| 405283483 | CV3218638 | single nucleotide variant | NM_004815.4(ARHGAP29):c.*1G>C | ARHGAP29-related disorder [RCV003957404] | likely benign | 1 | 94173868 | 94173868 | Human | | name , trait , alternate_id |
| 155645862 | CV1709218 | single nucleotide variant | NM_004815.4(ARHGAP29):c.697+6T>A | not provided [RCV002292094] | uncertain significance | 1 | 94205055 | 94205055 | Human | | name |
| 12912360 | CV243892 | single nucleotide variant | NM_004815.4(ARHGAP29):c.698-1G>C | Nonsyndromic cleft lip with or without cleft palate [RCV000491498] | pathogenic | 1 | 94203995 | 94203995 | Human | 1 | name |
| 405290011 | CV3205730 | single nucleotide variant | NM_004815.4(ARHGAP29):c.510+7T>C | ARHGAP29-related disorder [RCV003962086] | likely benign | 1 | 94208825 | 94208825 | Human | | name , trait , alternate_id |
| 405292031 | CV3207852 | single nucleotide variant | NM_004815.4(ARHGAP29):c.438-7T>C | ARHGAP29-related disorder [RCV003929528] | likely benign | 1 | 94208911 | 94208911 | Human | | name , trait , alternate_id |
| 12912159 | CV243894 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2109+1G>A | Nonsyndromic cleft lip with or without cleft palate [RCV000491061] | pathogenic | 1 | 94184871 | 94184871 | Human | 1 | name |
| 401913231 | CV2796855 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2796+5G>C | ARHGAP29-related disorder [RCV003427804] | uncertain significance | 1 | 94177847 | 94177847 | Human | | name , trait , alternate_id |
| 401902981 | CV2804770 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2481-1G>A | ARHGAP29-related disorder [RCV003394312] | likely pathogenic | 1 | 94178168 | 94178168 | Human | | name , trait , alternate_id |
| 405267252 | CV3202233 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1144-9T>A | ARHGAP29-related disorder [RCV003911701] | likely benign | 1 | 94201866 | 94201866 | Human | | name , trait , alternate_id |
| 15014841 | CV613609 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1920+1G>A | Nonsyndromic cleft lip with or without cleft palate [RCV000852348] | pathogenic | 1 | 94185341 | 94185341 | Human | 1 | name |
| 15111405 | CV778840 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2905+8G>A | not provided [RCV000961099] | benign|likely benign | 1 | 94177604 | 94177604 | Human | | name |
| 150472922 | CV1259379 | duplication | NM_004815.4(ARHGAP29):c.1144-26dup | not provided [RCV001684625] | benign | 1 | 94201874 | 94201875 | Human | | name |
| 405275932 | CV3199560 | deletion | NM_004815.4(ARHGAP29):c.873+11_873+15del | ARHGAP29-related disorder [RCV003916956] | likely benign | 1 | 94203085 | 94203089 | Human | | name , trait , alternate_id |
| 15196169 | CV762102 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1A>G (p.Met1Val) | not provided [RCV000934145] | likely benign | 1 | 94231611 | 94231611 | Human | | name |
| 155981885 | CV2351454 | single nucleotide variant | NM_004815.4(ARHGAP29):c.57A>C (p.Gln19His) | Inborn genetic diseases [RCV002946746]|not provided [RCV004697262] | uncertain significance | 1 | 94231555 | 94231555 | Human | 1 | name |
| 597692479 | CV3583794 | single nucleotide variant | NM_004815.4(ARHGAP29):c.76A>C (p.Thr26Pro) | Inborn genetic diseases [RCV004954348] | uncertain significance | 1 | 94231536 | 94231536 | Human | 1 | name |
| 15144997 | CV746685 | single nucleotide variant | NM_004815.4(ARHGAP29):c.489G>A (p.Leu163=) | not provided [RCV000922466] | likely benign | 1 | 94208853 | 94208853 | Human | | name |
| 15194028 | CV762101 | single nucleotide variant | NM_004815.4(ARHGAP29):c.351C>T (p.Phe117=) | not provided [RCV000933525] | likely benign | 1 | 94209340 | 94209340 | Human | | name |
| 405263600 | CV3189806 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2043A>G (p.Pro681=) | ARHGAP29-related disorder [RCV003896854] | likely benign | 1 | 94184938 | 94184938 | Human | | name , trait , alternate_id |
| 405277622 | CV3195943 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1227A>G (p.Glu409=) | ARHGAP29-related disorder [RCV003904467] | likely benign | 1 | 94201774 | 94201774 | Human | | name , trait , alternate_id |
