ClinVar Miner

Submissions for variant NM_145654.4(RDM1):c.73G>A (p.Gly25Arg)

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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 RCV004862954 SCV005492280 uncertain significance not specified 2024-08-14 criteria provided, single submitter clinical testing The c.73G>A (p.G25R) alteration is located in exon 1 (coding exon 1) of the RDM1 gene. This alteration results from a G to A substitution at nucleotide position 73, causing the glycine (G) at amino acid position 25 to be replaced by an arginine (R). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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