List of variants in gene EP300 reported as benign by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_001429.4(EP300):c.2053+8G>T	rs6002267	0.96326
NM_001429.4(EP300):c.3183T>A (p.Thr1061=)	rs20552	0.59984
NM_001429.4(EP300):c.4618-18C>T	rs2076578	0.25729
NM_001429.4(EP300):c.4452+20C>T	rs6002271	0.24366
NM_001429.4(EP300):c.4026-17C>A	rs2294976	0.07014
NM_001429.4(EP300):c.6668A>C (p.Gln2223Pro)	rs1046088	0.02418
NM_001429.4(EP300):c.2131+18T>A	rs9611506	0.02398
NM_001429.4(EP300):c.1283-8T>C	rs76827562	0.01914
NM_001429.4(EP300):c.942C>T (p.Gly314=)	rs20553	0.01913
NM_001429.4(EP300):c.2499G>A (p.Ser833=)	rs35560602	0.01700
NM_001429.4(EP300):c.631G>A (p.Gly211Ser)	rs142030651	0.00646
NM_001429.4(EP300):c.2773C>A (p.Pro925Thr)	rs148884710	0.00410
NM_001429.4(EP300):c.2091T>G (p.Ser697Arg)	rs61756764	0.00379
NM_001429.4(EP300):c.2064A>G (p.Leu688=)	rs61756763	0.00282
NM_001429.4(EP300):c.5814G>A (p.Thr1938=)	rs112948044	0.00258
NM_001429.4(EP300):c.6636G>A (p.Gln2212=)	rs142673005	0.00225
NM_001429.4(EP300):c.5259C>T (p.Cys1753=)	rs148040990	0.00172
NM_001429.4(EP300):c.2576T>C (p.Ile859Thr)	rs145714752	0.00072
NM_001429.4(EP300):c.4026-7T>C	rs187388966	0.00012
NM_001429.4(EP300):c.6729C>T (p.Gly2243=)	rs765194008	0.00008
NM_001429.4(EP300):c.*10GTA[1]	rs35508493
NM_001429.4(EP300):c.3143-4del	rs757931697
NM_001429.4(EP300):c.3143-4dup	rs757931697
NM_001429.4(EP300):c.3354C>T (p.Val1118=)	rs11704815
NM_001429.4(EP300):c.730-18_730-9del	rs61120041

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