| 405268213 | CV3198870 | single nucleotide variant | NM_004815.4(ARHGAP29):c.251G>A (p.Arg84His) | ARHGAP29-related disorder [RCV003911988] | benign | 1 | 94220347 | 94220347 | Human | | name , trait , alternate_id |
| 405275059 | CV3199990 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1491C>A (p.Ala497=) | ARHGAP29-related disorder [RCV003974001] | likely benign | 1 | 94189301 | 94189301 | Human | | name , trait , alternate_id |
| 405273302 | CV3210391 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2514C>T (p.Asn838=) | ARHGAP29-related disorder [RCV003914612] | likely benign | 1 | 94178134 | 94178134 | Human | | name , trait , alternate_id |
| 405274414 | CV3211755 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2844A>C (p.Thr948=) | ARHGAP29-related disorder [RCV003951551] | likely benign | 1 | 94177673 | 94177673 | Human | | name , trait , alternate_id |
| 408366068 | CV3514974 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1008A>G (p.Gln336=) | ARHGAP29-related disorder [RCV004755557] | likely benign | 1 | 94202679 | 94202679 | Human | | name , trait , alternate_id |
| 15202055 | CV719138 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2877G>A (p.Ala959=) | not provided [RCV000891368] | benign | 1 | 94177640 | 94177640 | Human | | name |
| 15155844 | CV732659 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2524T>C (p.Leu842=) | not provided [RCV000902216] | likely benign | 1 | 94178124 | 94178124 | Human | | name |
| 15187958 | CV732660 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1773A>G (p.Ser591=) | ARHGAP29-related disorder [RCV003902857]|not provided [RCV000909233] | benign|likely benign | 1 | 94186506 | 94186506 | Human | | name , trait , alternate_id |
| 15190661 | CV732661 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1527T>C (p.Ser509=) | ARHGAP29-related disorder [RCV003977968]|not provided [RCV000910017] | likely benign | 1 | 94189265 | 94189265 | Human | | name , trait , alternate_id |
| 15098132 | CV746683 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1881T>C (p.Cys627=) | not provided [RCV000914174] | likely benign | 1 | 94185381 | 94185381 | Human | | name |
| 15112176 | CV746684 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1188T>C (p.Val396=) | not provided [RCV000916865] | likely benign | 1 | 94201813 | 94201813 | Human | | name |
| 153303855 | CV1690514 | single nucleotide variant | NM_004815.4(ARHGAP29):c.326C>A (p.Thr109Asn) | not provided [RCV002269558] | uncertain significance | 1 | 94220272 | 94220272 | Human | | name |
| 155713383 | CV1760280 | single nucleotide variant | NM_004815.4(ARHGAP29):c.952A>G (p.Met318Val) | not provided [RCV002300786] | uncertain significance | 1 | 94202920 | 94202920 | Human | | name |
| 155800273 | CV1862871 | microsatellite | NM_004815.4(ARHGAP29):c.62_63del (p.Ser21fs) | ARHGAP29-related disorder [RCV004700769]|Cleft palate [RCV004786721] | pathogenic|likely pathogenic|uncertain significance | 1 | 94231549 | 94231550 | Human | | name , trait , alternate_id |
| 10407771 | CV213971 | single nucleotide variant | NM_004815.4(ARHGAP29):c.976A>T (p.Lys326Ter) | not provided [RCV000201264] | uncertain significance | 1 | 94202711 | 94202711 | Human | | name |
| 10450141 | CV215214 | single nucleotide variant | NM_004815.4(ARHGAP29):c.358G>T (p.Val120Phe) | not specified [RCV000202673] | uncertain significance | 1 | 94209333 | 94209333 | Human | | name |
| 156020793 | CV2226578 | single nucleotide variant | NM_004815.4(ARHGAP29):c.898A>G (p.Met300Val) | Inborn genetic diseases [RCV002757288] | uncertain significance | 1 | 94202974 | 94202974 | Human | 1 | name |
| 156077797 | CV2248180 | single nucleotide variant | NM_004815.4(ARHGAP29):c.640A>G (p.Thr214Ala) | Inborn genetic diseases [RCV002797770] | uncertain significance | 1 | 94205118 | 94205118 | Human | 1 | name |
| 156032289 | CV2259563 | single nucleotide variant | NM_004815.4(ARHGAP29):c.645G>T (p.Trp215Cys) | Inborn genetic diseases [RCV002821138] | uncertain significance | 1 | 94205113 | 94205113 | Human | 1 | name |
