ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.3421_3453del (p.Ala1141_Gly1151del)

dbSNP: rs1114167467
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000491788 SCV000579611 uncertain significance Hereditary cancer-predisposing syndrome 2016-12-07 criteria provided, single submitter clinical testing The c.3421_3453del33 variant (also known as p.A1141_G1151del) is located in coding exon 29 of the TSC2 gene. This variant results from an in-frame deletion of 33 nucleotides at positions 3421 to 3453. This results in the in-frame deletion of 11 amino acids at codons 1141 to 1151. This variant has been determined to be the result of a de novo mutation or germline mosaicism in one family. This amino acid position is poorly conserved in available vertebrate species. Since supporting evidence is limited at this time, the clinical significance of this variant remains unclear.

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