ClinVar Miner

List of variants in gene CUL4B reported as uncertain significance for X-linked syndromic intellectual disability

Included ClinVar conditions (168):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_003588.3(CUL4B):c.1005_1007TAT[1] (p.Ile337del) rs1556214312
NM_003588.3(CUL4B):c.1160A>G (p.Gln387Arg) rs1556213268
NM_003588.3(CUL4B):c.117A>T (p.Arg39Ser) rs757541076
NM_003588.3(CUL4B):c.193A>G (p.Ser65Gly)
NM_003588.3(CUL4B):c.2577G>C (p.Lys859Asn) rs1556181426
NM_003588.3(CUL4B):c.348G>T (p.Gln116His) rs755306871
NM_003588.3(CUL4B):c.373C>G (p.Leu125Val) rs760294805
NM_003588.3(CUL4B):c.943G>A (p.Val315Ile)

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