ClinVar Miner

Submissions for variant NM_001290043.2(TAP2):c.1144-5delinsAC

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago RCV003228182 SCV003924251 uncertain significance MHC class I deficiency 2021-03-30 criteria provided, single submitter clinical testing TAP2 NM_000544.3 exon 7 c.1144-6_1144-5delinsAC: This variant has not been reported in the literature and is not present in large control databases. This variant is present in ClinVar (Variation ID:466363). Evolutionary conservation and computational predictive tools for this variant are limited or unavailable. This variant is a deletion and insertion of 2 nucleotides at position 1144-6_1144-5; this variant is an intronic variant; splice prediction tools suggest that this variant may not affect splicing. However, further studies are needed to understand its impact. In summary, data on this variant is insufficient for disease classification. Therefore, the clinical significance of this variant is uncertain.

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