| 155703345 | CV1838436 | single nucleotide variant | NM_016032.4(ZDHHC9):c.*4A>G | Inborn genetic diseases [RCV002401818] | likely benign | X | 129806366 | 129806366 | Human | 1 | name |
| 150449636 | CV1275696 | single nucleotide variant | NM_016032.4(ZDHHC9):c.*105C>T | not provided [RCV001708151] | benign | X | 129806265 | 129806265 | Human | | name |
| 127246606 | CV1086257 | single nucleotide variant | NM_016032.4(ZDHHC9):c.979-6T>C | Syndromic X-linked intellectual disability Raymond type [RCV001394131] | likely benign | X | 129806492 | 129806492 | Human | 1 | name |
| 127254819 | CV1107998 | deletion | NM_016032.4(ZDHHC9):c.488-5del | Syndromic X-linked intellectual disability Raymond type [RCV001437347] | likely benign | X | 129814800 | 129814800 | Human | 1 | name |
| 127232807 | CV1107999 | single nucleotide variant | NM_016032.4(ZDHHC9):c.488-9C>A | Syndromic X-linked intellectual disability Raymond type [RCV001421452] | likely benign | X | 129814804 | 129814804 | Human | 1 | name |
| 127295254 | CV1129369 | single nucleotide variant | NM_016032.4(ZDHHC9):c.881+8G>C | Syndromic X-linked intellectual disability Raymond type [RCV001477054] | likely benign | X | 129811398 | 129811398 | Human | 1 | name |
| 151710133 | CV1403756 | duplication | NM_016032.4(ZDHHC9):c.329-2dup | Syndromic X-linked intellectual disability Raymond type [RCV001996957]|ZDHHC9-related disorder [RCV003407999] | uncertain significance | X | 129823838 | 129823839 | Human | 1 | name , trait , alternate_id |
| 152099569 | CV1606574 | single nucleotide variant | NM_016032.4(ZDHHC9):c.674+7T>C | Syndromic X-linked intellectual disability Raymond type [RCV002195369] | likely benign | X | 129813670 | 129813670 | Human | 1 | name |
| 156357284 | CV2020144 | single nucleotide variant | NM_016032.4(ZDHHC9):c.978+7G>A | Syndromic X-linked intellectual disability Raymond type [RCV002720621] | likely benign | X | 129810898 | 129810898 | Human | 1 | name |
| 156068545 | CV2065673 | single nucleotide variant | NM_016032.4(ZDHHC9):c.978+6T>G | Syndromic X-linked intellectual disability Raymond type [RCV002847001] | uncertain significance | X | 129810899 | 129810899 | Human | 1 | name |
| 8561842 | CV25749 | single nucleotide variant | NM_016032.4(ZDHHC9):c.167+5G>C | Syndromic X-linked intellectual disability Raymond type [RCV000011456] | pathogenic | X | 129841774 | 129841774 | Human | 1 | name |
| 402468270 | CV3028592 | single nucleotide variant | NM_016032.4(ZDHHC9):c.778-4G>C | Syndromic X-linked intellectual disability Raymond type [RCV003623397] | likely benign | X | 129811513 | 129811513 | Human | 1 | name |
| 405257232 | CV3222485 | single nucleotide variant | NM_016032.4(ZDHHC9):c.167+1G>A | Syndromic X-linked intellectual disability Raymond type [RCV003985981] | likely pathogenic | X | 129841778 | 129841778 | Human | 1 | name |
| 408390998 | CV3521094 | single nucleotide variant | NM_016032.4(ZDHHC9):c.487+6T>G | not provided [RCV004762916] | uncertain significance | X | 129823673 | 129823673 | Human | | name |
| 597873785 | CV3766072 | single nucleotide variant | NM_016032.4(ZDHHC9):c.979-8C>T | Syndromic X-linked intellectual disability Raymond type [RCV005108204] | likely benign | X | 129806494 | 129806494 | Human | 1 | name |
| 597949065 | CV3772270 | single nucleotide variant | NM_016032.4(ZDHHC9):c.488-2A>G | Syndromic X-linked intellectual disability Raymond type [RCV005120589] | likely pathogenic | X | 129814797 | 129814797 | Human | 1 | name |
| 597906722 | CV3781377 | single nucleotide variant | NM_016032.4(ZDHHC9):c.675-5C>A | Syndromic X-linked intellectual disability Raymond type [RCV005128065] | likely benign | X | 129812825 | 129812825 | Human | 1 | name |
| 597882865 | CV3857639 | single nucleotide variant | NM_016032.4(ZDHHC9):c.777+1G>A | Syndromic X-linked intellectual disability Raymond type [RCV005199266] | likely pathogenic | X | 129812717 | 129812717 | Human | 1 | name |
| 13520472 | CV495785 | single nucleotide variant | NM_016032.4(ZDHHC9):c.328+1G>A | not provided [RCV000598660] | pathogenic | X | 129828980 | 129828980 | Human | | name |
| 13525298 | CV507836 | single nucleotide variant | NM_016032.4(ZDHHC9):c.487+3G>A | not specified [RCV000602971] | likely benign | X | 129823676 | 129823676 | Human | | name |
| 13619496 | CV534482 | single nucleotide variant | NM_016032.4(ZDHHC9):c.674+9C>T | Syndromic X-linked intellectual disability Raymond type [RCV000646767]|not provided [RCV001727788]|not specified [RCV001702538] | benign|likely benign | X | 129813668 | 129813668 | Human | 1 | name |
| 13619489 | CV535014 | single nucleotide variant | NM_016032.4(ZDHHC9):c.881+3G>A | Autism spectrum disorder [RCV003126890]|Syndromic X-linked intellectual disability Raymond type [RCV000646763] | likely benign|uncertain significance | X | 129811403 | 129811403 | Human | 3 | name |
| 15141315 | CV776784 | single nucleotide variant | NM_016032.4(ZDHHC9):c.167+9C>T | Syndromic X-linked intellectual disability Raymond type [RCV001520044] | benign | X | 129841770 | 129841770 | Human | 1 | name |
| 38458124 | CV960362 | single nucleotide variant | NM_016032.4(ZDHHC9):c.487+8A>G | Syndromic X-linked intellectual disability Raymond type [RCV001228824] | likely benign|uncertain significance | X | 129823671 | 129823671 | Human | 1 | name |
| 40814601 | CV969509 | single nucleotide variant | NM_016032.4(ZDHHC9):c.881+1G>C | Intellectual disability [RCV001260845] | likely pathogenic | X | 129811405 | 129811405 | Human | 2 | name |
| 127283807 | CV1107997 | single nucleotide variant | NM_016032.4(ZDHHC9):c.881+10G>C | Syndromic X-linked intellectual disability Raymond type [RCV001448767] | likely benign | X | 129811396 | 129811396 | Human | 1 | name |
| 150411078 | CV1196299 | single nucleotide variant | NM_016032.4(ZDHHC9):c.-204+6G>T | Syndromic X-linked intellectual disability Raymond type [RCV002471124]|not provided [RCV001573474] | benign|likely benign | X | 129843690 | 129843690 | Human | 1 | name |
| 150463829 | CV1237689 | single nucleotide variant | NM_016032.4(ZDHHC9):c.675-22A>G | not provided [RCV001649695] | benign | X | 129812842 | 129812842 | Human | | name |
| 150497947 | CV1256794 | single nucleotide variant | NM_016032.4(ZDHHC9):c.487+14C>T | not provided [RCV001676286] | benign | X | 129823665 | 129823665 | Human | | name |
| 150468146 | CV1257012 | single nucleotide variant | NM_016032.4(ZDHHC9):c.882-62G>A | not provided [RCV001670658] | benign | X | 129811063 | 129811063 | Human | | name |
| 150438627 | CV1264850 | single nucleotide variant | NM_016032.4(ZDHHC9):c.167+33T>C | not provided [RCV001678843] | benign | X | 129841746 | 129841746 | Human | | name |
| 150456005 | CV1269017 | single nucleotide variant | NM_016032.4(ZDHHC9):c.675-80C>A | not provided [RCV001692841] | benign | X | 129812900 | 129812900 | Human | | name |
| 152118053 | CV1522263 | single nucleotide variant | NM_016032.4(ZDHHC9):c.328+17G>T | Syndromic X-linked intellectual disability Raymond type [RCV002081166] | likely benign | X | 129828964 | 129828964 | Human | 1 | name |
| 152152430 | CV1545885 | single nucleotide variant | NM_016032.4(ZDHHC9):c.979-18A>G | Syndromic X-linked intellectual disability Raymond type [RCV002179659] | benign | X | 129806504 | 129806504 | Human | 1 | name |
| 152139599 | CV1549709 | single nucleotide variant | NM_016032.4(ZDHHC9):c.674+20T>C | Syndromic X-linked intellectual disability Raymond type [RCV002156588] | benign | X | 129813657 | 129813657 | Human | 1 | name |
| 152148558 | CV1566305 | single nucleotide variant | NM_016032.4(ZDHHC9):c.168-18A>G | Syndromic X-linked intellectual disability Raymond type [RCV002139174] | benign | X | 129829159 | 129829159 | Human | 1 | name |
