8379[Gene ID] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155519	GRCh38/hg38 7p22.3-15.2(chr7:43360-27196404)x3	LOC129998085, LOC129998086 +904 more	Copy number gain	See cases	GPathogenic
Select item 155108	GRCh38/hg38 7p22.3-22.2(chr7:45130-3406236)x3	ADAP1, AMZ1 +246 more	Copy number gain	See cases	GUncertain significance
Select item 148758	GRCh38/hg38 7p22.3-15.3(chr7:45130-25221165)x3	RAC1, RADIL +823 more	Copy number gain	See cases	GPathogenic
Select item 148450	GRCh38/hg38 7p22.3-21.3(chr7:45130-7252065)x3	ACTB, ADAP1 +439 more	Copy number gain	See cases	GPathogenic
Select item 59675	GRCh38/hg38 7p22.3-22.1(chr7:45130-6270185)x3	BRAT1, ACTB +381 more	Copy number gain	See cases	GPathogenic
Select item 58492	GRCh38/hg38 7p22.3-22.1(chr7:45130-5880375)x1	ACTB, ADAP1 +357 more	Copy number loss	See cases	GPathogenic
Select item 154928	GRCh38/hg38 7p22.3-22.2(chr7:54165-3258775)x1	LOC126859917, LOC126859918 +245 more	Copy number loss	See cases	GPathogenic
Select item 160967	GRCh38/hg38 7p22.3(chr7:54185-1843584)x1	ADAP1, C7orf50 +140 more	Copy number loss	See cases	GPathogenic
Select item 147625	GRCh38/hg38 7p22.3-22.2(chr7:54185-3324143)x1	ADAP1, AMZ1 +246 more	Copy number loss	See cases	GPathogenic
Select item 147563	GRCh38/hg38 7p22.3-22.1(chr7:54185-6638027)x3	ACTB, ADAP1 +418 more	Copy number gain	See cases	GPathogenic
Select item 147357	GRCh38/hg38 7p22.3-15.2(chr7:54185-26827634)x3	HYCC1, ICA1 +879 more	Copy number gain	See cases	GPathogenic
Select item 146075	GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1	CUL1, CUX1 +4737 more	Copy number loss	See cases	GPathogenic
Select item 59678	GRCh38/hg38 7p22.3-14.2(chr7:54185-37089712)x3	LOC129998210, LOC129998211 +1148 more	Copy number gain	See cases	GPathogenic
Select item 57453	GRCh38/hg38 7p22.3-14.1(chr7:54185-41875885)x3	ABCB5, ACTB +1298 more	Copy number gain	See cases	GPathogenic
Select item 32434	GRCh38/hg38 7p22.3(chr7:54185-1843584)x1	ADAP1, C7orf50 +140 more	Copy number loss	See cases	GPathogenic
Select item 149269	GRCh38/hg38 7p22.3(chr7:689554-2031521)x3	ADAP1, C7orf50 +117 more	Copy number gain	See cases	GUncertain significance
Select item 147514	GRCh38/hg38 7p22.3(chr7:791215-1993065)x3	ADAP1, C7orf50 +105 more	Copy number gain	See cases	GUncertain significance
Select item 148752	GRCh38/hg38 7p22.3(chr7:1085248-2530644)x4	C7orf50, CHST12 +116 more	Copy number gain	See cases	GUncertain significance
Select item 147494	GRCh38/hg38 7p22.3(chr7:1330987-2530644)x1	CHST12, EIF3B +99 more	Copy number loss	See cases	GUncertain significance
Select item 154993	GRCh38/hg38 7p22.3-15.2(chr7:1698124-27207295)x3	ABCB5, ACTB +769 more	Copy number gain	See cases	GPathogenic
Select item 3121957	NM_001013836.2(MAD1L1):c.2153C>T (p.Ala718Val)	MAD1L1 (A174V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467196	NM_001013836.2(MAD1L1):c.2149G>A (p.Val717Met)	MAD1L1 (V173M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347017	NM_001013836.2(MAD1L1):c.2128G>A (p.Glu710Lys)	MAD1L1 (E166K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121956	NM_001013836.2(MAD1L1):c.2083C>T (p.Arg695Trp)	MAD1L1 (R151W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2657221	NM_001013836.2(MAD1L1):c.2031A>G (p.Leu677=)	MAD1L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 789755	NM_001013836.2(MAD1L1):c.1999-10T>C	MAD1L1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2232076	NM_001013836.2(MAD1L1):c.1997A>G (p.Lys666Arg)	MAD1L1 (K122R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248760	NM_001013836.2(MAD1L1):c.1995C>G (p.Phe665Leu)	MAD1L1 (F573L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 785208	NM_001013836.2(MAD1L1):c.1959G>A (p.Ser653=)	MAD1L1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2282674	NM_001013836.2(MAD1L1):c.1958C>G (p.Ser653Trp)	MAD1L1 (S109W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286884	NM_001013836.2(MAD1L1):c.1949G>T (p.Arg650Leu)	MAD1L1 (R650L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3238790	NM_001013836.2(MAD1L1):c.1948C>T (p.Arg650Trp)	MAD1L1 (R106W +2 more)	Single nucleotide variant (missense variant)	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition	GUncertain significance
Select item 6919	NM_001013836.2(MAD1L1):c.1947C>G (p.Tyr649Ter)	MAD1L1 (Y649* +2 more)	Single nucleotide variant (nonsense)	LYMPHOMA, DIFFUSE LARGE B-CELL, SOMATIC	GPathogenic
