ClinVar Miner

List of variants in gene MCCC1 reported as likely benign for not provided

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Total variants: 15
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HGVS dbSNP
NM_020166.5(MCCC1):c.108A>G (p.Gln36=) rs1577367769
NM_020166.5(MCCC1):c.1146C>T (p.Phe382=) rs762544072
NM_020166.5(MCCC1):c.1356G>A (p.Arg452=) rs1345111200
NM_020166.5(MCCC1):c.1416C>T (p.Asn472=) rs1560219940
NM_020166.5(MCCC1):c.1486T>C (p.Leu496=) rs768167603
NM_020166.5(MCCC1):c.156C>A (p.Val52=) rs398124353
NM_020166.5(MCCC1):c.1732-9T>A rs370660849
NM_020166.5(MCCC1):c.1764T>C (p.Asn588=) rs200025893
NM_020166.5(MCCC1):c.1851T>C (p.Thr617=) rs1577239619
NM_020166.5(MCCC1):c.189G>A (p.Arg63=) rs753180751
NM_020166.5(MCCC1):c.192G>A (p.Val64=) rs1360164882
NM_020166.5(MCCC1):c.2085G>A (p.Lys695=) rs762296041
NM_020166.5(MCCC1):c.300C>G (p.Pro100=) rs747409426
NM_020166.5(MCCC1):c.54G>A (p.Arg18=) rs1577376491
NM_020166.5(MCCC1):c.956-8C>T rs1577284365

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