ClinVar Miner

List of variants in gene TCTN3 reported as likely benign for Joubert syndrome

Included ClinVar conditions (57):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_015631.5(TCTN3):c.1425G>A (p.Arg475=) rs144543830
NM_015631.5(TCTN3):c.946A>G (p.Thr316Ala) rs200042949
NM_015631.5(TCTN3):c.9C>A (p.Thr3=) rs1471002377

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