ClinVar Miner

List of variants in gene CUX2 reported as benign for not provided

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_015267.4(CUX2):c.4414G>C (p.Val1472Leu) rs6490073 1.00000
NM_015267.4(CUX2):c.3918T>C (p.Asp1306=) rs3803167 0.35918
NM_015267.4(CUX2):c.2793G>C (p.Val931=) rs3742006 0.23200
NM_015267.4(CUX2):c.2270C>T (p.Ala757Val) rs114719470 0.01287
NM_015267.4(CUX2):c.2379C>T (p.Arg793=) rs112401949 0.01013
NM_015267.4(CUX2):c.436+4del rs145744067 0.00551
NM_015267.4(CUX2):c.1259-6T>C rs140435518 0.00419
NM_015267.4(CUX2):c.2643G>A (p.Pro881=) rs200061368 0.00401
NM_015267.4(CUX2):c.487C>T (p.Arg163Cys) rs202242120 0.00264
NM_015267.4(CUX2):c.81C>T (p.Val27=) rs190091435 0.00253
NM_015267.4(CUX2):c.1029G>A (p.Thr343=) rs199929446 0.00184
NM_015267.4(CUX2):c.4108G>A (p.Gly1370Arg) rs143575822 0.00124
NM_015267.4(CUX2):c.4010G>A (p.Gly1337Asp) rs201485891 0.00113
NM_015267.4(CUX2):c.417C>T (p.Pro139=) rs200963731 0.00101
NM_015267.4(CUX2):c.2604C>T (p.Tyr868=) rs183927879 0.00085
NM_015267.4(CUX2):c.3345C>T (p.Asn1115=) rs200333006 0.00083
NM_015267.4(CUX2):c.4298C>T (p.Pro1433Leu) rs200547493 0.00081
NM_015267.4(CUX2):c.2926+8C>T rs190095888 0.00066
NM_015267.4(CUX2):c.560+3G>A rs371759572 0.00001
NM_015267.4(CUX2):c.1796G>A (p.Arg599His)
NM_015267.4(CUX2):c.1944C>T (p.Asp648=)
NM_015267.4(CUX2):c.2500C>G (p.Pro834Ala)
NM_015267.4(CUX2):c.3754_3755insGCCCCC (p.Ser1252delinsCysProPro)
NM_015267.4(CUX2):c.430C>T (p.Pro144Ser)

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