ClinVar Miner

List of variants in gene INPP5E reported as uncertain significance for not provided

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_019892.6(INPP5E):c.-239C>G rs562519905 0.00588
NM_019892.6(INPP5E):c.1730C>G (p.Pro577Arg) rs147967974 0.00405
NM_019892.6(INPP5E):c.469G>T (p.Gly157Trp) rs78211353 0.00057
NM_019892.6(INPP5E):c.875G>A (p.Arg292His) rs199873582 0.00027
NM_019892.6(INPP5E):c.460C>T (p.Pro154Ser) rs565209005 0.00026
NM_019892.6(INPP5E):c.532G>A (p.Val178Met) rs376003129 0.00007
NM_019892.6(INPP5E):c.1325C>T (p.Thr442Ile) rs201043370 0.00006
NM_019892.6(INPP5E):c.1388C>T (p.Ala463Val) rs199956627 0.00006
NM_019892.6(INPP5E):c.311A>T (p.Glu104Val) rs748786705 0.00006
NM_019892.6(INPP5E):c.746C>T (p.Ser249Phe) rs550485638 0.00005
NM_019892.6(INPP5E):c.1178T>C (p.Val393Ala) rs930286679 0.00004
NM_019892.6(INPP5E):c.1456C>T (p.Arg486Cys) rs75939033 0.00004
NM_019892.6(INPP5E):c.593G>C (p.Ser198Thr) rs141286608 0.00004
NM_019892.6(INPP5E):c.1162G>T (p.Val388Leu) rs863225201 0.00003
NM_019892.6(INPP5E):c.1577C>T (p.Pro526Leu) rs746867724 0.00003
NM_019892.6(INPP5E):c.1133G>A (p.Arg378His) rs758951947 0.00002
NM_019892.6(INPP5E):c.1615G>A (p.Gly539Arg) rs375126841 0.00002
NM_019892.6(INPP5E):c.1732G>A (p.Gly578Arg) rs559636009 0.00002
NM_019892.6(INPP5E):c.1742C>T (p.Thr581Met) rs943471686 0.00002
NM_019892.6(INPP5E):c.982G>A (p.Asp328Asn) rs201857820 0.00002
NM_019892.6(INPP5E):c.1021G>A (p.Gly341Ser) rs780882740 0.00001
NM_019892.6(INPP5E):c.1549+17G>A rs776348228 0.00001
NM_019892.6(INPP5E):c.1630G>A (p.Asp544Asn) rs1161636527 0.00001
NM_019892.6(INPP5E):c.1787G>C (p.Arg596Thr) rs765327224 0.00001
NM_019892.6(INPP5E):c.1796G>A (p.Arg599Gln) rs750836133 0.00001
NM_019892.6(INPP5E):c.35A>G (p.Glu12Gly) rs1029781765 0.00001
NM_019892.6(INPP5E):c.874C>G (p.Arg292Gly) rs753742613 0.00001
NM_019892.6(INPP5E):c.877T>G (p.Tyr293Asp) rs1241112128 0.00001
NM_019892.6(INPP5E):c.1196C>G (p.Ser399Cys) rs1564433154
NM_019892.6(INPP5E):c.1430A>C (p.Asp477Ala) rs1835716590
NM_019892.6(INPP5E):c.1505C>T (p.Pro502Leu) rs769531967
NM_019892.6(INPP5E):c.1684A>G (p.Ser562Gly) rs863225197
NM_019892.6(INPP5E):c.1897C>G (p.Gln633Glu)
NM_019892.6(INPP5E):c.279G>T (p.Arg93Ser) rs1057520153
NM_019892.6(INPP5E):c.443_446del (p.Ser148fs) rs1564437356
NM_019892.6(INPP5E):c.61A>T (p.Arg21Trp) rs886042814
NM_019892.6(INPP5E):c.934_936del (p.Lys312del)
NM_019892.6(INPP5E):c.937-3C>G

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