ClinVar Miner

List of variants in gene EP300 reported as uncertain significance for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001429.4(EP300):c.1094A>G (p.Asn365Ser) rs747431211 0.00002
NM_001429.4(EP300):c.6526C>T (p.Pro2176Ser) rs779543207 0.00001
NM_001429.4(EP300):c.2596C>A (p.Pro866Thr)
NM_001429.4(EP300):c.3143-1G>T rs1230152737
NM_001429.4(EP300):c.3261+3A>G
NM_001429.4(EP300):c.3569C>T (p.Thr1190Ile)
NM_001429.4(EP300):c.3772T>C (p.Cys1258Arg) rs2145756430
NM_001429.4(EP300):c.3807-4T>G rs1337278789
NM_001429.4(EP300):c.3807-7C>T
NM_001429.4(EP300):c.458T>C (p.Met153Thr)
NM_001429.4(EP300):c.4934_4939del (p.Arg1645_Ala1647delinsPro)
NM_001429.4(EP300):c.5510G>A (p.Arg1837Gln) rs755471385
NM_001429.4(EP300):c.6177_6185dup (p.Arg2059_Pro2061dup) rs2145519648
NM_001429.4(EP300):c.6722A>G (p.Gln2241Arg)
NM_001429.4(EP300):c.6820C>G (p.Gln2274Glu)
NM_001429.4(EP300):c.6954_6965del (p.Gln2319_Pro2322del) rs2145523070
NM_001429.4(EP300):c.7041_7046del (p.His2348_Pro2349del) rs2145523559

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.