ClinVar Miner

Submissions for variant NM_001039029.3(LRTM2):c.244G>A (p.Ala82Thr)

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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 RCV004940481 SCV005615264 uncertain significance not specified 2024-11-08 criteria provided, single submitter clinical testing The c.244G>A (p.A82T) alteration is located in exon 4 (coding exon 2) of the LRTM2 gene. This alteration results from a G to A substitution at nucleotide position 244, causing the alanine (A) at amino acid position 82 to be replaced by a threonine (T). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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