ClinVar Miner

Submissions for variant NM_001761.3(CCNF):c.1655T>C (p.Phe552Ser)

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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 RCV004896041 SCV005550885 uncertain significance not specified 2024-07-10 criteria provided, single submitter clinical testing The c.1655T>C (p.F552S) alteration is located in exon 15 (coding exon 15) of the CCNF gene. This alteration results from a T to C substitution at nucleotide position 1655, causing the phenylalanine (F) at amino acid position 552 to be replaced by a serine (S). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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