ClinVar for Gene (Select 158358) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3261697	NM_001017969.3(BRD10):c.3874G>T (p.Val1292Leu)	BRD10 (V1292L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261696	NM_001017969.3(BRD10):c.4344T>G (p.Ser1448Arg)	BRD10 (S1448R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261695	NM_001017969.3(BRD10):c.5545A>G (p.Thr1849Ala)	BRD10 (T1849A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3261693	NM_001017969.3(BRD10):c.3808A>G (p.Lys1270Glu)	BRD10 (K1270E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261692	NM_001017969.3(BRD10):c.596A>G (p.His199Arg)	BRD10 (H199R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261691	NM_001017969.3(BRD10):c.4724T>C (p.Ile1575Thr)	BRD10 (I1575T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261690	NM_001017969.3(BRD10):c.5443A>G (p.Thr1815Ala)	BRD10 (T1815A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261689	NM_001017969.3(BRD10):c.1651A>G (p.Lys551Glu)	BRD10 (K551E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261688	NM_001017969.3(BRD10):c.5888C>T (p.Pro1963Leu)	BRD10 (P1963L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261687	NM_001017969.3(BRD10):c.5197C>G (p.Pro1733Ala)	BRD10 (P1733A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261686	NM_001017969.3(BRD10):c.3164A>G (p.His1055Arg)	BRD10 (H1055R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261685	NM_001017969.3(BRD10):c.4670C>T (p.Thr1557Ile)	BRD10 (T1557I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261684	NM_001017969.3(BRD10):c.4405C>G (p.Pro1469Ala)	BRD10 (P1469A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261683	NM_001017969.3(BRD10):c.4463C>G (p.Thr1488Ser)	BRD10 (T1488S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261682	NM_001017969.3(BRD10):c.3890A>G (p.Asn1297Ser)	BRD10 (N1297S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261681	NM_001017969.3(BRD10):c.3482C>A (p.Ser1161Tyr)	BRD10 (S1161Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261680	NM_001017969.3(BRD10):c.1193G>A (p.Gly398Glu)	BRD10 (G398E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261679	NM_001017969.3(BRD10):c.4859C>T (p.Thr1620Ile)	BRD10 (T1620I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261678	NM_001017969.3(BRD10):c.5992G>A (p.Val1998Ile)	BRD10 (V1998I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261677	NM_001017969.3(BRD10):c.1061G>A (p.Arg354His)	BRD10 (R354H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261676	NM_001017969.3(BRD10):c.2840T>C (p.Leu947Pro)	BRD10 (L947P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261675	NM_001017969.3(BRD10):c.2693T>C (p.Met898Thr)	BRD10 (M898T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261674	NM_001017969.3(BRD10):c.742A>G (p.Met248Val)	BRD10 (M248V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261672	NM_001017969.3(BRD10):c.5608C>T (p.Pro1870Ser)	BRD10 (P1870S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261671	NM_001017969.3(BRD10):c.6203T>A (p.Leu2068His)	BRD10 (L2068H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261670	NM_001017969.3(BRD10):c.3344A>G (p.Lys1115Arg)	BRD10 (K1115R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261669	NM_001017969.3(BRD10):c.4972G>A (p.Ala1658Thr)	BRD10 (A1658T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235688	NM_001017969.3(BRD10):c.710C>G (p.Ala237Gly)	BRD10 (A237G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235687	NM_001017969.3(BRD10):c.623T>A (p.Val208Asp)	BRD10 (V208D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235686	NM_001017969.3(BRD10):c.6214C>T (p.Leu2072Phe)	BRD10 (L2072F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235685	NM_001017969.3(BRD10):c.6176A>G (p.Asn2059Ser)	BRD10 (N2059S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235684	NM_001017969.3(BRD10):c.6116T>G (p.Leu2039Trp)	BRD10 (L2039W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235683	NM_001017969.3(BRD10):c.6076A>G (p.Ser2026Gly)	BRD10 (S2026G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235682	NM_001017969.3(BRD10):c.5975T>C (p.Val1992Ala)	BRD10 (V1992A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235681	NM_001017969.3(BRD10):c.5843A>G (p.Asn1948Ser)	BRD10 (N1948S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235680	NM_001017969.3(BRD10):c.5759G>A (p.Gly1920Glu)	BRD10 (G1920E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235679	NM_001017969.3(BRD10):c.5638A>G (p.Thr1880Ala)	BRD10 (T1880A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235678	NM_001017969.3(BRD10):c.5630T>C (p.Val1877Ala)	BRD10 (V1877A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235677	NM_001017969.3(BRD10):c.5597A>G (p.Gln1866Arg)	BRD10 (Q1866R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235676	NM_001017969.3(BRD10):c.5594G>A (p.Ser1865Asn)	BRD10 (S1865N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235675	NM_001017969.3(BRD10):c.5548A>G (p.Ile1850Val)	BRD10 (I1850V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235674	NM_001017969.3(BRD10):c.5351C>T (p.Thr1784Ile)	BRD10 (T1784I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235673	NM_001017969.3(BRD10):c.5168T>C (p.Leu1723Pro)	BRD10 (L1723P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235672	NM_001017969.3(BRD10):c.5068A>G (p.Arg1690Gly)	BRD10 (R1690G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235671	NM_001017969.3(BRD10):c.5035C>T (p.Pro1679Ser)	BRD10 (P1679S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235670	NM_001017969.3(BRD10):c.4820A>T (p.Glu1607Val)	BRD10 (E1607V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235669	NM_001017969.3(BRD10):c.4819G>A (p.Glu1607Lys)	BRD10 (E1607K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235668	NM_001017969.3(BRD10):c.4677A>G (p.Ile1559Met)	BRD10 (I1559M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235667	NM_001017969.3(BRD10):c.4636C>A (p.Pro1546Thr)	BRD10 (P1546T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235666	NM_001017969.3(BRD10):c.449A>G (p.Gln150Arg)	BRD10, LOC130001525 (Q150R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235665	NM_001017969.3(BRD10):c.4422G>C (p.Met1474Ile)	BRD10 (M1474I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235664	NM_001017969.3(BRD10):c.4406C>T (p.Pro1469Leu)	BRD10 (P1469L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235663	NM_001017969.3(BRD10):c.4286A>C (p.Asn1429Thr)	BRD10 (N1429T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235662	NM_001017969.3(BRD10):c.4166C>T (p.Thr1389Ile)	BRD10 (T1389I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235661	NM_001017969.3(BRD10):c.4115C>T (p.Thr1372Ile)	BRD10 (T1372I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235660	NM_001017969.3(BRD10):c.3997T>C (p.Phe1333Leu)	BRD10 (F1333L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235659	NM_001017969.3(BRD10):c.3643G>C (p.Val1215Leu)	BRD10 (V1215L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235658	NM_001017969.3(BRD10):c.3610A>T (p.Ser1204Cys)	BRD10 (S1204C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235657	NM_001017969.3(BRD10):c.3493C>T (p.Pro1165Ser)	BRD10 (P1165S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235656	NM_001017969.3(BRD10):c.3461T>C (p.Val1154Ala)	BRD10 (V1154A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235655	NM_001017969.3(BRD10):c.3428C>G (p.Thr1143Arg)	BRD10 (T1143R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235654	NM_001017969.3(BRD10):c.3270G>A (p.Met1090Ile)	BRD10 (M1090I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235653	NM_001017969.3(BRD10):c.3264G>C (p.Gln1088His)	BRD10 (Q1088H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235652	NM_001017969.3(BRD10):c.3253A>G (p.Ile1085Val)	BRD10 (I1085V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235651	NM_001017969.3(BRD10):c.3252G>C (p.Lys1084Asn)	BRD10 (K1084N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235650	NM_001017969.3(BRD10):c.3140C>G (p.Pro1047Arg)	BRD10 (P1047R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235649	NM_001017969.3(BRD10):c.2978C>T (p.Ser993Leu)	BRD10 (S993L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235648	