ClinVar Miner

Submissions for variant NM_001039029.3(LRTM2):c.955G>A (p.Gly319Ser)

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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 RCV004640139 SCV005133048 uncertain significance not specified 2024-04-20 criteria provided, single submitter clinical testing The c.955G>A (p.G319S) alteration is located in exon 5 (coding exon 3) of the LRTM2 gene. This alteration results from a G to A substitution at nucleotide position 955, causing the glycine (G) at amino acid position 319 to be replaced by a serine (S). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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