Select item 2443778	NM_001013836.2(MAD1L1):c.1882G>T (p.Glu628Ter)	MAD1L1 (E536* +1 more)	Single nucleotide variant (nonsense)	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition	GPathogenic
Select item 2539220	NM_001013836.2(MAD1L1):c.1880A>G (p.Gln627Arg)	MAD1L1 (Q535R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216089	NM_001013836.2(MAD1L1):c.1834G>A (p.Glu612Lys)	MAD1L1 (E68K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 144931	GRCh38/hg38 7p22.3(chr7:1918597-1993006)x1	LOC126859924, LOC126859925 +5 more	Copy number loss	See cases	GBenign
Select item 2318426	NM_001013836.2(MAD1L1):c.1790C>T (p.Ser597Leu)	MAD1L1 (S505L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467572	NM_001013836.2(MAD1L1):c.1750G>C (p.Val584Leu)	MAD1L1 (V584L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121954	NM_001013836.2(MAD1L1):c.1729G>A (p.Ala577Thr)	MAD1L1 (A33T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473078	NM_001013836.2(MAD1L1):c.1667G>T (p.Arg556Leu)	MAD1L1 (R556L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314086	NM_001013836.2(MAD1L1):c.1646C>A (p.Pro549His)	MAD1L1 (P457H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248165	NM_001013836.2(MAD1L1):c.1586G>A (p.Arg529Gln)	MAD1L1 (R529Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121952	NM_001013836.2(MAD1L1):c.1540C>T (p.Arg514Trp)	MAD1L1 (R422W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 147638	GRCh38/hg38 7p22.3(chr7:1967724-2035327)x1	LOC126859925, LOC129997789 +2 more	Copy number loss	See cases	GBenign
Select item 3121951	NM_001013836.2(MAD1L1):c.1475T>C (p.Leu492Pro)	LOC126859925, MAD1L1 (L400P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 771869	NM_001013836.2(MAD1L1):c.1461C>T (p.Ala487=)	LOC126859925, MAD1L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3121950	NM_001013836.2(MAD1L1):c.1429C>G (p.Leu477Val)	LOC126859925, MAD1L1 (L385V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2576571	NM_001013836.2(MAD1L1):c.1396C>T (p.Gln466Ter)	MAD1L1 (Q374* +1 more)	Single nucleotide variant (nonsense)	Mosaic variegated aneuploidy syndrome 1	GPathogenic
Select item 2657222	NM_001013836.2(MAD1L1):c.1377C>T (p.Ala459=)	MAD1L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2291182	NM_001013836.2(MAD1L1):c.1310A>T (p.Glu437Val)	MAD1L1 (E345V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121949	NM_001013836.2(MAD1L1):c.1303A>G (p.Met435Val)	MAD1L1 (M343V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1013533	NM_001013836.2(MAD1L1):c.1266G>A (p.Leu422=)	MAD1L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 758233	NM_001013836.2(MAD1L1):c.1263G>A (p.Glu421=)	MAD1L1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2492886	NM_001013836.2(MAD1L1):c.1240A>G (p.Ile414Val)	MAD1L1 (I414V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292522	NM_001013836.2(MAD1L1):c.1222C>T (p.Arg408Trp)	MAD1L1 (R408W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 155196	GRCh38/hg38 7p22.3(chr7:2031462-2653470)x3	BRAT1, CHST12 +63 more	Copy number gain	See cases	GLikely benign
Select item 3121948	NM_001013836.2(MAD1L1):c.1183C>T (p.Arg395Trp)	MAD1L1 (R303W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121947	NM_001013836.2(MAD1L1):c.1111G>C (p.Glu371Gln)	MAD1L1 (E279Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121946	NM_001013836.2(MAD1L1):c.1074C>T (p.Ser358=)	MAD1L1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 57287	GRCh38/hg38 7p22.3(chr7:2109441-2412551)x1	CHST12, EIF3B +37 more	Copy number loss	See cases	GUncertain significance
Select item 2486238	NM_001013836.2(MAD1L1):c.1066A>G (p.Thr356Ala)	MAD1L1 (T356A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292523	NM_001013836.2(MAD1L1):c.974G>C (p.Gly325Ala)	MAD1L1 (G233A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 787047	NM_001013836.2(MAD1L1):c.958C>T (p.Leu320=)	MAD1L1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2340304	NM_001013836.2(MAD1L1):c.874C>T (p.Arg292Cys)	MAD1L1 (R200C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2576570	NM_001013836.2(MAD1L1):c.820_823del (p.Glu274fs)	MAD1L1 (E182fs +1 more)	Microsatellite (frameshift variant)	Mosaic variegated aneuploidy syndrome 1	GPathogenic
