ClinVar Miner

List of variants in gene CUL4B reported as uncertain significance for developmental disorder of mental health

Included ClinVar conditions (728):
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Gene type:
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Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_001079872.2(CUL4B):c.1309G>A (p.Ala437Thr) rs757649304 0.00002
NM_001079872.2(CUL4B):c.1201A>C (p.Lys401Gln) rs750866615 0.00001
NM_001079872.2(CUL4B):c.889G>A (p.Val297Ile) rs367660624 0.00001
NM_001079872.2(CUL4B):c.1083A>G (p.Gln361=)
NM_001079872.2(CUL4B):c.1106A>G (p.Gln369Arg) rs1556213268
NM_001079872.2(CUL4B):c.1130G>A (p.Arg377Gln)
NM_001079872.2(CUL4B):c.1157T>C (p.Leu386Ser) rs1300720472
NM_001079872.2(CUL4B):c.1399G>T (p.Gly467Cys)
NM_001079872.2(CUL4B):c.1480G>A (p.Asp494Asn) rs2147329944
NM_001079872.2(CUL4B):c.1588T>C (p.Phe530Leu) rs1923920343
NM_001079872.2(CUL4B):c.1598T>G (p.Phe533Cys) rs1923919394
NM_001079872.2(CUL4B):c.1651T>A (p.Ser551Thr) rs2147328768
NM_001079872.2(CUL4B):c.1738T>C (p.Tyr580His) rs1923849803
NM_001079872.2(CUL4B):c.1743C>T (p.Gly581=)
NM_001079872.2(CUL4B):c.1747G>T (p.Asp583Tyr)
NM_001079872.2(CUL4B):c.1835T>C (p.Leu612Pro) rs2147328180
NM_001079872.2(CUL4B):c.1852+3A>G
NM_001079872.2(CUL4B):c.1853-13A>G
NM_001079872.2(CUL4B):c.2092C>T (p.His698Tyr) rs2147325555
NM_001079872.2(CUL4B):c.2356G>A (p.Asp786Asn)
NM_001079872.2(CUL4B):c.2390A>T (p.Lys797Ile)
NM_001079872.2(CUL4B):c.2404A>T (p.Arg802Trp)
NM_001079872.2(CUL4B):c.2506A>G (p.Ile836Val)
NM_001079872.2(CUL4B):c.2523G>C (p.Lys841Asn) rs1556181426
NM_001079872.2(CUL4B):c.2592+3A>T
NM_001079872.2(CUL4B):c.2650G>A (p.Asp884Asn) rs1922994124
NM_001079872.2(CUL4B):c.2652T>G (p.Asp884Glu) rs768424127
NM_001079872.2(CUL4B):c.2677dup (p.Tyr893fs) rs2147314730
NM_001079872.2(CUL4B):c.695A>T (p.Tyr232Phe)
NM_001079872.2(CUL4B):c.811A>T (p.Ile271Phe)
NM_001079872.2(CUL4B):c.881G>T (p.Arg294Ile) rs866840262
NM_001079872.2(CUL4B):c.911C>T (p.Pro304Leu)
NM_001079872.2(CUL4B):c.920+9G>A
NM_001079872.2(CUL4B):c.925A>T (p.Met309Leu)
NM_001079872.2(CUL4B):c.932T>A (p.Leu311Gln)
NM_001079872.2(CUL4B):c.951TAT[1] (p.Ile319del) rs1556214312
NM_001079872.2(CUL4B):c.986T>C (p.Ile329Thr)
NM_001079872.2(CUL4B):c.988G>C (p.Asp330His)
NM_001079872.2(CUL4B):c.995T>C (p.Ile332Thr) rs1924204795
NM_003588.4(CUL4B):c.29A>C (p.Asp10Ala) rs2147360370
NM_003588.4(CUL4B):c.46G>C (p.Ala16Pro)
NM_003588.4(CUL4B):c.5T>C (p.Met2Thr)

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