ClinVar Miner

List of variants in gene ZFYVE26 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 77
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
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.*583C>T rs72723172 0.00761
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.6588+7C>T rs186040735 0.00471
NM_015346.4(ZFYVE26):c.5484+13G>A rs140117984 0.00407
NM_015346.4(ZFYVE26):c.7055C>T (p.Thr2352Ile) rs151166497 0.00319
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.4401C>T (p.Pro1467=) rs138543433 0.00148
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.7533C>T (p.Ser2511=) rs147494935 0.00113
NM_015346.4(ZFYVE26):c.773G>A (p.Arg258Gln) rs150230201 0.00113
NM_015346.4(ZFYVE26):c.1945G>A (p.Val649Met) rs144790966 0.00107
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.2396C>T (p.Thr799Met) rs200179480 0.00014
NM_015346.4(ZFYVE26):c.5321-3C>T rs376234357 0.00011
NM_015346.4(ZFYVE26):c.4035G>T (p.Val1345=) rs374530573 0.00009
NM_015346.4(ZFYVE26):c.5767C>T (p.Arg1923Trp) rs544932478 0.00009
NM_015346.4(ZFYVE26):c.730C>A (p.Leu244Ile) rs148790248 0.00009
NM_015346.4(ZFYVE26):c.4324G>A (p.Asp1442Asn) rs534497092 0.00008
NM_015346.4(ZFYVE26):c.2253G>A (p.Glu751=) rs373115983 0.00006
NM_015346.4(ZFYVE26):c.2859A>T (p.Leu953=) rs189616103 0.00006
NM_015346.4(ZFYVE26):c.5768G>A (p.Arg1923Gln) rs199497582 0.00006
NM_015346.4(ZFYVE26):c.3780C>T (p.His1260=) rs749435914 0.00004
NM_015346.4(ZFYVE26):c.4125G>A (p.Glu1375=) rs374188915 0.00004
NM_015346.4(ZFYVE26):c.403G>A (p.Val135Met) rs771937001 0.00003
NM_015346.4(ZFYVE26):c.6456G>C (p.Gly2152=) rs140345788 0.00003
NM_015346.4(ZFYVE26):c.2529C>T (p.Arg843=) rs537194634 0.00002
NM_015346.4(ZFYVE26):c.5103C>T (p.Leu1701=) rs146148247 0.00002
NM_015346.4(ZFYVE26):c.6973G>A (p.Ala2325Thr) rs763267244 0.00002
NM_015346.4(ZFYVE26):c.1153A>T (p.Arg385Trp) rs529988015 0.00001
NM_015346.4(ZFYVE26):c.1170G>A (p.Leu390=) rs532292359 0.00001
NM_015346.4(ZFYVE26):c.295C>T (p.Arg99Trp) rs779962087 0.00001
NM_015346.4(ZFYVE26):c.5712A>G (p.Lys1904=) rs1391052284 0.00001
NM_015346.4(ZFYVE26):c.6870A>G (p.Ser2290=) rs766701632 0.00001
GRCh37/hg19 14q24.1(chr14:68248050-68282680)x1
NM_015346.4(ZFYVE26):c.1073T>C (p.Leu358Pro) rs2040164683
NM_015346.4(ZFYVE26):c.1233T>C (p.Ala411=) rs1351690810
NM_015346.4(ZFYVE26):c.1476T>C (p.Cys492=)
NM_015346.4(ZFYVE26):c.1639+7C>A rs2140246634
NM_015346.4(ZFYVE26):c.175G>T (p.Val59Leu) rs1555401096
NM_015346.4(ZFYVE26):c.1870G>A (p.Ala624Thr) rs531152715
NM_015346.4(ZFYVE26):c.2067C>T (p.Leu689=) rs141880939
NM_015346.4(ZFYVE26):c.2498C>T (p.Pro833Leu)
NM_015346.4(ZFYVE26):c.2614C>T (p.Arg872Cys)
NM_015346.4(ZFYVE26):c.2993G>A (p.Arg998His)
NM_015346.4(ZFYVE26):c.3017G>A (p.Arg1006Gln)
NM_015346.4(ZFYVE26):c.3097A>T (p.Ser1033Cys) rs1555397623
NM_015346.4(ZFYVE26):c.3248_3253del (p.Leu1083_Ser1084del) rs761454264
NM_015346.4(ZFYVE26):c.3681C>T (p.Ile1227=) rs141264277
NM_015346.4(ZFYVE26):c.3806C>T (p.Pro1269Leu) rs2140223671
NM_015346.4(ZFYVE26):c.3811T>C (p.Ser1271Pro) rs2039558721
NM_015346.4(ZFYVE26):c.4197C>T (p.Thr1399=) rs35018134
NM_015346.4(ZFYVE26):c.4408G>A (p.Asp1470Asn) rs1388977274
NM_015346.4(ZFYVE26):c.4525T>C (p.Cys1509Arg) rs1594911188
NM_015346.4(ZFYVE26):c.4569+2T>C rs779242644
NM_015346.4(ZFYVE26):c.5241A>G (p.Gln1747=)
NM_015346.4(ZFYVE26):c.528T>C (p.Leu176=) rs2040215930
NM_015346.4(ZFYVE26):c.5402C>G (p.Ala1801Gly)
NM_015346.4(ZFYVE26):c.5510G>A (p.Arg1837His) rs776920735
NM_015346.4(ZFYVE26):c.5510G>C (p.Arg1837Pro) rs776920735
NM_015346.4(ZFYVE26):c.5835G>A (p.Arg1945=)
NM_015346.4(ZFYVE26):c.5880G>A (p.Arg1960=) rs751183425
NM_015346.4(ZFYVE26):c.6008A>G (p.Asp2003Gly) rs890614624
NM_015346.4(ZFYVE26):c.6357C>T (p.Pro2119=)
NM_015346.4(ZFYVE26):c.715C>T (p.Leu239=)
NM_015346.4(ZFYVE26):c.984G>A (p.Leu328=)

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.