ClinVar Miner

Submissions for variant NM_006767.4(LZTR1):c.2059_2060insT (p.Ala687fs)

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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 RCV003168002 SCV003861235 pathogenic Hereditary cancer-predisposing syndrome; Cardiovascular phenotype 2023-02-03 criteria provided, single submitter clinical testing The c.2059_2060insT variant, located in coding exon 17 of the LZTR1 gene, results from an insertion of one nucleotide at position 2059, causing a translational frameshift with a predicted alternate stop codon (p.A687Vfs*7). This alteration is expected to result in loss of function by premature protein truncation or nonsense-mediated mRNA decay. Loss-of-function variants in LZTR1 are related to an increased risk for schwannomas and autosomal recessive Noonan syndrome; however, such associations with autosomal dominant Noonan syndrome have not been observed (Piotrowski A et al. Nat Genet. 2014 Feb;46:182-7; Yamamoto GL et al. J Med Genet. 2015 Jun;52:413-21; Johnston JJ et al. Genet Med. 2018 10;20:1175-1185). Based on the supporting evidence, this variant is pathogenic for an increased risk of LZTR1-related schwannomatosis (SWN) and would be expected to cause autosomal recessive Noonan syndrome when present along with a second pathogenic or likely pathogenic variant on the other allele; however, the association of this alteration with autosomal dominant Noonan syndrome is unlikely.

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