ClinVar Miner

List of variants in gene PCNT reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 93
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HGVS dbSNP
NM_006031.6(PCNT):c.-15C>G
NM_006031.6(PCNT):c.1107T>C (p.His369=) rs113731555
NM_006031.6(PCNT):c.1246A>G (p.Ile416Val) rs368199588
NM_006031.6(PCNT):c.1519C>G (p.Arg507Gly) rs138036524
NM_006031.6(PCNT):c.1640G>A (p.Gly547Glu) rs1057522262
NM_006031.6(PCNT):c.1761+14C>T rs368329088
NM_006031.6(PCNT):c.1784C>T (p.Ala595Val) rs143028464
NM_006031.6(PCNT):c.1885_1886delinsAA (p.Ser629Lys) rs1555955867
NM_006031.6(PCNT):c.1943C>G (p.Pro648Arg) rs752992538
NM_006031.6(PCNT):c.202G>C (p.Asp68His) rs1216804302
NM_006031.6(PCNT):c.2458C>T (p.Arg820Cys) rs369586175
NM_006031.6(PCNT):c.2575G>A (p.Asp859Asn) rs115369710
NM_006031.6(PCNT):c.267+163G>A
NM_006031.6(PCNT):c.2714A>G (p.Gln905Arg) rs112231246
NM_006031.6(PCNT):c.2833C>T (p.Arg945Cys) rs147358856
NM_006031.6(PCNT):c.2991T>C (p.Phe997=) rs767625587
NM_006031.6(PCNT):c.3108C>T (p.Thr1036=) rs182694054
NM_006031.6(PCNT):c.3423C>T (p.Leu1141=) rs113763153
NM_006031.6(PCNT):c.3553G>A (p.Glu1185Lys) rs920374957
NM_006031.6(PCNT):c.363A>C (p.Thr121=) rs150766997
NM_006031.6(PCNT):c.3647C>T (p.Pro1216Leu) rs200670500
NM_006031.6(PCNT):c.3648G>A (p.Pro1216=) rs756724097
NM_006031.6(PCNT):c.3748C>T (p.Arg1250Trp) rs117987006
NM_006031.6(PCNT):c.3749G>A (p.Arg1250Gln)
NM_006031.6(PCNT):c.3798C>T (p.Ala1266=) rs769080650
NM_006031.6(PCNT):c.3924G>A (p.Lys1308=) rs139543323
NM_006031.6(PCNT):c.4139C>T (p.Ala1380Val) rs201139850
NM_006031.6(PCNT):c.4140G>A (p.Ala1380=) rs372175239
NM_006031.6(PCNT):c.4142C>T (p.Ala1381Val) rs114383833
NM_006031.6(PCNT):c.4143G>A (p.Ala1381=) rs111697920
NM_006031.6(PCNT):c.4354G>A (p.Gly1452Arg) rs143796569
NM_006031.6(PCNT):c.4571C>G (p.Pro1524Arg) rs35513449
NM_006031.6(PCNT):c.467_505del (p.His156_Gln168del) rs587784306
NM_006031.6(PCNT):c.467_505dup (p.His156_Gln168dup) rs587784306
NM_006031.6(PCNT):c.4844C>T (p.Thr1615Met) rs139581644
NM_006031.6(PCNT):c.4910C>T (p.Pro1637Leu) rs34849154
NM_006031.6(PCNT):c.49A>G (p.Thr17Ala) rs1055522433
NM_006031.6(PCNT):c.5115+11A>G rs371474470
NM_006031.6(PCNT):c.5155G>A (p.Ala1719Thr) rs1290537073
NM_006031.6(PCNT):c.5199G>A (p.Lys1733=) rs61735808
NM_006031.6(PCNT):c.5253C>G (p.His1751Gln) rs114799541
NM_006031.6(PCNT):c.5323C>G (p.Leu1775Val) rs147409139
NM_006031.6(PCNT):c.5411G>A (p.Arg1804Gln)
NM_006031.6(PCNT):c.5477G>C (p.Gly1826Ala) rs199847432
