ClinVar Miner

Submissions for variant NM_021913.5(AXL):c.2566A>T (p.Thr856Ser)

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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 RCV005296793 SCV005961415 uncertain significance not specified 2024-12-23 criteria provided, single submitter clinical testing The c.2566A>T (p.T856S) alteration is located in exon 20 (coding exon 20) of the AXL gene. This alteration results from a A to T substitution at nucleotide position 2566, causing the threonine (T) at amino acid position 856 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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