ClinVar Miner

Submissions for variant NM_007129.5(ZIC2):c.1388_1389insAGCGGCGGCGGCAGCGGCGGCGGCAGCGGCGGC (p.Ala470_Val471insAlaAlaAlaAlaAlaAlaAlaAlaAlaAlaAla)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002894069 SCV003232545 likely pathogenic Holoprosencephaly 5 2022-11-22 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 holoprosencephaly (Invitae). In at least one individual the variant was observed to be de novo. This variant is not present in population databases (gnomAD no frequency). This variant, c.1388_1389insAGCGGCGGCGGCAGCGGCGGCGGCAGCGGCGGC, results in the insertion of 11 amino acid(s) of the ZIC2 protein (p.Ala460_Ala470dup), but otherwise preserves the integrity of the reading frame.

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