ClinVar Miner

List of variants studied for Spermatogenic failure 48

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Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_001321739.2(M1AP):c.676dup (p.Trp226fs) rs144217347 0.00238
NM_001321739.2(M1AP):c.797G>A (p.Arg266Gln) rs149272394 0.00017
NM_001321739.2(M1AP):c.949G>A (p.Gly317Arg) rs140179344 0.00011
NM_001321739.2(M1AP):c.344C>T (p.Ala115Val) rs563816801 0.00003
NM_001321739.2(M1AP):c.1166C>T (p.Pro389Leu) rs751126701 0.00001
NM_001321739.2(M1AP):c.1408C>T (p.Arg470Ter)
NM_001321739.2(M1AP):c.1435-1G>A rs1677697539
NM_001321739.2(M1AP):c.595+3A>G rs2530458075

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