BRD10[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 146018	GRCh38/hg38 9p24.3-q21.11(chr9:13997-68401065)x3	LOC130001767, LOC130001768 +1006 more	Copy number gain	See cases	GPathogenic
Select item 60415	GRCh38/hg38 9p24.3-22.3(chr9:111216-14650762)x1	AK3, BRD10 +270 more	Copy number loss	See cases	GPathogenic
Select item 152906	GRCh38/hg38 9p24.3-24.1(chr9:185579-7635806)x1	LOC130001516, LOC130001517 +217 more	Copy number loss	See cases	GPathogenic
Select item 160862	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC124210612, LOC124210613 +3786 more	Copy number gain	See cases	GPathogenic
Select item 154945	GRCh38/hg38 9p24.3-q21.31(chr9:193412-79877816)x3	CDKN2B, CDKN2B-AS1 +1214 more	Copy number gain	See cases	GPathogenic
Select item 150340	GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3	LOC121331326, LOC121331327 +3785 more	Copy number gain	See cases	GPathogenic
Select item 150050	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3	LOC126860737, LOC126860738 +3786 more	Copy number gain	See cases	GPathogenic
Select item 149828	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 146931	GRCh38/hg38 9p24.3-q21.12(chr9:193412-70630731)x3	LOC130001680, LOC130001681 +1062 more	Copy number gain	See cases	GPathogenic
Select item 146703	GRCh38/hg38 9p24.3-q21.13(chr9:193412-74615913)x3	LOC124210611, LOC124210612 +1120 more	Copy number gain	See cases	GPathogenic
Select item 59875	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3	LOC110121197, LOC110121234 +3786 more	Copy number gain	See cases	GPathogenic
Select item 33205	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC121331342, LOC121331343 +3786 more	Copy number gain	See cases	GPathogenic
Select item 60416	GRCh38/hg38 9p24.3-23(chr9:195399-11081440)x1	AK3, BRD10 +233 more	Copy number loss	See cases	GPathogenic
Select item 155344	GRCh38/hg38 9p24.3-13.1(chr9:203861-38381642)	LOC130001484, LOC130001485 +883 more	Copy number gain	See cases	GPathogenic
Select item 153821	GRCh38/hg38 9p24.3-24.1(chr9:203861-8172957)x1	AK3, BRD10 +223 more	Copy number loss	See cases	GPathogenic
Select item 153561	GRCh38/hg38 9p24.3-q22.1(chr9:203861-88130444)x4	LOC130001854, LOC130001855 +1367 more	Copy number gain	See cases	GPathogenic
Select item 153518	GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3	LOC113839542, LOC113839543 +3786 more	Copy number gain	See cases	GPathogenic
Select item 153184	GRCh38/hg38 9p24.3-21.1(chr9:203861-31423873)x4	LOC130001517, LOC130001518 +484 more	Copy number gain	See cases	GPathogenic
Select item 155409	GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 1684649	Single allele	LOC130001502, LOC130001503 +233 more	Deletion	Chromosome 9p deletion syndrome	GPathogenic
Select item 154897	GRCh38/hg38 9p24.3-22.3(chr9:204090-15260600)x1	AK3, BRD10 +271 more	Copy number loss	See cases	GPathogenic
Select item 150751	GRCh38/hg38 9p24.3-23(chr9:204090-9282864)x1	AK3, BRD10 +228 more	Copy number loss	See cases	GPathogenic
Select item 144686	GRCh38/hg38 9p24.3-23(chr9:204090-13146846)x1	LOC130001526, LOC130001527 +247 more	Copy number loss	See cases	GPathogenic
Select item 151712	GRCh38/hg38 9p24.3-24.1(chr9:204104-6322471)x1	LOC130001462, LOC130001463 +183 more	Copy number loss	See cases	GPathogenic