| 152069287 | CV1566838 | single nucleotide variant | NM_016032.4(ZDHHC9):c.328+11C>T | Syndromic X-linked intellectual disability Raymond type [RCV002111227] | likely benign | X | 129828970 | 129828970 | Human | 1 | name |
| 152175870 | CV1580122 | single nucleotide variant | NM_016032.4(ZDHHC9):c.488-15C>T | Syndromic X-linked intellectual disability Raymond type [RCV002164007] | likely benign | X | 129814810 | 129814810 | Human | 1 | name |
| 152123926 | CV1587330 | single nucleotide variant | NM_016032.4(ZDHHC9):c.487+17G>A | Syndromic X-linked intellectual disability Raymond type [RCV002136070] | benign | X | 129823662 | 129823662 | Human | 1 | name |
| 152136638 | CV1595178 | deletion | NM_016032.4(ZDHHC9):c.328+16del | Syndromic X-linked intellectual disability Raymond type [RCV002200033] | likely benign | X | 129828965 | 129828965 | Human | 1 | name |
| 152100596 | CV1606744 | single nucleotide variant | NM_016032.4(ZDHHC9):c.488-17C>T | Syndromic X-linked intellectual disability Raymond type [RCV002195497] | likely benign | X | 129814812 | 129814812 | Human | 1 | name |
| 152082839 | CV1608139 | single nucleotide variant | NM_016032.4(ZDHHC9):c.674+11C>T | Syndromic X-linked intellectual disability Raymond type [RCV002193249] | benign | X | 129813666 | 129813666 | Human | 1 | name |
| 152166258 | CV1620861 | single nucleotide variant | NM_016032.4(ZDHHC9):c.626-11C>T | Syndromic X-linked intellectual disability Raymond type [RCV002181897] | likely benign | X | 129813736 | 129813736 | Human | 1 | name |
| 152053231 | CV1659294 | single nucleotide variant | NM_016032.4(ZDHHC9):c.978+15C>T | Syndromic X-linked intellectual disability Raymond type [RCV002189664] | benign | X | 129810890 | 129810890 | Human | 1 | name |
| 152091296 | CV1662161 | single nucleotide variant | NM_016032.4(ZDHHC9):c.777+16C>T | Syndromic X-linked intellectual disability Raymond type [RCV002132078] | benign | X | 129812702 | 129812702 | Human | 1 | name |
| 156280592 | CV1896752 | single nucleotide variant | NM_016032.4(ZDHHC9):c.487+19A>T | Syndromic X-linked intellectual disability Raymond type [RCV003087099] | likely benign | X | 129823660 | 129823660 | Human | 1 | name |
| 10048534 | CV193633 | single nucleotide variant | NM_016032.4(ZDHHC9):c.167+10G>A | Syndromic X-linked intellectual disability Raymond type [RCV000646768]|ZDHHC9-related disorder [RCV003967420]|not specified [RCV000177289] | benign | X | 129841769 | 129841769 | Human | 1 | name , trait , alternate_id |
| 10048888 | CV194989 | single nucleotide variant | NM_016032.4(ZDHHC9):c.487+15A>G | Syndromic X-linked intellectual disability Raymond type [RCV002054125]|not provided [RCV001541409]|not specified [RCV000178962] | benign | X | 129823664 | 129823664 | Human | 1 | name |
| 156332707 | CV2000703 | single nucleotide variant | NM_016032.4(ZDHHC9):c.778-11T>G | Syndromic X-linked intellectual disability Raymond type [RCV002649908] | likely benign | X | 129811520 | 129811520 | Human | 1 | name |
| 155913284 | CV2011230 | single nucleotide variant | NM_016032.4(ZDHHC9):c.881+17A>G | Syndromic X-linked intellectual disability Raymond type [RCV002681870] | likely benign | X | 129811389 | 129811389 | Human | 1 | name |
| 156215050 | CV2028616 | single nucleotide variant | NM_016032.4(ZDHHC9):c.674+10G>A | Syndromic X-linked intellectual disability Raymond type [RCV002711916] | benign | X | 129813667 | 129813667 | Human | 1 | name |
| 156094876 | CV2030843 | single nucleotide variant | NM_016032.4(ZDHHC9):c.488-17C>G | Syndromic X-linked intellectual disability Raymond type [RCV002761086] | likely benign | X | 129814812 | 129814812 | Human | 1 | name |
| 156009739 | CV2045394 | single nucleotide variant | NM_016032.4(ZDHHC9):c.488-15C>G | Syndromic X-linked intellectual disability Raymond type [RCV002780075] | benign | X | 129814810 | 129814810 | Human | 1 | name |
| 156252329 | CV2082653 | single nucleotide variant | NM_016032.4(ZDHHC9):c.625+14G>A | Syndromic X-linked intellectual disability Raymond type [RCV002876986] | likely benign | X | 129814644 | 129814644 | Human | 1 | name |
| 156237724 | CV2108950 | single nucleotide variant | NM_016032.4(ZDHHC9):c.778-15G>T | Syndromic X-linked intellectual disability Raymond type [RCV002933085] | likely benign | X | 129811524 | 129811524 | Human | 1 | name |
| 402524906 | CV2891843 | single nucleotide variant | NM_016032.4(ZDHHC9):c.487+20C>T | Syndromic X-linked intellectual disability Raymond type [RCV003511138] | likely benign | X | 129823659 | 129823659 | Human | 1 | name |
| 402513676 | CV2925762 | single nucleotide variant | NM_016032.4(ZDHHC9):c.626-16C>T | Syndromic X-linked intellectual disability Raymond type [RCV003510207] | likely benign | X | 129813741 | 129813741 | Human | 1 | name |
| 402467991 | CV3010773 | single nucleotide variant | NM_016032.4(ZDHHC9):c.625+10C>T | Syndromic X-linked intellectual disability Raymond type [RCV003623322] | likely benign | X | 129814648 | 129814648 | Human | 1 | name |
| 402468808 | CV3024336 | single nucleotide variant | NM_016032.4(ZDHHC9):c.488-19C>T | Syndromic X-linked intellectual disability Raymond type [RCV003623538] | likely benign | X | 129814814 | 129814814 | Human | 1 | name |
| 402469682 | CV3047557 | single nucleotide variant | NM_016032.4(ZDHHC9):c.329-11T>C | Syndromic X-linked intellectual disability Raymond type [RCV003623775] | likely benign | X | 129823848 | 129823848 | Human | 1 | name |
| 405170453 | CV3064429 | single nucleotide variant | NM_016032.4(ZDHHC9):c.487+19A>G | Syndromic X-linked intellectual disability Raymond type [RCV003622065] | likely benign | X | 129823660 | 129823660 | Human | 1 | name |
| 405049662 | CV3137976 | duplication | NM_016032.4(ZDHHC9):c.882-19dup | Syndromic X-linked intellectual disability Raymond type [RCV003832014] | likely benign | X | 129811019 | 129811020 | Human | 1 | name |
| 597892637 | CV3809816 | single nucleotide variant | NM_016032.4(ZDHHC9):c.167+19G>C | Syndromic X-linked intellectual disability Raymond type [RCV005151537] | likely benign | X | 129841760 | 129841760 | Human | 1 | name |
| 13619494 | CV534598 | single nucleotide variant | NM_016032.4(ZDHHC9):c.626-10A>T | Syndromic X-linked intellectual disability Raymond type [RCV000646766] | benign | X | 129813735 | 129813735 | Human | 1 | name |
| 150513957 | CV1210786 | deletion | NM_016032.4(ZDHHC9):c.488-127del | not provided [RCV001598827] | benign | X | 129814922 | 129814922 | Human | | name |
| 150477517 | CV1218637 | duplication | NM_016032.4(ZDHHC9):c.329-222dup | not provided [RCV001616264] | benign | X | 129824051 | 129824052 | Human | | name |
| 150453401 | CV1231821 | single nucleotide variant | NM_016032.4(ZDHHC9):c.487+204C>T | not provided [RCV001648128] | benign | X | 129823475 | 129823475 | Human | | name |
| 150430086 | CV1231961 | single nucleotide variant | NM_016032.4(ZDHHC9):c.328+145C>T | not provided [RCV001641223] | benign | X | 129828836 | 129828836 | Human | | name |
| 150433868 | CV1243809 | duplication | NM_016032.4(ZDHHC9):c.488-141dup | not provided [RCV001665015] | benign | X | 129814921 | 129814922 | Human | | name |
| 150491877 | CV1253833 | single nucleotide variant | NM_016032.4(ZDHHC9):c.625+123A>G | not provided [RCV001674929] | benign | X | 129814535 | 129814535 | Human | | name |
| 150496918 | CV1256618 | single nucleotide variant | NM_016032.4(ZDHHC9):c.488-122A>G | not provided [RCV001676110] | benign | X | 129814917 | 129814917 | Human | | name |
| 150461275 | CV1270627 | single nucleotide variant | NM_016032.4(ZDHHC9):c.778-209T>C | not provided [RCV001693617] | benign | X | 129811718 | 129811718 | Human | | name |
