ClinVar Miner

Submissions for variant NM_003036.4(SKI):c.1528G>A (p.Ala510Thr) (rs61735580)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000195482 SCV000250681 uncertain significance not specified 2015-03-26 criteria provided, single submitter clinical testing p.Ala510Thr (A510T) GCC>ACC: c.1528 G>A in exon 5 of the SKI gene (NM_003036.3) A variant of unknown significance has been identified in the SKI gene. The A510T variant has not been published as a mutation or as a benign polymorphism to our knowledge. The A510T variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. In addition, this substitution occurs at a position that is conserved across mammals. However, in silico analysis is inconsistent in its predictions as to whether or not the variant is damaging to the protein structure/function. Additionally, the NHLBI Exome Sequencing Project reports A510T was observed in 7/4114 alleles (0.2%) from individuals of African American ancestry and the 1000 Genomes Project reports A510T was observed in 1/192 alleles (0.52%) from individuals of African Caribbean ancestry, indicating it may be a rare benign variant in these populations. Furthermore, no missense mutations in nearby residues have been reported in association with SGS, indicating this region of the protein may be tolerant of change. Therefore, based on the currently available information, it is unclear whether this variant is a pathogenic mutation or a rare benign variant. This variant was found in TAADV2-1
Invitae RCV000638898 SCV000760452 likely benign not provided 2018-12-25 criteria provided, single submitter clinical testing

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