| 405722098 | CV3292836 | single nucleotide variant | NM_006687.4(ACTL7A):c.41C>T (p.Thr14Ile) | not specified [RCV004428277] | uncertain significance | 9 | 108862363 | 108862363 | Human | | name |
| 405722489 | CV3292886 | single nucleotide variant | NM_006687.4(ACTL7A):c.80C>A (p.Ala27Asp) | not specified [RCV004428327] | uncertain significance | 9 | 108862402 | 108862402 | Human | | name |
| 156386599 | CV2225143 | single nucleotide variant | NM_006687.4(ACTL7A):c.296T>G (p.Val99Gly) | not specified [RCV004094950] | uncertain significance | 9 | 108862618 | 108862618 | Human | | name |
| 156073953 | CV2281407 | single nucleotide variant | NM_006687.4(ACTL7A):c.103G>A (p.Asp35Asn) | not specified [RCV004153744] | uncertain significance | 9 | 108862425 | 108862425 | Human | | name |
| 156284720 | CV2289001 | single nucleotide variant | NM_006687.4(ACTL7A):c.241T>C (p.Cys81Arg) | not specified [RCV004149953] | uncertain significance | 9 | 108862563 | 108862563 | Human | | name |
| 156343527 | CV2364125 | single nucleotide variant | NM_006687.4(ACTL7A):c.124G>A (p.Val42Met) | not specified [RCV004221501] | uncertain significance | 9 | 108862446 | 108862446 | Human | | name |
| 401751768 | CV2702899 | single nucleotide variant | NM_006687.4(ACTL7A):c.257C>G (p.Ala86Gly) | not specified [RCV004321237] | uncertain significance | 9 | 108862579 | 108862579 | Human | | name |
| 401829587 | CV2742893 | single nucleotide variant | NM_006687.4(ACTL7A):c.146C>G (p.Ser49Ter) | Spermatogenic failure 86 [RCV003325425] | pathogenic | 9 | 108862468 | 108862468 | Human | 1 | name |
| 405721982 | CV3292821 | single nucleotide variant | NM_006687.4(ACTL7A):c.188G>T (p.Arg63Met) | not specified [RCV004428262] | uncertain significance | 9 | 108862510 | 108862510 | Human | | name |
| 597793803 | CV3640650 | single nucleotide variant | NM_006687.4(ACTL7A):c.1161G>A (p.Pro387=) | not specified [RCV004903110] | likely benign | 9 | 108863483 | 108863483 | Human | | name |
| 598211157 | CV3939216 | single nucleotide variant | NM_006687.4(ACTL7A):c.152C>G (p.Pro51Arg) | not specified [RCV005315969] | uncertain significance | 9 | 108862474 | 108862474 | Human | | name |
| 598175604 | CV3949763 | single nucleotide variant | NM_006687.4(ACTL7A):c.100A>T (p.Arg34Trp) | not specified [RCV005309877] | uncertain significance | 9 | 108862422 | 108862422 | Human | | name |
| 598175665 | CV3949773 | single nucleotide variant | NM_006687.4(ACTL7A):c.158A>G (p.Glu53Gly) | not specified [RCV005309885] | uncertain significance | 9 | 108862480 | 108862480 | Human | | name |
| 156251076 | CV2273367 | single nucleotide variant | NM_006687.4(ACTL7A):c.866A>G (p.Glu289Gly) | not specified [RCV004132140] | uncertain significance | 9 | 108863188 | 108863188 | Human | | name |
| 156171535 | CV2312586 | single nucleotide variant | NM_006687.4(ACTL7A):c.883A>G (p.Ser295Gly) | not specified [RCV004169326] | uncertain significance | 9 | 108863205 | 108863205 | Human | | name |
| 155966319 | CV2329787 | single nucleotide variant | NM_006687.4(ACTL7A):c.607C>T (p.Arg203Cys) | not specified [RCV004183254] | uncertain significance | 9 | 108862929 | 108862929 | Human | | name |
| 156326444 | CV2331949 | single nucleotide variant | NM_006687.4(ACTL7A):c.569C>A (p.Ala190Asp) | not specified [RCV004187010] | uncertain significance | 9 | 108862891 | 108862891 | Human | | name |
| 156197984 | CV2334445 | single nucleotide variant | NM_006687.4(ACTL7A):c.379G>A (p.Val127Ile) | not specified [RCV004188418] | uncertain significance | 9 | 108862701 | 108862701 | Human | | name |
| 155983278 | CV2347976 | single nucleotide variant | NM_006687.4(ACTL7A):c.484C>T (p.Pro162Ser) | not specified [RCV004197663] | uncertain significance | 9 | 108862806 | 108862806 | Human | | name |
