ClinVar Miner

Submissions for variant NM_013275.6(ANKRD11):c.6052_6060del (p.Pro2018_Ala2020del)

dbSNP: rs775221712
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000785126 SCV000923688 uncertain significance KBG syndrome 2019-01-01 criteria provided, single submitter clinical testing
Invitae RCV000785126 SCV003227627 uncertain significance KBG syndrome 2024-01-08 criteria provided, single submitter clinical testing This variant, c.6052_6060del, results in the deletion of 3 amino acid(s) of the ANKRD11 protein (p.Pro2018_Ala2020del), but otherwise preserves the integrity of the reading frame. This variant is present in population databases (rs775221712, gnomAD 0.03%). This variant has not been reported in the literature in individuals affected with ANKRD11-related conditions. ClinVar contains an entry for this variant (Variation ID: 634602). Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.
Ambry Genetics RCV002536878 SCV003695490 likely benign Inborn genetic diseases 2022-06-03 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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