ClinVar Miner

List of variants in gene ZFYVE26 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_015346.4(ZFYVE26):c.5260G>A (p.Ala1754Thr) rs146968463 0.00045
NM_015346.4(ZFYVE26):c.6448C>T (p.Pro2150Ser) rs138423670 0.00042
NM_015346.4(ZFYVE26):c.3847A>G (p.Thr1283Ala) rs116139296 0.00036
NM_015346.4(ZFYVE26):c.3950C>T (p.Thr1317Met) rs143719747 0.00031
NM_015346.4(ZFYVE26):c.6154G>A (p.Val2052Ile) rs201273304 0.00018
NM_015346.4(ZFYVE26):c.3662T>A (p.Leu1221Gln) rs554371710 0.00015
NM_015346.4(ZFYVE26):c.4884C>A (p.His1628Gln) rs764247596 0.00014
NM_015346.4(ZFYVE26):c.5927C>T (p.Thr1976Met) rs149744465 0.00014
NM_015346.4(ZFYVE26):c.961A>C (p.Lys321Gln) rs375820273 0.00011
NM_015346.4(ZFYVE26):c.763C>T (p.Arg255Trp) rs267604034 0.00007
NM_015346.4(ZFYVE26):c.827G>A (p.Gly276Asp) rs201273988 0.00006
NM_015346.4(ZFYVE26):c.296G>A (p.Arg99Gln) rs758392268 0.00004
NM_015346.4(ZFYVE26):c.1436-3C>G rs775709247 0.00003
NM_015346.4(ZFYVE26):c.397G>A (p.Gly133Ser) rs199505106 0.00003
NM_015346.4(ZFYVE26):c.6190G>A (p.Gly2064Arg) rs368378082 0.00003
NM_015346.4(ZFYVE26):c.7231C>T (p.Arg2411Cys) rs375202089 0.00003
NM_015346.4(ZFYVE26):c.2539G>A (p.Ala847Thr) rs570114196 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.1228T>C (p.Trp410Arg) rs774078953 0.00001
NM_015346.4(ZFYVE26):c.1272-10T>C rs773153713 0.00001
NM_015346.4(ZFYVE26):c.3201G>A (p.Met1067Ile) rs752207692 0.00001
NM_015346.4(ZFYVE26):c.4427G>A (p.Arg1476Gln) rs202124427 0.00001
NM_015346.4(ZFYVE26):c.6679A>G (p.Ile2227Val) rs1018266195 0.00001
NM_015346.4(ZFYVE26):c.6757A>G (p.Ile2253Val) rs202150854 0.00001
NM_015346.4(ZFYVE26):c.7364C>T (p.Pro2455Leu) rs751465927 0.00001
NM_015346.4(ZFYVE26):c.2060C>A (p.Ala687Asp) rs1168269050
NM_015346.4(ZFYVE26):c.2228T>A (p.Val743Glu) rs2140242584
NM_015346.4(ZFYVE26):c.2747C>T (p.Ala916Val) rs2140233873
NM_015346.4(ZFYVE26):c.2909C>T (p.Pro970Leu)
NM_015346.4(ZFYVE26):c.308A>T (p.Glu103Val) rs750426190
NM_015346.4(ZFYVE26):c.3248_3253del (p.Leu1083_Ser1084del) rs761454264
NM_015346.4(ZFYVE26):c.3791G>A (p.Cys1264Tyr)
NM_015346.4(ZFYVE26):c.4015C>T (p.Leu1339Phe) rs2140223225
NM_015346.4(ZFYVE26):c.4048G>A (p.Glu1350Lys)
NM_015346.4(ZFYVE26):c.4108C>T (p.Leu1370Phe)
NM_015346.4(ZFYVE26):c.4198G>A (p.Val1400Ile)
NM_015346.4(ZFYVE26):c.4304T>G (p.Val1435Gly)
NM_015346.4(ZFYVE26):c.4804C>G (p.Arg1602Gly) rs558285072
NM_015346.4(ZFYVE26):c.5216G>A (p.Arg1739Gln) rs201566214
NM_015346.4(ZFYVE26):c.5321G>C (p.Gly1774Ala) rs756963060
NM_015346.4(ZFYVE26):c.5455A>G (p.Met1819Val)
NM_015346.4(ZFYVE26):c.5510G>T (p.Arg1837Leu)
NM_015346.4(ZFYVE26):c.5530A>G (p.Ser1844Gly)
NM_015346.4(ZFYVE26):c.5822T>C (p.Leu1941Pro) rs1064796739
NM_015346.4(ZFYVE26):c.5838_5839delinsTGCACAGT (p.Ser1947delinsAlaGlnCys) rs2140199578
NM_015346.4(ZFYVE26):c.6001C>T (p.Leu2001Phe) rs2140199238
NM_015346.4(ZFYVE26):c.6110G>C (p.Arg2037Thr)
NM_015346.4(ZFYVE26):c.6155T>C (p.Val2052Ala)
NM_015346.4(ZFYVE26):c.6415C>T (p.Leu2139Phe) rs771935696
NM_015346.4(ZFYVE26):c.6751T>C (p.Tyr2251His) rs947209355
NM_015346.4(ZFYVE26):c.6923G>A (p.Arg2308His)
NM_015346.4(ZFYVE26):c.737C>A (p.Ala246Asp)
NM_015346.4(ZFYVE26):c.7412A>G (p.Asn2471Ser) rs2038625442
NM_015346.4(ZFYVE26):c.7463T>C (p.Ile2488Thr) rs976321163
NM_015346.4(ZFYVE26):c.756T>G (p.Ser252Arg)
NM_015346.4(ZFYVE26):c.896A>T (p.Asp299Val) rs2140251095

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