ClinVar Miner

List of variants in gene ZFYVE27 reported as likely benign for Spastic paraplegia, autosomal dominant

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Gene type:
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Total variants: 21
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HGVS dbSNP
NM_144588.7(ZFYVE27):c.*1150C>T rs573448961
NM_144588.7(ZFYVE27):c.*1229dup rs373113574
NM_144588.7(ZFYVE27):c.*1310T>C rs147739377
NM_144588.7(ZFYVE27):c.*132C>T rs115982037
NM_144588.7(ZFYVE27):c.*1517G>C rs41290466
NM_144588.7(ZFYVE27):c.*163C>G rs41290464
NM_144588.7(ZFYVE27):c.*163C>T rs41290464
NM_144588.7(ZFYVE27):c.*413C>T rs181508408
NM_144588.7(ZFYVE27):c.*778C>T rs548911456
NM_144588.7(ZFYVE27):c.*894G>C rs534547830
NM_144588.7(ZFYVE27):c.1089+3G>A rs556454107
NM_144588.7(ZFYVE27):c.126C>T (p.Leu42=) rs17419023
NM_144588.7(ZFYVE27):c.244G>A (p.Val82Ile) rs17108378
NM_144588.7(ZFYVE27):c.32C>T (p.Pro11Leu) rs112316490
NM_144588.7(ZFYVE27):c.378G>A (p.Lys126=) rs75060573
NM_144588.7(ZFYVE27):c.508G>A (p.Ala170Thr) rs555051885
NM_144588.7(ZFYVE27):c.516C>T (p.Arg172=) rs116366646
NM_144588.7(ZFYVE27):c.572G>T (p.Gly191Val) rs35077384
NM_144588.7(ZFYVE27):c.62C>T (p.Ala21Val) rs140812293
NM_144588.7(ZFYVE27):c.79C>G (p.Pro27Ala) rs34979921
NM_144588.7(ZFYVE27):c.876+15C>T rs202196759

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