ClinVar Miner

Submissions for variant NM_001350162.2(TEX15):c.3279T>G (p.Tyr1093Ter)

dbSNP: rs864309485
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Research lab, Institute of Genetics and Molecular and Cellular Biology RCV000202575 SCV000222690 pathogenic Oligosynaptic infertility criteria provided, single submitter research autosomal recessive form of spermatogenic failure associated with defects in meiosis
OMIM RCV000626476 SCV000747131 pathogenic Spermatogenic failure 25 2015-10-01 no assertion criteria provided literature only

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