"Ambry Genetics"[submitter] AND "BRD10"[gene] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 1 to 100 of 192

<< First< Prev

Page of 2

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2400602	NM_005511.2(MLANA):c.68C>T (p.Thr23Met)	BRD10, MLANA (T23M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259217	NM_005511.2(MLANA):c.68C>A (p.Thr23Lys)	BRD10, MLANA (T23K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406025	NM_005511.2(MLANA):c.139T>C (p.Tyr47His)	BRD10, MLANA (Y47H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295667	NM_005511.2(MLANA):c.237T>G (p.Phe79Leu)	BRD10, MLANA (F79L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2244648	NM_005511.2(MLANA):c.242A>T (p.His81Leu)	BRD10, MLANA (H81L)	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 2401324	NM_001017969.3(BRD10):c.6278C>T (p.Ser2093Leu)	BRD10 (S2093L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204359	NM_001017969.3(BRD10):c.6262C>T (p.Pro2088Ser)	BRD10 (P2088S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378463	NM_001017969.3(BRD10):c.6260T>G (p.Phe2087Cys)	BRD10 (F2087C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404062	NM_001017969.3(BRD10):c.6248C>G (p.Pro2083Arg)	BRD10 (P2083R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351729	NM_001017969.3(BRD10):c.6242G>A (p.Arg2081Gln)	BRD10 (R2081Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280060	NM_001017969.3(BRD10):c.6227T>C (p.Val2076Ala)	BRD10 (V2076A)	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 2205594	NM_001017969.3(BRD10):c.6208C>G (p.Pro2070Ala)	BRD10 (P2070A)	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 3235685	NM_001017969.3(BRD10):c.6176A>G (p.Asn2059Ser)	BRD10 (N2059S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259963	NM_001017969.3(BRD10):c.6127G>A (p.Val2043Ile)	BRD10 (V2043I)	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 2551672	NM_001017969.3(BRD10):c.6083C>T (p.Pro2028Leu)	BRD10 (P2028L)	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 2494761	NM_001017969.3(BRD10):c.6057G>T (p.Leu2019Phe)	BRD10 (L2019F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347767	NM_001017969.3(BRD10):c.6053C>G (p.Ser2018Cys)	BRD10 (S2018C)	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 3235682	NM_001017969.3(BRD10):c.5975T>C (p.Val1992Ala)	BRD10 (V1992A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312383	NM_001017969.3(BRD10):c.5968G>A (p.Ala1990Thr)	BRD10 (A1990T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366794	NM_001017969.3(BRD10):c.5950C>G (p.Gln1984Glu)	BRD10 (Q1984E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269797	NM_001017969.3(BRD10):c.5929C>T (p.Pro1977Ser)	BRD10 (P1977S)	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 2383835	NM_001017969.3(BRD10):c.5885G>A (p.Ser1962Asn)	BRD10 (S1962N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516119	NM_001017969.3(BRD10):c.5863C>G (p.Pro1955Ala)	BRD10 (P1955A)	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 2281397	NM_001017969.3(BRD10):c.5711T>C (p.Leu1904Pro)	BRD10 (L1904P)	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 2306792	NM_001017969.3(BRD10):c.5634C>G (p.Ile1878Met)	BRD10 (I1878M)	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 3261672	NM_001017969.3(BRD10):c.5608C>T (p.Pro1870Ser)	BRD10 (P1870S)	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 2391840	NM_001017969.3(BRD10):c.5584C>G (p.Leu1862Val)	BRD10 (L1862V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
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 3261695	NM_001017969.3(BRD10):c.5545A>G (p.Thr1849Ala)	BRD10 (T1849A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
