ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 117
Download table as spreadsheet
HGVS dbSNP
NM_006031.6(PCNT):c.1220A>T (p.Asn407Ile) rs745322520
NM_006031.6(PCNT):c.1224G>A (p.Leu408=) rs797045874
NM_006031.6(PCNT):c.1246A>G (p.Ile416Val) rs368199588
NM_006031.6(PCNT):c.139G>C (p.Asp47His) rs112837071
NM_006031.6(PCNT):c.1457-5T>A rs769237607
NM_006031.6(PCNT):c.1457-9dup rs1486232846
NM_006031.6(PCNT):c.1463A>G (p.His488Arg) rs201966670
NM_006031.6(PCNT):c.1489C>A (p.Arg497Ser) rs371251124
NM_006031.6(PCNT):c.16G>C (p.Glu6Gln) rs761540486
NM_006031.6(PCNT):c.1743C>T (p.Leu581=) rs375581809
NM_006031.6(PCNT):c.175G>A (p.Glu59Lys) rs797045876
NM_006031.6(PCNT):c.1849G>C (p.Glu617Gln) rs747165033
NM_006031.6(PCNT):c.2154+7C>T rs376236418
NM_006031.6(PCNT):c.2154+8G>A rs778407564
NM_006031.6(PCNT):c.2247A>C (p.Glu749Asp) rs202246527
NM_006031.6(PCNT):c.2545G>A (p.Gly849Arg) rs776223654
NM_006031.6(PCNT):c.2575G>A (p.Asp859Asn) rs115369710
NM_006031.6(PCNT):c.2628A>G (p.Lys876=) rs758820636
NM_006031.6(PCNT):c.2809A>C (p.Lys937Gln) rs577883327
NM_006031.6(PCNT):c.2833C>T (p.Arg945Cys) rs147358856
NM_006031.6(PCNT):c.2834G>A (p.Arg945His) rs183691508
NM_006031.6(PCNT):c.2866G>A (p.Asp956Asn) rs146728385
NM_006031.6(PCNT):c.2899A>G (p.Ser967Gly) rs145451194
NM_006031.6(PCNT):c.3038C>T (p.Thr1013Ile) rs777758638
NM_006031.6(PCNT):c.3061C>T (p.Arg1021Trp) rs138361417
NM_006031.6(PCNT):c.321G>T (p.Lys107Asn) rs138834119
NM_006031.6(PCNT):c.3389G>A (p.Arg1130Gln) rs140003788
NM_006031.6(PCNT):c.3443T>C (p.Val1148Ala) rs762148129
NM_006031.6(PCNT):c.3469G>C (p.Ala1157Pro) rs778900170
NM_006031.6(PCNT):c.3550G>A (p.Gly1184Arg) rs752738005
NM_006031.6(PCNT):c.3564G>T (p.Gly1188=) rs1555973364
NM_006031.6(PCNT):c.3571C>T (p.Leu1191=) rs370240856
NM_006031.6(PCNT):c.3710A>G (p.His1237Arg) rs761299168
NM_006031.6(PCNT):c.4001A>C (p.Gln1334Pro) rs1318648644
NM_006031.6(PCNT):c.4078C>T (p.Arg1360Cys) rs202221024
NM_006031.6(PCNT):c.4163G>A (p.Arg1388His) rs775895650
NM_006031.6(PCNT):c.4216+9C>T rs369876466
NM_006031.6(PCNT):c.4311G>T (p.Lys1437Asn) rs765190339
NM_006031.6(PCNT):c.4351C>T (p.Arg1451Cys) rs200606073
NM_006031.6(PCNT):c.442G>T (p.Val148Phe) rs201815546
NM_006031.6(PCNT):c.442_519del (p.Val148_Thr173del) rs1555945478
NM_006031.6(PCNT):c.4518C>G (p.Leu1506=) rs954455553
NM_006031.6(PCNT):c.4552C>T (p.Arg1518Cys) rs763712724
NM_006031.6(PCNT):c.4563+9G>A rs750949882
NM_006031.6(PCNT):c.4625A>C (p.Glu1542Ala) rs797045877
NM_006031.6(PCNT):c.4687G>C (p.Glu1563Gln) rs746297554
NM_006031.6(PCNT):c.469G>A (p.Gly157Arg) rs1555945637
NM_006031.6(PCNT):c.4835T>C (p.Leu1612Pro) rs1296500904
NM_006031.6(PCNT):c.4838C>T (p.Ala1613Val) rs546562229
NM_006031.6(PCNT):c.484A>G (p.Ser162Gly) rs755909353
NM_006031.6(PCNT):c.4929G>C (p.Val1643=) rs569351854
NM_006031.6(PCNT):c.5074G>A (p.Val1692Ile) rs113342730
NM_006031.6(PCNT):c.5115G>A (p.Lys1705=) rs141860893
NM_006031.6(PCNT):c.5543A>G (p.Glu1848Gly) rs201943167
NM_006031.6(PCNT):c.5606C>T (p.Thr1869Met) rs775982969
NM_006031.6(PCNT):c.5705G>A (p.Arg1902His) rs201536644
NM_006031.6(PCNT):c.5756T>C (p.Leu1919Pro) rs755667206
NM_006031.6(PCNT):c.5792G>T (p.Arg1931Leu) rs776640595
NM_006031.6(PCNT):c.5855C>T (p.Ala1952Val) rs370664761
