| 155934511 | CV2225317 | single nucleotide variant | NM_032153.6(ZIC4):c.-7T>G | not specified [RCV004098954] | uncertain significance | 3 | 147402804 | 147402804 | Human | | name |
| 156366082 | CV1908483 | single nucleotide variant | NM_032153.6(ZIC4):c.689-5G>A | not provided [RCV002582074] | likely benign | 3 | 147391251 | 147391251 | Human | | name |
| 156131529 | CV1918009 | single nucleotide variant | NM_032153.6(ZIC4):c.71-10T>C | not provided [RCV002623330] | likely benign | 3 | 147396479 | 147396479 | Human | | name |
| 156391083 | CV2118657 | single nucleotide variant | NM_032153.6(ZIC4):c.-15-6A>G | not provided [RCV002943914] | benign | 3 | 147402818 | 147402818 | Human | | name |
| 405120237 | CV2952280 | single nucleotide variant | NM_032153.6(ZIC4):c.71-11T>A | not provided [RCV003671392] | likely benign | 3 | 147396480 | 147396480 | Human | | name |
| 156130827 | CV2022732 | single nucleotide variant | NM_032153.6(ZIC4):c.688+17G>A | not provided [RCV002740557] | likely benign | 3 | 147395835 | 147395835 | Human | | name |
| 156144430 | CV2033090 | single nucleotide variant | NM_032153.6(ZIC4):c.688+19C>T | not provided [RCV002741014] | likely benign | 3 | 147395833 | 147395833 | Human | | name |
| 156024047 | CV2145505 | single nucleotide variant | NM_032153.6(ZIC4):c.689-14G>A | not provided [RCV003018368] | likely benign | 3 | 147391260 | 147391260 | Human | | name |
| 405147948 | CV2960148 | single nucleotide variant | NM_032153.6(ZIC4):c.688+10C>A | not provided [RCV003669841] | likely benign | 3 | 147395842 | 147395842 | Human | | name |
| 405224757 | CV2979492 | deletion | NM_032153.6(ZIC4):c.-15-20del | not provided [RCV003681234] | likely benign | 3 | 147402832 | 147402832 | Human | | name |
| 597974048 | CV3821056 | single nucleotide variant | NM_032153.6(ZIC4):c.1004+7G>A | not provided [RCV005168377] | likely benign | 3 | 147390924 | 147390924 | Human | | name |
| 156133626 | CV2195967 | single nucleotide variant | NM_032153.6(ZIC4):c.-16+901C>T | not specified [RCV004072221] | uncertain significance | 3 | 147405462 | 147405462 | Human | | name |
| 156054817 | CV2320489 | single nucleotide variant | NM_032153.6(ZIC4):c.-16+952G>A | not specified [RCV004172123] | likely benign | 3 | 147405411 | 147405411 | Human | | name |
| 156392747 | CV2386647 | single nucleotide variant | NM_032153.6(ZIC4):c.-16+986C>T | not specified [RCV004230988] | uncertain significance | 3 | 147405377 | 147405377 | Human | | name |
| 405140722 | CV3029742 | single nucleotide variant | NM_032153.6(ZIC4):c.1005-15A>C | not provided [RCV003702397] | benign | 3 | 147388874 | 147388874 | Human | | name |
| 407459794 | CV3490353 | single nucleotide variant | NM_032153.6(ZIC4):c.-16+967A>T | not specified [RCV004687226] | uncertain significance | 3 | 147405396 | 147405396 | Human | | name |
| 597728716 | CV3625060 | single nucleotide variant | NM_032153.6(ZIC4):c.-16+928G>C | not specified [RCV004888576] | uncertain significance | 3 | 147405435 | 147405435 | Human | | name |
| 598159412 | CV3934083 | single nucleotide variant | NM_032153.6(ZIC4):c.-16+961G>T | not specified [RCV005306567] | uncertain significance | 3 | 147405402 | 147405402 | Human | | name |
| 156137556 | CV1902164 | single nucleotide variant | NM_032153.6(ZIC4):c.-15-1282C>T | not provided [RCV003082074] | uncertain significance | 3 | 147404094 | 147404094 | Human | | name |