| 156068323 | CV2289509 | single nucleotide variant | NM_004815.4(ARHGAP29):c.928C>T (p.Leu310Phe) | Inborn genetic diseases [RCV002886743] | uncertain significance | 1 | 94202944 | 94202944 | Human | 1 | name |
| 156147515 | CV2311162 | single nucleotide variant | NM_004815.4(ARHGAP29):c.830T>C (p.Leu277Ser) | Inborn genetic diseases [RCV002915183] | uncertain significance | 1 | 94203143 | 94203143 | Human | 1 | name |
| 155913195 | CV2341729 | single nucleotide variant | NM_004815.4(ARHGAP29):c.589G>A (p.Val197Met) | Inborn genetic diseases [RCV002968257] | likely benign | 1 | 94205169 | 94205169 | Human | 1 | name |
| 156003716 | CV2357485 | single nucleotide variant | NM_004815.4(ARHGAP29):c.451C>T (p.Leu151Phe) | Inborn genetic diseases [RCV002997204] | uncertain significance | 1 | 94208891 | 94208891 | Human | 1 | name |
| 329382093 | CV2438429 | single nucleotide variant | NM_004815.4(ARHGAP29):c.485G>A (p.Arg162Gln) | Inborn genetic diseases [RCV003175888] | uncertain significance | 1 | 94208857 | 94208857 | Human | 1 | name |
| 329382451 | CV2465151 | single nucleotide variant | NM_004815.4(ARHGAP29):c.821G>A (p.Ser274Asn) | Inborn genetic diseases [RCV003213362] | uncertain significance | 1 | 94203152 | 94203152 | Human | 1 | name |
| 401743673 | CV2684757 | single nucleotide variant | NM_004815.4(ARHGAP29):c.912G>T (p.Arg304Ser) | Inborn genetic diseases [RCV003251996] | uncertain significance | 1 | 94202960 | 94202960 | Human | 1 | name |
| 401773250 | CV2698147 | single nucleotide variant | NM_004815.4(ARHGAP29):c.805A>G (p.Asn269Asp) | Inborn genetic diseases [RCV003285333] | uncertain significance | 1 | 94203168 | 94203168 | Human | 1 | name |
| 401762956 | CV2720142 | single nucleotide variant | NM_004815.4(ARHGAP29):c.329C>A (p.Ala110Glu) | Inborn genetic diseases [RCV003300389] | uncertain significance | 1 | 94220269 | 94220269 | Human | 1 | name |
| 401937597 | CV2798794 | duplication | NM_004815.4(ARHGAP29):c.1834dup (p.Thr612fs) | ARHGAP29-related disorder [RCV003416661] | uncertain significance | 1 | 94185427 | 94185428 | Human | | name , trait , alternate_id |
| 405269414 | CV3201632 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3759C>T (p.Leu1253=) | ARHGAP29-related disorder [RCV003899541] | likely benign | 1 | 94173896 | 94173896 | Human | | name , trait , alternate_id |
| 405685345 | CV3282795 | single nucleotide variant | NM_004815.4(ARHGAP29):c.419C>T (p.Ala140Val) | Inborn genetic diseases [RCV004422606] | uncertain significance | 1 | 94209272 | 94209272 | Human | 1 | name |
| 405685352 | CV3282796 | single nucleotide variant | NM_004815.4(ARHGAP29):c.769A>G (p.Met257Val) | Inborn genetic diseases [RCV004422607] | uncertain significance | 1 | 94203204 | 94203204 | Human | 1 | name |
| 407499051 | CV3468506 | single nucleotide variant | NM_004815.4(ARHGAP29):c.413C>A (p.Thr138Asn) | Inborn genetic diseases [RCV004669222] | uncertain significance | 1 | 94209278 | 94209278 | Human | 1 | name |
| 407499369 | CV3468555 | single nucleotide variant | NM_004815.4(ARHGAP29):c.712A>G (p.Arg238Gly) | Inborn genetic diseases [RCV004669242] | uncertain significance | 1 | 94203980 | 94203980 | Human | 1 | name |
| 597692494 | CV3583816 | single nucleotide variant | NM_004815.4(ARHGAP29):c.940G>C (p.Glu314Gln) | Inborn genetic diseases [RCV004954350] | uncertain significance | 1 | 94202932 | 94202932 | Human | 1 | name |
| 597692500 | CV3583827 | single nucleotide variant | NM_004815.4(ARHGAP29):c.841A>G (p.Ile281Val) | Inborn genetic diseases [RCV004954351] | uncertain significance | 1 | 94203132 | 94203132 | Human | 1 | name |
| 598176204 | CV4007090 | single nucleotide variant | NM_004815.4(ARHGAP29):c.463G>T (p.Val155Leu) | Inborn genetic diseases [RCV005393604] | uncertain significance | 1 | 94208879 | 94208879 | Human | 1 | name |
| 15194769 | CV696916 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3345G>A (p.Gly1115=) | not provided [RCV000955735] | benign | 1 | 94174310 | 94174310 | Human | | name |
| 15183335 | CV707597 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3282T>C (p.Thr1094=) | ARHGAP29-related disorder [RCV003918577]|not provided [RCV000974851] | benign | 1 | 94174373 | 94174373 | Human | | name , trait , alternate_id |
