ClinVar Miner

Submissions for variant NM_003386.3(ZAN):c.2624C>T (p.Thr875Met)

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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 RCV004268627 SCV003887244 uncertain significance not specified 2023-01-23 criteria provided, single submitter clinical testing The c.2624C>T (p.T875M) alteration is located in exon 14 (coding exon 13) of the ZAN gene. This alteration results from a C to T substitution at nucleotide position 2624, causing the threonine (T) at amino acid position 875 to be replaced by a methionine (M). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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