NM_001017969.3(BRD10):c.2956G>C (p.Glu986Gln)	BRD10 (E986Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235647	NM_001017969.3(BRD10):c.2857G>A (p.Ala953Thr)	BRD10 (A953T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235646	NM_001017969.3(BRD10):c.2713T>A (p.Phe905Ile)	BRD10 (F905I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235645	NM_001017969.3(BRD10):c.2653C>G (p.Leu885Val)	BRD10 (L885V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235644	NM_001017969.3(BRD10):c.2642C>T (p.Ser881Leu)	BRD10 (S881L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3235642	NM_001017969.3(BRD10):c.2585G>A (p.Gly862Asp)	BRD10 (G862D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235641	NM_001017969.3(BRD10):c.2255A>T (p.Lys752Ile)	BRD10 (K752I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235640	NM_001017969.3(BRD10):c.2243C>T (p.Thr748Ile)	BRD10 (T748I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235638	NM_001017969.3(BRD10):c.2179A>C (p.Lys727Gln)	BRD10 (K727Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235637	NM_001017969.3(BRD10):c.2110C>T (p.Arg704Cys)	BRD10 (R704C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235636	NM_001017969.3(BRD10):c.2097C>G (p.Asn699Lys)	BRD10 (N699K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235635	NM_001017969.3(BRD10):c.19C>T (p.Pro7Ser)	BRD10 (P7S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235634	NM_001017969.3(BRD10):c.1954C>T (p.Pro652Ser)	BRD10 (P652S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235633	NM_001017969.3(BRD10):c.1885C>A (p.Pro629Thr)	BRD10 (P629T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235632	NM_001017969.3(BRD10):c.1724G>A (p.Arg575Lys)	BRD10 (R575K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235631	NM_001017969.3(BRD10):c.1531A>G (p.Lys511Glu)	BRD10 (K511E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235629	NM_001017969.3(BRD10):c.134G>T (p.Arg45Met)	BRD10 (R45M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235628	NM_001017969.3(BRD10):c.1250C>G (p.Pro417Arg)	BRD10 (P417R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235627	NM_001017969.3(BRD10):c.1199G>C (p.Cys400Ser)	BRD10 (C400S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192758	NM_005511.2(MLANA):c.296A>G (p.Asn99Ser)	BRD10, MLANA (N99S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063123	GRCh37/hg19 9p24.3-24.1(chr9:203862-8548307)x1	AK3, BRD10 +37 more	Copy number loss	not specified	GPathogenic
Select item 3063089	GRCh37/hg19 9p24.3-23(chr9:203861-9128400)x1	AK3, BRD10 +37 more	Copy number loss	not specified	GPathogenic
Select item 3063080	GRCh37/hg19 9p24.3-22.3(chr9:203861-15508556)x1	AK3, BRD10 +47 more	Copy number loss	not specified	GPathogenic
Select item 3063071	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3	DMAC1, DMRT1 +769 more	Copy number gain	not specified	GPathogenic
Select item 3063070	GRCh37/hg19 9p24.3-22.1(chr9:203861-19302836)x1	ADAMTSL1, AK3 +57 more	Copy number loss	not specified	GPathogenic
Select item 2685336	GRCh37/hg19 9p24.1(chr9:5849390-6017252)x1	BRD10, MLANA +1 more	Copy number loss	not provided	GUncertain significance
Select item 2684569	GRCh37/hg19 9p24.3-13.1(chr9:1475882-38771831)x3	CREB3, STOML2 +188 more	Copy number gain	not provided	GPathogenic
Select item 2671611	Single allele	AK3, BNC2 +49 more	Deletion	not provided	GPathogenic
Select item 2659058	NM_001017969.3(BRD10):c.963A>G (p.Pro321=)	BRD10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2659057	NM_001017969.3(BRD10):c.3516A>G (p.Thr1172=)	BRD10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2659056	NM_001017969.3(BRD10):c.4294ATT[1] (p.Ile1433del)	BRD10 (I1433del)	Microsatellite (inframe_deletion)	not provided	GLikely benign
Select item 2561178	NM_001017969.3(BRD10):c.2719A>G (p.Met907Val)	BRD10 (M907V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561018	NM_001017969.3(BRD10):c.2399G>A (p.Arg800Gln)	BRD10 (R800Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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