| 15187955 | CV732658 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3366T>A (p.Thr1122=) | ARHGAP29-related disorder [RCV003902856]|not provided [RCV000909232] | benign|likely benign | 1 | 94174289 | 94174289 | Human | | name , trait , alternate_id |
| 151661301 | CV1329822 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1865C>T (p.Thr622Met) | Isolated cleft palate [RCV001823022] | uncertain significance | 1 | 94185397 | 94185397 | Human | 1 | name |
| 156105635 | CV2217653 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1381C>G (p.Gln461Glu) | Inborn genetic diseases [RCV002706866] | uncertain significance | 1 | 94189984 | 94189984 | Human | 1 | name |
| 155979222 | CV2222823 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1799C>T (p.Thr600Ile) | Inborn genetic diseases [RCV002732313] | uncertain significance | 1 | 94185463 | 94185463 | Human | 1 | name |
| 156131458 | CV2235239 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1151A>C (p.Glu384Ala) | Inborn genetic diseases [RCV002762963] | uncertain significance | 1 | 94201850 | 94201850 | Human | 1 | name |
| 156271139 | CV2237112 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2726A>C (p.Lys909Thr) | Inborn genetic diseases [RCV002792480] | uncertain significance | 1 | 94177922 | 94177922 | Human | 1 | name |
| 156038705 | CV2260069 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2395A>C (p.Ile799Leu) | Inborn genetic diseases [RCV002821584] | uncertain significance | 1 | 94179810 | 94179810 | Human | 1 | name |
| 155997234 | CV2288601 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2206T>C (p.Ser736Pro) | Inborn genetic diseases [RCV002882953] | uncertain significance | 1 | 94184192 | 94184192 | Human | 1 | name |
| 155932643 | CV2290785 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2576C>T (p.Pro859Leu) | Inborn genetic diseases [RCV002861203] | uncertain significance | 1 | 94178072 | 94178072 | Human | 1 | name |
| 155941293 | CV2294227 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1288G>A (p.Val430Ile) | Inborn genetic diseases [RCV002879681] | uncertain significance | 1 | 94190077 | 94190077 | Human | 1 | name |
| 156014792 | CV2360177 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2273G>T (p.Arg758Leu) | Inborn genetic diseases [RCV002998160] | uncertain significance | 1 | 94179932 | 94179932 | Human | 1 | name |
| 156392629 | CV2386555 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2876C>T (p.Ala959Val) | Inborn genetic diseases [RCV002725132] | uncertain significance | 1 | 94177641 | 94177641 | Human | 1 | name |
| 12912154 | CV243891 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1475C>A (p.Ser492Ter) | Nonsyndromic cleft lip with or without cleft palate [RCV000491051] | pathogenic | 1 | 94189317 | 94189317 | Human | 1 | name |
| 329353716 | CV2439577 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2804A>G (p.His935Arg) | Inborn genetic diseases [RCV003201508] | uncertain significance | 1 | 94177713 | 94177713 | Human | 1 | name |
| 329365272 | CV2440213 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1088A>G (p.Asn363Ser) | Inborn genetic diseases [RCV003207175] | uncertain significance | 1 | 94202599 | 94202599 | Human | 1 | name |
| 329401770 | CV2457396 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1054G>C (p.Glu352Gln) | Inborn genetic diseases [RCV003198784] | uncertain significance | 1 | 94202633 | 94202633 | Human | 1 | name |
| 329360921 | CV2463112 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2398C>A (p.Leu800Ile) | Inborn genetic diseases [RCV003205254] | uncertain significance | 1 | 94179807 | 94179807 | Human | 1 | name |
| 329362176 | CV2466085 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1691A>T (p.His564Leu) | Inborn genetic diseases [RCV003205891] | uncertain significance | 1 | 94186588 | 94186588 | Human | 1 | name |
| 329395055 | CV2473014 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1940G>A (p.Arg647Gln) | not provided [RCV003218997] | uncertain significance | 1 | 94185041 | 94185041 | Human | | name |
