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. 2022 Jul 14;41(2):422–433. doi: 10.5534/wjmh.220009

Table 3. Variants with uncertain significance in genes identified in patients with non-obstructive azoospermia and their clinical characteristics.

Gene symbol (OMIM number) Patient code Notes FSH (IU/l) Testis histology Left/right testicular volume (mL) Nucleotide change Amino acid change rs ID Minor allele frequency (%)
CATSPER1 (606389) 143808128 Varicocele NA Mixed atrophy NA NM_053054.4:c.1270T>C NP_444282.3:p.Trp424Arg rs139761671 0.006
CFAP44 (617559) 115748838 Idiopathic N Hypospermatogenesis NA NM_018338.3:c.2202_2204del NP_060808.2:p.Glu737del rs749873759 -
DNAH1 (603332) 111008936 Idiopathic 7.9 Hypospermatogenesis NA NM_015512.5:c.4739C>G NP_056327.4:p.Ala1580Gly rs754588837 0.0008
DPY19L2 (613893) 125687856 Idiopathic N Hypospermatogenesis NA NM_173812.5:c.1025A>C NP_776173.3:p.Gln342Pro - -
NANOS1 (608226) 105816704 Varicocele 8.7 Hypospermatogenesis NA NM_199461.4:c.830_833del NP_955631.1:p.Pro277Argfs*73 rs746095721 0.002
131919035 Varicocele 26.05 Mixed atrophy NA NM_199461.4:c.830_833del NP_955631.1:p.Pro277Argfs*73 rs746095721 0.002
PLK4 (605031) 100132259 Varicocele 6.3 Hypospermatogenesis NA NM_014264.5:c.17G>A NP_055079.3:p.Gly6Glu rs149003893 0.1
113090176 Varicocele 18 Mixed atrophy 3.5/3.5 NM_014264.5:c.17G>A NP_055079.3:p.Gly6Glu rs149003893 0.1
SYCE1 (611486) 163680875 Idiopathic N Hypospermatogenesis NA NM_130784.3:c.52G>C NP_570140.1:p.Glu18Gln rs756386589 0.003
SYCP3 (604759) 130059718 Varicocele 27.3 SCOS 7.5/10 NM_001177948.1:c.643del NP_001171419.1:p.Ile215Leufs*2 rs761136347 0.004
SUN5 (613942) 111008936 Idiopathic 7.9 Hypospermatogenesis NA NM_080675.4:c.476G>A NP_542406.2:p.Arg159Gln rs144823079 0.09
TEX11 (300311) 125687856 Idiopathic N Hypospermatogenesis NA NM_001003811.2:c.2186-6_2186-3del - - -
TEX15 (605795) 148743930 Idiopathic 23 SCOS NA NM_001350162.2:c.541-4_541-3del - rs35279485 0.003
100132259 Varicocele 6.3 Hypospermatogenesis NA NM_001350162.2:c.541-4_541-3del - rs35279485 0.003
USP9Y (400005) 122354337 Idiopathic NA Maturation arrest NA NM_004654.4:c.7434+14del - rs760325957 0.004
125687856 Idiopathic N Hypospermatogenesis NA NM_004654.4:c.7434+14del - rs760325957 0.004
128766983 Idiopathic N Mixed atrophy NA NM_004654.4:c.6574del NP_004645.2:p.Ala2192Glnfs*7 - -
128766983 Idiopathic N Mixed atrophy NA NM_004654.4:c.7434+14del - rs760325957 0.004
130424034 Idiopathic 28.9; 37 Mixed atrophy 12.6/7 NM_004654.4:c.7434+14del - rs760325957 0.004
148743930 Idiopathic 23 SCOS NA NM_004654.4:c.7434+14del - rs760325957 0.004
151184989 Idiopathic 28.9 SCOS/mixed atrophy N NM_004654.4:c.7434+14del - rs760325957 0.004
156833670 Idiopathic NA Hypospermatogenesis/ mixed atrophy N NM_004654.4:c.7434+14del - rs760325957 0.004
125938310 Cryptorchidism NA Hypospermatogenesis NA NM_004654.4:c.449T>C NP_004645.2:Ile150Thr - -
125938310 Cryptorchidism NA Hypospermatogenesis NA NM_004654.4:c.7434+14del - rs760325957 0.004
141879319 Cryptorchidism 11.3 Mixed atrophy Smaller than normal NM_004654.4:c.7434+14del - rs760325957 0.004
USP9Y (400005) 142201659 Cryptorchidism 26 SCOS/Mixed atrophy N/ Smaller than normal NM_004654.4:c.7434+13_7434+14del - - -
143296311 Cryptorchidism NA Hypospermatogenesis NA NM_004654.4:c.7434+14dup - rs760325957 0.08
114516827 Varicocele N Mixed atrophy NA NM_004654.4:c.7434+14del - rs760325957 0.004
114709776 Varicocele N Mixed atrophy NA NM_004654.4:c.7434+14del - rs760325957 0.004
143808128 Varicocele NA Mixed atrophy NA NM_004654.4:c.7434+14dup - rs760325957 0.08
ZMYND15 (614312) 101797172 Idiopathic 6.39 SCOS NA NM_001136046.3:c.1262G>A NP_001129518.1:p.Arg421Gln rs748907962 0.005
163680875 Idiopathic N Hypospermatogenesis NA NM_001136046.3:c.1260_1262del NP_001129518.1:p.Arg421del rs866053815 0.0004
ZPBP (608498) 120151485 Idiopathic 20 SCOS Smaller than normal NM_007009.3:c.128-6del - rs202222027 0.02

OMIM: Online Mendelian Inheritance in Man, FSH: follicle stimulating hormone, NA: not assessed, N: normal, SCOS: Sertoli cell only syndrome, -: not available.