ClinVar Miner

Submissions for variant NM_001101648.2(NPC1L1):c.2116G>A (p.Val706Met)

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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 RCV005387706 SCV006036927 uncertain significance not specified 2025-02-08 criteria provided, single submitter clinical testing The c.2116G>A (p.V706M) alteration is located in exon 6 (coding exon 6) of the NPC1L1 gene. This alteration results from a G to A substitution at nucleotide position 2116, causing the valine (V) at amino acid position 706 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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