ClinVar Miner

Submissions for variant NM_012140.5(SLC25A10):c.763-37G>A

gnomAD frequency: 0.00053  dbSNP: rs200706742
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003457715 SCV004185092 likely benign not provided 2024-06-01 criteria provided, single submitter clinical testing SLC25A10: BP4, BS1
Mendelics RCV003492087 SCV004232620 benign Mitochondrial DNA depletion syndrome 19 2024-01-23 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003979918 SCV004786709 likely benign SLC25A10-related disorder 2024-01-27 criteria provided, single submitter clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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