ClinVar Miner

List of variants in gene ZFYVE26 reported as uncertain significance for Hereditary spastic paraplegia

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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_015346.4(ZFYVE26):c.-70A>T rs17192296 0.02937
NM_015346.4(ZFYVE26):c.5260G>A (p.Ala1754Thr) rs146968463 0.00045
NM_015346.4(ZFYVE26):c.624T>C (p.Asp208=) rs140128583 0.00034
NM_015346.4(ZFYVE26):c.6154G>A (p.Val2052Ile) rs201273304 0.00018
NM_015346.4(ZFYVE26):c.5927C>T (p.Thr1976Met) rs149744465 0.00014
NM_015346.4(ZFYVE26):c.879G>A (p.Ser293=) rs199794711 0.00013
NM_015346.4(ZFYVE26):c.4035G>T (p.Val1345=) rs374530573 0.00009
NM_015346.4(ZFYVE26):c.5834G>A (p.Arg1945Gln) rs200595749 0.00009
NM_015346.4(ZFYVE26):c.951C>T (p.Ala317=) rs142029189 0.00009
NM_015346.4(ZFYVE26):c.4293G>C (p.Gln1431His) rs373740172 0.00008
NM_015346.4(ZFYVE26):c.6789C>T (p.Asp2263=) rs372463199 0.00007
NM_015346.4(ZFYVE26):c.763C>T (p.Arg255Trp) rs267604034 0.00007
NM_015346.4(ZFYVE26):c.2097C>A (p.Ile699=) rs142972003 0.00006
NM_015346.4(ZFYVE26):c.3036C>T (p.His1012=) rs551159891 0.00006
NM_015346.4(ZFYVE26):c.5320G>A (p.Gly1774Ser) rs372819280 0.00006
NM_015346.4(ZFYVE26):c.5768G>A (p.Arg1923Gln) rs199497582 0.00006
NM_015346.4(ZFYVE26):c.2426G>A (p.Gly809Asp) rs149519213 0.00005
NM_015346.4(ZFYVE26):c.2756-7C>T rs200721800 0.00005
NM_015346.4(ZFYVE26):c.1387C>T (p.Leu463Phe) rs556064894 0.00004
NM_015346.4(ZFYVE26):c.416A>G (p.Asn139Ser) rs754388575 0.00004
NM_015346.4(ZFYVE26):c.4694A>G (p.Glu1565Gly) rs759468816 0.00004
NM_015346.4(ZFYVE26):c.540C>T (p.Asp180=) rs150289689 0.00004
NM_015346.4(ZFYVE26):c.1435+8G>A rs779576115 0.00003
NM_015346.4(ZFYVE26):c.4027A>G (p.Arg1343Gly) rs777319379 0.00003
NM_015346.4(ZFYVE26):c.4955C>T (p.Ala1652Val) rs752388667 0.00003
NM_015346.4(ZFYVE26):c.6876A>G (p.Leu2292=) rs773663147 0.00003
NM_015346.4(ZFYVE26):c.308A>C (p.Glu103Ala) rs750426190 0.00002
NM_015346.4(ZFYVE26):c.4073G>A (p.Arg1358His) rs138424288 0.00002
NM_015346.4(ZFYVE26):c.5791-6G>A rs771906344 0.00002
NM_015346.4(ZFYVE26):c.6973G>A (p.Ala2325Thr) rs763267244 0.00002
NM_015346.4(ZFYVE26):c.764G>A (p.Arg255Gln) rs200023667 0.00002
NM_015346.4(ZFYVE26):c.1378G>A (p.Glu460Lys) rs764112580 0.00001
NM_015346.4(ZFYVE26):c.1399C>G (p.Gln467Glu) rs373177554 0.00001
NM_015346.4(ZFYVE26):c.2183G>A (p.Arg728Gln) rs770927853 0.00001
NM_015346.4(ZFYVE26):c.2756-6G>A rs750576685 0.00001
NM_015346.4(ZFYVE26):c.3259C>G (p.Leu1087Val) rs1279334070 0.00001
NM_015346.4(ZFYVE26):c.3652A>C (p.Asn1218His) rs1306939952 0.00001
NM_015346.4(ZFYVE26):c.4203C>T (p.Leu1401=) rs941752233 0.00001
NM_015346.4(ZFYVE26):c.4452G>C (p.Arg1484Ser) rs368241137 0.00001
NM_015346.4(ZFYVE26):c.4663C>T (p.Leu1555=) rs2039462773 0.00001
NM_015346.4(ZFYVE26):c.5791-3C>T rs1334379838 0.00001
NM_015346.4(ZFYVE26):c.5981G>A (p.Gly1994Asp) rs1359433577 0.00001
NM_015346.4(ZFYVE26):c.1141G>C (p.Glu381Gln) rs2040162265
NM_015346.4(ZFYVE26):c.1659A>C (p.Ser553=) rs2140243482
NM_015346.4(ZFYVE26):c.1944T>C (p.His648=) rs1466130502
NM_015346.4(ZFYVE26):c.2174G>T (p.Arg725Leu) rs374310868
NM_015346.4(ZFYVE26):c.227C>A (p.Ala76Asp) rs770415843
NM_015346.4(ZFYVE26):c.2553+8G>A rs1355900379
NM_015346.4(ZFYVE26):c.266G>A (p.Arg89Gln) rs138664542
NM_015346.4(ZFYVE26):c.3129A>C (p.Gln1043His) rs2140227998
NM_015346.4(ZFYVE26):c.3248_3253del (p.Leu1083_Ser1084del) rs761454264
NM_015346.4(ZFYVE26):c.4024C>G (p.Arg1342Gly) rs368778263
NM_015346.4(ZFYVE26):c.4975-5A>G rs2140212689
NM_015346.4(ZFYVE26):c.5073G>A (p.Val1691=) rs2140212459
NM_015346.4(ZFYVE26):c.5434G>A (p.Asp1812Asn) rs2140207374
NM_015346.4(ZFYVE26):c.5771G>A (p.Ser1924Asn) rs2039094968
NM_015346.4(ZFYVE26):c.6033G>A (p.Val2011=) rs2140194830
NM_015346.4(ZFYVE26):c.6253_6255del (p.Lys2085del) rs1555394387
NM_015346.4(ZFYVE26):c.6897G>A (p.Leu2299=) rs2140184412

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