ClinVar Miner

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

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Total variants: 8
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HGVS dbSNP
GRCh37/hg19 10p13(chr10:16949550-16975190)x3
GRCh37/hg19 10p13(chr10:17086636-17133683)x1
GRCh37/hg19 10p13(chr10:17098935-17101476)x1
NM_001081.3(CUBN):c.10265C>T (p.Thr3422Ile) rs1801230
NM_001081.3(CUBN):c.2188C>T (p.His730Tyr) rs7905349
NM_001081.3(CUBN):c.3522C>T (p.Gly1174=) rs1873469
NM_001081.3(CUBN):c.5098G>A (p.Asp1700Asn) rs116114483
NM_001081.3(CUBN):c.5803A>G (p.Ser1935Gly) rs41289305

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