ClinVar Miner

List of variants studied for Spermatogenic failure 25

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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_001350162.2(TEX15):c.3563C>T (p.Ala1188Val) rs117788795 0.00427
NM_001350162.2(TEX15):c.4945G>A (p.Val1649Ile) rs76147771 0.00252
NM_001350162.2(TEX15):c.8838T>G (p.Ile2946Met) rs145215857 0.00218
NM_001350162.2(TEX15):c.3838A>G (p.Thr1280Ala) rs144234582 0.00074
NM_001350162.2(TEX15):c.1261G>A (p.Gly421Ser) rs951031727 0.00025
NM_001350162.2(TEX15):c.8083C>T (p.Arg2695Ter) rs763654373 0.00004
NM_001350162.2(TEX15):c.1624A>T (p.Ile542Phe)
NM_001350162.2(TEX15):c.1774A>G (p.Ile592Val)
NM_001350162.2(TEX15):c.2134C>T (p.Gln712Ter)
NM_001350162.2(TEX15):c.2441C>T (p.Pro814Leu)
NM_001350162.2(TEX15):c.2549G>T (p.Trp850Leu)
NM_001350162.2(TEX15):c.2672A>T (p.His891Leu)
NM_001350162.2(TEX15):c.3279T>G (p.Tyr1093Ter) rs864309485
NM_001350162.2(TEX15):c.3323T>C (p.Leu1108Pro) rs1807627307
NM_001350162.2(TEX15):c.3568A>T (p.Lys1190Ter) rs1554492164
NM_001350162.2(TEX15):c.3953T>C (p.Leu1318Ser)
NM_001350162.2(TEX15):c.3958C>T (p.Arg1320Ter)
NM_001350162.2(TEX15):c.4119C>A (p.Ser1373Arg)
NM_001350162.2(TEX15):c.4189del (p.Ser1397fs) rs1554491783
NM_001350162.2(TEX15):c.4944C>G (p.Asp1648Glu) rs117362953
NM_001350162.2(TEX15):c.5315G>A (p.Cys1772Tyr)
NM_001350162.2(TEX15):c.5590G>C (p.Glu1864Gln)
NM_001350162.2(TEX15):c.6118T>G (p.Cys2040Gly)
NM_001350162.2(TEX15):c.6127G>A (p.Glu2043Lys)
NM_001350162.2(TEX15):c.6823G>A (p.Ala2275Thr)
NM_001350162.2(TEX15):c.6848_6849del (p.Arg2283fs) rs550195743
NM_001350162.2(TEX15):c.6869_6872del (p.Lys2290fs)
NM_001350162.2(TEX15):c.6874_6877del (p.Ser2292fs)
NM_001350162.2(TEX15):c.688-6T>C
NM_001350162.2(TEX15):c.7414C>T (p.Arg2472Ter)
NM_001350162.2(TEX15):c.8164-17G>A
NM_001350162.2(TEX15):c.8806T>C (p.Ser2936Pro)
NM_001350162.2(TEX15):c.933C>G (p.Phe311Leu)

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