| 156442123 | CV1938026 | single nucleotide variant | NM_032153.6(ZIC4):c.-15-1225G>A | not provided [RCV003112460]|not specified [RCV004686767] | uncertain significance | 3 | 147404037 | 147404037 | Human | | name |
| 402500358 | CV2872789 | single nucleotide variant | NM_032153.6(ZIC4):c.-15-1159G>A | not provided [RCV003545836] | uncertain significance | 3 | 147403971 | 147403971 | Human | | name |
| 405238390 | CV2891386 | single nucleotide variant | NM_032153.6(ZIC4):c.-15-1271A>C | not provided [RCV003556855] | likely benign | 3 | 147404083 | 147404083 | Human | | name |
| 405145097 | CV3027254 | single nucleotide variant | NM_032153.6(ZIC4):c.-15-1133C>G | not provided [RCV003702763] | likely benign | 3 | 147403945 | 147403945 | Human | | name |
| 405144572 | CV3027344 | single nucleotide variant | NM_032153.6(ZIC4):c.-15-1138C>T | not provided [RCV003702807] | likely benign | 3 | 147403950 | 147403950 | Human | | name |
| 405133019 | CV3051366 | single nucleotide variant | NM_032153.6(ZIC4):c.-15-1142C>G | not provided [RCV003724998] | likely benign | 3 | 147403954 | 147403954 | Human | | name |
| 405154804 | CV3068809 | single nucleotide variant | NM_032153.6(ZIC4):c.-15-1245T>C | not provided [RCV003726669] | likely benign | 3 | 147404057 | 147404057 | Human | | name |
| 405246199 | CV3162254 | single nucleotide variant | NM_032153.6(ZIC4):c.-15-1272T>C | not provided [RCV003868773] | likely benign | 3 | 147404084 | 147404084 | Human | | name |
| 597976386 | CV3829634 | single nucleotide variant | NM_032153.6(ZIC4):c.-15-1253C>T | not provided [RCV005169901] | uncertain significance | 3 | 147404065 | 147404065 | Human | | name |
| 12896529 | CV389565 | single nucleotide variant | NM_032153.6(ZIC4):c.-15-1152G>A | not provided [RCV002522753]|not specified [RCV000455473] | benign | 3 | 147403964 | 147403964 | Human | 5 | name |
| 12896529 | CV389565 | single nucleotide variant | NM_032153.6(ZIC4):c.-15-1152G>A | not provided [RCV002522753]|not specified [RCV000455473] | benign | 3 | 147403964 | 147403965 | Human | 5 | name |
| 15178034 | CV733860 | single nucleotide variant | NM_032153.6(ZIC4):c.-15-1281G>A | not provided [RCV000906782]|not specified [RCV004887661] | likely benign | 3 | 147404093 | 147404093 | Human | | name |
| 402506904 | CV3039217 | single nucleotide variant | NM_032153.6(ZIC4):c.37T>C (p.Leu13=) | not provided [RCV003715289] | likely benign | 3 | 147402761 | 147402761 | Human | | name |
| 156245062 | CV1894097 | single nucleotide variant | NM_032153.6(ZIC4):c.273T>C (p.Ala91=) | not provided [RCV003085891] | likely benign | 3 | 147396267 | 147396267 | Human | | name |
| 156361611 | CV1900576 | single nucleotide variant | NM_032153.6(ZIC4):c.105C>T (p.Thr35=) | not provided [RCV002581764] | likely benign | 3 | 147396435 | 147396435 | Human | | name |
| 156131303 | CV1917975 | single nucleotide variant | NM_032153.6(ZIC4):c.132G>A (p.Pro44=) | not provided [RCV002623321] | likely benign | 3 | 147396408 | 147396408 | Human | | name |
| 156417883 | CV1920640 | single nucleotide variant | NM_032153.6(ZIC4):c.198G>C (p.Gly66=) | not provided [RCV002611051] | likely benign | 3 | 147396342 | 147396342 | Human | | name |
| 597936615 | CV3764877 | single nucleotide variant | NM_032153.6(ZIC4):c.276C>T (p.Ala92=) | not provided [RCV005117576] | likely benign | 3 | 147396264 | 147396264 | Human | | name |
| 597913451 | CV3833797 | single nucleotide variant | NM_032153.6(ZIC4):c.258C>T (p.Ser86=) | not provided [RCV005183156] | likely benign | 3 | 147396282 | 147396282 | Human | | name |
