ClinVar Miner

Submissions for variant NM_001761.3(CCNF):c.1808G>C (p.Ser603Thr)

dbSNP: rs1282355532
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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 RCV004299247 SCV003962468 uncertain significance not specified 2023-03-24 criteria provided, single submitter clinical testing The c.1808G>C (p.S603T) alteration is located in exon 16 (coding exon 16) of the CCNF gene. This alteration results from a G to C substitution at nucleotide position 1808, causing the serine (S) at amino acid position 603 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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