NM_006031.6(PCNT):c.5607G>A (p.Thr1869=) rs763347923
NM_006031.6(PCNT):c.5710G>A (p.Ala1904Thr) rs200426591
NM_006031.6(PCNT):c.5736C>T (p.Ala1912=) rs766460016
NM_006031.6(PCNT):c.5803G>C (p.Val1935Leu) rs774248299
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.5994+4G>A rs781737632
NM_006031.6(PCNT):c.6032C>T (p.Ala2011Val) rs145119952
NM_006031.6(PCNT):c.6072C>T (p.Thr2024=) rs143671774
NM_006031.6(PCNT):c.6080A>G (p.Gln2027Arg) rs147189224
NM_006031.6(PCNT):c.6093G>A (p.Gln2031=) rs138543824
NM_006031.6(PCNT):c.6635G>A (p.Arg2212Gln) rs201503338
NM_006031.6(PCNT):c.6645G>A (p.Pro2215=) rs144342729
NM_006031.6(PCNT):c.6822G>A (p.Pro2274=) rs375741970
NM_006031.6(PCNT):c.688C>T (p.Arg230Cys) rs143560718
NM_006031.6(PCNT):c.6933C>T (p.Val2311=) rs148444313
NM_006031.6(PCNT):c.6986C>G (p.Pro2329Arg) rs35848602
NM_006031.6(PCNT):c.6991G>A (p.Gly2331Arg) rs775387368
NM_006031.6(PCNT):c.7040T>C (p.Phe2347Ser) rs150704986
NM_006031.6(PCNT):c.7059G>A (p.Pro2353=) rs149413536
NM_006031.6(PCNT):c.7162C>T (p.Arg2388Cys) rs201562329
NM_006031.6(PCNT):c.7179+18G>A rs370492724
NM_006031.6(PCNT):c.721-13T>G rs748762743
NM_006031.6(PCNT):c.724G>A (p.Val242Met) rs147931950
NM_006031.6(PCNT):c.7281C>T (p.Asp2427=) rs138588682
NM_006031.6(PCNT):c.7332C>T (p.Thr2444=) rs150882711
NM_006031.6(PCNT):c.7398G>A (p.Glu2466=) rs114739559
NM_006031.6(PCNT):c.7413G>A (p.Glu2471=) rs191561981
NM_006031.6(PCNT):c.7459C>G (p.Leu2487Val) rs201185279
NM_006031.6(PCNT):c.7495-13A>G rs114588443
NM_006031.6(PCNT):c.7803G>A (p.Ala2601=) rs144869229
NM_006031.6(PCNT):c.7833C>T (p.Ser2611=) rs139227909
NM_006031.6(PCNT):c.7914-4G>A rs76287849
NM_006031.6(PCNT):c.7914-5C>T rs114120845
NM_006031.6(PCNT):c.8172C>T (p.Ile2724=) rs146717642
NM_006031.6(PCNT):c.8365G>A (p.Ala2789Thr) rs753073203
NM_006031.6(PCNT):c.8528T>G (p.Leu2843Arg) rs569737144
NM_006031.6(PCNT):c.8646G>C (p.Leu2882Phe) rs141771795
NM_006031.6(PCNT):c.8889G>A (p.Ser2963=) rs151325202
NM_006031.6(PCNT):c.8924T>C (p.Leu2975Pro) rs35881595
NM_006031.6(PCNT):c.9291T>C (p.Ala3097=) rs150554265
NM_006031.6(PCNT):c.9334C>T (p.Pro3112Ser) rs534490490
NM_006031.6(PCNT):c.9352C>A (p.Pro3118Thr) rs1057520975
NM_006031.6(PCNT):c.9623+8C>T rs75758339
NM_006031.6(PCNT):c.9707G>A (p.Arg3236Gln) rs113591604
NM_006031.6(PCNT):c.9720G>A (p.Pro3240=) rs141991283
NM_006031.6(PCNT):c.9840-15G>C rs564095021
NM_006031.6(PCNT):c.9949T>C (p.Leu3317=) rs111389121
NM_006031.6(PCNT):c.9967+18C>T rs369414311

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