BRD1[gene] and "single gene"[properties] - ClinVar

Search results

Items: 84

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 722639	NM_001304808.3(BRD1):c.3549C>T (p.Ser1183=)	BRD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2240958	NM_001304808.3(BRD1):c.3535G>A (p.Gly1179Arg)	BRD1 (G534R +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 746333	NM_001304808.3(BRD1):c.3528C>T (p.Arg1176=)	BRD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2340657	NM_001304808.3(BRD1):c.3505C>T (p.Arg1169Cys)	BRD1 (R1164C +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2207254	NM_001304808.3(BRD1):c.3436A>G (p.Ile1146Val)	BRD1 (I1015V +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370574	NM_001304808.3(BRD1):c.3319G>C (p.Glu1107Gln)	BRD1 (E1102Q +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489491	NM_001304808.3(BRD1):c.3314T>C (p.Ile1105Thr)	BRD1 (I1098T +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2653349	NM_001304808.3(BRD1):c.3309G>A (p.Leu1103=)	BRD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 724375	NM_001304808.3(BRD1):c.3279C>G (p.Val1093=)	BRD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2601385	NM_001304808.3(BRD1):c.3253C>T (p.Arg1085Cys)	BRD1 (R1078C +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 719862	NM_001304808.3(BRD1):c.3159C>T (p.Ala1053=)	BRD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3134949	NM_001304808.3(BRD1):c.3133A>G (p.Ser1045Gly)	BRD1 (S1045G +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3134948	NM_001304808.3(BRD1):c.3128G>C (p.Gly1043Ala)	BRD1 (G1041A +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380059	NM_001304808.3(BRD1):c.3127G>A (p.Gly1043Ser)	BRD1 (G529S +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 763917	NM_001304808.3(BRD1):c.3122-4G>A	BRD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2227753	NM_001304808.3(BRD1):c.3115G>A (p.Ala1039Thr)	BRD1 (A908T +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3261668	NM_001304808.3(BRD1):c.3074C>T (p.Ser1025Phe)	BRD1 (S1023F +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3134947	NM_001304808.3(BRD1):c.3062G>C (p.Ser1021Thr)	BRD1 (S890T +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 781531	NM_001304808.3(BRD1):c.3060C>T (p.Arg1020=)	BRD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2246710	NM_001304808.3(BRD1):c.3059G>A (p.Arg1020His)	BRD1 (R1013H +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3261666	NM_001304808.3(BRD1):c.2986G>T (p.Asp996Tyr)	BRD1 (D914Y +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312016	NM_001304808.3(BRD1):c.2981T>C (p.Leu994Pro)	BRD1 (L480P +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508110	NM_001304808.3(BRD1):c.2978C>T (p.Pro993Leu)	BRD1 (P862L +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3261664	NM_001304808.3(BRD1):c.2977C>A (p.Pro993Thr)	BRD1 (P993T +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3261662	NM_001304808.3(BRD1):c.2969G>A (p.Ser990Asn)	BRD1 (S859N +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2218423	NM_001304808.3(BRD1):c.2936G>A (p.Arg979Gln)	BRD1 (R848Q +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2383354	NM_001304808.3(BRD1):c.2923G>C (p.Ala975Pro)	BRD1 (A893P +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2330938	NM_001304808.3(BRD1):c.2905G>A (p.Gly969Ser)	BRD1 (G838S +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2234449	NM_001304808.3(BRD1):c.2882C>T (p.Ala961Val)	BRD1 (A447V +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3134946	NM_001304808.3(BRD1):c.2879G>A (p.Gly960Asp)	BRD1 (G446D +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3134945	NM_001304808.3(BRD1):c.2846G>A (p.Arg949His)	BRD1 (R435H +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 721966	NM_001304808.3(BRD1):c.2808C>T (p.Cys936=)	BRD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2203959	NM_001304808.3(BRD1):c.2798G>A (p.Arg933Gln)	BRD1 (R802Q +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509473	NM_001304808.3(BRD1):c.2797C>G (p.Arg933Gly)	BRD1 (R931G +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212714	NM_001304808.3(BRD1):c.2786G>C (p.Arg929Thr)	BRD1 (R284T +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 755857	NM_001304808.3(BRD1):c.2349G>A (p.Ala783=)	BRD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2594189	NM_001304808.3(BRD1):c.2348C>T (p.Ala783Val)	BRD1 (A269V +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2622118	NM_001304808.3(BRD1):c.2342C>T (p.Pro781Leu)	BRD1 (P776L +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2211142	NM_001304808.3(BRD1):c.2333C>T (p.Ala778Val)	BRD1 (A771V +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 781532	NM_001304808.3(BRD1):c.2326G>A (p.Gly776Arg)	BRD1 (G262R +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 784425	NM_001304808.3(BRD1):c.2313C>T (p.Gly771=)	BRD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2264613	NM_001304808.3(BRD1):c.2248C>T (p.Leu750Phe)	BRD1 (L236F +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2569814	NM_001304808.3(BRD1):c.2203G>T (p.Gly735Cys)	BRD1 (G221C +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1226634	NM_001304808.3(BRD1):c.2188G>A (p.Ala730Thr)	BRD1 (A216T +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 789249	NM_001304808.3(BRD1):c.2118C>A (p.Pro706=)	BRD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2460374	NM_001304808.3(BRD1):c.2072C>T (p.Pro691Leu)	BRD1 (P177L +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 717985	NM_001304808.3(BRD1):c.2066C>T (p.Ala689Val)	BRD1 (A175V +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2570019	NM_001304808.3(BRD1):c.2057G>A (p.Arg686Gln)	BRD1 (R686Q +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620117	NM_001304808.3(BRD1):c.2056C>T (p.Arg686Trp)	BRD1 (R679W +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3261663	NM_001304808.3(BRD1):c.2017A>G (p.Ile673Val)	BRD1 (I666V +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3134944	NM_001304808.3(BRD1):c.2000G>A (p.Arg667Gln)	BRD1 (R665Q +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3261661	NM_001304808.3(BRD1):c.1939G>A (p.Val647Met)	BRD1 (V645M +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3261660	NM_001304808.3(BRD1):c.1885G>A (p.Glu629Lys)	BRD1 (E622K +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518655	NM_001304808.3(BRD1):c.1874A>G (p.His625Arg)	BRD1 (H111R +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 733982	NM_001304808.3(BRD1):c.1860G>A (p.Gly620=)	BRD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2289578	NM_001304808.3(BRD1):c.1859G>A (p.Gly620Glu)	BRD1 (G615E +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 740214	NM_001304808.3(BRD1):c.1764G>A (p.Ala588=)	BRD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2239396	NM_001304808.3(BRD1):c.1694C>G (p.Thr565Ser)	BRD1 (T51S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458722	NM_001304808.3(BRD1):c.1688G>A (p.Arg563Gln)	BRD1 (R49Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2224922	NM_001304808.3(BRD1):c.1675G>A (p.Ala559Thr)	BRD1 (A45T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320313	NM_001304808.3(BRD1):c.1666G>A (p.Glu556Lys)	BRD1 (E42K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 718307	NM_001304808.3(BRD1):c.1657-4C>T	BRD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2379296	NM_001304808.3(BRD1):c.1591G>A (p.Asp531Asn)	BRD1 (D585N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 734087	NM_001304808.3(BRD1):c.1536T>C (p.Asp512=)	BRD1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3134943	NM_001304808.3(BRD1):c.1378A>T (p.Ile460Phe)	BRD1 (I460F +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3134942	NM_001304808.3(BRD1):c.1345G>A (p.Ala449Thr)	BRD1 (A449T)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 725820	NM_001304808.3(BRD1):c.1327G>A (p.Val443Ile)	BRD1 (V443I)	Single nucleotide variant (missense variant +3 more)	not provided	GLikely benign
Select item 719240	NM_001304808.3(BRD1):c.1241A>G (p.Glu414Gly)	BRD1 (E414G)	Single nucleotide variant (missense variant +3 more)	not provided	GLikely benign
Select item 710389	NM_001304808.3(BRD1):c.1208A>G (p.Asp403Gly)	BRD1 (D403G)	Single nucleotide variant (missense variant +3 more)	not provided	GBenign
Select item 733158	NM_001304808.3(BRD1):c.1203C>T (p.Tyr401=)	BRD1	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 760731	NM_001304808.3(BRD1):c.1116C>T (p.Gly372=)	BRD1	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 748434	NM_001304808.3(BRD1):c.1044A>G (p.Thr348=)	BRD1	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 3261667	NM_001304808.3(BRD1):c.991A>C (p.Lys331Gln)	BRD1 (K331Q)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2342687	NM_001304808.3(BRD1):c.706A>G (p.Met236Val)	BRD1 (M236V)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 1343930	NM_001304808.3(BRD1):c.579C>T (p.Phe193=)	BRD1	Single nucleotide variant (synonymous variant +3 more)	not provided	GBenign
Select item 3134951	NM_001304808.3(BRD1):c.568A>C (p.Met190Leu)	BRD1 (M190L)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2298543	NM_001304808.3(BRD1):c.416A>G (p.Tyr139Cys)	BRD1 (Y139C)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3134950	NM_001304808.3(BRD1):c.389C>T (p.Pro130Leu)	BRD1 (P130L)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2653350	NM_001304808.3(BRD1):c.372C>T (p.Ile124=)	BRD1	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 787512	NM_001304808.3(BRD1):c.333G>A (p.Pro111=)	BRD1	Single nucleotide variant (synonymous variant +3 more)	not provided	GBenign
Select item 2385195	NM_001304808.3(BRD1):c.332C>T (p.Pro111Leu)	BRD1 (P111L)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 773097	NM_001304808.3(BRD1):c.317G>C (p.Ser106Thr)	BRD1 (S106T)	Single nucleotide variant (missense variant +3 more)	not provided	GBenign
Select item 2328747	NM_001304808.3(BRD1):c.123G>T (p.Glu41Asp)	BRD1 (E41D)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 715753	NM_001304808.3(BRD1):c.99C>T (p.Tyr33=)	BRD1	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign

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Items: 84