| 329952534 | CV2669954 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1672A>G (p.Ile558Val) | not provided [RCV003233167] | uncertain significance | 1 | 94188846 | 94188846 | Human | | name |
| 401754273 | CV2685218 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1240C>T (p.Leu414Phe) | Inborn genetic diseases [RCV003254943] | uncertain significance | 1 | 94201761 | 94201761 | Human | 1 | name |
| 401717696 | CV2710552 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2705T>C (p.Val902Ala) | Inborn genetic diseases [RCV003242807] | uncertain significance | 1 | 94177943 | 94177943 | Human | 1 | name |
| 401881950 | CV2784897 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1409C>G (p.Thr470Arg) | Inborn genetic diseases [RCV003365111] | uncertain significance | 1 | 94189956 | 94189956 | Human | 1 | name |
| 401931867 | CV2801689 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1706G>A (p.Arg569Gln) | ARHGAP29-related disorder [RCV003408525]|not provided [RCV004812487] | uncertain significance | 1 | 94186573 | 94186573 | Human | | name , trait , alternate_id |
| 401926306 | CV2803542 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1229T>G (p.Ile410Ser) | ARHGAP29-related disorder [RCV003405910] | uncertain significance | 1 | 94201772 | 94201772 | Human | | name , trait , alternate_id |
| 405265507 | CV3185726 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1571T>C (p.Ile524Thr) | not provided [RCV003886290] | likely benign | 1 | 94189221 | 94189221 | Human | | name |
| 405274192 | CV3211612 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2864G>A (p.Arg955His) | ARHGAP29-related disorder [RCV003951438] | likely benign | 1 | 94177653 | 94177653 | Human | | name , trait , alternate_id |
| 405685286 | CV3282784 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1270A>G (p.Thr424Ala) | Inborn genetic diseases [RCV004422595] | uncertain significance | 1 | 94201731 | 94201731 | Human | 1 | name |
| 405685291 | CV3282785 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1462A>G (p.Ser488Gly) | Inborn genetic diseases [RCV004422596] | uncertain significance | 1 | 94189330 | 94189330 | Human | 1 | name |
| 405685296 | CV3282786 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1694G>A (p.Arg565Gln) | Inborn genetic diseases [RCV004422597] | uncertain significance | 1 | 94186585 | 94186585 | Human | 1 | name |
| 405685300 | CV3282787 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2050A>G (p.Ile684Val) | Inborn genetic diseases [RCV004422598] | uncertain significance | 1 | 94184931 | 94184931 | Human | 1 | name |
| 405685306 | CV3282788 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2315A>T (p.His772Leu) | Inborn genetic diseases [RCV004422599] | uncertain significance | 1 | 94179890 | 94179890 | Human | 1 | name |
| 405685312 | CV3282789 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2434G>A (p.Ala812Thr) | Inborn genetic diseases [RCV004422600] | uncertain significance | 1 | 94179771 | 94179771 | Human | 1 | name |
| 405685317 | CV3282790 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2549T>C (p.Leu850Pro) | Inborn genetic diseases [RCV004422601] | uncertain significance | 1 | 94178099 | 94178099 | Human | 1 | name |
| 405685323 | CV3282791 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2620T>A (p.Leu874Met) | Inborn genetic diseases [RCV004422602] | uncertain significance | 1 | 94178028 | 94178028 | Human | 1 | name |
| 405685328 | CV3282792 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2971A>G (p.Thr991Ala) | Inborn genetic diseases [RCV004422603] | uncertain significance | 1 | 94174684 | 94174684 | Human | 1 | name |
| 407499015 | CV3468478 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2318T>G (p.Val773Gly) | Inborn genetic diseases [RCV004669213] | uncertain significance | 1 | 94179887 | 94179887 | Human | 1 | name |
| 407472829 | CV3468489 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1493A>C (p.Asn498Thr) | Inborn genetic diseases [RCV004662593] | uncertain significance | 1 | 94189299 | 94189299 | Human | 1 | name |
