ClinVar Miner

List of variants in gene CUBN reported by Mayo Clinic Laboratories, Mayo Clinic

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_001081.4(CUBN):c.6125-2A>G rs75386064 0.00226
NM_001081.4(CUBN):c.10119C>A (p.Val3373=) rs139596037 0.00163
NM_001081.4(CUBN):c.5069C>T (p.Ala1690Val) rs141640975 0.00155
NM_001081.4(CUBN):c.10105A>G (p.Ser3369Gly) rs145023719 0.00070
NM_001081.4(CUBN):c.3G>T (p.Met1Ile) rs11254385 0.00068
NM_001081.4(CUBN):c.4669C>T (p.Leu1557Phe) rs140970422 0.00064
NM_001081.4(CUBN):c.5626T>G (p.Ser1876Ala) rs145026134 0.00055
NM_001081.4(CUBN):c.6091A>G (p.Thr2031Ala) rs150392211 0.00034
NM_001081.4(CUBN):c.3116A>G (p.Tyr1039Cys) rs150014503 0.00031
NM_001081.4(CUBN):c.8071G>A (p.Gly2691Arg) rs1801237 0.00022
NM_001081.4(CUBN):c.5926+5G>A rs143301088 0.00019
NM_001081.4(CUBN):c.7837A>C (p.Ile2613Leu) rs144626884 0.00016
NM_001081.4(CUBN):c.6764C>T (p.Pro2255Leu) rs368964066 0.00015
NM_001081.4(CUBN):c.2738G>C (p.Ser913Thr) rs201589187 0.00012
NM_001081.4(CUBN):c.4A>G (p.Met2Val) rs200499216 0.00007
NM_001081.4(CUBN):c.5758G>A (p.Ala1920Thr) rs770772474 0.00002
NM_001081.4(CUBN):c.6916T>C (p.Trp2306Arg) rs1322005237 0.00002
NM_001081.4(CUBN):c.3829+1G>A rs1349644537 0.00001
NM_001081.4(CUBN):c.4268C>T (p.Thr1423Met) rs483352704 0.00001
NM_001081.4(CUBN):c.5738A>G (p.Tyr1913Cys) rs1474834640 0.00001
NM_001081.4(CUBN):c.2753A>G (p.Asn918Ser)
NM_001081.4(CUBN):c.349-6T>A rs1837201696
NM_001081.4(CUBN):c.3491-24T>C
NM_001081.4(CUBN):c.3823C>T (p.Arg1275Trp) rs189294363
NM_001081.4(CUBN):c.4838G>T (p.Arg1613Leu) rs147343635
NM_001081.4(CUBN):c.6959A>G (p.Asn2320Ser)

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