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

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2361150	NM_207189.4(BRDT):c.212A>C (p.Lys71Thr)	BRDT (K71T)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2612474	NM_207189.4(BRDT):c.214A>T (p.Asn72Tyr)	BRDT (N72Y)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	GUncertain significance
Select item 2242619	NM_207189.4(BRDT):c.349C>T (p.Leu117Phe)	BRDT (L44F +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2513479	NM_207189.4(BRDT):c.713A>T (p.Lys238Ile)	BRDT (K238I +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2295681	NM_207189.4(BRDT):c.733A>T (p.Ile245Leu)	BRDT (I245L +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2261867	NM_207189.4(BRDT):c.839T>C (p.Leu280Pro)	BRDT (L234P +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2307302	NM_207189.4(BRDT):c.863A>C (p.His288Pro)	BRDT (H242P +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2610630	NM_207189.4(BRDT):c.904A>C (p.Asn302His)	BRDT (N229H +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2287102	NM_207189.4(BRDT):c.955C>A (p.Leu319Ile)	BRDT (L323I +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2554036	NM_207189.4(BRDT):c.1003T>A (p.Tyr335Asn)	BRDT (Y335N +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2280335	NM_207189.4(BRDT):c.1018G>C (p.Asp340His)	BRDT (D340H +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2528229	NM_207189.4(BRDT):c.1129C>A (p.Pro377Thr)	BRDT (P304T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2554153	NM_207189.4(BRDT):c.1130C>G (p.Pro377Arg)	BRDT (P381R +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2264537	NM_207189.4(BRDT):c.1133T>C (p.Ile378Thr)	BRDT (I305T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2389086	NM_207189.4(BRDT):c.1166T>C (p.Ile389Thr)	BRDT (I316T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2558118	NM_207189.4(BRDT):c.1207A>G (p.Asn403Asp)	BRDT (N330D +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2526518	NM_207189.4(BRDT):c.1240G>T (p.Asp414Tyr)	BRDT (D368Y +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2483060	NM_207189.4(BRDT):c.1264C>T (p.Arg422Cys)	BRDT (R349C +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2355027	NM_207189.4(BRDT):c.1907G>A (p.Arg636Gln)	BRDT (R590Q +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2399322	NM_207189.4(BRDT):c.1934G>A (p.Ser645Asn)	BRDT (S572N +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2508762	NM_207189.4(BRDT):c.1936A>G (p.Ser646Gly)	BRDT (S573G +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2294997	NM_207189.4(BRDT):c.2060T>G (p.Val687Gly)	BRDT (V614G +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2608729	NM_207189.4(BRDT):c.2467G>T (p.Asp823Tyr)	BRDT (D777Y +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2244747	NM_207189.4(BRDT):c.2501T>C (p.Ile834Thr)	BRDT (I761T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2484625	NM_207189.4(BRDT):c.2693C>G (p.Ala898Gly)	BRDT (A825G +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2332601	NM_207189.4(BRDT):c.2703A>T (p.Lys901Asn)	BRDT (K828N +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2279481	NM_207189.4(BRDT):c.2710C>T (p.Leu904Phe)	BRDT (L831F +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2610383	NM_207189.4(BRDT):c.2729G>A (p.Arg910His)	BRDT (R864H +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 30