NM_006031.6(PCNT):c.591C>G (p.Ile197Met) rs559031201
NM_006031.6(PCNT):c.5940C>T (p.Gly1980=) rs150436577
NM_006031.6(PCNT):c.5954C>T (p.Ser1985Phe) rs140398533
NM_006031.6(PCNT):c.6080A>G (p.Gln2027Arg) rs147189224
NM_006031.6(PCNT):c.6141C>T (p.Asp2047=) rs144445891
NM_006031.6(PCNT):c.6150+3G>A rs760779996
NM_006031.6(PCNT):c.6195T>G (p.Asp2065Glu) rs148389745
NM_006031.6(PCNT):c.6349G>A (p.Gly2117Arg) rs749897159
NM_006031.6(PCNT):c.644G>A (p.Cys215Tyr) rs138962786
NM_006031.6(PCNT):c.6651G>T (p.Gly2217=) rs755119869
NM_006031.6(PCNT):c.6819G>A (p.Gly2273=) rs200610141
NM_006031.6(PCNT):c.6933C>T (p.Val2311=) rs148444313
NM_006031.6(PCNT):c.7104T>C (p.Pro2368=) rs576187743
NM_006031.6(PCNT):c.7118G>A (p.Gly2373Glu) rs147670568
NM_006031.6(PCNT):c.7180-8C>T rs143511166
NM_006031.6(PCNT):c.7198C>T (p.Arg2400Cys) rs751297741
NM_006031.6(PCNT):c.7259C>T (p.Pro2420Leu) rs144633170
NM_006031.6(PCNT):c.7282G>A (p.Glu2428Lys) rs778163048
NM_006031.6(PCNT):c.7300C>A (p.Leu2434Ile) rs112633352
NM_006031.6(PCNT):c.7304A>G (p.His2435Arg) rs373432697
NM_006031.6(PCNT):c.7309G>C (p.Gly2437Arg) rs148384323
NM_006031.6(PCNT):c.7332C>T (p.Thr2444=) rs150882711
NM_006031.6(PCNT):c.7342G>A (p.Asp2448Asn) rs748347210
NM_006031.6(PCNT):c.7354G>T (p.Asp2452Tyr) rs1006896204
NM_006031.6(PCNT):c.7424G>A (p.Arg2475Gln) rs149779006
NM_006031.6(PCNT):c.7454G>T (p.Ser2485Ile) rs797045880
NM_006031.6(PCNT):c.7459C>G (p.Leu2487Val) rs201185279
NM_006031.6(PCNT):c.7541G>A (p.Arg2514Gln) rs370021414
NM_006031.6(PCNT):c.7634C>T (p.Ala2545Val) rs150303409
NM_006031.6(PCNT):c.7803G>A (p.Ala2601=) rs144869229
NM_006031.6(PCNT):c.7988G>A (p.Arg2663His) rs778334017
NM_006031.6(PCNT):c.8128C>T (p.His2710Tyr) rs987345147
NM_006031.6(PCNT):c.8284C>T (p.Arg2762Trp) rs761885630
NM_006031.6(PCNT):c.8401G>C (p.Val2801Leu) rs138868039
NM_006031.6(PCNT):c.8564G>A (p.Arg2855Gln) rs568559091
NM_006031.6(PCNT):c.8646G>C (p.Leu2882Phe) rs141771795
NM_006031.6(PCNT):c.8659G>A (p.Gly2887Arg) rs797045881
NM_006031.6(PCNT):c.8786A>C (p.His2929Pro) rs1556003819
NM_006031.6(PCNT):c.8820C>A (p.Asp2940Glu) rs797045882
NM_006031.6(PCNT):c.8930C>T (p.Ala2977Val) rs146657011
NM_006031.6(PCNT):c.8951C>G (p.Ser2984Cys) rs376696104
NM_006031.6(PCNT):c.8956G>A (p.Ala2986Thr) rs201877661
NM_006031.6(PCNT):c.8997G>A (p.Arg2999=) rs1288558445
NM_006031.6(PCNT):c.9028A>G (p.Lys3010Glu) rs797045883
NM_006031.6(PCNT):c.9035T>C (p.Val3012Ala) rs557745291
NM_006031.6(PCNT):c.9051C>G (p.His3017Gln) rs1556004960
NM_006031.6(PCNT):c.9155A>G (p.Asn3052Ser) rs779546932
NM_006031.6(PCNT):c.9163C>A (p.Leu3055Ile) rs754586558
NM_006031.6(PCNT):c.9293G>T (p.Trp3098Leu) rs797045884
NM_006031.6(PCNT):c.9304G>A (p.Glu3102Lys) rs775636867
NM_006031.6(PCNT):c.9331C>T (p.Arg3111Cys) rs1007600831
NM_006031.6(PCNT):c.9393+8C>T rs750108017
NM_006031.6(PCNT):c.9618A>G (p.Ile3206Met) rs372895276
NM_006031.6(PCNT):c.9707G>A (p.Arg3236Gln) rs113591604
NM_006031.6(PCNT):c.9826C>T (p.His3276Tyr) rs202170105
NM_006031.6(PCNT):c.9866T>C (p.Leu3289Ser) rs199737174
NM_006031.6(PCNT):c.9871A>G (p.Arg3291Gly) rs147637351
NM_006031.6(PCNT):c.9886T>C (p.Ser3296Pro) rs752708321

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.