359G>C (p.Glu453Asp)	BRDT (E380D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135007	NM_207189.4(BRDT):c.1787C>T (p.Ser596Leu)	BRDT (S523L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135008	NM_207189.4(BRDT):c.1904C>G (p.Ser635Cys)	BRDT (S562C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355027	NM_207189.4(BRDT):c.1907G>A (p.Arg636Gln)	BRDT (R590Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399322	NM_207189.4(BRDT):c.1934G>A (p.Ser645Asn)	BRDT (S572N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508762	NM_207189.4(BRDT):c.1936A>G (p.Ser646Gly)	BRDT (S573G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135009	NM_207189.4(BRDT):c.2036A>G (p.Asn679Ser)	BRDT (N683S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294997	NM_207189.4(BRDT):c.2060T>G (p.Val687Gly)	BRDT (V614G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261751	NM_207189.4(BRDT):c.2177C>T (p.Pro726Leu)	BRDT (P680L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135010	NM_207189.4(BRDT):c.2359G>A (p.Glu787Lys)	BRDT (E714K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135011	NM_207189.4(BRDT):c.2392A>G (p.Ile798Val)	BRDT (I725V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608729	NM_207189.4(BRDT):c.2467G>T (p.Asp823Tyr)	BRDT (D777Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244747	NM_207189.4(BRDT):c.2501T>C (p.Ile834Thr)	BRDT (I761T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261752	NM_207189.4(BRDT):c.2528A>G (p.Gln843Arg)	BRDT (Q770R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135012	NM_207189.4(BRDT):c.2645A>G (p.Asn882Ser)	BRDT (N886S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484625	NM_207189.4(BRDT):c.2693C>G (p.Ala898Gly)	BRDT (A825G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332601	NM_207189.4(BRDT):c.2703A>T (p.Lys901Asn)	BRDT (K828N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135013	NM_207189.4(BRDT):c.2704T>A (p.Ser902Thr)	BRDT (S856T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279481	NM_207189.4(BRDT):c.2710C>T (p.Leu904Phe)	BRDT (L831F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610383	NM_207189.4(BRDT):c.2729G>A (p.Arg910His)	BRDT (R864H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135014	NM_207189.4(BRDT):c.2801T>G (p.Leu934Arg)	BRDT (L861R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 49