ClinVar Miner

List of variants in gene HSPD1 reported as likely benign for Spastic paraplegia, autosomal dominant

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Total variants: 11
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HGVS dbSNP
NM_002156.4(HSPD1):c.-66T>C rs34519984
NM_002156.5(HSPD1):c.-3+15C>T rs59701865
NM_002156.5(HSPD1):c.1216-9C>T rs189395138
NM_002156.5(HSPD1):c.1360T>C (p.Leu454=) rs147135152
NM_002156.5(HSPD1):c.1446T>C (p.Asn482=) rs2303884
NM_002156.5(HSPD1):c.144C>T (p.Ala48=) rs11551346
NM_002156.5(HSPD1):c.1688G>C (p.Gly563Ala) rs41265953
NM_002156.5(HSPD1):c.18A>G (p.Thr6=) rs79630442
NM_002156.5(HSPD1):c.27C>G (p.Arg9=) rs11551349
NM_002156.5(HSPD1):c.561T>C (p.Ser187=) rs141357756
NM_002156.5(HSPD1):c.603A>G (p.Val201=) rs146598485

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