| 8661114 | CV136234 | single nucleotide variant | NM_032153.6(ZIC4):c.966G>C (p.Ser322=) | not provided [RCV002515803]|not specified [RCV000118906] | benign|likely benign|conflicting interpretations of pathogenicity | 3 | 147390969 | 147390969 | Human | | name |
| 156408104 | CV1911465 | single nucleotide variant | NM_032153.6(ZIC4):c.765G>A (p.Ser255=) | not provided [RCV002607119] | likely benign | 3 | 147391170 | 147391170 | Human | | name |
| 156269171 | CV1915185 | single nucleotide variant | NM_032153.6(ZIC4):c.849G>A (p.Lys283=) | not provided [RCV002628030] | likely benign | 3 | 147391086 | 147391086 | Human | | name |
| 156314229 | CV1931479 | single nucleotide variant | NM_032153.6(ZIC4):c.49C>T (p.Arg17Ter) | not provided [RCV002629957] | uncertain significance | 3 | 147402749 | 147402749 | Human | | name |
| 155916486 | CV1941566 | single nucleotide variant | NM_032153.6(ZIC4):c.74G>A (p.Ser25Asn) | not provided [RCV003111729]|not specified [RCV004189749] | uncertain significance | 3 | 147396466 | 147396466 | Human | | name |
| 156133071 | CV2022824 | single nucleotide variant | NM_032153.6(ZIC4):c.35G>A (p.Arg12Gln) | not provided [RCV002740636] | uncertain significance | 3 | 147402763 | 147402763 | Human | | name |
| 155938630 | CV2041482 | single nucleotide variant | NM_032153.6(ZIC4):c.28A>G (p.Arg10Gly) | not provided [RCV002775046] | uncertain significance | 3 | 147402770 | 147402770 | Human | | name |
| 156017119 | CV2046925 | single nucleotide variant | NM_032153.6(ZIC4):c.744C>T (p.Ser248=) | not provided [RCV002756994] | likely benign | 3 | 147391191 | 147391191 | Human | | name |
| 155906507 | CV2080378 | single nucleotide variant | NM_032153.6(ZIC4):c.459G>A (p.Glu153=) | not provided [RCV002858187] | likely benign | 3 | 147396081 | 147396081 | Human | | name |
| 156103086 | CV2113451 | single nucleotide variant | NM_032153.6(ZIC4):c.468G>A (p.Thr156=) | not provided [RCV002952811] | likely benign | 3 | 147396072 | 147396072 | Human | | name |
| 156018477 | CV2114678 | single nucleotide variant | NM_032153.6(ZIC4):c.831C>T (p.His277=) | not provided [RCV002909495] | likely benign | 3 | 147391104 | 147391104 | Human | | name |
| 156306764 | CV2115642 | single nucleotide variant | NM_032153.6(ZIC4):c.699C>T (p.Pro233=) | not provided [RCV002922857] | likely benign | 3 | 147391236 | 147391236 | Human | | name |
| 156070696 | CV2168857 | single nucleotide variant | NM_032153.6(ZIC4):c.307C>T (p.Leu103=) | not provided [RCV003037558] | likely benign | 3 | 147396233 | 147396233 | Human | | name |
| 155959090 | CV2193736 | single nucleotide variant | NM_032153.6(ZIC4):c.40C>T (p.Arg14Trp) | not specified [RCV004074499] | uncertain significance | 3 | 147402758 | 147402758 | Human | | name |
| 156347238 | CV2375404 | single nucleotide variant | NM_032153.6(ZIC4):c.50G>A (p.Arg17Gln) | not provided [RCV003548965]|not specified [RCV004232799] | uncertain significance | 3 | 147402748 | 147402748 | Human | | name |
| 404996820 | CV2851494 | single nucleotide variant | NM_032153.6(ZIC4):c.34C>T (p.Arg12Ter) | not provided [RCV003491856] | uncertain significance | 3 | 147402764 | 147402764 | Human | | name |
| 405223677 | CV2887580 | single nucleotide variant | NM_032153.6(ZIC4):c.963C>T (p.Ser321=) | not provided [RCV003554306] | likely benign | 3 | 147390972 | 147390972 | Human | | name |
| 405128459 | CV2954907 | single nucleotide variant | NM_032153.6(ZIC4):c.900G>C (p.Ser300=) | not provided [RCV003668158] | likely benign | 3 | 147391035 | 147391035 | Human | | name |
