ClinVar Miner

Submissions for variant NM_001101648.2(NPC1L1):c.1529T>C (p.Met510Thr)

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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 RCV005387707 SCV006036928 uncertain significance not specified 2025-02-09 criteria provided, single submitter clinical testing The c.1529T>C (p.M510T) alteration is located in exon 2 (coding exon 2) of the NPC1L1 gene. This alteration results from a T to C substitution at nucleotide position 1529, causing the methionine (M) at amino acid position 510 to be replaced by a threonine (T). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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