ClinVar Miner

Submissions for variant NM_021913.5(AXL):c.1202A>G (p.Asn401Ser)

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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 RCV005296786 SCV005961405 uncertain significance not specified 2024-12-11 criteria provided, single submitter clinical testing The c.1202A>G (p.N401S) alteration is located in exon 9 (coding exon 9) of the AXL gene. This alteration results from a A to G substitution at nucleotide position 1202, causing the asparagine (N) at amino acid position 401 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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