| 405222176 | CV3056911 | single nucleotide variant | NM_032153.6(ZIC4):c.966G>T (p.Ser322=) | not provided [RCV003733480] | likely benign | 3 | 147390969 | 147390969 | Human | | name |
| 405211162 | CV3146306 | single nucleotide variant | NM_032153.6(ZIC4):c.354C>T (p.Arg118=) | not provided [RCV003845837] | likely benign | 3 | 147396186 | 147396186 | Human | | name |
| 597728708 | CV3625061 | single nucleotide variant | NM_032153.6(ZIC4):c.41G>A (p.Arg14Gln) | not specified [RCV004888577] | uncertain significance | 3 | 147402757 | 147402757 | Human | | name |
| 597860909 | CV3826072 | single nucleotide variant | NM_032153.6(ZIC4):c.957G>A (p.Val319=) | not provided [RCV005174971] | likely benign | 3 | 147390978 | 147390978 | Human | | name |
| 15163035 | CV733859 | single nucleotide variant | NM_032153.6(ZIC4):c.840G>T (p.Ser280=) | not provided [RCV000903684] | benign | 3 | 147391095 | 147391095 | Human | | name |
| 156181176 | CV1901757 | single nucleotide variant | NM_032153.6(ZIC4):c.209A>G (p.Asp70Gly) | not provided [RCV002595067] | uncertain significance | 3 | 147396331 | 147396331 | Human | | name |
| 156400715 | CV1907881 | single nucleotide variant | NM_032153.6(ZIC4):c.277G>T (p.Ala93Ser) | not provided [RCV002584845]|not specified [RCV004073379] | uncertain significance | 3 | 147396263 | 147396263 | Human | | name |
| 155990585 | CV2026935 | single nucleotide variant | NM_032153.6(ZIC4):c.152C>T (p.Pro51Leu) | not provided [RCV002755732] | uncertain significance | 3 | 147396388 | 147396388 | Human | | name |
| 155935262 | CV2063767 | single nucleotide variant | NM_032153.6(ZIC4):c.161C>G (p.Ser54Cys) | not provided [RCV002839031] | uncertain significance | 3 | 147396379 | 147396379 | Human | | name |
| 156211395 | CV2103318 | single nucleotide variant | NM_032153.6(ZIC4):c.248C>T (p.Ala83Val) | not provided [RCV002918176] | likely benign | 3 | 147396292 | 147396292 | Human | | name |
| 155934190 | CV2113997 | single nucleotide variant | NM_032153.6(ZIC4):c.295G>C (p.Gly99Arg) | not provided [RCV002904011] | benign|likely benign | 3 | 147396245 | 147396245 | Human | | name |
| 156236310 | CV2118436 | single nucleotide variant | NM_032153.6(ZIC4):c.274G>C (p.Ala92Pro) | not provided [RCV002958704] | uncertain significance | 3 | 147396266 | 147396266 | Human | | name |
| 156368737 | CV2193774 | single nucleotide variant | NM_032153.6(ZIC4):c.236C>T (p.Pro79Leu) | not specified [RCV004074533] | uncertain significance | 3 | 147396304 | 147396304 | Human | | name |
| 156084782 | CV2249284 | single nucleotide variant | NM_032153.6(ZIC4):c.182G>C (p.Gly61Ala) | not specified [RCV004118310] | uncertain significance | 3 | 147396358 | 147396358 | Human | | name |
| 156346915 | CV2353802 | single nucleotide variant | NM_032153.6(ZIC4):c.127T>G (p.Phe43Val) | not provided [RCV005098996]|not specified [RCV004201807] | uncertain significance | 3 | 147396413 | 147396413 | Human | | name |
| 156006541 | CV2401207 | single nucleotide variant | NM_032153.6(ZIC4):c.149C>G (p.Pro50Arg) | not provided [RCV005099222]|not specified [RCV004245761] | uncertain significance | 3 | 147396391 | 147396391 | Human | | name |
| 401863561 | CV2776980 | single nucleotide variant | NM_032153.6(ZIC4):c.140A>G (p.His47Arg) | not specified [RCV004351790] | uncertain significance | 3 | 147396400 | 147396400 | Human | | name |
| 402519628 | CV2946239 | single nucleotide variant | NM_032153.6(ZIC4):c.169C>T (p.Arg57Cys) | not provided [RCV003663204] | uncertain significance | 3 | 147396371 | 147396371 | Human | | name |
