"PreventionGenetics, part of Exact Sciences"[submitter] AND "BRD4"[gen - ClinVar

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Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 778171	NM_001379291.1(BRD4):c.4020+9G>T	BRD4	Single nucleotide variant (intron variant)	BRD4-related condition +1 more	GBenign/Likely benign
Select item 710756	NM_001379291.1(BRD4):c.3927C>T (p.Thr1309=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition +1 more	GBenign
Select item 2075753	NM_001379291.1(BRD4):c.3822G>A (p.Arg1274=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition +1 more	GLikely benign
Select item 775116	NM_001379291.1(BRD4):c.3810G>C (p.Glu1270Asp)	BRD4 (E1270D)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 2056059	NM_001379291.1(BRD4):c.3567G>A (p.Ala1189=)	BRD4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 710757	NM_001379291.1(BRD4):c.3489G>A (p.Arg1163=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition +1 more	GBenign
Select item 2063727	NM_001379291.1(BRD4):c.3334GAG[1] (p.Glu1113del)	BRD4 (E1113del)	Microsatellite (inframe_deletion)	not provided +1 more	GBenign
Select item 2066261	NM_001379291.1(BRD4):c.3336G>A (p.Glu1112=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition +1 more	GBenign/Likely benign
Select item 3044479	NM_001379291.1(BRD4):c.3156C>T (p.Asp1052=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition	GLikely benign
Select item 2175499	NM_001379291.1(BRD4):c.3061C>A (p.His1021Asn)	BRD4 (H1021N)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2126109	NM_001379291.1(BRD4):c.2909_2923dup (p.Pro974_Pro975insLeuGlnGlnGlnPro)	BRD4	Duplication (inframe_insertion)	not provided +1 more	GBenign/Likely benign
Select item 2073270	NM_001379291.1(BRD4):c.2922G>A (p.Pro974=)	BRD4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1575397	NM_001379291.1(BRD4):c.2913G>A (p.Gln971=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition +1 more	GLikely benign
Select item 2041369	NM_001379291.1(BRD4):c.2856C>T (p.Ser952=)	BRD4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3029281	NM_001379291.1(BRD4):c.2843T>C (p.Val948Ala)	BRD4 (V948A)	Single nucleotide variant (missense variant)	BRD4-related condition	GUncertain significance
Select item 793016	NM_001379291.1(BRD4):c.2811G>A (p.Lys937=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition +1 more	GLikely benign
Select item 2068700	NM_001379291.1(BRD4):c.2397C>T (p.Pro799=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition +1 more	GLikely benign
Select item 3051601	NM_001379291.1(BRD4):c.2385C>A (p.Ser795=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition	GLikely benign
Select item 3036267	NM_001379291.1(BRD4):c.2367A>T (p.Ala789=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition	GLikely benign
Select item 3040579	NM_001379291.1(BRD4):c.2271G>A (p.Pro757=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition	GLikely benign
Select item 710758	NM_001379291.1(BRD4):c.2241G>A (p.Gln747=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition +1 more	GBenign
Select item 3032667	NM_001379291.1(BRD4):c.2158+499G>A	BRD4	Single nucleotide variant (synonymous variant +1 more)	BRD4-related condition	GLikely benign
Select item 3052100	NM_001379291.1(BRD4):c.2158+424C>T	BRD4	Single nucleotide variant (synonymous variant +1 more)	BRD4-related condition	GLikely benign
Select item 2633318	NM_001379291.1(BRD4):c.2041C>T (p.Pro681Ser)	BRD4 (P681S)	Single nucleotide variant (missense variant)	BRD4-related condition	GUncertain significance
Select item 2056304	NM_001379291.1(BRD4):c.1881C>T (p.Gly627=)	BRD4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 2058463	NM_001379291.1(BRD4):c.1688G>A (p.Ser563Asn)	BRD4 (S563N)	Single nucleotide variant (missense variant)	BRD4-related condition +1 more	GBenign
Select item 2064564	NM_001379291.1(BRD4):c.1644A>G (p.Lys548=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition +1 more	GLikely benign
Select item 735642	NM_001379291.1(BRD4):c.1590G>A (p.Gln530=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition +1 more	GBenign/Likely benign
Select item 2065052	NM_001379291.1(BRD4):c.1458C>T (p.Ser486=)	BRD4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1976364	NM_001379291.1(BRD4):c.1374G>A (p.Pro458=)	BRD4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 743575	NM_001379291.1(BRD4):c.1342-8C>T	BRD4	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 3038717	NM_001379291.1(BRD4):c.1219C>T (p.Leu407=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition	GLikely benign
Select item 771515	NM_001379291.1(BRD4):c.801C>T (p.Pro267=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition +1 more	GBenign
Select item 2632926	NM_001379291.1(BRD4):c.577G>C (p.Val193Leu)	BRD4 (V193L)	Single nucleotide variant (missense variant)	BRD4-related condition	GUncertain significance
Select item 3051567	NM_001379291.1(BRD4):c.132C>T (p.Asn44=)	BRD4	Single nucleotide variant (synonymous variant)	BRD4-related condition	GLikely benign
Select item 3046799	NM_001379291.1(BRD4):c.28A>G (p.Arg10Gly)	BRD4 (R10G)	Single nucleotide variant (missense variant)	BRD4-related condition	GUncertain significance

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Items: 36