ClinVar Miner

List of variants in gene PLCE1 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (902):
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Gene type:
ClinVar version:
Total variants: 68
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HGVS dbSNP
NM_016341.4(PLCE1):c.-160G>A rs186468483
NM_016341.4(PLCE1):c.-165T>C rs183919560
NM_016341.4(PLCE1):c.-226del rs886047492
NM_016341.4(PLCE1):c.-287G>A rs17506379
NM_016341.4(PLCE1):c.-351T>G rs533595233
NM_016341.4(PLCE1):c.-433G>T rs886047491
NM_016341.4(PLCE1):c.-468A>G rs886047490
NM_016341.4(PLCE1):c.-47A>G rs11187771
NM_016341.4(PLCE1):c.-537G>A rs573255713
NM_016341.4(PLCE1):c.-54G>T rs41291122
NM_016341.4(PLCE1):c.-616_-615dup rs554480714
NM_016341.4(PLCE1):c.1090A>G (p.Ile364Val) rs372621219
NM_016341.4(PLCE1):c.1290G>A (p.Glu430=) rs867246620
NM_016341.4(PLCE1):c.1313T>C (p.Val438Ala) rs199689540
NM_016341.4(PLCE1):c.1383A>G (p.Ser461=) rs756176410
NM_016341.4(PLCE1):c.1389G>A (p.Ser463=) rs750894632
NM_016341.4(PLCE1):c.1421C>T (p.Thr474Ile) rs886047499
NM_016341.4(PLCE1):c.1461T>C (p.Phe487=) rs374646299
NM_016341.4(PLCE1):c.1495C>T (p.Arg499Cys) rs61751493
NM_016341.4(PLCE1):c.1567A>G (p.Ile523Val) rs61751494
NM_016341.4(PLCE1):c.1698T>A (p.Pro566=) rs377307234
NM_016341.4(PLCE1):c.1729G>A (p.Ala577Thr) rs141639885
NM_016341.4(PLCE1):c.2214+7C>T rs201418194
NM_016341.4(PLCE1):c.227C>A (p.Ala76Glu) rs61749238
NM_016341.4(PLCE1):c.2323C>T (p.Arg775Trp) rs761776701
NM_016341.4(PLCE1):c.2428A>G (p.Ile810Val) rs78217273
NM_016341.4(PLCE1):c.2598G>C (p.Thr866=) rs368426208
NM_016341.4(PLCE1):c.2635C>T (p.Arg879Cys) rs372756642
NM_016341.4(PLCE1):c.2728G>A (p.Val910Ile) rs61751497
NM_016341.4(PLCE1):c.2770G>A (p.Gly924Ser) rs758463243
NM_016341.4(PLCE1):c.296C>T (p.Ala99Val) rs761055810
NM_016341.4(PLCE1):c.3133G>T (p.Ala1045Ser) rs200419008
NM_016341.4(PLCE1):c.3183C>T (p.Pro1061=) rs367640320
NM_016341.4(PLCE1):c.323A>G (p.Asn108Ser) rs886047493
NM_016341.4(PLCE1):c.3279+12T>C rs139184808
NM_016341.4(PLCE1):c.3279+4G>T rs886047500
NM_016341.4(PLCE1):c.3281G>C (p.Gly1094Ala) rs61732523
NM_016341.4(PLCE1):c.3579C>T (p.His1193=) rs368956195
NM_016341.4(PLCE1):c.3876G>A (p.Ser1292=) rs886047501
NM_016341.4(PLCE1):c.3990C>T (p.Asn1330=) rs368399893
NM_016341.4(PLCE1):c.4165G>A (p.Glu1389Lys) rs886047502
NM_016341.4(PLCE1):c.4341G>A (p.Met1447Ile) rs766196444
NM_016341.4(PLCE1):c.4341G>C (p.Met1447Ile) rs766196444
NM_016341.4(PLCE1):c.4412G>A (p.Arg1471His) rs199793703
NM_016341.4(PLCE1):c.441G>A (p.Lys147=) rs758420946
NM_016341.4(PLCE1):c.4447A>G (p.Ile1483Val) rs886047503
NM_016341.4(PLCE1):c.459A>G (p.Gln153=) rs886047494
NM_016341.4(PLCE1):c.4733A>T (p.Asn1578Ile) rs61732525
NM_016341.4(PLCE1):c.4810G>T (p.Asp1604Tyr) rs765634224
NM_016341.4(PLCE1):c.4924G>A (p.Asp1642Asn) rs886047504
NM_016341.4(PLCE1):c.4935G>A (p.Leu1645=) rs369632735
NM_016341.4(PLCE1):c.5099T>C (p.Ile1700Thr) rs886047505
NM_016341.4(PLCE1):c.5139A>T (p.Thr1713=) rs747614650
NM_016341.4(PLCE1):c.513G>A (p.Val171=) rs61749239
NM_016341.4(PLCE1):c.5168-6G>T rs148239915
NM_016341.4(PLCE1):c.5175T>C (p.Cys1725=) rs752359550
NM_016341.4(PLCE1):c.5313G>T (p.Arg1771Ser) rs781690094
NM_016341.4(PLCE1):c.5549G>A (p.Cys1850Tyr) rs776276690
NM_016341.4(PLCE1):c.576A>C (p.Glu192Asp) rs886047495
NM_016341.4(PLCE1):c.5782G>A (p.Val1928Ile) rs202171627
NM_016341.4(PLCE1):c.5840C>T (p.Ala1947Val) rs763348713
NM_016341.4(PLCE1):c.633C>T (p.Asp211=) rs201117145
NM_016341.4(PLCE1):c.642A>T (p.Gly214=) rs149064632
NM_016341.4(PLCE1):c.664G>C (p.Gly222Arg) rs373215088
NM_016341.4(PLCE1):c.699T>C (p.Tyr233=) rs886047496
NM_016341.4(PLCE1):c.724A>C (p.Lys242Gln) rs886047497
NM_016341.4(PLCE1):c.72G>A (p.Ser24=) rs558409444
NM_016341.4(PLCE1):c.950G>A (p.Ser317Asn) rs886047498

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