| 152140493 | CV1613857 | microsatellite | NM_016032.4(ZDHHC9):c.488-19CT[3] | Syndromic X-linked intellectual disability Raymond type [RCV002084089] | benign | X | 129814807 | 129814808 | Human | | name |
| 597937508 | CV3807859 | microsatellite | NM_016032.4(ZDHHC9):c.882-18CT[2] | Syndromic X-linked intellectual disability Raymond type [RCV005158238] | likely benign | X | 129811014 | 129811015 | Human | | name |
| 15119553 | CV773752 | single nucleotide variant | NM_016032.4(ZDHHC9):c.9G>A (p.Val3=) | Syndromic X-linked intellectual disability Raymond type [RCV001438620] | likely benign | X | 129841937 | 129841937 | Human | 1 | name |
| 127312264 | CV1150414 | single nucleotide variant | NM_016032.4(ZDHHC9):c.51C>T (p.Leu17=) | Syndromic X-linked intellectual disability Raymond type [RCV001481642] | likely benign | X | 129841895 | 129841895 | Human | 1 | name |
| 152031676 | CV1571835 | inversion | NM_016032.4(ZDHHC9):c.487+14_487+15inv | Inborn genetic diseases [RCV002337201]|Syndromic X-linked intellectual disability Raymond type [RCV002186750] | benign|likely benign | X | 129823664 | 129823665 | Human | | name |
| 402518302 | CV2856512 | single nucleotide variant | NM_016032.4(ZDHHC9):c.36G>A (p.Arg12=) | Syndromic X-linked intellectual disability Raymond type [RCV003510601] | likely benign | X | 129841910 | 129841910 | Human | 1 | name |
| 596946683 | CV3548512 | single nucleotide variant | NM_016032.4(ZDHHC9):c.84C>T (p.Arg28=) | not provided [RCV004810339] | likely benign | X | 129841862 | 129841862 | Human | | name |
| 597860033 | CV3850385 | single nucleotide variant | NM_016032.4(ZDHHC9):c.7G>A (p.Val3Met) | Syndromic X-linked intellectual disability Raymond type [RCV005195718] | uncertain significance | X | 129841939 | 129841939 | Human | 1 | name |
| 616935454 | CV4016057 | single nucleotide variant | NM_016032.4(ZDHHC9):c.30G>A (p.Val10=) | not provided [RCV005414922] | uncertain significance | X | 129841916 | 129841916 | Human | | name |
| 15197401 | CV773751 | single nucleotide variant | NM_016032.4(ZDHHC9):c.36G>C (p.Arg12=) | Syndromic X-linked intellectual disability Raymond type [RCV001468042] | likely benign | X | 129841910 | 129841910 | Human | 1 | name |
| 126774351 | CV1035342 | single nucleotide variant | NM_016032.4(ZDHHC9):c.20G>C (p.Arg7Thr) | Syndromic X-linked intellectual disability Raymond type [RCV001347129] | uncertain significance | X | 129841926 | 129841926 | Human | 1 | name |
| 152126389 | CV1548980 | single nucleotide variant | NM_016032.4(ZDHHC9):c.144A>G (p.Thr48=) | Syndromic X-linked intellectual disability Raymond type [RCV002082275] | likely benign | X | 129841802 | 129841802 | Human | 1 | name |
| 152106632 | CV1560115 | single nucleotide variant | NM_016032.4(ZDHHC9):c.159C>T (p.Phe53=) | Syndromic X-linked intellectual disability Raymond type [RCV002133934] | likely benign | X | 129841787 | 129841787 | Human | 1 | name |
| 152035637 | CV1590446 | single nucleotide variant | NM_016032.4(ZDHHC9):c.136C>T (p.Leu46=) | Inborn genetic diseases [RCV002382311]|Syndromic X-linked intellectual disability Raymond type [RCV002205529] | likely benign | X | 129841810 | 129841810 | Human | 2 | name |
| 156226260 | CV2140655 | single nucleotide variant | NM_016032.4(ZDHHC9):c.180G>A (p.Leu60=) | Syndromic X-linked intellectual disability Raymond type [RCV003007570] | likely benign|uncertain significance | X | 129829129 | 129829129 | Human | 1 | name |
| 402464745 | CV2970220 | single nucleotide variant | NM_016032.4(ZDHHC9):c.23A>G (p.Lys8Arg) | Syndromic X-linked intellectual disability Raymond type [RCV003622485] | uncertain significance | X | 129841923 | 129841923 | Human | 1 | name |
| 402467123 | CV2997327 | single nucleotide variant | NM_016032.4(ZDHHC9):c.153C>T (p.Leu51=) | Syndromic X-linked intellectual disability Raymond type [RCV003623091] | likely benign | X | 129841793 | 129841793 | Human | 1 | name |
| 402466873 | CV3000062 | single nucleotide variant | NM_016032.4(ZDHHC9):c.120G>T (p.Leu40=) | Syndromic X-linked intellectual disability Raymond type [RCV003623028] | likely benign | X | 129841826 | 129841826 | Human | 1 | name |
| 597910896 | CV3782230 | single nucleotide variant | NM_016032.4(ZDHHC9):c.285T>C (p.Pro95=) | Syndromic X-linked intellectual disability Raymond type [RCV005128723] | likely benign | X | 129829024 | 129829024 | Human | 1 | name |
| 13215851 | CV430650 | single nucleotide variant | NM_016032.4(ZDHHC9):c.144A>T (p.Thr48=) | Syndromic X-linked intellectual disability Raymond type [RCV001509624]|not provided [RCV004704030]|not specified [RCV000503026] | benign|likely benign | X | 129841802 | 129841802 | Human | 1 | name |
| 15101514 | CV758285 | single nucleotide variant | NM_016032.4(ZDHHC9):c.291G>A (p.Ala97=) | Syndromic X-linked intellectual disability Raymond type [RCV000914795]|not provided [RCV003438585] | benign|likely benign | X | 129829018 | 129829018 | Human | 1 | name |
| 15113039 | CV773750 | single nucleotide variant | NM_016032.4(ZDHHC9):c.141G>A (p.Gly47=) | Syndromic X-linked intellectual disability Raymond type [RCV001471572] | likely benign | X | 129841805 | 129841805 | Human | 1 | name |
| 127235985 | CV1086258 | single nucleotide variant | NM_016032.4(ZDHHC9):c.549C>T (p.Tyr183=) | Syndromic X-linked intellectual disability Raymond type [RCV001391992] | likely benign | X | 129814734 | 129814734 | Human | 1 | name |
| 127270657 | CV1108000 | single nucleotide variant | NM_016032.4(ZDHHC9):c.429A>G (p.Thr143=) | Syndromic X-linked intellectual disability Raymond type [RCV001441523] | likely benign | X | 129823737 | 129823737 | Human | 1 | name |
| 127235935 | CV1108001 | single nucleotide variant | NM_016032.4(ZDHHC9):c.384T>C (p.Asn128=) | Syndromic X-linked intellectual disability Raymond type [RCV001433224] | likely benign | X | 129823782 | 129823782 | Human | 1 | name |
| 127326808 | CV1150410 | single nucleotide variant | NM_016032.4(ZDHHC9):c.861G>T (p.Leu287=) | Syndromic X-linked intellectual disability Raymond type [RCV001506410] | likely benign | X | 129811426 | 129811426 | Human | 1 | name |
| 127311347 | CV1150411 | single nucleotide variant | NM_016032.4(ZDHHC9):c.414G>T (p.Leu138=) | Syndromic X-linked intellectual disability Raymond type [RCV001481429] | likely benign | X | 129823752 | 129823752 | Human | 1 | name |
| 127317537 | CV1150412 | single nucleotide variant | NM_016032.4(ZDHHC9):c.357C>A (p.Gly119=) | Syndromic X-linked intellectual disability Raymond type [RCV001503415] | likely benign | X | 129823809 | 129823809 | Human | 1 | name |
| 127300253 | CV1150413 | single nucleotide variant | NM_016032.4(ZDHHC9):c.324G>A (p.Glu108=) | Syndromic X-linked intellectual disability Raymond type [RCV001498552] | likely benign | X | 129828985 | 129828985 | Human | 1 | name |
| 127291213 | CV1159339 | single nucleotide variant | NM_016032.4(ZDHHC9):c.984C>G (p.Pro328=) | Syndromic X-linked intellectual disability Raymond type [RCV001510245] | benign | X | 129806481 | 129806481 | Human | 1 | name |
| 150553110 | CV1298134 | single nucleotide variant | NM_016032.4(ZDHHC9):c.58A>T (p.Arg20Trp) | not provided [RCV001768747] | uncertain significance | X | 129841888 | 129841888 | Human | | name |
| 152058510 | CV1531896 | single nucleotide variant | NM_016032.4(ZDHHC9):c.795A>T (p.Thr265=) | Syndromic X-linked intellectual disability Raymond type [RCV002089984] | likely benign | X | 129811492 | 129811492 | Human | 1 | name |
| 152123594 | CV1570608 | single nucleotide variant | NM_016032.4(ZDHHC9):c.666T>A (p.Thr222=) | Syndromic X-linked intellectual disability Raymond type [RCV002217106] | likely benign | X | 129813685 | 129813685 | Human | 1 | name |
