ClinVar Miner

List of variants reported as likely pathogenic for Abnormal facial shape; Abnormality of blood and blood-forming tissues; Abnormality of the immune system; Postnatal growth retardation; Neurodevelopmental abnormality

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Total variants: 9
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NM_001791.4(CDC42):c.191A>G (p.Tyr64Cys) rs864309721
NM_001791.4(CDC42):c.196A>G (p.Arg66Gly) rs797044870
NM_001791.4(CDC42):c.203G>A (p.Arg68Gln) rs1553196096
NM_001791.4(CDC42):c.242G>T (p.Cys81Phe) rs1553196100
NM_001791.4(CDC42):c.247T>C (p.Ser83Pro) rs1553196101
NM_001791.4(CDC42):c.476C>T (p.Ala159Val) rs1553196134
NM_001791.4(CDC42):c.511G>A (p.Glu171Lys) rs1553196539
NM_001791.4(CDC42):c.62T>C (p.Ile21Thr) rs1064795845
NM_001791.4(CDC42):c.68A>G (p.Tyr23Cys) rs797044916

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