| 407499089 | CV3468526 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1614T>A (p.Phe538Leu) | Inborn genetic diseases [RCV004669231] | uncertain significance | 1 | 94188904 | 94188904 | Human | 1 | name |
| 407499101 | CV3468537 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2375T>C (p.Met792Thr) | Inborn genetic diseases [RCV004669234] | likely benign | 1 | 94179830 | 94179830 | Human | 1 | name |
| 407472973 | CV3468545 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2773T>G (p.Ser925Ala) | Inborn genetic diseases [RCV004662629] | uncertain significance | 1 | 94177875 | 94177875 | Human | 1 | name |
| 408365556 | CV3507585 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1244G>A (p.Arg415Gln) | ARHGAP29-related disorder [RCV004755085] | uncertain significance | 1 | 94201757 | 94201757 | Human | | name , trait , alternate_id |
| 408391777 | CV3523400 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2623G>A (p.Val875Ile) | not provided [RCV004770774] | uncertain significance | 1 | 94178025 | 94178025 | Human | | name |
| 408386615 | CV3524118 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1726A>G (p.Met576Val) | not provided [RCV004767992] | uncertain significance | 1 | 94186553 | 94186553 | Human | | name |
| 408393044 | CV3528344 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1108A>G (p.Lys370Glu) | not provided [RCV004776112] | uncertain significance | 1 | 94202579 | 94202579 | Human | | name |
| 597692517 | CV3583849 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1778C>T (p.Thr593Ile) | Inborn genetic diseases [RCV004954353] | uncertain significance | 1 | 94186501 | 94186501 | Human | 1 | name |
| 597692522 | CV3583860 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1976A>G (p.His659Arg) | Inborn genetic diseases [RCV004954354] | uncertain significance | 1 | 94185005 | 94185005 | Human | 1 | name |
| 597692530 | CV3583871 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1070G>A (p.Ser357Asn) | Inborn genetic diseases [RCV004954355] | uncertain significance | 1 | 94202617 | 94202617 | Human | 1 | name |
| 597692537 | CV3583880 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2551A>C (p.Ile851Leu) | Inborn genetic diseases [RCV004954356] | uncertain significance | 1 | 94178097 | 94178097 | Human | 1 | name |
| 597692551 | CV3583892 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2956A>G (p.Ile986Val) | Inborn genetic diseases [RCV004954358] | uncertain significance | 1 | 94174699 | 94174699 | Human | 1 | name |
| 597692556 | CV3583899 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2618G>T (p.Arg873Leu) | Inborn genetic diseases [RCV004954359] | uncertain significance | 1 | 94178030 | 94178030 | Human | 1 | name |
| 597692634 | CV3583912 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2863C>T (p.Arg955Cys) | Inborn genetic diseases [RCV004954371] | uncertain significance | 1 | 94177654 | 94177654 | Human | 1 | name |
| 597692685 | CV3583921 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2768T>C (p.Met923Thr) | Inborn genetic diseases [RCV004954378] | uncertain significance | 1 | 94177880 | 94177880 | Human | 1 | name |
| 597833940 | CV3735135 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2549T>A (p.Leu850His) | not provided [RCV005054868] | uncertain significance | 1 | 94178099 | 94178099 | Human | | name |
| 597834034 | CV3735161 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1597T>A (p.Trp533Arg) | not provided [RCV005054894] | uncertain significance | 1 | 94188921 | 94188921 | Human | | name |
| 597843484 | CV3735924 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1837C>G (p.His613Asp) | not provided [RCV005065273] | uncertain significance | 1 | 94185425 | 94185425 | Human | | name |
| 598175547 | CV4006993 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2887T>C (p.Cys963Arg) | Inborn genetic diseases [RCV005393507] | uncertain significance | 1 | 94177630 | 94177630 | Human | 1 | name |
