ClinVar Miner

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

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_016341.4(PLCE1):c.2157C>T (p.Gly719=) rs200164874 0.00208
NM_016341.4(PLCE1):c.2999G>A (p.Ser1000Asn) rs61751498 0.00200
NM_016341.4(PLCE1):c.1567A>G (p.Ile523Val) rs61751494 0.00188
NM_016341.4(PLCE1):c.2076A>T (p.Thr692=) rs147203844 0.00155
NM_016341.4(PLCE1):c.3595G>A (p.Gly1199Ser) rs199781223 0.00127
NM_016341.4(PLCE1):c.5782G>A (p.Val1928Ile) rs202171627 0.00101
NM_016341.4(PLCE1):c.3133G>T (p.Ala1045Ser) rs200419008 0.00013
NM_016341.4(PLCE1):c.5778C>T (p.Phe1926=) rs78828338 0.00012
NM_016341.4(PLCE1):c.1313T>C (p.Val438Ala) rs199689540 0.00010
NM_016341.4(PLCE1):c.5979T>C (p.Ser1993=) rs200943442 0.00009
NM_016341.4(PLCE1):c.5670G>A (p.Pro1890=) rs370864800 0.00002
NM_016341.4(PLCE1):c.599C>T (p.Thr200Ile) rs777436865 0.00002
NM_016341.4(PLCE1):c.621C>T (p.Asn207=) rs780591486 0.00002
NM_016341.4(PLCE1):c.1207-42904C>T
NM_016341.4(PLCE1):c.1207-43013G>A
NM_016341.4(PLCE1):c.1260C>T (p.Leu420=)
NM_016341.4(PLCE1):c.1332A>G (p.Gln444=)
NM_016341.4(PLCE1):c.1371C>T (p.Leu457=)
NM_016341.4(PLCE1):c.1401C>T (p.Thr467=)
NM_016341.4(PLCE1):c.1512T>C (p.Ser504=)
NM_016341.4(PLCE1):c.1560G>A (p.Lys520=)
NM_016341.4(PLCE1):c.1927G>T (p.Ala643Ser) rs61886330
NM_016341.4(PLCE1):c.1956-10C>T
NM_016341.4(PLCE1):c.2154C>T (p.Asp718=)
NM_016341.4(PLCE1):c.2769G>T (p.Leu923=)
NM_016341.4(PLCE1):c.297G>A (p.Ala99=)
NM_016341.4(PLCE1):c.3281G>T (p.Gly1094Val) rs61732523
NM_016341.4(PLCE1):c.3492G>A (p.Thr1164=)
NM_016341.4(PLCE1):c.3565A>G (p.Ser1189Gly)
NM_016341.4(PLCE1):c.3677+5A>T
NM_016341.4(PLCE1):c.3795C>T (p.Ser1265=)
NM_016341.4(PLCE1):c.3996C>T (p.Phe1332=)
NM_016341.4(PLCE1):c.4053+7G>A
NM_016341.4(PLCE1):c.4332C>T (p.Asp1444=)
NM_016341.4(PLCE1):c.4390-6T>C
NM_016341.4(PLCE1):c.4795+8A>G
NM_016341.4(PLCE1):c.4902T>C (p.Ala1634=) rs886038624
NM_016341.4(PLCE1):c.5458+10C>G
NM_016341.4(PLCE1):c.651A>G (p.Val217=) rs886038625

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