ClinVar Miner

List of variants in gene PIEZO1 reported as uncertain significance for not specified

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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_001142864.4(PIEZO1):c.3602C>T (p.Thr1201Met) rs372935580 0.00080
NM_001142864.4(PIEZO1):c.6905G>A (p.Arg2302His) rs200555745 0.00058
NM_001142864.4(PIEZO1):c.7471C>T (p.Arg2491Trp) rs201746476 0.00030
NM_001142864.4(PIEZO1):c.6154G>A (p.Val2052Ile) rs564395221 0.00024
NM_001142864.4(PIEZO1):c.3922C>G (p.Leu1308Val) rs532112751 0.00019
NM_001142864.4(PIEZO1):c.5068C>T (p.Leu1690Phe) rs992621550 0.00011
NM_001142864.4(PIEZO1):c.5822C>T (p.Pro1941Leu) rs761049480 0.00006
NM_001142864.4(PIEZO1):c.5615G>A (p.Arg1872His) rs1004130638 0.00004
NM_001142864.4(PIEZO1):c.352G>A (p.Ala118Thr) rs752004128 0.00003
NM_001142864.4(PIEZO1):c.3556G>A (p.Gly1186Arg) rs536842871 0.00001
NM_001142864.4(PIEZO1):c.3740T>G (p.Phe1247Cys) rs907173644 0.00001
NM_001142864.4(PIEZO1):c.5284C>T (p.Arg1762Cys) rs1184084921 0.00001
NM_001142864.4(PIEZO1):c.6421G>A (p.Asp2141Asn) rs781566440 0.00001
NM_001142864.4(PIEZO1):c.4211G>C (p.Arg1404Pro) rs565593847
NM_001142864.4(PIEZO1):c.4246G>A (p.Gly1416Arg)
NM_001142864.4(PIEZO1):c.4957C>T (p.Arg1653Cys)
NM_001142864.4(PIEZO1):c.5181G>C (p.Lys1727Asn)
NM_001142864.4(PIEZO1):c.5296A>C (p.Lys1766Gln)

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