ClinVar Miner

Submissions for variant NM_013385.5(CYTH4):c.40G>A (p.Gly14Arg)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV004907850 SCV005570756 uncertain significance not specified 2024-08-07 criteria provided, single submitter clinical testing The c.40G>A (p.G14R) alteration is located in exon 2 (coding exon 2) of the CYTH4 gene. This alteration results from a G to A substitution at nucleotide position 40, causing the glycine (G) at amino acid position 14 to be replaced by an arginine (R). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.
Department of Clinical Pathology, School of Medicine, Fujita Health University RCV004560221 SCV004217879 likely benign EBV-positive nodal T- and NK-cell lymphoma no assertion criteria provided research

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