| 156345541 | CV2356273 | single nucleotide variant | NM_006687.4(ACTL7A):c.891T>G (p.His297Gln) | not specified [RCV004206083] | uncertain significance | 9 | 108863213 | 108863213 | Human | | name |
| 156141259 | CV2358391 | single nucleotide variant | NM_006687.4(ACTL7A):c.336T>G (p.Asn112Lys) | not specified [RCV004207286] | uncertain significance | 9 | 108862658 | 108862658 | Human | | name |
| 156190317 | CV2384972 | single nucleotide variant | NM_006687.4(ACTL7A):c.961A>T (p.Met321Leu) | not specified [RCV004226200] | uncertain significance | 9 | 108863283 | 108863283 | Human | | name |
| 329382036 | CV2438365 | single nucleotide variant | NM_006687.4(ACTL7A):c.497C>A (p.Ala166Glu) | not specified [RCV004259527] | uncertain significance | 9 | 108862819 | 108862819 | Human | | name |
| 329373553 | CV2439342 | single nucleotide variant | NM_006687.4(ACTL7A):c.515C>T (p.Pro172Leu) | not specified [RCV004249645] | uncertain significance | 9 | 108862837 | 108862837 | Human | | name |
| 401743993 | CV2684828 | single nucleotide variant | NM_006687.4(ACTL7A):c.691G>A (p.Glu231Lys) | not specified [RCV004293900] | uncertain significance | 9 | 108863013 | 108863013 | Human | | name |
| 401829583 | CV2742890 | single nucleotide variant | NM_006687.4(ACTL7A):c.733G>A (p.Ala245Thr) | Spermatogenic failure 86 [RCV003325422] | pathogenic | 9 | 108863055 | 108863055 | Human | 1 | name |
| 401829584 | CV2742891 | single nucleotide variant | NM_006687.4(ACTL7A):c.463C>T (p.Arg155Ter) | Spermatogenic failure 86 [RCV003325423] | pathogenic | 9 | 108862785 | 108862785 | Human | 1 | name |
| 401829588 | CV2742894 | single nucleotide variant | NM_006687.4(ACTL7A):c.737G>C (p.Gly246Ala) | Spermatogenic failure 86 [RCV003325426] | pathogenic | 9 | 108863059 | 108863059 | Human | 1 | name |
| 401877898 | CV2757678 | single nucleotide variant | NM_006687.4(ACTL7A):c.421G>A (p.Val141Met) | not specified [RCV004334787] | uncertain significance | 9 | 108862743 | 108862743 | Human | | name |
| 405722087 | CV3292835 | single nucleotide variant | NM_006687.4(ACTL7A):c.383A>G (p.His128Arg) | not specified [RCV004428276] | likely benign | 9 | 108862705 | 108862705 | Human | | name |
| 405722168 | CV3292845 | single nucleotide variant | NM_006687.4(ACTL7A):c.464G>A (p.Arg155Gln) | not specified [RCV004428286] | uncertain significance | 9 | 108862786 | 108862786 | Human | | name |
| 405722270 | CV3292858 | single nucleotide variant | NM_006687.4(ACTL7A):c.586A>G (p.Met196Val) | not specified [RCV004428299] | uncertain significance | 9 | 108862908 | 108862908 | Human | | name |
| 405722327 | CV3292865 | single nucleotide variant | NM_006687.4(ACTL7A):c.667G>A (p.Val223Met) | not specified [RCV004428306] | uncertain significance | 9 | 108862989 | 108862989 | Human | | name |
| 405722364 | CV3292870 | single nucleotide variant | NM_006687.4(ACTL7A):c.718G>A (p.Gly240Arg) | not specified [RCV004428311] | uncertain significance | 9 | 108863040 | 108863040 | Human | | name |
| 405722403 | CV3292875 | single nucleotide variant | NM_006687.4(ACTL7A):c.769C>A (p.Leu257Met) | not specified [RCV004428316] | likely benign | 9 | 108863091 | 108863091 | Human | | name |
| 405722456 | CV3292882 | single nucleotide variant | NM_006687.4(ACTL7A):c.787G>A (p.Glu263Lys) | not specified [RCV004428323] | uncertain significance | 9 | 108863109 | 108863109 | Human | | name |
| 405722481 | CV3292885 | single nucleotide variant | NM_006687.4(ACTL7A):c.808G>T (p.Gly270Cys) | not specified [RCV004428326] | uncertain significance | 9 | 108863130 | 108863130 | Human | | name |
| 407483312 | CV3418225 | single nucleotide variant | NM_006687.4(ACTL7A):c.580C>G (p.Pro194Ala) | not specified [RCV004602830] | uncertain significance | 9 | 108862902 | 108862902 | Human | | name |
| 407483391 | CV3418237 | single nucleotide variant | NM_006687.4(ACTL7A):c.307T>C (p.Tyr103His) | not specified [RCV004602842] | uncertain significance | 9 | 108862629 | 108862629 | Human | | name |