Select item 3121964	NM_001013836.2(MAD1L1):c.812A>C (p.Glu271Ala)	MAD1L1 (E271A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 722376	NM_001013836.2(MAD1L1):c.810-10G>A	MAD1L1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2526393	NM_001013836.2(MAD1L1):c.799G>A (p.Ala267Thr)	MAD1L1 (A175T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2599619	NM_001013836.2(MAD1L1):c.752G>A (p.Arg251Gln)	MAD1L1 (R159Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292521	NM_001013836.2(MAD1L1):c.719C>G (p.Ala240Gly)	MAD1L1 (A148G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3024872	NM_001013836.2(MAD1L1):c.708G>C (p.Glu236Asp)	MAD1L1 (E144D +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3292524	NM_001013836.2(MAD1L1):c.682C>G (p.Leu228Val)	MAD1L1 (L136V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288319	NM_001013836.2(MAD1L1):c.547C>A (p.Leu183Met)	MAD1L1 (L183M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289859	NM_001013836.2(MAD1L1):c.544C>T (p.Arg182Cys)	MAD1L1 (R90C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121963	NM_001013836.2(MAD1L1):c.403C>G (p.Gln135Glu)	MAD1L1 (Q135E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121962	NM_001013836.2(MAD1L1):c.388C>T (p.Arg130Cys)	MAD1L1 (R130C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121961	NM_001013836.2(MAD1L1):c.374A>G (p.Gln125Arg)	MAD1L1 (Q125R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2657223	NM_001013836.2(MAD1L1):c.323C>T (p.Thr108Met)	MAD1L1 (T108M)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2389096	NM_001013836.2(MAD1L1):c.323C>A (p.Thr108Lys)	MAD1L1 (T108K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524344	NM_001013836.2(MAD1L1):c.286T>C (p.Tyr96His)	MAD1L1 (Y96H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2265492	NM_001013836.2(MAD1L1):c.277G>A (p.Ala93Thr)	MAD1L1 (A93T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121959	NM_001013836.2(MAD1L1):c.241G>A (p.Ala81Thr)	MAD1L1 (A81T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121958	NM_001013836.2(MAD1L1):c.225G>T (p.Glu75Asp)	MAD1L1 (E75D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121955	NM_001013836.2(MAD1L1):c.206G>A (p.Arg69Gln)	MAD1L1 (R69Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2443777	NM_001013836.2(MAD1L1):c.196C>T (p.Gln66Ter)	MAD1L1	Single nucleotide variant (nonsense +1 more)	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition	GPathogenic
Select item 6920	NM_001013836.2(MAD1L1):c.175C>T (p.Arg59Cys)	MAD1L1 (R59C)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GBenign
Select item 2265956	NM_001013836.2(MAD1L1):c.109G>T (p.Ala37Ser)	MAD1L1 (A37S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2266246	NM_001013836.2(MAD1L1):c.40C>G (p.Leu14Val)	MAD1L1 (L14V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3062980	GRCh37/hg19 7p22.3-22.2(chr7:2163435-2987198)x3	AMZ1, BRAT1 +11 more	Copy number gain	not specified	GUncertain significance
Select item 3062963	GRCh37/hg19 7p22.3-22.2(chr7:2088540-3127784)x3	AMZ1, BRAT1 +11 more	Copy number gain	not specified	GUncertain significance
Select item 3062959	GRCh37/hg19 7p22.3(chr7:43360-2020306)x1	ADAP1, C7orf50 +19 more	Copy number loss	not specified	GPathogenic
Select item 2685228	GRCh37/hg19 7p22.3(chr7:1775509-1905919)x1	ELFN1, MAD1L1	Copy number loss	not provided	GUncertain significance
Select item 2684473	GRCh37/hg19 7p22.3(chr7:2163436-2610093)x3	BRAT1, CHST12 +7 more	Copy number gain	not provided	GUncertain significance
Select item 2684470	GRCh37/hg19 7p22.3-22.1(chr7:43361-5965440)x3	RNF216, SDK1 +48 more	Copy number gain	not provided	GPathogenic
Select item 2684469	GRCh37/hg19 7p22.3-21.3(chr7:43361-8890475)x3	PSMG3, RAC1 +73 more	Copy number gain	not provided	GPathogenic
Select item 1808366	GRCh37/hg19 7p22.3(chr7:2262524-2433729)x3	EIF3B, MAD1L1 +3 more	Copy number gain	not provided	GUncertain significance
Select item 1711132	GRCh37/hg19 7p22.3-21.3(chr7:43360-9649794)x3	MAD1L1, MAFK +73 more	Copy number gain	See cases	GPathogenic
Select item 1708459	GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1	AASS, ABCA13 +896 more	Copy number loss	See cases	GUncertain significance
Select item 1708194	GRCh37/hg19 7p22.3-21.1(chr7:43360-19485604)x3	ACTB, ADAP1 +98 more	Copy number gain	See cases	GPathogenic

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