ClinVar Miner

Variants in gene PCNT with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 57
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HGVS dbSNP
NM_006031.6(PCNT):c.-16G>T rs138595914
NM_006031.6(PCNT):c.1616C>T (p.Thr539Ile) rs2249060
NM_006031.6(PCNT):c.3339T>C (p.Ser1113=) rs61735805
NM_006031.6(PCNT):c.3487C>T (p.Arg1163Cys) rs7279204
NM_006031.6(PCNT):c.3580G>A (p.Ala1194Thr) rs35044802
NM_006031.6(PCNT):c.3615G>A (p.Ala1205=) rs61735806
NM_006031.6(PCNT):c.4285C>T (p.Arg1429Cys) rs62224222
NM_006031.6(PCNT):c.4345C>G (p.Gln1449Glu) rs139432601
NM_006031.6(PCNT):c.4354G>A (p.Gly1452Arg) rs143796569
NM_006031.6(PCNT):c.4572G>A (p.Pro1524=) rs116431741
NM_006031.6(PCNT):c.467A>G (p.His156Arg) rs61735825
NM_006031.6(PCNT):c.4910C>T (p.Pro1637Leu) rs34849154
NM_006031.6(PCNT):c.4962+10G>A rs114474454
NM_006031.6(PCNT):c.498A>G (p.Pro166=) rs61735824
NM_006031.6(PCNT):c.520A>G (p.Ile174Val) rs61735822
NM_006031.6(PCNT):c.54+6C>T rs80017051
NM_006031.6(PCNT):c.5535G>A (p.Arg1845=) rs61735543
NM_006031.6(PCNT):c.5634C>T (p.Asp1878=) rs61735811
NM_006031.6(PCNT):c.5742G>A (p.Ala1914=) rs61735810
NM_006031.6(PCNT):c.5771C>T (p.Ala1924Val) rs184420466
NM_006031.6(PCNT):c.5858G>A (p.Arg1953His) rs34268261
NM_006031.6(PCNT):c.5879G>A (p.Arg1960Gln) rs34813667
NM_006031.6(PCNT):c.6384A>G (p.Thr2128=) rs60444527
NM_006031.6(PCNT):c.6571T>C (p.Ser2191Pro) rs34151633
NM_006031.6(PCNT):c.6579G>A (p.Pro2193=) rs150756913
NM_006031.6(PCNT):c.6616A>G (p.Thr2206Ala) rs9981448
NM_006031.6(PCNT):c.6634C>T (p.Arg2212Trp) rs144471022
NM_006031.6(PCNT):c.6739C>T (p.His2247Tyr) rs61735812
NM_006031.6(PCNT):c.6822G>A (p.Pro2274=) rs375741970
NM_006031.6(PCNT):c.6918T>C (p.Ala2306=) rs61738290
NM_006031.6(PCNT):c.6957T>G (p.Phe2319Leu) rs61735813
NM_006031.6(PCNT):c.6986C>G (p.Pro2329Arg) rs35848602
NM_006031.6(PCNT):c.7074T>C (p.Pro2358=) rs61735815
NM_006031.6(PCNT):c.711T>G (p.His237Gln) rs34500739
NM_006031.6(PCNT):c.7130C>T (p.Pro2377Leu) rs61735814
NM_006031.6(PCNT):c.7159G>A (p.Val2387Met) rs75024419
NM_006031.6(PCNT):c.720+17T>C rs9982233
NM_006031.6(PCNT):c.7404G>C (p.Gln2468His) rs77075366
NM_006031.6(PCNT):c.7485C>T (p.Ile2495=) rs61735817
NM_006031.6(PCNT):c.7536G>A (p.Pro2512=) rs61735818
NM_006031.6(PCNT):c.7652C>T (p.Ala2551Val) rs12481791
NM_006031.6(PCNT):c.7867C>T (p.Leu2623=) rs61735821
NM_006031.6(PCNT):c.7874G>A (p.Arg2625Gln) rs8131693
NM_006031.6(PCNT):c.7914-16C>T rs2839257
NM_006031.6(PCNT):c.7914-4G>A rs76287849
NM_006031.6(PCNT):c.8258G>A (p.Arg2753His) rs743346
NM_006031.6(PCNT):c.8418G>A (p.Ala2806=) rs9983522
NM_006031.6(PCNT):c.8671G>A (p.Ala2891Thr) rs33956783
NM_006031.6(PCNT):c.8752-5A>C rs149444205
NM_006031.6(PCNT):c.8811A>G (p.Thr2937=) rs17371795
NM_006031.6(PCNT):c.8895G>A (p.Ala2965=) rs572222540
NM_006031.6(PCNT):c.8924T>C (p.Leu2975Pro) rs35881595
NM_006031.6(PCNT):c.8988C>T (p.Ala2996=) rs61735826
NM_006031.6(PCNT):c.9015G>A (p.Thr3005=) rs79359463
NM_006031.6(PCNT):c.9271A>G (p.Ser3091Gly) rs4818842
NM_006031.6(PCNT):c.9274-3C>T rs200348425
NM_006031.6(PCNT):c.9394-4T>C rs2839260

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