Select item 150819	GRCh38/hg38 9p24.3-21.2(chr9:204104-27963369)x3	ACER2, ADAMTSL1 +458 more	Copy number gain	See cases	GPathogenic
Select item 150341	GRCh38/hg38 9p24.3-q21.11(chr9:204104-67549861)x3	LOC130001585, LOC130001586 +984 more	Copy number gain	See cases	GPathogenic
Select item 150242	GRCh38/hg38 9p24.3-13.1(chr9:204104-38768294)x3	LOC130001507, LOC130001508 +899 more	Copy number gain	See cases	GPathogenic
Select item 150116	GRCh38/hg38 9p24.3-13.3(chr9:204104-34151476)x3	ACER2, ACO1 +582 more	Copy number gain	See cases	GPathogenic
Select item 149060	GRCh38/hg38 9p24.3-23(chr9:204104-10023901)x1	AK3, BRD10 +230 more	Copy number loss	See cases	GPathogenic
Select item 148823	GRCh38/hg38 9p24.3-q21.11(chr9:204104-66233120)x4	LOC130001746, LOC130001747 +980 more	Copy number gain	See cases	GPathogenic
Select item 148677	GRCh38/hg38 9p24.3-24.1(chr9:204104-7133443)x1	AK3, BRD10 +215 more	Copy number loss	See cases	GPathogenic
Select item 148598	GRCh38/hg38 9p24.3-23(chr9:204104-14182668)x1	AK3, BRD10 +256 more	Copy number loss	See cases	GPathogenic
Select item 148381	GRCh38/hg38 9p24.3-24.1(chr9:204104-8266492)x1	AK3, BRD10 +224 more	Copy number loss	See cases	GPathogenic
Select item 148307	GRCh38/hg38 9p24.3-23(chr9:204104-11610300)x3	AK3, BRD10 +233 more	Copy number gain	See cases	GPathogenic
Select item 146684	GRCh38/hg38 9p24.3-23(chr9:204104-11298187)x1	AK3, BRD10 +233 more	Copy number loss	See cases	GPathogenic
Select item 146394	GRCh38/hg38 9p24.3-22.1(chr9:204104-18882281)x1	SNORD137, SPATA6L +303 more	Copy number loss	See cases	GPathogenic
Select item 160921	GRCh38/hg38 9p24.3-13.1(chr9:204193-38815478)x3	ACER2, ACO1 +899 more	Copy number gain	See cases	GPathogenic
Select item 147839	GRCh38/hg38 9p24.3-23(chr9:204193-11435662)x1	AK3, BRD10 +233 more	Copy number loss	See cases	GPathogenic
Select item 146719	GRCh38/hg38 9p24.3-22.2(chr9:204193-16897580)x1	SMARCA2, SNAPC3 +290 more	Copy number loss	See cases	GPathogenic
Select item 146254	GRCh38/hg38 9p24.3-23(chr9:204193-10852686)x1	AK3, BRD10 +232 more	Copy number loss	See cases	GPathogenic
Select item 146231	GRCh38/hg38 9p24.3-24.1(chr9:204193-6968724)x1	LOC130001441, LOC130001442 +215 more	Copy number loss	See cases	GPathogenic
Select item 144441	GRCh38/hg38 9p24.3-23(chr9:204193-11277770)x1	AK3, BRD10 +233 more	Copy number loss	See cases	GPathogenic
Select item 144391	GRCh38/hg38 9p24.3-23(chr9:204193-10473327)x1	AK3, BRD10 +230 more	Copy number loss	See cases	GPathogenic
Select item 144343	GRCh38/hg38 9p24.3-22.2(chr9:204193-18073359)x1	LOC130001522, LOC130001523 +297 more	Copy number loss	See cases	GPathogenic
Select item 144309	GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445)	LOC130002189, LOC130002190 +3786 more	Copy number gain	See cases	GPathogenic
Select item 144246	GRCh38/hg38 9p24.3-23(chr9:204193-10164955)x1	RCL1, RFX3 +230 more	Copy number loss	See cases	GPathogenic
Select item 60431	GRCh38/hg38 9p24.3-23(chr9:204193-10340779)x1	AK3, BRD10 +230 more	Copy number loss	See cases	GPathogenic
Select item 59839	GRCh38/hg38 9p24.3-13.3(chr9:204193-33284638)x3	ACER2, ACO1 +539 more	Copy number gain	See cases	GPathogenic
