ClinVar Miner

Submissions for variant NM_000038.6(APC):c.4271C>T (p.Pro1424Leu)

dbSNP: rs1580645953
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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 RCV001022190 SCV001183893 uncertain significance Hereditary cancer-predisposing syndrome 2019-02-19 criteria provided, single submitter clinical testing The p.P1424L variant (also known as c.4271C>T), located in coding exon 15 of the APC gene, results from a C to T substitution at nucleotide position 4271. The proline at codon 1424 is replaced by leucine, an amino acid with similar properties. This amino acid position is highly conserved in available vertebrate species. In addition, the in silico prediction for this alteration is inconclusive. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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