ClinVar Miner

Submissions for variant NM_000168.6(GLI3):c.4010del (p.Ala1337fs)

dbSNP: rs1583728570
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001009115 SCV001168926 pathogenic not provided 2018-11-20 criteria provided, single submitter clinical testing The c.4010delC variant in the GLI3 gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. The c.4010delC variant causes a frameshift starting with codon Alanine 1337, changes this amino acid to a Glutamic acid residue, and creates a premature Stop codon at position 82 of the new reading frame, denoted p.Ala1337GlufsX82. This variant is predicted to cause loss of normal protein function through protein truncation. The c.4010delC variant is not observed in large population cohorts (Lek et al., 2016). We interpret c.4010delC as a pathogenic variant.

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