ClinVar Miner

List of variants in gene CUL3 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (916):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_003590.5(CUL3):c.*1774G>T rs13016316
NM_003590.5(CUL3):c.*2073A>G rs10498161
NM_003590.5(CUL3):c.*2192T>C rs3768898
NM_003590.5(CUL3):c.*2193G>A rs73993899
NM_003590.5(CUL3):c.*2431G>T rs10498160
NM_003590.5(CUL3):c.*2653G>A rs3768899
NM_003590.5(CUL3):c.*3148A>G rs17479770
NM_003590.5(CUL3):c.*3367T>C rs4674908
NM_003590.5(CUL3):c.*3672T>C rs2396092
NM_003590.5(CUL3):c.*3736del rs5839066
NM_003590.5(CUL3):c.*3789C>T rs4234054
NM_003590.5(CUL3):c.*3991A>G rs12470077
NM_003590.5(CUL3):c.*940C>T rs3768897
NM_003590.5(CUL3):c.1485+13G>A rs3754629
NM_003590.5(CUL3):c.1699G>A (p.Val567Ile) rs3738952
NM_003590.5(CUL3):c.1992A>G (p.Gln664=) rs2070127

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