| 598175680 | CV4007013 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2618G>A (p.Arg873His) | Inborn genetic diseases [RCV005393527] | uncertain significance | 1 | 94178030 | 94178030 | Human | 1 | name |
| 598175754 | CV4007024 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2279A>G (p.Tyr760Cys) | Inborn genetic diseases [RCV005393538] | uncertain significance | 1 | 94179926 | 94179926 | Human | 1 | name |
| 598175825 | CV4007034 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2890G>A (p.Asp964Asn) | Inborn genetic diseases [RCV005393548] | uncertain significance | 1 | 94177627 | 94177627 | Human | 1 | name |
| 598175960 | CV4007053 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1999C>T (p.His667Tyr) | Inborn genetic diseases [RCV005393567] | uncertain significance | 1 | 94184982 | 94184982 | Human | 1 | name |
| 598176024 | CV4007061 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2225T>G (p.Val742Gly) | Inborn genetic diseases [RCV005393575] | uncertain significance | 1 | 94184173 | 94184173 | Human | 1 | name |
| 598176156 | CV4007082 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1514G>A (p.Arg505His) | Inborn genetic diseases [RCV005393596] | uncertain significance | 1 | 94189278 | 94189278 | Human | 1 | name |
| 598185294 | CV4007100 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1388A>T (p.Tyr463Phe) | Inborn genetic diseases [RCV005395590] | uncertain significance | 1 | 94189977 | 94189977 | Human | 1 | name |
| 598185329 | CV4007106 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1126G>A (p.Glu376Lys) | Inborn genetic diseases [RCV005395596] | uncertain significance | 1 | 94202561 | 94202561 | Human | 1 | name |
| 616940085 | CV4014611 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2365T>C (p.Trp789Arg) | not provided [RCV005414105] | uncertain significance | 1 | 94179840 | 94179840 | Human | | name |
| 15106527 | CV707598 | single nucleotide variant | NM_004815.4(ARHGAP29):c.2393G>A (p.Arg798Gln) | ARHGAP29-related disorder [RCV003916014]|not provided [RCV000960095] | likely benign | 1 | 94179812 | 94179812 | Human | | name , trait , alternate_id |
| 15192151 | CV732662 | single nucleotide variant | NM_004815.4(ARHGAP29):c.1252G>A (p.Val418Ile) | ARHGAP29-related disorder [RCV003913004]|not provided [RCV000910454] | benign | 1 | 94201749 | 94201749 | Human | | name , trait , alternate_id |
| 8629732 | CV84879 | single nucleotide variant | NM_004815.3(ARHGAP29):c.2272C>T (p.Arg758Ter) | Malignant melanoma [RCV000064961] | not provided | 1 | 94179933 | 94179933 | Human | | name |
| 8629733 | CV84880 | single nucleotide variant | NM_004815.3(ARHGAP29):c.1859C>T (p.Ser620Phe) | Malignant melanoma [RCV000064962] | not provided | 1 | 94185403 | 94185403 | Human | | name |
| 10449879 | CV215213 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3181G>A (p.Ala1061Thr) | not specified [RCV000203045] | uncertain significance | 1 | 94174474 | 94174474 | Human | | name |
| 156246243 | CV2219063 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3010A>G (p.Asn1004Asp) | Inborn genetic diseases [RCV002702153] | uncertain significance | 1 | 94174645 | 94174645 | Human | 1 | name |
| 155920196 | CV2279553 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3688C>T (p.Leu1230Phe) | Inborn genetic diseases [RCV002859564] | uncertain significance | 1 | 94173967 | 94173967 | Human | 1 | name |
| 155997252 | CV2288602 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3212G>T (p.Gly1071Val) | Inborn genetic diseases [RCV002882954] | uncertain significance | 1 | 94174443 | 94174443 | Human | 1 | name |
| 156191013 | CV2301772 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3701A>G (p.Asp1234Gly) | Inborn genetic diseases [RCV002892539] | uncertain significance | 1 | 94173954 | 94173954 | Human | 1 | name |
| 155906757 | CV2303374 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3197G>T (p.Cys1066Phe) | Inborn genetic diseases [RCV002901918] | uncertain significance | 1 | 94174458 | 94174458 | Human | 1 | name |
| 155934494 | CV2372475 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3235A>G (p.Lys1079Glu) | Inborn genetic diseases [RCV002684657] | uncertain significance | 1 | 94174420 | 94174420 | Human | 1 | name |
