ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.3662T>C (p.Leu1221Pro)

dbSNP: rs1597720167
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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 RCV002319272 SCV001182359 uncertain significance Hereditary cancer-predisposing syndrome; Cardiovascular phenotype 2023-03-09 criteria provided, single submitter clinical testing The p.L1221P variant (also known as c.3662T>C), located in coding exon 27 of the NF1 gene, results from a T to C substitution at nucleotide position 3662. The leucine at codon 1221 is replaced by proline, an amino acid with similar properties. This amino acid position is highly conserved in available vertebrate species. In addition, this alteration is predicted to be deleterious by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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