List of variants in gene EP300 reported as likely benign for not specified

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: 26

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HGVS	dbSNP	gnomAD frequency
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.6636G>A (p.Gln2212=)	rs142673005	0.00225
NM_001429.4(EP300):c.1878+9C>G	rs186198699	0.00138
NM_001429.4(EP300):c.5061+10G>A	rs78432056	0.00135
NM_001429.4(EP300):c.5147G>C (p.Ser1716Thr)	rs147676363	0.00112
NM_001429.4(EP300):c.6390G>A (p.Met2130Ile)	rs147973806	0.00101
NM_001429.4(EP300):c.6969C>G (p.Pro2323=)	rs111489369	0.00100
NM_001429.4(EP300):c.6417C>T (p.Gly2139=)	rs111315183	0.00045
NM_001429.4(EP300):c.6481A>G (p.Met2161Val)	rs188035979	0.00029
NM_001429.4(EP300):c.324C>T (p.Ala108=)	rs138876937	0.00020
NM_001429.4(EP300):c.2240C>T (p.Pro747Leu)	rs193026103	0.00019
NM_001429.4(EP300):c.2242-8T>C	rs199931034	0.00018
NM_001429.4(EP300):c.7161T>C (p.Gly2387=)	rs143148170	0.00016
NM_001429.4(EP300):c.1782G>C (p.Thr594=)	rs17002307	0.00013
NM_001429.4(EP300):c.6729C>T (p.Gly2243=)	rs765194008	0.00008
NM_001429.4(EP300):c.4482A>G (p.Arg1494=)	rs149471059	0.00006
NM_001429.4(EP300):c.2359G>A (p.Gly787Ser)	rs564786569	0.00004
NM_001429.4(EP300):c.2756G>A (p.Ser919Asn)	rs141403873	0.00004
NM_001429.4(EP300):c.5914A>G (p.Met1972Val)	rs373725137	0.00002
NM_001429.4(EP300):c.5440C>A (p.Arg1814=)	rs757325753	0.00001
NM_001429.4(EP300):c.5601G>A (p.Gln1867=)	rs1250353355	0.00001
NM_001429.4(EP300):c.6660A>G (p.Pro2220=)	rs886038484	0.00001
NM_001429.4(EP300):c.6798_6800del (p.Gln2268del)	rs533875300
NM_001429.4(EP300):c.7245G>A (p.Ter2415=)	rs587783622
NM_001429.4(EP300):c.730-5C>T

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