| 156150432 | CV2394652 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3218A>G (p.Asp1073Gly) | Inborn genetic diseases [RCV002764081] | uncertain significance | 1 | 94174437 | 94174437 | Human | 1 | name |
| 401737763 | CV2679971 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3007A>G (p.Thr1003Ala) | Inborn genetic diseases [RCV003239938] | uncertain significance | 1 | 94174648 | 94174648 | Human | 1 | name |
| 401730632 | CV2711424 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3635C>A (p.Ala1212Glu) | Inborn genetic diseases [RCV003271455] | uncertain significance | 1 | 94174020 | 94174020 | Human | 1 | name |
| 401888897 | CV2765043 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3712A>G (p.Met1238Val) | Inborn genetic diseases [RCV003353631] | uncertain significance | 1 | 94173943 | 94173943 | Human | 1 | name |
| 401865487 | CV2778785 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3761A>G (p.Glu1254Gly) | Inborn genetic diseases [RCV003359699] | uncertain significance | 1 | 94173894 | 94173894 | Human | 1 | name |
| 405685335 | CV3282793 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3224A>C (p.Gln1075Pro) | Inborn genetic diseases [RCV004422604] | uncertain significance | 1 | 94174431 | 94174431 | Human | 1 | name |
| 405685340 | CV3282794 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3587A>T (p.His1196Leu) | Inborn genetic diseases [RCV004422605] | uncertain significance | 1 | 94174068 | 94174068 | Human | 1 | name |
| 407499033 | CV3468496 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3586C>G (p.His1196Asp) | Inborn genetic diseases [RCV004669218] | uncertain significance | 1 | 94174069 | 94174069 | Human | 1 | name |
| 407472895 | CV3468516 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3744A>T (p.Gln1248His) | Inborn genetic diseases [RCV004662609] | uncertain significance | 1 | 94173911 | 94173911 | Human | 1 | name |
| 408365596 | CV3508303 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3070A>G (p.Arg1024Gly) | ARHGAP29-related disorder [RCV004755128] | uncertain significance | 1 | 94174585 | 94174585 | Human | | name , trait , alternate_id |
| 408386410 | CV3528912 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3630C>G (p.Asp1210Glu) | not provided [RCV004772745] | uncertain significance | 1 | 94174025 | 94174025 | Human | | name |
| 597692507 | CV3583838 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3598G>A (p.Gly1200Ser) | Inborn genetic diseases [RCV004954352] | uncertain significance | 1 | 94174057 | 94174057 | Human | 1 | name |
| 597692544 | CV3583885 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3703G>C (p.Val1235Leu) | Inborn genetic diseases [RCV004954357] | uncertain significance | 1 | 94173952 | 94173952 | Human | 1 | name |
| 597692584 | CV3583904 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3142T>G (p.Cys1048Gly) | Inborn genetic diseases [RCV004954363] | uncertain significance | 1 | 94174513 | 94174513 | Human | 1 | name |
| 597936084 | CV3863723 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3238A>G (p.Ile1080Val) | not provided [RCV005207536] | uncertain significance | 1 | 94174417 | 94174417 | Human | | name |
| 598175616 | CV4007003 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3254A>T (p.Tyr1085Phe) | Inborn genetic diseases [RCV005393517] | uncertain significance | 1 | 94174401 | 94174401 | Human | 1 | name |
| 598175902 | CV4007044 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3646C>T (p.Pro1216Ser) | Inborn genetic diseases [RCV005393558] | uncertain significance | 1 | 94174009 | 94174009 | Human | 1 | name |
| 598176090 | CV4007071 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3034A>G (p.Arg1012Gly) | Inborn genetic diseases [RCV005393585] | uncertain significance | 1 | 94174621 | 94174621 | Human | 1 | name |
| 598176214 | CV4007092 | single nucleotide variant | NM_004815.4(ARHGAP29):c.3416C>T (p.Ser1139Phe) | Inborn genetic diseases [RCV005393606] | uncertain significance | 1 | 94174239 | 94174239 | Human | 1 | name |
