ClinVar Miner

Submissions for variant NM_000089.4(COL1A2):c.3583_3597del (p.Cys1195_Thr1199del)

dbSNP: rs2115962258
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001969229 SCV002255379 likely pathogenic Osteogenesis imperfecta type I; Ehlers-Danlos syndrome, classic type, 1 2022-06-13 criteria provided, single submitter clinical testing In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has been observed in individual(s) with autosomal dominant osteogenesis imperfecta (Invitae). This variant is not present in population databases (gnomAD no frequency). This variant, c.3583_3597del, results in the deletion of 5 amino acid(s) of the COL1A2 protein (p.Cys1195_Thr1199del), but otherwise preserves the integrity of the reading frame.

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