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 3235674	NM_001017969.3(BRD10):c.5351C>T (p.Thr1784Ile)	BRD10 (T1784I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243866	NM_001017969.3(BRD10):c.5280C>A (p.Asn1760Lys)	BRD10 (N1760K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282303	NM_001017969.3(BRD10):c.5267C>T (p.Pro1756Leu)	BRD10 (P1756L)	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 3235673	NM_001017969.3(BRD10):c.5168T>C (p.Leu1723Pro)	BRD10 (L1723P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318288	NM_001017969.3(BRD10):c.5090A>G (p.Asn1697Ser)	BRD10 (N1697S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349365	NM_001017969.3(BRD10):c.5089A>G (p.Asn1697Asp)	BRD10 (N1697D)	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 2456429	NM_001017969.3(BRD10):c.5036C>T (p.Pro1679Leu)	BRD10 (P1679L)	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 2351992	NM_001017969.3(BRD10):c.5027C>T (p.Ala1676Val)	BRD10 (A1676V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219007	NM_001017969.3(BRD10):c.5012C>T (p.Ser1671Phe)	BRD10 (S1671F)	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 2331521	NM_001017969.3(BRD10):c.4969G>A (p.Gly1657Arg)	BRD10 (G1657R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213699	NM_001017969.3(BRD10):c.4948G>A (p.Val1650Ile)	BRD10 (V1650I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352574	NM_001017969.3(BRD10):c.4922A>C (p.Glu1641Ala)	BRD10 (E1641A)	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 2560716	NM_001017969.3(BRD10):c.4859C>G (p.Thr1620Arg)	BRD10 (T1620R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474270	NM_001017969.3(BRD10):c.4826A>C (p.Lys1609Thr)	BRD10 (K1609T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473497	NM_001017969.3(BRD10):c.4825A>G (p.Lys1609Glu)	BRD10 (K1609E)	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 2525398	NM_001017969.3(BRD10):c.4777A>G (p.Ile1593Val)	BRD10 (I1593V)	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 3235668	NM_001017969.3(BRD10):c.4677A>G (p.Ile1559Met)	BRD10 (I1559M)	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 3235667	NM_001017969.3(BRD10):c.4636C>A (p.Pro1546Thr)	BRD10 (P1546T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326291	NM_001017969.3(BRD10):c.4492T>C (p.Ser1498Pro)	BRD10 (S1498P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511576	NM_001017969.3(BRD10):c.4490C>A (p.Thr1497Lys)	BRD10 (T1497K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243935	NM_001017969.3(BRD10):c.4475T>C (p.Met1492Thr)	BRD10 (M1492T)	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 3235665	NM_001017969.3(BRD10):c.4422G>C (p.Met1474Ile)	BRD10 (M1474I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494395	NM_001017969.3(BRD10):c.4420A>C (p.Met1474Leu)	BRD10 (M1474L)	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 3261684	NM_001017969.3(BRD10):c.4405C>G (p.Pro1469Ala)	BRD10 (P1469A)	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 2543333	NM_001017969.3(BRD10):c.4333A>G (p.Ile1445Val)	BRD10 (I1445V)	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 2296513	NM_001017969.3(BRD10):c.4051A>C (p.Thr1351Pro)	BRD10 (T1351P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216833	NM_001017969.3(BRD10):c.4028C>G (p.Ser1343Cys)	BRD10 (S1343C)	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 2268422	NM_001017969.3(BRD10):c.3983C>G (p.Thr1328Ser)	BRD10 (T1328S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370844	NM_001017969.3(BRD10):c.3925A>G (p.Ser1309Gly)	BRD10 (S1309G)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2523399	NM_001017969.3(BRD10):c.3920C>G (p.Ser1307Cys)	BRD10 (S1307C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372448	NM_001017969.3(BRD10):c.3916G>C (p.Val1306Leu)	BRD10 (V1306L)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
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 3261697	NM_001017969.3(BRD10):c.3874G>T (p.Val1292Leu)	BRD10 (V1292L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 2253310	NM_001017969.3(BRD10):c.3794C>G (p.Ala1265Gly)	BRD10 (A1265G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236112	NM_001017969.3(BRD10):c.3778G>A (p.Ala1260Thr)	BRD10 (A1260T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304496	NM_001017969.3(BRD10):c.3660C>G (p.Phe1220Leu)	BRD10 (F1220L)	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 2461343	NM_001017969.3(BRD10):c.3517A>G (p.Ile1173Val)	BRD10 (I1173V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3235657	NM_001017969.3(BRD10):c.3493C>T (p.Pro1165Ser)	BRD10 (P1165S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

<< First< Prev

Page of 2