ClinVar Miner

Submissions for variant NM_021913.5(AXL):c.1829G>T (p.Arg610Leu)

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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 RCV004880064 SCV005535956 uncertain significance not specified 2024-11-15 criteria provided, single submitter clinical testing The c.1829G>T (p.R610L) alteration is located in exon 16 (coding exon 16) of the AXL gene. This alteration results from a G to T substitution at nucleotide position 1829, causing the arginine (R) at amino acid position 610 to be replaced by a leucine (L). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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