ClinVar Miner

Submissions for variant NM_001761.3(CCNF):c.1072G>A (p.Ala358Thr)

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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 RCV004604834 SCV005096507 uncertain significance not specified 2024-06-04 criteria provided, single submitter clinical testing The c.1072G>A (p.A358T) alteration is located in exon 10 (coding exon 10) of the CCNF gene. This alteration results from a G to A substitution at nucleotide position 1072, causing the alanine (A) at amino acid position 358 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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