ClinVar Miner

Submissions for variant NM_012140.5(SLC25A10):c.657C>T (p.Pro219=)

gnomAD frequency: 0.00091  dbSNP: rs114621664
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV002248748 SCV002519365 uncertain significance not specified 2022-05-04 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003456408 SCV004185091 likely benign not provided 2023-11-01 criteria provided, single submitter clinical testing SLC25A10: BP4, BS1
Breakthrough Genomics, Breakthrough Genomics RCV003456408 SCV005193181 uncertain significance not provided criteria provided, single submitter not provided

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