ClinVar Miner

List of variants in gene CUL7 reported as likely benign for Three M syndrome

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Total variants: 8
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HGVS dbSNP
NM_014780.4(CUL7):c.-168C>T rs3737186
NM_014780.4(CUL7):c.1027C>T (p.Pro343Ser) rs113845886
NM_014780.4(CUL7):c.1202G>A (p.Arg401Gln) rs73733791
NM_014780.4(CUL7):c.1846A>G (p.Ser616Gly) rs7774330
NM_014780.4(CUL7):c.2555G>A (p.Arg852Gln) rs34574340
NM_014780.4(CUL7):c.3096C>T (p.Asp1032=) rs138276478
NM_014780.4(CUL7):c.4794G>A (p.Lys1598=) rs61437700
NM_014780.4(CUL7):c.4898C>T (p.Thr1633Met) rs139249497

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