| 407483489 | CV3418255 | single nucleotide variant | NM_006687.4(ACTL7A):c.337C>T (p.Arg113Cys) | not specified [RCV004602858] | uncertain significance | 9 | 108862659 | 108862659 | Human | | name |
| 407483521 | CV3418266 | single nucleotide variant | NM_006687.4(ACTL7A):c.944G>A (p.Arg315Gln) | not specified [RCV004602866] | uncertain significance | 9 | 108863266 | 108863266 | Human | | name |
| 597793746 | CV3640623 | single nucleotide variant | NM_006687.4(ACTL7A):c.860T>C (p.Ile287Thr) | not specified [RCV004903090] | likely benign | 9 | 108863182 | 108863182 | Human | | name |
| 597793794 | CV3640644 | single nucleotide variant | NM_006687.4(ACTL7A):c.434C>T (p.Thr145Ile) | not specified [RCV004903107] | uncertain significance | 9 | 108862756 | 108862756 | Human | | name |
| 597793824 | CV3640658 | single nucleotide variant | NM_006687.4(ACTL7A):c.446T>A (p.Ile149Asn) | not specified [RCV004903117] | uncertain significance | 9 | 108862768 | 108862768 | Human | | name |
| 597750330 | CV3640679 | single nucleotide variant | NM_006687.4(ACTL7A):c.616A>G (p.Met206Val) | not specified [RCV004892561] | uncertain significance | 9 | 108862938 | 108862938 | Human | | name |
| 598175503 | CV3939226 | single nucleotide variant | NM_006687.4(ACTL7A):c.772A>T (p.Asn258Tyr) | not specified [RCV005309862] | uncertain significance | 9 | 108863094 | 108863094 | Human | | name |
| 598175565 | CV3949754 | single nucleotide variant | NM_006687.4(ACTL7A):c.723G>C (p.Arg241Ser) | not specified [RCV005309871] | uncertain significance | 9 | 108863045 | 108863045 | Human | | name |
| 156079654 | CV2300939 | single nucleotide variant | NM_006687.4(ACTL7A):c.1249G>A (p.Val417Ile) | not specified [RCV004158125] | uncertain significance | 9 | 108863571 | 108863571 | Human | | name |
| 156049471 | CV2319309 | single nucleotide variant | NM_006687.4(ACTL7A):c.1087G>A (p.Gly363Ser) | not specified [RCV004180135] | uncertain significance | 9 | 108863409 | 108863409 | Human | | name |
| 156137443 | CV2375756 | single nucleotide variant | NM_006687.4(ACTL7A):c.1147C>T (p.Pro383Ser) | not specified [RCV004224349] | uncertain significance | 9 | 108863469 | 108863469 | Human | | name |
| 156152192 | CV2394832 | single nucleotide variant | NM_006687.4(ACTL7A):c.1183A>G (p.Arg395Gly) | not specified [RCV004234494] | uncertain significance | 9 | 108863505 | 108863505 | Human | | name |
| 401829585 | CV2742892 | single nucleotide variant | NM_006687.4(ACTL7A):c.1084G>A (p.Gly362Arg) | Spermatogenic failure 86 [RCV003325424] | pathogenic | 9 | 108863406 | 108863406 | Human | 1 | name |
| 407483564 | CV3418277 | single nucleotide variant | NM_006687.4(ACTL7A):c.1010C>A (p.Thr337Asn) | not specified [RCV004602875] | uncertain significance | 9 | 108863332 | 108863332 | Human | | name |
| 596928244 | CV3541341 | single nucleotide variant | NM_006687.4(ACTL7A):c.1204G>A (p.Gly402Ser) | Spermatogenic failure 86 [RCV004797212] | likely pathogenic | 9 | 108863526 | 108863526 | Human | 1 | name |
| 597793766 | CV3640633 | single nucleotide variant | NM_006687.4(ACTL7A):c.1256G>A (p.Arg419His) | not specified [RCV004903097] | uncertain significance | 9 | 108863578 | 108863578 | Human | | name |
| 597793843 | CV3640669 | single nucleotide variant | NM_006687.4(ACTL7A):c.1142T>C (p.Met381Thr) | not specified [RCV004903124] | uncertain significance | 9 | 108863464 | 108863464 | Human | | name |
| 597793892 | CV3640688 | single nucleotide variant | NM_006687.4(ACTL7A):c.1145G>A (p.Cys382Tyr) | not specified [RCV004903140] | uncertain significance | 9 | 108863467 | 108863467 | Human | | name |
| 151741739 | CV1335525 | microsatellite | NM_006687.4(ACTL7A):c.149_150del (p.Glu50fs) | Male infertility with normal semen parameters [RCV001845046] | pathogenic | 9 | 108862469 | 108862470 | Human | | name |
