ClinVar Miner

List of variants in gene CDK4 reported as uncertain significance for not provided

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Total variants: 21
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HGVS dbSNP
NM_000075.4(CDK4):c.-2G>A rs771607042
NM_000075.4(CDK4):c.122A>G (p.Asn41Ser) rs144890720
NM_000075.4(CDK4):c.132_143del (p.Gly45_Gly48del) rs749094206
NM_000075.4(CDK4):c.133G>T (p.Gly45Cys) rs876660318
NM_000075.4(CDK4):c.14G>A (p.Arg5Gln) rs1031329993
NM_000075.4(CDK4):c.219-10C>T rs759302811
NM_000075.4(CDK4):c.229G>A (p.Val77Ile) rs730881670
NM_000075.4(CDK4):c.245G>A (p.Arg82Gln) rs3211612
NM_000075.4(CDK4):c.255G>T (p.Arg85=) rs1565806692
NM_000075.4(CDK4):c.307T>A (p.Tyr103Asn) rs752767372
NM_000075.4(CDK4):c.352A>C (p.Lys118Gln) rs772689692
NM_000075.4(CDK4):c.364C>T (p.Arg122Cys) rs587778185
NM_000075.4(CDK4):c.385G>A (p.Asp129Asn) rs876660606
NM_000075.4(CDK4):c.397G>A (p.Ala133Thr) rs751684879
NM_000075.4(CDK4):c.409G>A (p.Val137Ile) rs150281463
NM_000075.4(CDK4):c.409G>C (p.Val137Leu) rs150281463
NM_000075.4(CDK4):c.431A>G (p.Glu144Gly) rs863224603
NM_000075.4(CDK4):c.458C>T (p.Thr153Ile) rs1443076952
NM_000075.4(CDK4):c.460G>C (p.Val154Leu) rs563692823
NM_000075.4(CDK4):c.553G>A (p.Val185Ile)
NM_000075.4(CDK4):c.625C>T (p.Arg209Cys) rs140644696

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