ClinVar Miner

List of variants in gene CREBBP reported as benign by Genetic Services Laboratory, University of Chicago

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Total variants: 25
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HGVS dbSNP
NM_001079846.1(CREBBP):c.1537C>A (p.Leu513Ile) rs61753381
NM_001079846.1(CREBBP):c.1839T>C (p.Tyr613=) rs130003
NM_001079846.1(CREBBP):c.2458C>T (p.Pro820Ser) rs145733598
NM_001079846.1(CREBBP):c.2670G>A (p.Pro890=) rs3025694
NM_001079846.1(CREBBP):c.2827G>A (p.Ala943Thr) rs61753380
NM_001079846.1(CREBBP):c.2859C>T (p.Asp953=) rs142528559
NM_001079846.1(CREBBP):c.2860G>A (p.Val954Ile) rs61731383
NM_001079846.1(CREBBP):c.3723-8C>T rs3025684
NM_001079846.1(CREBBP):c.3786C>A (p.Ile1262=) rs129974
NM_001079846.1(CREBBP):c.4019+19T>C rs202204380
NM_001079846.1(CREBBP):c.4446+14A>G rs200934101
NM_001079846.1(CREBBP):c.4446+7G>A rs587783498
NM_001079846.1(CREBBP):c.459G>A (p.Pro153=) rs56388626
NM_001079846.1(CREBBP):c.4615-14G>C rs130008
NM_001079846.1(CREBBP):c.5322C>G (p.Thr1774=) rs61731405
NM_001079846.1(CREBBP):c.5340G>A (p.Val1780=) rs61754523
NM_001079846.1(CREBBP):c.5819A>G (p.Asn1940Ser) rs112906840
NM_001079846.1(CREBBP):c.5874C>T (p.Ala1958=) rs181646656
NM_001079846.1(CREBBP):c.5889T>C (p.Asn1963=) rs200998860
NM_001079846.1(CREBBP):c.6507A>G (p.Gln2169=) rs55960450
NM_001079846.1(CREBBP):c.6510A>C (p.Gln2170His) rs142545779
NM_001079846.1(CREBBP):c.6597C>T (p.Pro2199=) rs3751845
NM_001079846.1(CREBBP):c.6984G>C (p.Arg2328=) rs587783513
NM_001079846.1(CREBBP):c.7098A>G (p.Glu2366=) rs55916120
NM_001079846.1(CREBBP):c.939T>C (p.Asp313=) rs3025702

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