ClinVar Miner

List of variants in gene PLCE1 reported as benign by PreventionGenetics, part of Exact Sciences

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_016341.4(PLCE1):c.810T>C (p.Cys270=) rs17109671 0.40626
NM_016341.4(PLCE1):c.960G>A (p.Glu320=) rs17109674 0.32407
NM_016341.4(PLCE1):c.5330C>T (p.Thr1777Ile) rs3765524 0.31528
NM_016341.4(PLCE1):c.5780A>G (p.His1927Arg) rs2274223 0.31202
NM_016341.4(PLCE1):c.5035+12C>A rs3736901 0.28787
NM_016341.4(PLCE1):c.1643G>T (p.Arg548Leu) rs17417407 0.15541
NM_016341.4(PLCE1):c.5458+7G>A rs17516758 0.13792
NM_016341.4(PLCE1):c.4263G>A (p.Ser1421=) rs41291134 0.05210
NM_016341.4(PLCE1):c.1405T>A (p.Ser469Thr) rs17508082 0.02979
NM_016341.4(PLCE1):c.3132C>T (p.His1044=) rs61732522 0.02481
NM_016341.4(PLCE1):c.5669C>T (p.Pro1890Leu) rs58539480 0.01296
NM_016341.4(PLCE1):c.4059C>T (p.Phe1353=) rs61751499 0.00977
NM_016341.4(PLCE1):c.2124G>A (p.Val708=) rs61751496 0.00975
NM_016341.4(PLCE1):c.1729G>A (p.Ala577Thr) rs141639885 0.00444
NM_016341.4(PLCE1):c.227C>T (p.Ala76Val) rs61749238 0.00315
NM_016341.4(PLCE1):c.2428A>G (p.Ile810Val) rs78217273 0.00251
NM_016341.4(PLCE1):c.513G>A (p.Val171=) rs61749239 0.00101
NM_016341.4(PLCE1):c.1207-43089G>A
NM_016341.4(PLCE1):c.4724G>C (p.Arg1575Pro) rs2274224

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