ClinVar Miner

List of variants in gene ZFYVE27 reported as benign for Spastic paraplegia

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_001385875.1(ZFYVE27):c.413G>T (p.Gly138Val) rs10882993 0.74523
NM_001385875.1(ZFYVE27):c.665-20G>T rs3750614 0.61549
NM_001385875.1(ZFYVE27):c.-1G>A rs3818876 0.51770
NM_001385875.1(ZFYVE27):c.456-12C>T rs12264401 0.04525
NM_001385875.1(ZFYVE27):c.244G>A (p.Val82Ile) rs17108378 0.02833
NM_001385875.1(ZFYVE27):c.572G>T (p.Gly191Val) rs35077384 0.02717
NM_001385875.1(ZFYVE27):c.378G>A (p.Lys126=) rs75060573 0.01901
NM_001385875.1(ZFYVE27):c.516C>T (p.Arg172=) rs116366646 0.00608
NM_001385875.1(ZFYVE27):c.32C>T (p.Pro11Leu) rs112316490 0.00564
NM_001385875.1(ZFYVE27):c.126C>T (p.Leu42=) rs17419023 0.00508
NM_001385875.1(ZFYVE27):c.62C>T (p.Ala21Val) rs140812293 0.00388
NM_001385875.1(ZFYVE27):c.238C>T (p.Leu80Phe) rs145356389 0.00204
NM_001385875.1(ZFYVE27):c.79C>G (p.Pro27Ala) rs34979921 0.00179
NM_001385875.1(ZFYVE27):c.876+15C>T rs202196759 0.00124
NM_001385875.1(ZFYVE27):c.269-16G>A rs117049029 0.00092
NM_001385875.1(ZFYVE27):c.522G>A (p.Leu174=) rs143515214 0.00035
NM_001385875.1(ZFYVE27):c.508G>A (p.Ala170Thr) rs555051885 0.00022
NM_001385875.1(ZFYVE27):c.1089+3G>A rs556454107
NM_001385875.1(ZFYVE27):c.897+19G>A

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