ClinVar Miner

List of variants in gene CUBN studied for not specified

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Total variants: 21
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HGVS dbSNP
NM_001081.3(CUBN):c.10295C>G (p.Thr3432Ser) rs7898873
NM_001081.3(CUBN):c.1681G>A (p.Asp561Asn) rs147449194
NM_001081.3(CUBN):c.2487G>A (p.Ser829=) rs1801225
NM_001081.3(CUBN):c.2496dup (p.Pro833fs) rs1554816715
NM_001081.3(CUBN):c.2594G>A (p.Ser865Asn) rs138083522
NM_001081.3(CUBN):c.2791+130G>A rs4747297
NM_001081.3(CUBN):c.2791+6A>C rs78549445
NM_001081.3(CUBN):c.4268C>T (p.Thr1423Met) rs483352704
NM_001081.3(CUBN):c.4376C>G (p.Ser1459Cys) rs138022214
NM_001081.3(CUBN):c.5069C>T (p.Ala1690Val) rs141640975
NM_001081.3(CUBN):c.5081-106_5081-105insTAGTGGCAAA rs778548191
NM_001081.3(CUBN):c.5304C>T (p.Ile1768=) rs61841454
NM_001081.3(CUBN):c.5856A>G (p.Ser1952=) rs1801234
NM_001081.3(CUBN):c.6479A>G (p.Asp2160Gly) rs144704318
NM_001081.3(CUBN):c.6613G>A (p.Gly2205Arg) rs140883483
NM_001081.3(CUBN):c.8720C>A (p.Ala2907Glu) rs758557930
NM_001081.3(CUBN):c.8894T>C (p.Phe2965Ser) rs117620008
NM_001081.3(CUBN):c.8905+137T>A rs780847
NM_001081.3(CUBN):c.8950A>G (p.Ile2984Val) rs1801239
NM_001081.3(CUBN):c.8968G>A (p.Val2990Ile) rs115888073
NM_001081.3(CUBN):c.9340G>A (p.Gly3114Ser) rs117035284

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