Select item 59836	GRCh38/hg38 9p24.3-21.3(chr9:204193-22086858)x3	LOC130001520, LOC130001521 +410 more	Copy number gain	See cases	GPathogenic
Select item 57406	GRCh38/hg38 9p24.3-13.1(chr9:204193-38741440)x3	SPATA31F3, SPATA31G1 +898 more	Copy number gain	See cases	GPathogenic
Select item 57180	GRCh38/hg38 9p24.3-23(chr9:204193-13974100)x1	AK3, BRD10 +255 more	Copy number loss	See cases	GPathogenic
Select item 32288	GRCh38/hg38 9p24.3-13.1(chr9:204193-38815478)x3	ANKRD18B, APTX +899 more	Copy number gain	See cases	GPathogenic
Select item 152907	GRCh38/hg38 9p24.3-23(chr9:211086-11457340)x1	AK3, BRD10 +233 more	Copy number loss	See cases	GPathogenic
Select item 151916	GRCh38/hg38 9p24.3-24.1(chr9:211086-7444397)x1	AK3, BRD10 +217 more	Copy number loss	See cases	GPathogenic
Select item 60441	GRCh38/hg38 9p24.3-23(chr9:211086-11867480)x1	AK3, BRD10 +233 more	Copy number loss	See cases	GPathogenic
Select item 60440	GRCh38/hg38 9p24.3-24.1(chr9:211086-6106482)x1	AK3, BRD10 +179 more	Copy number loss	See cases	GPathogenic
Select item 59060	GRCh38/hg38 9p24.3-23(chr9:211087-13754567)x1	AK3, BRD10 +252 more	Copy number loss	See cases	GPathogenic
Select item 147703	GRCh38/hg38 9p24.3-22.3(chr9:214367-16307944)x1	LOC130001455, LOC130001456 +280 more	Copy number loss	See cases	GPathogenic
Select item 154621	GRCh38/hg38 9p24.3-24.1(chr9:220253-7733826)x1	AK3, BRD10 +213 more	Copy number loss	See cases	GPathogenic
Select item 146356	GRCh38/hg38 9p24.3-22.1(chr9:220253-18708805)x1	LOC105375972, LOC105375976 +295 more	Copy number loss	See cases	GPathogenic
Select item 146111	GRCh38/hg38 9p24.3-24.1(chr9:220253-8866675)x1	LOC121331319, LOC121740737 +222 more	Copy number loss	See cases	GPathogenic
Select item 59876	GRCh38/hg38 9p24.3-13.1(chr9:220253-38815419)x3	ACER2, ACO1 +894 more	Copy number gain	See cases	GPathogenic
Select item 59065	GRCh38/hg38 9p24.3-24.1(chr9:220253-6968724)x1	LOC124210609, LOC124210610 +210 more	Copy number loss	See cases	GPathogenic
Select item 59064	GRCh38/hg38 9p24.3-22.2(chr9:220253-18073359)x1	ADAMTSL1, AK3 +292 more	Copy number loss	See cases	GPathogenic
Select item 59062	GRCh38/hg38 9p24.3-24.1(chr9:220253-6073001)x1	LOC130001490, LOC130001491 +172 more	Copy number loss	See cases	GPathogenic
Select item 144555	GRCh38/hg38 9p24.3-21.1(chr9:220257-29424848)x3	SLC1A1, SLC24A2 +461 more	Copy number gain	See cases	GPathogenic
Select item 152943	GRCh38/hg38 9p24.3-22.3(chr9:322690-16401656)x1	AK3, BRD10 +273 more	Copy number loss	See cases	GPathogenic
Select item 149484	GRCh38/hg38 9p24.3-21.3(chr9:459131-24207894)x3	CDKN2B, CDKN2B-AS1 +412 more	Copy number gain	See cases	GPathogenic
Select item 57027	GRCh38/hg38 9p24.3-23(chr9:1592306-12387899)x3	AK3, BRD10 +204 more	Copy number gain	See cases	GPathogenic
Select item 147561	GRCh38/hg38 9p24.2-23(chr9:3591159-9361786)x3	AK3, BRD10 +153 more	Copy number gain	See cases	GPathogenic
Select item 147623	GRCh38/hg38 9p24.2-24.1(chr9:4152060-8518353)x1	AK3, BRD10 +144 more	Copy number loss	See cases	GPathogenic
Select item 147501	GRCh38/hg38 9p24.1-21.2(chr9:4661872-27661572)x3	LOC126860594, LOC126860595 +355 more	Copy number gain	See cases	GPathogenic
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

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