| 405245281 | CV2969068 | single nucleotide variant | NM_032153.6(ZIC4):c.202C>G (p.Pro68Ala) | not provided [RCV003685111] | uncertain significance | 3 | 147396338 | 147396338 | Human | | name |
| 405210267 | CV2970554 | single nucleotide variant | NM_032153.6(ZIC4):c.224C>T (p.Pro75Leu) | not provided [RCV003679297] | uncertain significance | 3 | 147396316 | 147396316 | Human | | name |
| 404982801 | CV2979531 | single nucleotide variant | NM_032153.6(ZIC4):c.210C>G (p.Asp70Glu) | not provided [RCV003691481] | uncertain significance | 3 | 147396330 | 147396330 | Human | | name |
| 405226491 | CV3039323 | single nucleotide variant | NM_032153.6(ZIC4):c.295G>A (p.Gly99Arg) | not provided [RCV003710739] | uncertain significance | 3 | 147396245 | 147396245 | Human | | name |
| 405208607 | CV3065458 | single nucleotide variant | NM_032153.6(ZIC4):c.281C>A (p.Ala94Asp) | not provided [RCV003731669] | uncertain significance | 3 | 147396259 | 147396259 | Human | | name |
| 405020634 | CV3139167 | single nucleotide variant | NM_032153.6(ZIC4):c.199C>T (p.Leu67Phe) | not provided [RCV003829809] | uncertain significance | 3 | 147396341 | 147396341 | Human | | name |
| 405681911 | CV3357139 | single nucleotide variant | NM_032153.6(ZIC4):c.235C>A (p.Pro79Thr) | not specified [RCV004488865] | uncertain significance | 3 | 147396305 | 147396305 | Human | | name |
| 407459786 | CV3490351 | single nucleotide variant | NM_032153.6(ZIC4):c.136C>A (p.Leu46Ile) | not specified [RCV004687224] | uncertain significance | 3 | 147396404 | 147396404 | Human | | name |
| 407459790 | CV3490352 | single nucleotide variant | NM_032153.6(ZIC4):c.188T>A (p.Leu63Gln) | not specified [RCV004687225] | uncertain significance | 3 | 147396352 | 147396352 | Human | | name |
| 597728679 | CV3625066 | single nucleotide variant | NM_032153.6(ZIC4):c.168C>A (p.Ser56Arg) | not specified [RCV004888581] | uncertain significance | 3 | 147396372 | 147396372 | Human | | name |
| 597875789 | CV3775877 | single nucleotide variant | NM_032153.6(ZIC4):c.166A>C (p.Ser56Arg) | not provided [RCV005123404] | uncertain significance | 3 | 147396374 | 147396374 | Human | | name |
| 598260375 | CV3934082 | single nucleotide variant | NM_032153.6(ZIC4):c.185T>A (p.Leu62His) | not specified [RCV005300412] | uncertain significance | 3 | 147396355 | 147396355 | Human | | name |
| 598260380 | CV3934084 | single nucleotide variant | NM_032153.6(ZIC4):c.107C>T (p.Ala36Val) | not specified [RCV005300413] | uncertain significance | 3 | 147396433 | 147396433 | Human | | name |
| 156169651 | CV1874057 | single nucleotide variant | NM_032153.6(ZIC4):c.487G>T (p.Val163Phe) | not provided [RCV003083189] | uncertain significance | 3 | 147396053 | 147396053 | Human | | name |
| 156447070 | CV1944705 | single nucleotide variant | NM_032153.6(ZIC4):c.334G>A (p.Gly112Ser) | not provided [RCV003118597] | uncertain significance | 3 | 147396206 | 147396206 | Human | | name |
| 155951056 | CV2026221 | single nucleotide variant | NM_032153.6(ZIC4):c.455A>G (p.His152Arg) | not provided [RCV002730683] | uncertain significance | 3 | 147396085 | 147396085 | Human | | name |
| 156111955 | CV2038844 | single nucleotide variant | NM_032153.6(ZIC4):c.899C>G (p.Ser300Trp) | not provided [RCV002785434] | uncertain significance | 3 | 147391036 | 147391036 | Human | | name |
| 156149870 | CV2091028 | single nucleotide variant | NM_032153.6(ZIC4):c.506C>G (p.Ala169Gly) | not provided [RCV002890616] | benign | 3 | 147396034 | 147396034 | Human | | name |