| 152124035 | CV1587345 | single nucleotide variant | NM_016032.4(ZDHHC9):c.936C>T (p.Pro312=) | Syndromic X-linked intellectual disability Raymond type [RCV002136084] | likely benign | X | 129810947 | 129810947 | Human | 1 | name |
| 152132599 | CV1588071 | single nucleotide variant | NM_016032.4(ZDHHC9):c.954T>C (p.Ser318=) | Syndromic X-linked intellectual disability Raymond type [RCV002199519] | likely benign | X | 129810929 | 129810929 | Human | 1 | name |
| 152148729 | CV1616596 | single nucleotide variant | NM_016032.4(ZDHHC9):c.981C>T (p.Ala327=) | Syndromic X-linked intellectual disability Raymond type [RCV002201634]|not provided [RCV003438981] | likely benign | X | 129806484 | 129806484 | Human | 1 | name |
| 152078584 | CV1661425 | single nucleotide variant | NM_016032.4(ZDHHC9):c.561C>T (p.Phe187=) | Syndromic X-linked intellectual disability Raymond type [RCV002130548] | likely benign | X | 129814722 | 129814722 | Human | 1 | name |
| 155267348 | CV1699561 | deletion | NM_016032.4(ZDHHC9):c.267del (p.Ser89fs) | Syndromic X-linked intellectual disability Raymond type [RCV002283354] | pathogenic|likely pathogenic | X | 129829042 | 129829042 | Human | 1 | name |
| 155641676 | CV1707095 | single nucleotide variant | NM_016032.4(ZDHHC9):c.35G>A (p.Arg12Gln) | not provided [RCV002288025] | uncertain significance | X | 129841911 | 129841911 | Human | | name |
| 155737400 | CV1774536 | single nucleotide variant | NM_016032.4(ZDHHC9):c.76G>A (p.Asp26Asn) | Syndromic X-linked intellectual disability Raymond type [RCV002301992]|not provided [RCV003317589] | uncertain significance | X | 129841870 | 129841870 | Human | 1 | name |
| 156058810 | CV1876072 | single nucleotide variant | NM_016032.4(ZDHHC9):c.345G>A (p.Ala115=) | Syndromic X-linked intellectual disability Raymond type [RCV003053267] | likely benign | X | 129823821 | 129823821 | Human | 1 | name |
| 156441699 | CV1941028 | single nucleotide variant | NM_016032.4(ZDHHC9):c.495C>T (p.Phe165=) | Syndromic X-linked intellectual disability Raymond type [RCV003112028] | likely benign | X | 129814788 | 129814788 | Human | 1 | name |
| 155903504 | CV2007168 | single nucleotide variant | NM_016032.4(ZDHHC9):c.807C>A (p.Arg269=) | Syndromic X-linked intellectual disability Raymond type [RCV002681248] | likely benign | X | 129811480 | 129811480 | Human | 1 | name |
| 156186666 | CV2033893 | single nucleotide variant | NM_016032.4(ZDHHC9):c.336C>T (p.Thr112=) | Syndromic X-linked intellectual disability Raymond type [RCV002765783] | likely benign | X | 129823830 | 129823830 | Human | 1 | name |
| 155955957 | CV2069997 | single nucleotide variant | NM_016032.4(ZDHHC9):c.516G>A (p.Val172=) | Syndromic X-linked intellectual disability Raymond type [RCV002816515] | likely benign|uncertain significance | X | 129814767 | 129814767 | Human | 1 | name |
| 156140477 | CV2109886 | single nucleotide variant | NM_016032.4(ZDHHC9):c.807C>T (p.Arg269=) | Syndromic X-linked intellectual disability Raymond type [RCV002928536] | likely benign | X | 129811480 | 129811480 | Human | 1 | name |
| 405168295 | CV2940435 | single nucleotide variant | NM_016032.4(ZDHHC9):c.612C>T (p.Val204=) | Syndromic X-linked intellectual disability Raymond type [RCV003621762] | likely benign | X | 129814671 | 129814671 | Human | 1 | name |
| 402466305 | CV2986245 | single nucleotide variant | NM_016032.4(ZDHHC9):c.531A>G (p.Gly177=) | Syndromic X-linked intellectual disability Raymond type [RCV003622818] | likely benign | X | 129814752 | 129814752 | Human | 1 | name |
| 402468099 | CV3014264 | single nucleotide variant | NM_016032.4(ZDHHC9):c.396C>T (p.Asn132=) | Syndromic X-linked intellectual disability Raymond type [RCV003623352] | likely benign | X | 129823770 | 129823770 | Human | 1 | name |
| 405171518 | CV3059653 | single nucleotide variant | NM_016032.4(ZDHHC9):c.597C>T (p.Phe199=) | Syndromic X-linked intellectual disability Raymond type [RCV003622161] | likely benign | X | 129814686 | 129814686 | Human | 1 | name |
| 405170304 | CV3060891 | single nucleotide variant | NM_016032.4(ZDHHC9):c.714C>T (p.Ser238=) | Syndromic X-linked intellectual disability Raymond type [RCV003622051] | benign | X | 129812781 | 129812781 | Human | 1 | name |
| 405172766 | CV3079558 | single nucleotide variant | NM_016032.4(ZDHHC9):c.987A>C (p.Thr329=) | Syndromic X-linked intellectual disability Raymond type [RCV003622282] | benign | X | 129806478 | 129806478 | Human | 1 | name |
| 405209483 | CV3145858 | single nucleotide variant | NM_016032.4(ZDHHC9):c.621C>T (p.Ala207=) | Syndromic X-linked intellectual disability Raymond type [RCV003845588] | benign | X | 129814662 | 129814662 | Human | 1 | name |
| 405239620 | CV3165970 | single nucleotide variant | NM_016032.4(ZDHHC9):c.411A>G (p.Lys137=) | Syndromic X-linked intellectual disability Raymond type [RCV003866982] | likely benign | X | 129823755 | 129823755 | Human | 1 | name |
| 405248848 | CV3180107 | single nucleotide variant | NM_016032.4(ZDHHC9):c.747C>T (p.Leu249=) | Syndromic X-linked intellectual disability Raymond type [RCV003869567] | likely benign | X | 129812748 | 129812748 | Human | 1 | name |
| 405269810 | CV3187498 | single nucleotide variant | NM_016032.4(ZDHHC9):c.885G>A (p.Val295=) | not provided [RCV003887582] | likely benign | X | 129810998 | 129810998 | Human | | name |
| 596944544 | CV3543426 | single nucleotide variant | NM_016032.4(ZDHHC9):c.34C>T (p.Arg12Trp) | not provided [RCV004801547] | uncertain significance | X | 129841912 | 129841912 | Human | | name |
| 597950363 | CV3797869 | single nucleotide variant | NM_016032.4(ZDHHC9):c.465C>T (p.Cys155=) | Syndromic X-linked intellectual disability Raymond type [RCV005135863] | likely benign | X | 129823701 | 129823701 | Human | 1 | name |
| 597973426 | CV3801135 | single nucleotide variant | NM_016032.4(ZDHHC9):c.83G>A (p.Arg28His) | Syndromic X-linked intellectual disability Raymond type [RCV005143330] | uncertain significance | X | 129841863 | 129841863 | Human | 1 | name |
| 597919400 | CV3842607 | single nucleotide variant | NM_016032.4(ZDHHC9):c.717C>T (p.Val239=) | Syndromic X-linked intellectual disability Raymond type [RCV005184092] | likely benign | X | 129812778 | 129812778 | Human | 1 | name |
| 13464855 | CV470473 | single nucleotide variant | NM_016032.4(ZDHHC9):c.489G>A (p.Glu163=) | Syndromic X-linked intellectual disability Raymond type [RCV000544164] | likely benign | X | 129814794 | 129814794 | Human | 1 | name |
| 13468306 | CV471686 | single nucleotide variant | NM_016032.4(ZDHHC9):c.900T>C (p.Gly300=) | Syndromic X-linked intellectual disability Raymond type [RCV000558046] | likely benign | X | 129810983 | 129810983 | Human | 1 | name |
| 13465086 | CV471687 | single nucleotide variant | NM_016032.4(ZDHHC9):c.876C>T (p.Pro292=) | Syndromic X-linked intellectual disability Raymond type [RCV000545362] | likely benign | X | 129811411 | 129811411 | Human | 1 | name |
| 13467939 | CV471688 | single nucleotide variant | NM_016032.4(ZDHHC9):c.519G>A (p.Gly173=) | Syndromic X-linked intellectual disability Raymond type [RCV000556555] | likely benign | X | 129814764 | 129814764 | Human | 1 | name |
| 13499769 | CV472051 | single nucleotide variant | NM_016032.4(ZDHHC9):c.975C>T (p.Ser325=) | History of neurodevelopmental disorder [RCV000720979]|Syndromic X-linked intellectual disability Raymond type [RCV000534077]|not provided [RCV004704081]|not specified [RCV001821562] | benign|likely benign | X | 129810908 | 129810908 | Human | 1 | name |
