ClinVar Miner

List of variants in gene ZFYVE26 studied for Hereditary spastic paraplegia

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 117
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_015346.4(ZFYVE26):c.5672A>G (p.Asn1891Ser) rs3742883 0.93729
NM_015346.4(ZFYVE26):c.2559G>A (p.Leu853=) rs7143196 0.14152
NM_015346.4(ZFYVE26):c.3365C>T (p.Ala1122Val) rs3742884 0.04741
NM_015346.4(ZFYVE26):c.3308C>T (p.Pro1103Leu) rs3742885 0.04730
NM_015346.4(ZFYVE26):c.3118T>A (p.Ser1040Thr) rs112787369 0.03993
NM_015346.4(ZFYVE26):c.3757C>T (p.Leu1253=) rs34296097 0.03528
NM_015346.4(ZFYVE26):c.1224G>T (p.Gly408=) rs17104689 0.03409
NM_015346.4(ZFYVE26):c.7232G>A (p.Arg2411His) rs34373049 0.03090
NM_015346.4(ZFYVE26):c.-70A>T rs17192296 0.02937
NM_015346.4(ZFYVE26):c.2332+7del rs145183291 0.02598
NM_015346.4(ZFYVE26):c.2852C>T (p.Thr951Met) rs35471427 0.02295
NM_015346.4(ZFYVE26):c.6921C>T (p.Ser2307=) rs35917338 0.01911
NM_015346.4(ZFYVE26):c.7407T>C (p.Asp2469=) rs35106153 0.01846
NM_015346.4(ZFYVE26):c.5784T>C (p.Tyr1928=) rs34852231 0.01623
NM_015346.4(ZFYVE26):c.6987-3C>T rs76728509 0.01610
NM_015346.4(ZFYVE26):c.5612G>A (p.Cys1871Tyr) rs61746722 0.00962
NM_015346.4(ZFYVE26):c.1844C>T (p.Ser615Phe) rs117228915 0.00888
NM_015346.4(ZFYVE26):c.2826G>A (p.Met942Ile) rs117367857 0.00826
NM_015346.4(ZFYVE26):c.6229G>A (p.Gly2077Arg) rs140540720 0.00750
NM_015346.4(ZFYVE26):c.5678G>T (p.Ser1893Ile) rs34952009 0.00716
NM_015346.4(ZFYVE26):c.2887G>C (p.Val963Leu) rs116890187 0.00606
NM_015346.4(ZFYVE26):c.7586C>G (p.Pro2529Arg) rs143198225 0.00510
NM_015346.4(ZFYVE26):c.6588+7C>T rs186040735 0.00471
NM_015346.4(ZFYVE26):c.6819G>A (p.Arg2273=) rs144007962 0.00349
NM_015346.4(ZFYVE26):c.7055C>T (p.Thr2352Ile) rs151166497 0.00319
NM_015346.4(ZFYVE26):c.5121A>C (p.Gly1707=) rs143981992 0.00291
NM_015346.4(ZFYVE26):c.4264G>A (p.Val1422Met) rs148552744 0.00276
NM_015346.4(ZFYVE26):c.3722G>A (p.Arg1241Gln) rs140756827 0.00258
NM_015346.4(ZFYVE26):c.1184G>T (p.Gly395Val) rs35512910 0.00250
NM_015346.4(ZFYVE26):c.4854C>T (p.Leu1618=) rs151287975 0.00246
NM_015346.4(ZFYVE26):c.7417-5G>C rs201771769 0.00236
NM_015346.4(ZFYVE26):c.6405G>A (p.Leu2135=) rs76327447 0.00220
NM_015346.4(ZFYVE26):c.453C>T (p.Ser151=) rs75391113 0.00203
NM_015346.4(ZFYVE26):c.1933A>G (p.Met645Val) rs77129887 0.00201
NM_015346.4(ZFYVE26):c.4066T>G (p.Cys1356Gly) rs149276487 0.00166
NM_015346.4(ZFYVE26):c.677G>A (p.Arg226His) rs147919567 0.00147
NM_015346.4(ZFYVE26):c.6086T>C (p.Ile2029Thr) rs139163400 0.00130
NM_015346.4(ZFYVE26):c.5799C>T (p.Ser1933=) rs145858625 0.00115
NM_015346.4(ZFYVE26):c.7533C>T (p.Ser2511=) rs147494935 0.00113
NM_015346.4(ZFYVE26):c.4734C>T (p.Ile1578=) rs200243306 0.00105
NM_015346.4(ZFYVE26):c.3051T>C (p.Ala1017=) rs138895639 0.00064
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.748G>A (p.Glu250Lys) rs200340910 0.00019
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.4324G>A (p.Asp1442Asn) rs534497092 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.1597G>A (p.Ala533Thr) rs551062468 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.2105G>A (p.Arg702His) rs201339450 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.3382C>T (p.Gln1128Ter) rs988442865 0.00001
NM_015346.4(ZFYVE26):c.3652A>C (p.Asn1218His) rs1306939952 0.00001
NM_015346.4(ZFYVE26):c.4114_4115insGAAGGGC (p.Ala1372fs) rs950356390 0.00001
NM_015346.4(ZFYVE26):c.4181G>A (p.Trp1394Ter) rs370828455 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.6296dup (p.Asn2100fs) rs1555394376 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.1870G>A (p.Ala624Thr) rs531152715
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.2609_2633del (p.Met870fs) rs2140234090
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.3210C>G (p.Pro1070=) rs7156492
NM_015346.4(ZFYVE26):c.3210C>T (p.Pro1070=) rs7156492
NM_015346.4(ZFYVE26):c.3248_3253del (p.Leu1083_Ser1084del) rs761454264
NM_015346.4(ZFYVE26):c.363+1G>A rs935301743
NM_015346.4(ZFYVE26):c.3642_3643insCCACACTTAG (p.Ala1215fs) rs773333879
NM_015346.4(ZFYVE26):c.4024C>G (p.Arg1342Gly) rs368778263
NM_015346.4(ZFYVE26):c.4197C>T (p.Thr1399=) rs35018134
NM_015346.4(ZFYVE26):c.4370G>A (p.Cys1457Tyr) rs2235967
NM_015346.4(ZFYVE26):c.4455del (p.Trp1485fs) rs1566881181
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
NM_015346.4(ZFYVE26):c.7617G>A (p.Lys2539=) rs550301037

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.