| 155922046 | CV2102462 | single nucleotide variant | NM_032153.6(ZIC4):c.493G>A (p.Gly165Ser) | not provided [RCV002903400] | benign | 3 | 147396047 | 147396047 | Human | | name |
| 156018625 | CV2114690 | single nucleotide variant | NM_032153.6(ZIC4):c.794C>T (p.Thr265Met) | not provided [RCV002909501]|not specified [RCV004066241] | uncertain significance | 3 | 147391141 | 147391141 | Human | | name |
| 156236837 | CV2193511 | single nucleotide variant | NM_032153.6(ZIC4):c.971C>A (p.Ala324Glu) | not specified [RCV004072992] | uncertain significance | 3 | 147390964 | 147390964 | Human | | name |
| 155951823 | CV2238851 | single nucleotide variant | NM_032153.6(ZIC4):c.326C>A (p.Ala109Glu) | not specified [RCV004109765] | uncertain significance | 3 | 147396214 | 147396214 | Human | | name |
| 155932492 | CV2290684 | single nucleotide variant | NM_032153.6(ZIC4):c.968C>G (p.Ala323Gly) | not specified [RCV004149209] | uncertain significance | 3 | 147390967 | 147390967 | Human | | name |
| 156356651 | CV2320829 | single nucleotide variant | NM_032153.6(ZIC4):c.550C>G (p.Pro184Ala) | not specified [RCV004172659] | uncertain significance | 3 | 147395990 | 147395990 | Human | | name |
| 401724756 | CV2693408 | single nucleotide variant | NM_032153.6(ZIC4):c.815A>G (p.Asp272Gly) | not specified [RCV004295362] | uncertain significance | 3 | 147391120 | 147391120 | Human | | name |
| 401759835 | CV2707163 | single nucleotide variant | NM_032153.6(ZIC4):c.783C>G (p.Asp261Glu) | not specified [RCV004315527] | uncertain significance | 3 | 147391152 | 147391152 | Human | | name |
| 401770824 | CV2726272 | single nucleotide variant | NM_032153.6(ZIC4):c.351C>A (p.Phe117Leu) | not specified [RCV004326721] | uncertain significance | 3 | 147396189 | 147396189 | Human | | name |
| 401891609 | CV2780574 | single nucleotide variant | NM_032153.6(ZIC4):c.529G>A (p.Glu177Lys) | not specified [RCV004351946] | uncertain significance | 3 | 147396011 | 147396011 | Human | | name |
| 401888471 | CV2785011 | single nucleotide variant | NM_032153.6(ZIC4):c.793A>C (p.Thr265Pro) | not specified [RCV004355033] | uncertain significance | 3 | 147391142 | 147391142 | Human | | name |
| 401877607 | CV2790229 | single nucleotide variant | NM_032153.6(ZIC4):c.790T>C (p.Tyr264His) | not specified [RCV004364141] | uncertain significance | 3 | 147391145 | 147391145 | Human | | name |
| 402479204 | CV2853899 | single nucleotide variant | NM_032153.6(ZIC4):c.865G>T (p.Gly289Trp) | not provided [RCV003543835] | uncertain significance | 3 | 147391070 | 147391070 | Human | | name |
| 405236105 | CV2887850 | single nucleotide variant | NM_032153.6(ZIC4):c.547A>G (p.Lys183Glu) | not provided [RCV003556419] | uncertain significance | 3 | 147395993 | 147395993 | Human | | name |
| 405151478 | CV2888539 | single nucleotide variant | NM_032153.6(ZIC4):c.626C>T (p.Pro209Leu) | not provided [RCV003561763] | uncertain significance | 3 | 147395914 | 147395914 | Human | | name |
| 402522485 | CV2940268 | single nucleotide variant | NM_032153.6(ZIC4):c.503A>T (p.Gln168Leu) | not provided [RCV003663413] | uncertain significance | 3 | 147396037 | 147396037 | Human | | name |
| 405136564 | CV2963133 | single nucleotide variant | NM_032153.6(ZIC4):c.913G>C (p.Ala305Pro) | not provided [RCV003668839] | uncertain significance | 3 | 147391022 | 147391022 | Human | | name |