| 13500567 | CV472052 | single nucleotide variant | NM_016032.4(ZDHHC9):c.777C>T (p.Asp259=) | Syndromic X-linked intellectual disability Raymond type [RCV000537419] | likely benign|uncertain significance | X | 129812718 | 129812718 | Human | 1 | name |
| 13619498 | CV534472 | single nucleotide variant | NM_016032.4(ZDHHC9):c.858G>T (p.Val286=) | Syndromic X-linked intellectual disability Raymond type [RCV000646769] | likely benign | X | 129811429 | 129811429 | Human | 1 | name |
| 13619493 | CV534504 | single nucleotide variant | NM_016032.4(ZDHHC9):c.873G>A (p.Leu291=) | Syndromic X-linked intellectual disability Raymond type [RCV000646765] | likely benign | X | 129811414 | 129811414 | Human | 1 | name |
| 15188628 | CV729401 | single nucleotide variant | NM_016032.4(ZDHHC9):c.369G>A (p.Pro123=) | Syndromic X-linked intellectual disability Raymond type [RCV001517335] | benign | X | 129823797 | 129823797 | Human | 1 | name |
| 15113867 | CV773749 | single nucleotide variant | NM_016032.4(ZDHHC9):c.789A>G (p.Ser263=) | Syndromic X-linked intellectual disability Raymond type [RCV001415357] | likely benign | X | 129811498 | 129811498 | Human | 1 | name |
| 15111719 | CV786699 | single nucleotide variant | NM_016032.4(ZDHHC9):c.579C>T (p.Leu193=) | Syndromic X-linked intellectual disability Raymond type [RCV001481952] | likely benign | X | 129814704 | 129814704 | Human | 1 | name |
| 26898977 | CV822215 | single nucleotide variant | NM_016032.4(ZDHHC9):c.85G>A (p.Val29Ile) | Syndromic X-linked intellectual disability Raymond type [RCV001034433] | likely benign | X | 129841861 | 129841861 | Human | 1 | name |
| 38466422 | CV939422 | single nucleotide variant | NM_016032.4(ZDHHC9):c.98G>A (p.Arg33Gln) | Inborn genetic diseases [RCV005306316]|See cases [RCV001810497]|Syndromic X-linked intellectual disability Raymond type [RCV001212778] | uncertain significance | X | 129841848 | 129841848 | Human | 2 | name |
| 38479934 | CV951589 | single nucleotide variant | NM_016032.4(ZDHHC9):c.53C>G (p.Pro18Arg) | Syndromic X-linked intellectual disability Raymond type [RCV001234524] | uncertain significance | X | 129841893 | 129841893 | Human | 1 | name |
| 38458113 | CV959160 | single nucleotide variant | NM_016032.4(ZDHHC9):c.888G>A (p.Leu296=) | Syndromic X-linked intellectual disability Raymond type [RCV001246233] | likely benign|uncertain significance | X | 129810995 | 129810995 | Human | 1 | name |
| 126913379 | CV1052267 | single nucleotide variant | NM_016032.4(ZDHHC9):c.274G>A (p.Gly92Arg) | Syndromic X-linked intellectual disability Raymond type [RCV001370081]|not provided [RCV002466668] | uncertain significance | X | 129829035 | 129829035 | Human | 1 | name |
| 127322238 | CV1159337 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1032C>T (p.Pro344=) | Syndromic X-linked intellectual disability Raymond type [RCV001523441] | benign | X | 129806433 | 129806433 | Human | 1 | name |
| 127313611 | CV1159338 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1014G>A (p.Pro338=) | Syndromic X-linked intellectual disability Raymond type [RCV001519306] | benign | X | 129806451 | 129806451 | Human | 1 | name |
| 150552009 | CV1300811 | deletion | NM_016032.4(ZDHHC9):c.984del (p.Thr329fs) | Syndromic X-linked intellectual disability Raymond type [RCV003509685]|not provided [RCV001754671] | uncertain significance | X | 129806481 | 129806481 | Human | 1 | name |
| 151801189 | CV1403444 | single nucleotide variant | NM_016032.4(ZDHHC9):c.244A>G (p.Thr82Ala) | Syndromic X-linked intellectual disability Raymond type [RCV001923595]|not provided [RCV003322904] | uncertain significance | X | 129829065 | 129829065 | Human | 1 | name |
| 156396863 | CV1959086 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1038G>A (p.Glu346=) | Syndromic X-linked intellectual disability Raymond type [RCV002584442] | likely benign | X | 129806427 | 129806427 | Human | 1 | name |
| 156205982 | CV2000601 | single nucleotide variant | NM_016032.4(ZDHHC9):c.220A>G (p.Met74Val) | Syndromic X-linked intellectual disability Raymond type [RCV002666667] | uncertain significance | X | 129829089 | 129829089 | Human | 1 | name |
| 156006862 | CV2041999 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1032C>G (p.Pro344=) | Syndromic X-linked intellectual disability Raymond type [RCV002756475] | likely benign | X | 129806433 | 129806433 | Human | 1 | name |
| 156369775 | CV2174342 | single nucleotide variant | NM_016032.4(ZDHHC9):c.266G>C (p.Ser89Thr) | Syndromic X-linked intellectual disability Raymond type [RCV003049610] | uncertain significance | X | 129829043 | 129829043 | Human | 1 | name |
| 156149557 | CV2175257 | single nucleotide variant | NM_016032.4(ZDHHC9):c.222G>A (p.Met74Ile) | Syndromic X-linked intellectual disability Raymond type [RCV003040325] | uncertain significance | X | 129829087 | 129829087 | Human | 1 | name |
| 401740932 | CV2702706 | single nucleotide variant | NM_016032.4(ZDHHC9):c.202A>G (p.Ile68Val) | Inborn genetic diseases [RCV003292484] | uncertain significance | X | 129829107 | 129829107 | Human | 1 | name |
| 402510828 | CV2854658 | single nucleotide variant | NM_016032.4(ZDHHC9):c.197C>T (p.Pro66Leu) | Syndromic X-linked intellectual disability Raymond type [RCV003509938] | uncertain significance | X | 129829112 | 129829112 | Human | 1 | name |
| 402518809 | CV2865989 | single nucleotide variant | NM_016032.4(ZDHHC9):c.184G>A (p.Val62Ile) | Syndromic X-linked intellectual disability Raymond type [RCV003510561] | uncertain significance | X | 129829125 | 129829125 | Human | 1 | name |
| 405711427 | CV3225896 | single nucleotide variant | NM_016032.4(ZDHHC9):c.155T>C (p.Phe52Ser) | Syndromic X-linked intellectual disability Raymond type [RCV003990955] | uncertain significance | X | 129841791 | 129841791 | Human | 1 | name |
| 407426651 | CV3411453 | single nucleotide variant | NM_016032.4(ZDHHC9):c.290C>T (p.Ala97Val) | not provided [RCV004590631] | uncertain significance | X | 129829019 | 129829019 | Human | | name |
| 408384371 | CV3505186 | single nucleotide variant | NM_016032.4(ZDHHC9):c.116A>G (p.Tyr39Cys) | Syndromic X-linked intellectual disability Raymond type [RCV005103617]|ZDHHC9-related disorder [RCV004731754] | uncertain significance | X | 129841830 | 129841830 | Human | 1 | name , trait , alternate_id |
| 597846247 | CV3880600 | single nucleotide variant | NM_016032.4(ZDHHC9):c.257C>G (p.Thr86Ser) | not provided [RCV005227488] | uncertain significance | X | 129829052 | 129829052 | Human | | name |
| 12894886 | CV411124 | single nucleotide variant | NM_016032.4(ZDHHC9):c.251T>C (p.Leu84Ser) | not provided [RCV000484510] | likely pathogenic | X | 129829058 | 129829058 | Human | | name |
| 12913239 | CV421144 | single nucleotide variant | NM_016032.4(ZDHHC9):c.286C>T (p.Arg96Trp) | Syndromic X-linked intellectual disability Raymond type [RCV000493569]|not provided [RCV001575552] | pathogenic|likely pathogenic | X | 129829023 | 129829023 | Human | 1 | name |
| 13464753 | CV471251 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1056C>T (p.Pro352=) | Syndromic X-linked intellectual disability Raymond type [RCV000543804] | likely benign | X | 129806409 | 129806409 | Human | 1 | name |
| 14395615 | CV611441 | single nucleotide variant | NM_016032.4(ZDHHC9):c.268G>A (p.Asp90Asn) | Syndromic X-linked intellectual disability Raymond type [RCV000760177] | likely pathogenic | X | 129829041 | 129829041 | Human | 1 | name |
| 38491525 | CV959162 | single nucleotide variant | NM_016032.4(ZDHHC9):c.160G>A (p.Ala54Thr) | Syndromic X-linked intellectual disability Raymond type [RCV001239527] | uncertain significance | X | 129841786 | 129841786 | Human | 1 | name |
