List of variants in gene EP300 reported as benign by PreventionGenetics, part of Exact Sciences

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: 27

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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.2380-15T>C	rs17002316	0.04125
NM_001429.4(EP300):c.95-16T>C	rs5758235	0.04095
NM_001429.4(EP300):c.1168+18G>A	rs3818120	0.04073
NM_001429.4(EP300):c.3348G>A (p.Gln1116=)	rs20554	0.04022
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.5061+9C>T	rs73176628	0.02054
NM_001429.4(EP300):c.2019T>C (p.Pro673=)	rs2230110	0.01054
NM_001429.4(EP300):c.631G>A (p.Gly211Ser)	rs142030651	0.00646
NM_001429.4(EP300):c.2064A>G (p.Leu688=)	rs61756763	0.00282
NM_001429.4(EP300):c.865A>G (p.Met289Val)	rs2230111	0.00258
NM_001429.4(EP300):c.678C>G (p.Gly226=)	rs147244947	0.00158
NM_001429.4(EP300):c.4311A>C (p.Ala1437=)	rs150941761	0.00150
NM_001429.4(EP300):c.6210G>A (p.Val2070=)	rs11912899	0.00142
NM_001429.4(EP300):c.3143-9T>C	rs199773872	0.00083
NM_001429.4(EP300):c.1519A>G (p.Ser507Gly)	rs146242251	0.00070
NM_001429.4(EP300):c.6481A>G (p.Met2161Val)	rs188035979	0.00029
NM_001429.4(EP300):c.*10GTA[1]	rs35508493
NM_001429.4(EP300):c.2242-5_2242-4dup
NM_001429.4(EP300):c.2534C>G (p.Thr845Ser)
NM_001429.4(EP300):c.4798C>G (p.Leu1600Val)	rs140154690
NM_001429.4(EP300):c.730-18_730-9del	rs61120041

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