| 405246608 | CV2966365 | single nucleotide variant | NM_032153.6(ZIC4):c.311C>G (p.Thr104Arg) | not provided [RCV003685464] | uncertain significance | 3 | 147396229 | 147396229 | Human | | name |
| 402507735 | CV2979103 | single nucleotide variant | NM_032153.6(ZIC4):c.454C>A (p.His152Asn) | not provided [RCV003689229] | uncertain significance | 3 | 147396086 | 147396086 | Human | | name |
| 405233475 | CV2985376 | single nucleotide variant | NM_032153.6(ZIC4):c.731G>T (p.Arg244Leu) | not provided [RCV003711766] | uncertain significance | 3 | 147391204 | 147391204 | Human | | name |
| 405143503 | CV3056160 | single nucleotide variant | NM_032153.6(ZIC4):c.482A>G (p.Glu161Gly) | not provided [RCV003725855] | uncertain significance | 3 | 147396058 | 147396058 | Human | | name |
| 405188637 | CV3069162 | single nucleotide variant | NM_032153.6(ZIC4):c.875C>T (p.Pro292Leu) | not provided [RCV003729510] | uncertain significance | 3 | 147391060 | 147391060 | Human | | name |
| 405255199 | CV3175726 | single nucleotide variant | NM_032153.6(ZIC4):c.988G>A (p.Ala330Thr) | not provided [RCV003871994] | uncertain significance | 3 | 147390947 | 147390947 | Human | | name |
| 402515161 | CV3178867 | single nucleotide variant | NM_032153.6(ZIC4):c.965C>G (p.Ser322Trp) | not provided [RCV003879300] | uncertain significance | 3 | 147390970 | 147390970 | Human | | name |
| 405681915 | CV3357140 | single nucleotide variant | NM_032153.6(ZIC4):c.427C>T (p.Leu143Phe) | not provided [RCV005104786]|not specified [RCV004488866] | uncertain significance | 3 | 147396113 | 147396113 | Human | | name |
| 405681921 | CV3357141 | single nucleotide variant | NM_032153.6(ZIC4):c.776C>G (p.Thr259Ser) | not specified [RCV004488867] | uncertain significance | 3 | 147391159 | 147391159 | Human | | name |
| 597728702 | CV3625063 | single nucleotide variant | NM_032153.6(ZIC4):c.422C>G (p.Pro141Arg) | not specified [RCV004888578] | uncertain significance | 3 | 147396118 | 147396118 | Human | | name |
| 597728695 | CV3625064 | single nucleotide variant | NM_032153.6(ZIC4):c.881C>T (p.Pro294Leu) | not specified [RCV004888579] | uncertain significance | 3 | 147391054 | 147391054 | Human | | name |
| 597728687 | CV3625065 | single nucleotide variant | NM_032153.6(ZIC4):c.907C>A (p.Pro303Thr) | not specified [RCV004888580] | uncertain significance | 3 | 147391028 | 147391028 | Human | | name |
| 597728672 | CV3625067 | single nucleotide variant | NM_032153.6(ZIC4):c.440C>G (p.Thr147Ser) | not specified [RCV004888582] | uncertain significance | 3 | 147396100 | 147396100 | Human | | name |
| 597728420 | CV3625068 | single nucleotide variant | NM_032153.6(ZIC4):c.908C>G (p.Pro303Arg) | not specified [RCV004888583] | uncertain significance | 3 | 147391027 | 147391027 | Human | | name |
| 597728171 | CV3625069 | single nucleotide variant | NM_032153.6(ZIC4):c.869G>C (p.Arg290Pro) | not specified [RCV004888584] | uncertain significance | 3 | 147391066 | 147391066 | Human | | name |
| 597942924 | CV3816353 | single nucleotide variant | NM_032153.6(ZIC4):c.996G>T (p.Leu332Phe) | not provided [RCV005159414] | uncertain significance | 3 | 147390939 | 147390939 | Human | | name |
| 598260385 | CV3934085 | single nucleotide variant | NM_032153.6(ZIC4):c.471C>A (p.His157Gln) | not specified [RCV005300414] | uncertain significance | 3 | 147396069 | 147396069 | Human | | name |
| 15100394 | CV697872 | single nucleotide variant | NM_032153.6(ZIC4):c.965C>T (p.Ser322Leu) | not provided [RCV000958908] | benign | 3 | 147390970 | 147390970 | Human | | name |