| 40889548 | CV972702 | single nucleotide variant | NM_016032.4(ZDHHC9):c.287G>A (p.Arg96Gln) | Neurodevelopmental abnormality [RCV001264623] | uncertain significance | X | 129829022 | 129829022 | Human | 2 | name |
| 40887034 | CV974302 | duplication | NM_016032.4(ZDHHC9):c.743dup (p.Leu249fs) | Inborn genetic diseases [RCV001266420] | pathogenic | X | 129812751 | 129812752 | Human | 1 | name |
| 40886584 | CV974303 | single nucleotide variant | NM_016032.4(ZDHHC9):c.267T>G (p.Ser89Arg) | Inborn genetic diseases [RCV001265737] | uncertain significance | X | 129829042 | 129829042 | Human | 1 | name |
| 126746496 | CV1018906 | single nucleotide variant | NM_016032.4(ZDHHC9):c.421T>C (p.Cys141Arg) | Syndromic X-linked intellectual disability Raymond type [RCV001330898] | uncertain significance | X | 129823745 | 129823745 | Human | 1 | name |
| 126726621 | CV1035341 | single nucleotide variant | NM_016032.4(ZDHHC9):c.331G>T (p.Ala111Ser) | Syndromic X-linked intellectual disability Raymond type [RCV001348507] | uncertain significance | X | 129823835 | 129823835 | Human | 1 | name |
| 126921300 | CV1052263 | single nucleotide variant | NM_016032.4(ZDHHC9):c.989A>G (p.Glu330Gly) | Syndromic X-linked intellectual disability Raymond type [RCV001363398] | uncertain significance | X | 129806476 | 129806476 | Human | 1 | name |
| 126917459 | CV1052264 | single nucleotide variant | NM_016032.4(ZDHHC9):c.614A>G (p.Tyr205Cys) | Syndromic X-linked intellectual disability Raymond type [RCV001361180] | uncertain significance | X | 129814669 | 129814669 | Human | 1 | name |
| 126923448 | CV1052265 | single nucleotide variant | NM_016032.4(ZDHHC9):c.443G>A (p.Arg148Gln) | Syndromic X-linked intellectual disability Raymond type [RCV001365857] | uncertain significance | X | 129823723 | 129823723 | Human | 1 | name |
| 126924110 | CV1052266 | single nucleotide variant | NM_016032.4(ZDHHC9):c.313A>G (p.Ile105Val) | Syndromic X-linked intellectual disability Raymond type [RCV001366642] | uncertain significance | X | 129828996 | 129828996 | Human | 1 | name |
| 150552969 | CV1295649 | single nucleotide variant | NM_016032.4(ZDHHC9):c.304G>A (p.Ala102Thr) | not provided [RCV001768581] | uncertain significance | X | 129829005 | 129829005 | Human | | name |
| 150553968 | CV1298362 | single nucleotide variant | NM_016032.4(ZDHHC9):c.418T>C (p.Tyr140His) | not provided [RCV001770561] | uncertain significance | X | 129823748 | 129823748 | Human | | name |
| 150551805 | CV1298907 | single nucleotide variant | NM_016032.4(ZDHHC9):c.496G>A (p.Asp166Asn) | Syndromic X-linked intellectual disability Raymond type [RCV001754546]|not provided [RCV003321869] | likely pathogenic|conflicting interpretations of pathogenicity | X | 129814787 | 129814787 | Human | 1 | name |
| 150553352 | CV1303336 | single nucleotide variant | NM_016032.4(ZDHHC9):c.425A>T (p.Tyr142Phe) | not provided [RCV001769026] | uncertain significance | X | 129823741 | 129823741 | Human | | name |
| 150553950 | CV1309629 | single nucleotide variant | NM_016032.4(ZDHHC9):c.346G>A (p.Val116Met) | not provided [RCV003238674] | uncertain significance | X | 129823820 | 129823820 | Human | | name |
| 151714758 | CV1401782 | single nucleotide variant | NM_016032.4(ZDHHC9):c.544C>T (p.Arg182Cys) | Syndromic X-linked intellectual disability Raymond type [RCV002017156]|not provided [RCV004797982] | conflicting interpretations of pathogenicity|uncertain significance | X | 129814739 | 129814739 | Human | 1 | name |
| 151797531 | CV1435233 | single nucleotide variant | NM_016032.4(ZDHHC9):c.344C>T (p.Ala115Val) | Syndromic X-linked intellectual disability Raymond type [RCV001916191] | uncertain significance | X | 129823822 | 129823822 | Human | 1 | name |
| 151830826 | CV1515856 | single nucleotide variant | NM_016032.4(ZDHHC9):c.778A>G (p.Ile260Val) | Syndromic X-linked intellectual disability Raymond type [RCV001984051] | uncertain significance | X | 129811509 | 129811509 | Human | 1 | name |
| 152037372 | CV1669109 | single nucleotide variant | NM_016032.4(ZDHHC9):c.412C>A (p.Leu138Met) | Syndromic X-linked intellectual disability Raymond type [RCV003774650]|not provided [RCV002224161] | uncertain significance | X | 129823754 | 129823754 | Human | 1 | name |
| 153000948 | CV1683972 | single nucleotide variant | NM_016032.4(ZDHHC9):c.523T>G (p.Cys175Gly) | Syndromic X-linked intellectual disability Raymond type [RCV002254828] | uncertain significance | X | 129814760 | 129814760 | Human | 1 | name |
| 153346549 | CV1691830 | single nucleotide variant | NM_016032.4(ZDHHC9):c.601T>C (p.Phe201Leu) | Syndromic X-linked intellectual disability Raymond type [RCV002273313] | uncertain significance | X | 129814682 | 129814682 | Human | 1 | name |
| 155267811 | CV1701377 | single nucleotide variant | NM_016032.4(ZDHHC9):c.566T>C (p.Leu189Pro) | Syndromic X-linked intellectual disability Raymond type [RCV002283602] | uncertain significance | X | 129814717 | 129814717 | Human | 1 | name |
| 155694431 | CV1771917 | single nucleotide variant | NM_016032.4(ZDHHC9):c.770A>G (p.Asn257Ser) | Syndromic X-linked intellectual disability Raymond type [RCV002299503]|not provided [RCV005051957] | uncertain significance | X | 129812725 | 129812725 | Human | 1 | name |
| 155709651 | CV1775753 | single nucleotide variant | NM_016032.4(ZDHHC9):c.952A>T (p.Ser318Cys) | Syndromic X-linked intellectual disability Raymond type [RCV002296139] | uncertain significance | X | 129810931 | 129810931 | Human | 1 | name |
| 156048626 | CV1867601 | single nucleotide variant | NM_016032.4(ZDHHC9):c.979G>C (p.Ala327Pro) | not provided [RCV002510073] | uncertain significance | X | 129806486 | 129806486 | Human | | name |
| 156412688 | CV1904548 | single nucleotide variant | NM_016032.4(ZDHHC9):c.698T>C (p.Phe233Ser) | Syndromic X-linked intellectual disability Raymond type [RCV002587911] | uncertain significance | X | 129812797 | 129812797 | Human | 1 | name |
| 156382371 | CV1941571 | single nucleotide variant | NM_016032.4(ZDHHC9):c.979G>A (p.Ala327Thr) | Inborn genetic diseases [RCV002722764]|Syndromic X-linked intellectual disability Raymond type [RCV003111664] | uncertain significance | X | 129806486 | 129806486 | Human | 2 | name |
| 156103744 | CV2061109 | single nucleotide variant | NM_016032.4(ZDHHC9):c.718G>A (p.Val240Met) | Syndromic X-linked intellectual disability Raymond type [RCV002824651]|not provided [RCV003458155] | uncertain significance | X | 129812777 | 129812777 | Human | 1 | name |
| 155943024 | CV2072325 | single nucleotide variant | NM_016032.4(ZDHHC9):c.328G>A (p.Glu110Lys) | Syndromic X-linked intellectual disability Raymond type [RCV002861902] | uncertain significance | X | 129828981 | 129828981 | Human | 1 | name |
| 156335627 | CV2178090 | single nucleotide variant | NM_016032.4(ZDHHC9):c.361C>T (p.Arg121Ter) | Syndromic X-linked intellectual disability Raymond type [RCV003047458]|not provided [RCV004775276] | pathogenic | X | 129823805 | 129823805 | Human | 1 | name |
| 156224621 | CV2219407 | single nucleotide variant | NM_016032.4(ZDHHC9):c.892C>T (p.Arg298Ter) | Inborn genetic diseases [RCV002712354]|Syndromic X-linked intellectual disability Raymond type [RCV003225255] | pathogenic|likely pathogenic | X | 129810991 | 129810991 | Human | 2 | name |
| 156050795 | CV2237846 | single nucleotide variant | NM_016032.4(ZDHHC9):c.983C>G (p.Pro328Arg) | Inborn genetic diseases [RCV002782008] | uncertain significance | X | 129806482 | 129806482 | Human | 1 | name |
| 11051309 | CV225835 | single nucleotide variant | NM_016032.4(ZDHHC9):c.893G>A (p.Arg298Gln) | Syndromic X-linked intellectual disability Raymond type [RCV000209872] | uncertain significance | X | 129810990 | 129810990 | Human | 1 | name |
