ClinVar Miner

List of variants in gene ZFYVE27 studied for Spastic paraplegia, autosomal dominant

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Gene type:
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Total variants: 47
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HGVS dbSNP
NM_001002261.3(ZFYVE27):c.*1074C>G rs543023183
NM_001002261.3(ZFYVE27):c.*1148C>T rs371748674
NM_001002261.3(ZFYVE27):c.*1150C>T rs573448961
NM_001002261.3(ZFYVE27):c.*1195C>T rs540494473
NM_001002261.3(ZFYVE27):c.*1229dupG rs373113574
NM_001002261.3(ZFYVE27):c.*1283C>T rs886047531
NM_001002261.3(ZFYVE27):c.*1308A>C rs1047537
NM_001002261.3(ZFYVE27):c.*1310T>C rs147739377
NM_001002261.3(ZFYVE27):c.*132C>T rs115982037
NM_001002261.3(ZFYVE27):c.*1340G>C rs886047532
NM_001002261.3(ZFYVE27):c.*1379G>A rs13389
NM_001002261.3(ZFYVE27):c.*1411A>G rs567464767
NM_001002261.3(ZFYVE27):c.*1450G>A rs886047533
NM_001002261.3(ZFYVE27):c.*1472C>T rs528359630
NM_001002261.3(ZFYVE27):c.*1517G>C rs41290466
NM_001002261.3(ZFYVE27):c.*163C>G rs41290464
NM_001002261.3(ZFYVE27):c.*163C>T rs41290464
NM_001002261.3(ZFYVE27):c.*223G>C rs886047527
NM_001002261.3(ZFYVE27):c.*248T>C rs3814559
NM_001002261.3(ZFYVE27):c.*367G>A rs3814560
NM_001002261.3(ZFYVE27):c.*40A>G rs1981237
NM_001002261.3(ZFYVE27):c.*413C>T rs181508408
NM_001002261.3(ZFYVE27):c.*678A>C rs886047528
NM_001002261.3(ZFYVE27):c.*696G>A rs4244329
NM_001002261.3(ZFYVE27):c.*778C>T rs548911456
NM_001002261.3(ZFYVE27):c.*894G>C rs534547830
NM_001002261.3(ZFYVE27):c.*945G>A rs886047529
NM_001002261.3(ZFYVE27):c.-1G>A rs3818876
NM_001002261.3(ZFYVE27):c.1104+3G>A rs556454107
NM_001002261.3(ZFYVE27):c.1182C>A (p.Ala394=) rs768113258
NM_001002261.3(ZFYVE27):c.126C>T (p.Leu42=) rs17419023
NM_001002261.3(ZFYVE27):c.244G>A (p.Val82Ile) rs17108378
NM_001002261.3(ZFYVE27):c.32C>T (p.Pro11Leu) rs112316490
NM_001002261.3(ZFYVE27):c.378G>A (p.Lys126=) rs75060573
NM_001002261.3(ZFYVE27):c.386G>A (p.Ser129Asn) rs763464659
NM_001002261.3(ZFYVE27):c.413G>T (p.Gly138Val) rs10882993
NM_001002261.3(ZFYVE27):c.424C>T (p.Arg142Cys) rs145746084
NM_001002261.3(ZFYVE27):c.456-12C>T rs12264401
NM_001002261.3(ZFYVE27):c.508G>A (p.Ala170Thr) rs555051885
NM_001002261.3(ZFYVE27):c.516C>T (p.Arg172=) rs116366646
NM_001002261.3(ZFYVE27):c.522G>A (p.Leu174=) rs143515214
NM_001002261.3(ZFYVE27):c.572G>T (p.Gly191Val) rs35077384
NM_001002261.3(ZFYVE27):c.62C>T (p.Ala21Val) rs140812293
NM_001002261.3(ZFYVE27):c.797C>T (p.Pro266Leu) rs886047525
NM_001002261.3(ZFYVE27):c.79C>G (p.Pro27Ala) rs34979921
NM_001002261.3(ZFYVE27):c.891+15C>T rs202196759
NM_001002261.3(ZFYVE27):c.929C>T (p.Ala310Val) rs886047526

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