ClinVar Miner

List of variants in gene CUBN reported as likely benign for not provided

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Gene type:
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Total variants: 35
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HGVS dbSNP
NM_001081.3(CUBN):c.1681G>A (p.Asp561Asn) rs147449194
NM_001081.3(CUBN):c.1811C>T (p.Pro604Leu) rs200537125
NM_001081.3(CUBN):c.2656G>A (p.Glu886Lys) rs138545198
NM_001081.3(CUBN):c.2922C>T (p.Phe974=) rs201802902
NM_001081.3(CUBN):c.4206C>T (p.Phe1402=) rs563089365
NM_001081.3(CUBN):c.9267C>T (p.Thr3089=) rs200124646
NM_001081.4(CUBN):c.10605G>A (p.Thr3535=) rs779258017
NM_001081.4(CUBN):c.10722G>A (p.Gly3574=) rs1461042186
NM_001081.4(CUBN):c.1236T>C (p.Thr412=) rs201404467
NM_001081.4(CUBN):c.1659C>T (p.Leu553=) rs1588641562
NM_001081.4(CUBN):c.1765+9G>A rs780944597
NM_001081.4(CUBN):c.2632A>G (p.Ser878Gly) rs563114115
NM_001081.4(CUBN):c.2706G>T (p.Val902=) rs375569366
NM_001081.4(CUBN):c.4998C>T (p.His1666=) rs1588511492
NM_001081.4(CUBN):c.5151C>T (p.Val1717=) rs533873170
NM_001081.4(CUBN):c.5196C>T (p.Thr1732=) rs182162293
NM_001081.4(CUBN):c.5757C>T (p.His1919=) rs79184887
NM_001081.4(CUBN):c.5841C>T (p.Ser1947=) rs199868206
NM_001081.4(CUBN):c.5949G>A (p.Arg1983=) rs1202641067
NM_001081.4(CUBN):c.6048C>T (p.Thr2016=) rs770723197
NM_001081.4(CUBN):c.6125-5C>T rs767744034
NM_001081.4(CUBN):c.6312G>A (p.Thr2104=) rs768950272
NM_001081.4(CUBN):c.6366C>A (p.Val2122=) rs774532398
NM_001081.4(CUBN):c.6822-6C>T rs762758607
NM_001081.4(CUBN):c.6849G>A (p.Arg2283=) rs373804380
NM_001081.4(CUBN):c.7215C>T (p.Asn2405=) rs762398338
NM_001081.4(CUBN):c.7300G>A (p.Gly2434Ser) rs144565631
NM_001081.4(CUBN):c.7346T>G (p.Met2449Arg) rs41301097
NM_001081.4(CUBN):c.7534-5A>G rs769047632
NM_001081.4(CUBN):c.7557C>T (p.Asn2519=) rs1588639145
NM_001081.4(CUBN):c.783G>A (p.Thr261=) rs770878354
NM_001081.4(CUBN):c.7899C>T (p.Leu2633=) rs751019710
NM_001081.4(CUBN):c.8613T>G (p.Thr2871=) rs775837120
NM_001081.4(CUBN):c.8874C>T (p.Val2958=) rs763368350
NM_001081.4(CUBN):c.9237-10C>T rs768128551

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