| 243051950 | CV2404235 | single nucleotide variant | NM_016032.4(ZDHHC9):c.806G>A (p.Arg269His) | Syndromic X-linked intellectual disability Raymond type [RCV005060947]|not provided [RCV003129261] | uncertain significance | X | 129811481 | 129811481 | Human | 1 | name |
| 329363093 | CV2445820 | single nucleotide variant | NM_016032.4(ZDHHC9):c.754C>G (p.Leu252Val) | Inborn genetic diseases [RCV003181193] | likely benign | X | 129812741 | 129812741 | Human | 1 | name |
| 8598602 | CV25750 | single nucleotide variant | NM_016032.4(ZDHHC9):c.442C>T (p.Arg148Trp) | Intellectual disability [RCV001260822]|Syndromic X-linked intellectual disability Raymond type [RCV000011457]|not provided [RCV001091717] | pathogenic|likely pathogenic | X | 129823724 | 129823724 | Human | 3 | name |
| 8598603 | CV25751 | single nucleotide variant | NM_016032.4(ZDHHC9):c.448C>T (p.Pro150Ser) | Syndromic X-linked intellectual disability Raymond type [RCV000011458] | pathogenic | X | 129823718 | 129823718 | Human | 1 | name |
| 401797088 | CV2740875 | single nucleotide variant | NM_016032.4(ZDHHC9):c.792G>A (p.Trp264Ter) | not provided [RCV003322039] | likely pathogenic | X | 129811495 | 129811495 | Human | | name |
| 401855105 | CV2752760 | single nucleotide variant | NM_016032.4(ZDHHC9):c.805C>T (p.Arg269Cys) | Syndromic X-linked intellectual disability Raymond type [RCV003337814] | uncertain significance | X | 129811482 | 129811482 | Human | 1 | name |
| 401915820 | CV2795357 | single nucleotide variant | NM_016032.4(ZDHHC9):c.496G>C (p.Asp166His) | Neurodevelopmental disorder [RCV003389192] | uncertain significance | X | 129814787 | 129814787 | Human | 1 | name |
| 401912862 | CV2801459 | single nucleotide variant | NM_016032.4(ZDHHC9):c.565C>T (p.Leu189Phe) | Syndromic X-linked intellectual disability Raymond type [RCV005062893]|ZDHHC9-related disorder [RCV003399997] | uncertain significance | X | 129814718 | 129814718 | Human | 1 | name , trait , alternate_id |
| 402520760 | CV2877883 | single nucleotide variant | NM_016032.4(ZDHHC9):c.961C>T (p.Leu321Phe) | Syndromic X-linked intellectual disability Raymond type [RCV003510693] | uncertain significance | X | 129810922 | 129810922 | Human | 1 | name |
| 402511664 | CV2914457 | single nucleotide variant | NM_016032.4(ZDHHC9):c.586A>G (p.Ile196Val) | Syndromic X-linked intellectual disability Raymond type [RCV003510034] | uncertain significance | X | 129814697 | 129814697 | Human | 1 | name |
| 405169377 | CV2954896 | single nucleotide variant | NM_016032.4(ZDHHC9):c.373C>T (p.Arg125Cys) | Syndromic X-linked intellectual disability Raymond type [RCV003621966] | uncertain significance | X | 129823793 | 129823793 | Human | 1 | name |
| 402465172 | CV2965257 | single nucleotide variant | NM_016032.4(ZDHHC9):c.715G>A (p.Val239Ile) | Syndromic X-linked intellectual disability Raymond type [RCV003622588] | uncertain significance | X | 129812780 | 129812780 | Human | 1 | name |
| 402467037 | CV2997119 | single nucleotide variant | NM_016032.4(ZDHHC9):c.491G>A (p.Arg164His) | Syndromic X-linked intellectual disability Raymond type [RCV003623069] | uncertain significance | X | 129814792 | 129814792 | Human | 1 | name |
| 402466755 | CV2999551 | single nucleotide variant | NM_016032.4(ZDHHC9):c.913G>C (p.Glu305Gln) | Syndromic X-linked intellectual disability Raymond type [RCV003622997] | uncertain significance | X | 129810970 | 129810970 | Human | 1 | name |
| 402467616 | CV3015916 | single nucleotide variant | NM_016032.4(ZDHHC9):c.562A>G (p.Ile188Val) | Syndromic X-linked intellectual disability Raymond type [RCV003623222] | uncertain significance | X | 129814721 | 129814721 | Human | 1 | name |
| 402469259 | CV3034037 | single nucleotide variant | NM_016032.4(ZDHHC9):c.790T>C (p.Trp264Arg) | Syndromic X-linked intellectual disability Raymond type [RCV003623659] | uncertain significance | X | 129811497 | 129811497 | Human | 1 | name |
| 405223199 | CV3151121 | single nucleotide variant | NM_016032.4(ZDHHC9):c.956G>A (p.Ser319Asn) | Syndromic X-linked intellectual disability Raymond type [RCV003847546] | likely benign | X | 129810927 | 129810927 | Human | 1 | name |
| 407508905 | CV3496415 | single nucleotide variant | NM_016032.4(ZDHHC9):c.620C>T (p.Ala207Val) | not provided [RCV004698256] | uncertain significance | X | 129814663 | 129814663 | Human | | name |
| 408366886 | CV3500301 | single nucleotide variant | NM_016032.4(ZDHHC9):c.844A>T (p.Asn282Tyr) | not provided [RCV004722344] | uncertain significance | X | 129811443 | 129811443 | Human | | name |
| 408388957 | CV3520942 | single nucleotide variant | NM_016032.4(ZDHHC9):c.575C>T (p.Ser192Phe) | not provided [RCV004761775] | uncertain significance | X | 129814708 | 129814708 | Human | | name |
| 597631391 | CV3631132 | single nucleotide variant | NM_016032.4(ZDHHC9):c.824G>A (p.Ser275Asn) | Inborn genetic diseases [RCV004967679] | uncertain significance | X | 129811463 | 129811463 | Human | 1 | name |
| 597916544 | CV3779387 | single nucleotide variant | NM_016032.4(ZDHHC9):c.764C>T (p.Thr255Ile) | Syndromic X-linked intellectual disability Raymond type [RCV005129528] | uncertain significance | X | 129812731 | 129812731 | Human | 1 | name |
| 597888328 | CV3787724 | single nucleotide variant | NM_016032.4(ZDHHC9):c.754C>T (p.Leu252Phe) | Syndromic X-linked intellectual disability Raymond type [RCV005125291] | uncertain significance | X | 129812741 | 129812741 | Human | 1 | name |
| 597958939 | CV3848512 | single nucleotide variant | NM_016032.4(ZDHHC9):c.679C>A (p.Leu227Ile) | Syndromic X-linked intellectual disability Raymond type [RCV005192213] | uncertain significance | X | 129812816 | 129812816 | Human | 1 | name |
| 616938313 | CV4012998 | single nucleotide variant | NM_016032.4(ZDHHC9):c.878C>T (p.Pro293Leu) | not provided [RCV005410464] | uncertain significance | X | 129811409 | 129811409 | Human | | name |
| 13472887 | CV446494 | single nucleotide variant | NM_016032.4(ZDHHC9):c.805C>G (p.Arg269Gly) | not provided [RCV000519244]|not specified [RCV002248754] | uncertain significance | X | 129811482 | 129811482 | Human | | name |
| 13499076 | CV471689 | single nucleotide variant | NM_016032.4(ZDHHC9):c.397A>C (p.Asn133His) | Syndromic X-linked intellectual disability Raymond type [RCV000531396] | uncertain significance | X | 129823769 | 129823769 | Human | 1 | name |
| 13619491 | CV534485 | single nucleotide variant | NM_016032.4(ZDHHC9):c.332C>T (p.Ala111Val) | Syndromic X-linked intellectual disability Raymond type [RCV000646764] | likely benign|uncertain significance | X | 129823834 | 129823834 | Human | 1 | name |
| 13705338 | CV536546 | single nucleotide variant | NM_016032.4(ZDHHC9):c.928C>T (p.Arg310Ter) | not provided [RCV000657798] | uncertain significance | X | 129810955 | 129810955 | Human | | name |
| 13801883 | CV574272 | single nucleotide variant | NM_016032.4(ZDHHC9):c.929G>A (p.Arg310Gln) | Inborn genetic diseases [RCV004965687]|Intellectual disability [RCV001260851]|Syndromic X-linked intellectual disability Raymond type [RCV000698036] | uncertain significance | X | 129810954 | 129810954 | Human | 4 | name |
| 13820758 | CV574274 | single nucleotide variant | NM_016032.4(ZDHHC9):c.598G>A (p.Ala200Thr) | Syndromic X-linked intellectual disability Raymond type [RCV000695094] | likely benign|uncertain significance | X | 129814685 | 129814685 | Human | 1 | name |
| 14714032 | CV649668 | single nucleotide variant | NM_016032.4(ZDHHC9):c.399C>A (p.Asn133Lys) | Syndromic X-linked intellectual disability Raymond type [RCV000794288] | uncertain significance | X | 129823767 | 129823767 | Human | 1 | name |
