ClinVar Miner

List of variants in gene CAMK2B reported by Ambry Genetics

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Gene type:
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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_001220.5(CAMK2B):c.1340-2A>T rs142386444 0.00046
NM_001220.5(CAMK2B):c.1276C>T (p.Pro426Ser) rs376228133 0.00039
NM_001220.5(CAMK2B):c.1597+2T>C rs772511617 0.00012
NM_001220.5(CAMK2B):c.1568C>T (p.Pro523Leu) rs371087765 0.00006
NM_001220.5(CAMK2B):c.1645G>A (p.Val549Ile) rs771606853 0.00006
NM_001220.5(CAMK2B):c.1939G>A (p.Asp647Asn) rs1489151076 0.00003
NM_001220.5(CAMK2B):c.1642G>A (p.Ala548Thr) rs373065396 0.00002
NM_001220.5(CAMK2B):c.1067C>T (p.Thr356Met) rs774876084 0.00001
NM_001220.5(CAMK2B):c.1361T>C (p.Leu454Pro) rs1344342135 0.00001
NM_001220.5(CAMK2B):c.1369G>A (p.Val457Met) rs755307162 0.00001
NM_001220.5(CAMK2B):c.1399G>A (p.Glu467Lys) rs374476287 0.00001
NM_001220.5(CAMK2B):c.1010T>C (p.Leu337Pro)
NM_001220.5(CAMK2B):c.1031T>C (p.Leu344Ser)
NM_001220.5(CAMK2B):c.1117C>T (p.Pro373Ser)
NM_001220.5(CAMK2B):c.125C>G (p.Ala42Gly)
NM_001220.5(CAMK2B):c.1267T>G (p.Ser423Ala)
NM_001220.5(CAMK2B):c.416C>T (p.Pro139Leu) rs1554389088
NM_001220.5(CAMK2B):c.448G>C (p.Gly150Arg) rs2096701703
NM_001220.5(CAMK2B):c.4G>T (p.Ala2Ser)
NM_001220.5(CAMK2B):c.523G>A (p.Ala175Thr) rs2096699885
NM_001220.5(CAMK2B):c.764T>C (p.Ile255Thr)
NM_001220.5(CAMK2B):c.901A>G (p.Lys301Glu) rs1554385111
NM_001220.5(CAMK2B):c.977T>G (p.Met326Arg) rs1239169240

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