ClinVar Miner

List of variants in gene CREBBP reported as likely benign for not specified

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Total variants: 34
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HGVS dbSNP
NM_004380.2(CREBBP):c.1211G>C (p.Cys404Ser) rs587783462
NM_004380.2(CREBBP):c.1216+20C>A rs200567815
NM_004380.2(CREBBP):c.1331-4A>G rs756291909
NM_004380.2(CREBBP):c.1633T>C (p.Leu545=) rs371285951
NM_004380.2(CREBBP):c.2409C>T (p.Ser803=) rs139207930
NM_004380.2(CREBBP):c.2463+6G>A rs1555482647
NM_004380.2(CREBBP):c.2616G>A (p.Thr872=) rs781112420
NM_004380.2(CREBBP):c.2728A>G (p.Thr910Ala) rs143247685
NM_004380.2(CREBBP):c.333C>T (p.Asn111=) rs150229705
NM_004380.2(CREBBP):c.3698+7G>A rs374345970
NM_004380.2(CREBBP):c.383C>G (p.Ser128Cys) rs55790011
NM_004380.2(CREBBP):c.3889C>T (p.His1297Tyr) rs1057521558
NM_004380.2(CREBBP):c.4133+19T>C rs202204380
NM_004380.2(CREBBP):c.4280+8T>C rs376814421
NM_004380.2(CREBBP):c.4350C>T (p.Tyr1450=) rs144832179
NM_004380.2(CREBBP):c.4494A>G (p.Arg1498=) rs149560660
NM_004380.2(CREBBP):c.458C>T (p.Pro153Leu) rs146538907
NM_004380.2(CREBBP):c.4617T>C (p.Tyr1539=) rs727503891
NM_004380.2(CREBBP):c.5436C>G (p.Thr1812=) rs61731405
NM_004380.2(CREBBP):c.5829G>A (p.Pro1943=) rs546554430
NM_004380.2(CREBBP):c.5886C>A (p.Ile1962=) rs370565083
NM_004380.2(CREBBP):c.5934C>T (p.Asn1978=) rs754282387
NM_004380.2(CREBBP):c.6090G>A (p.Gln2030=) rs374969185
NM_004380.2(CREBBP):c.6606_6620del15 (p.Gln2212_Gln2216del) rs1555470941
NM_004380.2(CREBBP):c.6609A>G (p.Gln2203=) rs62636220
NM_004380.2(CREBBP):c.6618_6620dupGCA (p.Gln2216_Gly2217insGln) rs779647460
NM_004380.2(CREBBP):c.6624A>G (p.Gln2208=) rs142545779
NM_004380.2(CREBBP):c.6633_6641delACAGCAGCA (p.Gln2214_Gln2216del) rs746989288
NM_004380.2(CREBBP):c.701C>T (p.Ala234Val) rs727503892
NM_004380.2(CREBBP):c.7040C>T (p.Ala2347Val) rs182347573
NM_004380.2(CREBBP):c.712G>C (p.Val238Leu) rs146887252
NM_004380.2(CREBBP):c.7293G>A (p.Thr2431=) rs587783514
NM_004380.2(CREBBP):c.7302G>A (p.Thr2434=) rs144609433
NM_004380.2(CREBBP):c.760G>A (p.Ala254Thr) rs148781922

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