| 26898837 | CV822214 | single nucleotide variant | NM_016032.4(ZDHHC9):c.808G>A (p.Val270Ile) | Inborn genetic diseases [RCV005298671]|Syndromic X-linked intellectual disability Raymond type [RCV001034122] | likely benign|uncertain significance | X | 129811479 | 129811479 | Human | 2 | name |
| 26907645 | CV849602 | single nucleotide variant | NM_016032.4(ZDHHC9):c.925A>G (p.Ser309Gly) | Syndromic X-linked intellectual disability Raymond type [RCV001070420] | uncertain significance | X | 129810958 | 129810958 | Human | 1 | name |
| 34896042 | CV917359 | single nucleotide variant | NM_016032.4(ZDHHC9):c.949A>T (p.Thr317Ser) | Syndromic X-linked intellectual disability Raymond type [RCV002560163]|not specified [RCV001193307] | uncertain significance | X | 129810934 | 129810934 | Human | 1 | name |
| 38463745 | CV919974 | duplication | NM_016032.4(ZDHHC9):c.852dup (p.Glu285Ter) | Syndromic X-linked intellectual disability Raymond type [RCV001199032] | likely pathogenic | X | 129811434 | 129811435 | Human | 1 | name |
| 38462332 | CV919975 | single nucleotide variant | NM_016032.4(ZDHHC9):c.354G>C (p.Gln118His) | Syndromic X-linked intellectual disability Raymond type [RCV001198121] | benign | X | 129823812 | 129823812 | Human | 1 | name |
| 38456795 | CV939421 | single nucleotide variant | NM_016032.4(ZDHHC9):c.362G>A (p.Arg121Gln) | Syndromic X-linked intellectual disability Raymond type [RCV001210933] | uncertain significance | X | 129823804 | 129823804 | Human | 1 | name |
| 38495187 | CV959161 | single nucleotide variant | NM_016032.4(ZDHHC9):c.673A>G (p.Thr225Ala) | Syndromic X-linked intellectual disability Raymond type [RCV001241781] | uncertain significance | X | 129813678 | 129813678 | Human | 1 | name |
| 40888083 | CV974301 | single nucleotide variant | NM_016032.4(ZDHHC9):c.748G>A (p.Val250Met) | Inborn genetic diseases [RCV001267624] | uncertain significance | X | 129812747 | 129812747 | Human | 1 | name |
| 126733868 | CV999601 | single nucleotide variant | NM_016032.4(ZDHHC9):c.764C>A (p.Thr255Lys) | Inborn genetic diseases [RCV004686652]|Syndromic X-linked intellectual disability Raymond type [RCV001294819] | likely pathogenic|uncertain significance | X | 129812731 | 129812731 | Human | 2 | name |
| 126766070 | CV999602 | single nucleotide variant | NM_016032.4(ZDHHC9):c.718G>C (p.Val240Leu) | Syndromic X-linked intellectual disability Raymond type [RCV001301739] | conflicting interpretations of pathogenicity|uncertain significance | X | 129812777 | 129812777 | Human | 1 | name |
| 126751094 | CV1035340 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1025G>A (p.Ser342Asn) | Syndromic X-linked intellectual disability Raymond type [RCV001352371] | uncertain significance | X | 129806440 | 129806440 | Human | 1 | name |
| 150410505 | CV1178671 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1045C>T (p.Pro349Ser) | Syndromic X-linked intellectual disability Raymond type [RCV002032563]|not provided [RCV001546678] | likely benign|uncertain significance | X | 129806420 | 129806420 | Human | 1 | name |
| 151801684 | CV1431564 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1028C>T (p.Thr343Ile) | Syndromic X-linked intellectual disability Raymond type [RCV001924440] | uncertain significance | X | 129806437 | 129806437 | Human | 1 | name |
| 151711126 | CV1468319 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1054C>A (p.Pro352Thr) | Syndromic X-linked intellectual disability Raymond type [RCV002001031] | uncertain significance | X | 129806411 | 129806411 | Human | 1 | name |
| 151711186 | CV1498399 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1055C>G (p.Pro352Arg) | Syndromic X-linked intellectual disability Raymond type [RCV002001367] | uncertain significance | X | 129806410 | 129806410 | Human | 1 | name |
| 156082465 | CV1883754 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1030C>T (p.Pro344Ser) | Syndromic X-linked intellectual disability Raymond type [RCV003079915] | likely benign | X | 129806435 | 129806435 | Human | 1 | name |
| 156444969 | CV1949022 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1084G>C (p.Ala362Pro) | Syndromic X-linked intellectual disability Raymond type [RCV003115903] | uncertain significance | X | 129806381 | 129806381 | Human | 1 | name |
| 156186065 | CV2164113 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1021A>G (p.Ser341Gly) | Syndromic X-linked intellectual disability Raymond type [RCV003023981] | uncertain significance | X | 129806444 | 129806444 | Human | 1 | name |
| 329380653 | CV2464274 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1081G>A (p.Glu361Lys) | Inborn genetic diseases [RCV003212832] | uncertain significance | X | 129806384 | 129806384 | Human | 1 | name |
| 401869512 | CV2772427 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1034A>C (p.Glu345Ala) | Inborn genetic diseases [RCV003345824]|Syndromic X-linked intellectual disability Raymond type [RCV003621701] | likely benign|uncertain significance | X | 129806431 | 129806431 | Human | 2 | name |
| 402464685 | CV2956060 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1003A>T (p.Asn335Tyr) | Syndromic X-linked intellectual disability Raymond type [RCV003622469] | uncertain significance | X | 129806462 | 129806462 | Human | 1 | name |
| 405869462 | CV3396743 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1057C>T (p.Pro353Ser) | Syndromic X-linked intellectual disability Raymond type [RCV004566623] | uncertain significance | X | 129806408 | 129806408 | Human | 1 | name |
| 596947176 | CV3548726 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1021A>C (p.Ser341Arg) | not provided [RCV004811050] | uncertain significance | X | 129806444 | 129806444 | Human | | name |
| 13806203 | CV572196 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1001C>T (p.Ser334Leu) | Syndromic X-linked intellectual disability Raymond type [RCV000700466] | uncertain significance | X | 129806464 | 129806464 | Human | 1 | name |
| 13814231 | CV574270 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1013C>T (p.Pro338Leu) | Inborn genetic diseases [RCV005298582]|Syndromic X-linked intellectual disability Raymond type [RCV000690755]|not specified [RCV004702324] | uncertain significance | X | 129806452 | 129806452 | Human | 2 | name |
| 15201946 | CV758284 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1033G>A (p.Glu345Lys) | Syndromic X-linked intellectual disability Raymond type [RCV000913293] | benign | X | 129806432 | 129806432 | Human | 1 | name |
| 38491957 | CV929560 | single nucleotide variant | NM_016032.4(ZDHHC9):c.1075G>A (p.Ala359Thr) | Syndromic X-linked intellectual disability Raymond type [RCV001223206] | uncertain significance | X | 129806390 | 129806390 | Human | 1 | name |
| 8561841 | CV25748 | deletion | NM_016032.4(ZDHHC9):c.172_175del (p.Arg58fs) | Syndromic X-linked intellectual disability Raymond type [RCV000011455] | pathogenic | X | 129829134 | 129829137 | Human | 1 | name |
| 13611547 | CV514791 | deletion | NM_016032.4(ZDHHC9):c.717_738del (p.Val240fs) | not provided [RCV000627547] | pathogenic | X | 129812757 | 129812778 | Human | | name |
| 13533097 | CV512587 | deletion | NM_016032.4(ZDHHC9):c.679del (p.Val226_Leu227insTer) | Inborn genetic diseases [RCV000624868] | pathogenic | X | 129812816 | 129812816 | Human | 1 | name |
| 13467633 | CV471250 | insertion | NM_016032.4(ZDHHC9):c.1064_1065insCCCACAGCC (p.Pro355_Gln357dup) | Syndromic X-linked intellectual disability Raymond type [RCV000555375] | likely benign|uncertain significance | X | 129806400 | 129806401 | Human | 1 | name |
