ClinVar Miner

List of variants in gene POP1 reported as benign for not provided

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Gene type:
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Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_001145860.2(POP1):c.2057+21A>G rs4735530 0.70291
NM_001145860.2(POP1):c.143-213C>T rs4735529 0.49478
NM_001145860.2(POP1):c.1903-79T>C rs7000738 0.43328
NM_001145860.2(POP1):c.-2-127A>G rs11997551 0.43171
NM_001145860.2(POP1):c.1903-245T>C rs10112133 0.30397
NM_001145860.2(POP1):c.1566A>C (p.Lys522Asn) rs17184326 0.13671
NM_001145860.2(POP1):c.1711-207A>C rs9969669 0.13622
NM_001145860.2(POP1):c.1594+170G>T rs16896671 0.13466
NM_001145860.2(POP1):c.1363-123T>C rs28645170 0.13459
NM_001145860.2(POP1):c.1363-136C>T rs28549107 0.13456
NM_001145860.2(POP1):c.1363-176G>T rs28668499 0.13447
NM_001145860.2(POP1):c.1363-347G>A rs72678802 0.13405
NM_001145860.2(POP1):c.1595-192G>A rs62522197 0.12914
NM_001145860.2(POP1):c.1595-18A>G rs17184704 0.12910
NM_001145860.2(POP1):c.1595-205A>G rs72680613 0.12905
NM_001145860.2(POP1):c.1902+93C>T rs72680615 0.12879
NM_001145860.2(POP1):c.1711-86T>C rs9969536 0.12875
NM_001145860.2(POP1):c.2058-232G>A rs7012074 0.11201
NM_001145860.2(POP1):c.1594+44C>T rs17184361 0.11128
NM_001145860.2(POP1):c.824-95A>C rs16896659 0.10894
NM_001145860.2(POP1):c.1594+10C>T rs28575522 0.10208
NM_001145860.2(POP1):c.1475-124A>G rs17184298 0.08550
NM_001145860.2(POP1):c.2420+181T>C rs75235928 0.07908
NM_001145860.2(POP1):c.736-229G>A rs73701266 0.07432
NM_001145860.2(POP1):c.736-73C>T rs73701267 0.07427
NM_001145860.2(POP1):c.824-38C>T rs73701269 0.07426
NM_001145860.2(POP1):c.824-193T>A rs73701268 0.07423
NM_001145860.2(POP1):c.1012-53G>A rs75347577 0.07412
NM_001145860.2(POP1):c.1012-69C>A rs115741751 0.07390
NM_001145860.2(POP1):c.1012-94T>G rs76745470 0.07384
NM_001145860.2(POP1):c.2163T>C (p.Ala721=) rs16896695 0.06990
NM_001145860.2(POP1):c.2980C>G (p.Leu994Val) rs17856355 0.04270
NM_001145860.2(POP1):c.2532T>C (p.Ala844=) rs12541183 0.02748
NM_001145860.2(POP1):c.1128T>A (p.Pro376=) rs62639698 0.01514
NM_001145860.2(POP1):c.1012-11T>C rs78782053 0.01344
NM_001145860.2(POP1):c.933C>T (p.Ile311=) rs34680723 0.01342
NM_001145860.2(POP1):c.1795T>C (p.Leu599=) rs34635625 0.00575
NM_001145860.2(POP1):c.2013G>C (p.Leu671=) rs142987843 0.00429
NM_001145860.2(POP1):c.221A>G (p.Gln74Arg) rs141161667 0.00426
NM_001145860.2(POP1):c.1362+7G>A rs182805220 0.00211
NM_001145860.2(POP1):c.1379A>C (p.Glu460Ala) rs2306131 0.00186
NM_001145860.2(POP1):c.10G>A (p.Ala4Thr) rs145484648 0.00067
NM_001145860.2(POP1):c.1227A>G (p.Leu409=) rs146559376 0.00028
NM_001145860.2(POP1):c.1908T>C (p.Tyr636=) rs139387262 0.00028
NM_001145860.2(POP1):c.2488C>T (p.Arg830Trp) rs145798300 0.00026
NM_001145860.2(POP1):c.2262G>A (p.Gln754=) rs552172526 0.00005
NM_001145860.2(POP1):c.2091G>A (p.Lys697=) rs200715007 0.00004
NM_001145860.2(POP1):c.2469T>A (p.Ser823=) rs770831980 0.00004
NM_001145860.2(POP1):c.171G>A (p.Arg57=) rs184763875 0.00003
NM_001145860.2(POP1):c.1902+9C>T rs369328781 0.00001
NM_001145860.2(POP1):c.1363-180G>A rs28695425
NM_001145860.2(POP1):c.142+311dup rs1274675081
NM_001145860.2(POP1):c.142+80A>G rs28556674
NM_001145860.2(POP1):c.2058-140TG[19] rs58936294
NM_001145860.2(POP1):c.2058-140TG[20] rs58936294
NM_001145860.2(POP1):c.2058-140TG[24] rs58936294
NM_001145860.2(POP1):c.2058-140TG[25] rs58936294
NM_001145860.2(POP1):c.2058-140TG[26] rs58936294
NM_001145860.2(POP1):c.2499C>T (p.Pro833=) rs111665863
NM_001145860.2(POP1):c.310+218T>G rs3802195
NM_001145860.2(POP1):c.311-214T>G rs3802196
NM_001145860.2(POP1):c.311-49= rs2447508
NM_001145860.2(POP1):c.380C>T (p.Ser127Leu)
NM_001145860.2(POP1):c.735+324_735+326del rs34286627

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