ClinVar Miner

List of variants in gene INPP5E reported as benign for not provided

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Gene type:
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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_019892.6(INPP5E):c.1035-138T>A rs10735662 0.45396
NM_019892.6(INPP5E):c.1248T>C (p.Thr416=) rs10781542 0.42574
NM_019892.6(INPP5E):c.1284T>C (p.Gly428=) rs10870194 0.42571
NM_019892.6(INPP5E):c.*703A>G rs1128874 0.42476
NM_019892.6(INPP5E):c.1034+120A>G rs10781543 0.41467
NM_019892.6(INPP5E):c.*328T>C rs35763810 0.41134
NM_019892.6(INPP5E):c.*816A>G rs8413 0.40078
NM_019892.6(INPP5E):c.937-136C>A rs7851507 0.37410
NM_019892.6(INPP5E):c.1549+23A>G rs11146014 0.28999
NM_019892.6(INPP5E):c.1802+155G>A rs72775768 0.28718
NM_019892.6(INPP5E):c.1279+131C>T rs34619169 0.25890
NM_019892.6(INPP5E):c.1280-26T>C rs34302850 0.25844
NM_019892.6(INPP5E):c.1280-24C>T rs34936112 0.25833
NM_019892.6(INPP5E):c.1794G>T (p.Gly598=) rs33982662 0.22912
NM_019892.6(INPP5E):c.1035-127C>T rs11146021 0.20968
NM_019892.6(INPP5E):c.1280-116G>A rs34985258 0.20728
NM_019892.6(INPP5E):c.1280-105G>A rs35531907 0.20727
NM_019892.6(INPP5E):c.*98G>A rs35873563 0.20643
NM_019892.6(INPP5E):c.1802+156A>G rs68142670 0.20348
NM_019892.6(INPP5E):c.1802+49G>A rs4451431 0.15392
NM_019892.6(INPP5E):c.1034+266G>T rs10870197 0.11959
NM_019892.6(INPP5E):c.936+266G>A rs7864967 0.10896
NM_019892.6(INPP5E):c.1665+263C>T rs10870184 0.10875
NM_019892.6(INPP5E):c.972A>G (p.Pro324=) rs10870199 0.10324
NM_019892.6(INPP5E):c.1665+100C>G rs73566940 0.05561
NM_019892.6(INPP5E):c.1359C>T (p.Pro453=) rs35774078 0.05472
NM_019892.6(INPP5E):c.1035-128G>A rs112904493 0.05122
NM_019892.6(INPP5E):c.1387+150G>A rs56704890 0.02984
NM_019892.6(INPP5E):c.1803-68C>T rs77350282 0.02540
NM_019892.6(INPP5E):c.33C>G (p.Ser11=) rs79161998 0.02475
NM_019892.6(INPP5E):c.-174G>A rs544247720 0.01935
NM_019892.6(INPP5E):c.981C>T (p.Ala327=) rs35498378 0.01340
NM_019892.6(INPP5E):c.636C>A (p.Val212=) rs34071122 0.01252
NM_019892.6(INPP5E):c.531C>A (p.Ala177=) rs58206296 0.01135
NM_019892.6(INPP5E):c.791G>A (p.Arg264His) rs202197173 0.00415
NM_019892.6(INPP5E):c.1730C>G (p.Pro577Arg) rs147967974 0.00405
NM_019892.6(INPP5E):c.1159+8C>T rs73566945 0.00276
NM_019892.6(INPP5E):c.1299G>A (p.Ala433=) rs56931633 0.00272
NC_000009.12:g.136439848G>A rs111413675
NM_019892.6(INPP5E):c.1159+33_1159+34insGGTGGGCGCGGCTGGAGGGGTGGGCGCGGCTGGAGG rs1239490197
NM_019892.6(INPP5E):c.1159+7_1159+8insGGTGGGCGTGGCTAGAGG rs71269007
NM_019892.6(INPP5E):c.1159+7_1159+8insGGTGGGCGTGGCTGGAGG rs71269007
NM_019892.6(INPP5E):c.1387+115G>A rs10870193
NM_019892.6(INPP5E):c.1521C>T (p.His507=) rs10870188
NM_019892.6(INPP5E):c.1550-72G>A rs68002978
NM_019892.6(INPP5E):c.1791G>A (p.Pro597=) rs10870182
NM_019892.6(INPP5E):c.1791G>C (p.Pro597=) rs10870182
NM_019892.6(INPP5E):c.1802+213_1802+215del rs34184721
NM_019892.6(INPP5E):c.812+7_812+10del rs5901103
NM_019892.6(INPP5E):c.813-141G>C rs76470602

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