ClinVar Miner

List of variants in gene CUBN reported by Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare

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Gene type:
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Total variants: 23
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HGVS dbSNP
NM_001081.3(CUBN):c.349C>A (p.Leu117Met) rs1588661287
NM_001081.3(CUBN):c.4459C>T (p.Arg1487Ter) rs145661597
NM_001081.3(CUBN):c.4921del (p.Tyr1641fs) rs1564443979
NM_001081.3(CUBN):c.4964C>G (p.Pro1655Arg) rs532968940
NM_001081.3(CUBN):c.5428C>T (p.Arg1810Ter) rs143944436
NM_001081.3(CUBN):c.5511dup (p.Gly1838fs) rs1168074679
NM_001081.3(CUBN):c.5600del (p.Phe1867fs) rs747417629
NM_001081.3(CUBN):c.6225G>A (p.Ser2075=) rs75737363
NM_001081.3(CUBN):c.7797C>G (p.Cys2599Trp) rs138758085
NM_001081.3(CUBN):c.8894T>C (p.Phe2965Ser) rs117620008
NM_001081.3(CUBN):c.9079G>A (p.Gly3027Arg) rs150202444
NM_001081.3(CUBN):c.9524C>A (p.Ser3175Ter) rs368697251
NM_001081.3(CUBN):c.9922T>C (p.Trp3308Arg) rs752843169
NM_001081.3(CUBN):c.9949C>T (p.Gln3317Ter) rs1564379463
NM_001081.4(CUBN):c.3473G>A (p.Trp1158Ter) rs1564492988
NM_001081.4(CUBN):c.3929T>C (p.Ile1310Thr) rs1588604587
NM_001081.4(CUBN):c.489+2_489+4dup rs1588658746
NM_001081.4(CUBN):c.4973del (p.Asn1658fs) rs1588511533
NM_001081.4(CUBN):c.5549-2A>C rs1564435513
NM_001081.4(CUBN):c.6088C>T (p.Arg2030Ter) rs374417889
NM_001081.4(CUBN):c.6125-2A>G rs75386064
NM_001081.4(CUBN):c.7534-1G>T rs1588639188
NM_001081.4(CUBN):c.9053A>C (p.Tyr3018Ser) rs370778353

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