ClinVar Miner

Submissions for variant NM_001350162.2(TEX15):c.9223G>A (p.Gly3075Arg)

gnomAD frequency: 0.00147  dbSNP: rs150606321
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000971550 SCV001119205 likely benign not provided 2017-07-14 criteria provided, single submitter clinical testing
Institute of Reproductive Genetics, University of Münster RCV001261893 SCV001439223 uncertain significance Non-obstructive azoospermia 2020-06-07 criteria provided, single submitter research
CeGaT Center for Human Genetics Tuebingen RCV000971550 SCV004164574 likely benign not provided 2023-08-01 criteria provided, single submitter clinical testing TEX15: BP4, BS2

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