ClinVar Miner

List of variants in gene ZFYVE26 reported as likely benign for not specified

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Gene type:
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Total variants: 37
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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.1224G>T (p.Gly408=) rs17104689 0.03409
NM_015346.4(ZFYVE26):c.5484+13G>A rs140117984 0.00407
NM_015346.4(ZFYVE26):c.7371+18C>T rs149769693 0.00272
NM_015346.4(ZFYVE26):c.3722G>A (p.Arg1241Gln) rs140756827 0.00258
NM_015346.4(ZFYVE26):c.6405G>A (p.Leu2135=) rs76327447 0.00220
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.773G>A (p.Arg258Gln) rs150230201 0.00113
NM_015346.4(ZFYVE26):c.3051T>C (p.Ala1017=) rs138895639 0.00064
NM_015346.4(ZFYVE26):c.5654-10C>G rs183559101 0.00043
NM_015346.4(ZFYVE26):c.1369C>G (p.Leu457Val) rs201917832 0.00017
NM_015346.4(ZFYVE26):c.4035G>T (p.Val1345=) rs374530573 0.00009
NM_015346.4(ZFYVE26):c.6135C>T (p.Ala2045=) rs146209388 0.00009
NM_015346.4(ZFYVE26):c.4293G>C (p.Gln1431His) rs373740172 0.00008
NM_015346.4(ZFYVE26):c.684C>T (p.Pro228=) rs369761894 0.00008
NM_015346.4(ZFYVE26):c.991A>G (p.Asn331Asp) rs199630965 0.00007
NM_015346.4(ZFYVE26):c.4125G>A (p.Glu1375=) rs374188915 0.00004
NM_015346.4(ZFYVE26):c.6423G>A (p.Thr2141=) rs142448052 0.00004
NM_015346.4(ZFYVE26):c.2427C>T (p.Gly809=) rs144063215 0.00002
NM_015346.4(ZFYVE26):c.1819G>A (p.Gly607Arg) rs142015707 0.00001
NM_015346.4(ZFYVE26):c.2985C>T (p.Ala995=) rs772468217 0.00001
NM_015346.4(ZFYVE26):c.3819G>A (p.Pro1273=) rs752013494 0.00001
NM_015346.4(ZFYVE26):c.6645G>A (p.Gly2215=) rs1278427910 0.00001
NM_015346.4(ZFYVE26):c.864G>A (p.Pro288=) rs1360412471 0.00001
NM_015346.4(ZFYVE26):c.2067C>T (p.Leu689=) rs141880939
NM_015346.4(ZFYVE26):c.3210C>G (p.Pro1070=) rs7156492
NM_015346.4(ZFYVE26):c.3846T>G (p.Pro1282=) rs1057523453
NM_015346.4(ZFYVE26):c.4370G>A (p.Cys1457Tyr) rs2235967
NM_015346.4(ZFYVE26):c.4502C>T (p.Thr1501Met) rs201034965
NM_015346.4(ZFYVE26):c.6299A>G (p.Asn2100Ser) rs1043960451
NM_015346.4(ZFYVE26):c.7143G>A (p.Gly2381=) rs1555393351
NM_015346.4(ZFYVE26):c.887-13G>A

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