| 401935723 | CV2817915 | single nucleotide variant | NM_153813.3(ZFPM1):c.171G>A (p.Pro57=) | not provided [RCV003413027] | likely benign | 16 | 88489056 | 88489056 | Human | | name |
| 401903551 | CV2817916 | single nucleotide variant | NM_153813.3(ZFPM1):c.282G>A (p.Pro94=) | not provided [RCV003419486] | likely benign | 16 | 88514400 | 88514400 | Human | | name |
| 150472913 | CV1217258 | single nucleotide variant | NM_153813.3(ZFPM1):c.64A>G (p.Arg22Gly) | not provided [RCV001615553] | benign | 16 | 88485962 | 88485962 | Human | | name |
| 155915318 | CV2243734 | single nucleotide variant | NM_153813.3(ZFPM1):c.86G>T (p.Gly29Val) | not specified [RCV004114433] | uncertain significance | 16 | 88485984 | 88485984 | Human | | name |
| 405265381 | CV3185607 | single nucleotide variant | NM_153813.3(ZFPM1):c.699C>T (p.Thr233=) | not provided [RCV003886171]|not specified [RCV004369689] | likely benign | 16 | 88528225 | 88528225 | Human | | name |
| 407458084 | CV3490187 | single nucleotide variant | NM_153813.3(ZFPM1):c.73G>A (p.Val25Met) | not specified [RCV004686566] | likely benign | 16 | 88485971 | 88485971 | Human | | name |
| 598159042 | CV3937760 | single nucleotide variant | NM_153813.3(ZFPM1):c.29G>A (p.Arg10Gln) | not specified [RCV005306474] | uncertain significance | 16 | 88453667 | 88453667 | Human | | name |
| 15152356 | CV715163 | single nucleotide variant | NM_153813.3(ZFPM1):c.477C>T (p.Ala159=) | not provided [RCV000968334] | benign | 16 | 88526888 | 88526888 | Human | | name |
| 156253026 | CV2366110 | single nucleotide variant | NM_153813.3(ZFPM1):c.170C>T (p.Pro57Leu) | not specified [RCV004210145] | uncertain significance | 16 | 88489055 | 88489055 | Human | | name |
| 329356292 | CV2430676 | single nucleotide variant | NM_153813.3(ZFPM1):c.247G>A (p.Gly83Ser) | not specified [RCV004253865] | likely benign | 16 | 88489132 | 88489132 | Human | | name |
| 401903553 | CV2817917 | single nucleotide variant | NM_153813.3(ZFPM1):c.1005C>T (p.Cys335=) | not provided [RCV003419487] | likely benign | 16 | 88532672 | 88532672 | Human | | name |
| 401903554 | CV2817918 | single nucleotide variant | NM_153813.3(ZFPM1):c.1596G>A (p.Gly532=) | not provided [RCV003419488] | likely benign | 16 | 88533554 | 88533554 | Human | | name |
| 401911924 | CV2817919 | single nucleotide variant | NM_153813.3(ZFPM1):c.2265G>C (p.Pro755=) | not provided [RCV003426889] | likely benign | 16 | 88534223 | 88534223 | Human | | name |
| 401911926 | CV2817920 | single nucleotide variant | NM_153813.3(ZFPM1):c.2274G>C (p.Pro758=) | not provided [RCV003426890] | likely benign | 16 | 88534232 | 88534232 | Human | | name |
| 405669356 | CV3360355 | single nucleotide variant | NM_153813.3(ZFPM1):c.112A>C (p.Thr38Pro) | not specified [RCV004486162] | uncertain significance | 16 | 88486010 | 88486010 | Human | | name |
| 405669370 | CV3360358 | single nucleotide variant | NM_153813.3(ZFPM1):c.136C>A (p.Pro46Thr) | not specified [RCV004486165] | uncertain significance | 16 | 88486034 | 88486034 | Human | | name |
| 407459187 | CV3490195 | single nucleotide variant | NM_153813.3(ZFPM1):c.142G>A (p.Ala48Thr) | not specified [RCV004687068] | likely benign | 16 | 88486040 | 88486040 | Human | | name |
| 597800250 | CV3628187 | single nucleotide variant | NM_153813.3(ZFPM1):c.214G>A (p.Glu72Lys) | not specified [RCV004880143] | uncertain significance | 16 | 88489099 | 88489099 | Human | | name |
| 598259745 | CV3937753 | single nucleotide variant | NM_153813.3(ZFPM1):c.245C>T (p.Pro82Leu) | not specified [RCV005300288] | uncertain significance | 16 | 88489130 | 88489130 | Human | | name |
| 15139720 | CV715162 | single nucleotide variant | NM_153813.3(ZFPM1):c.209G>C (p.Gly70Ala) | not provided [RCV000966014] | benign | 16 | 88489094 | 88489094 | Human | | name |
| 155901395 | CV2241995 | single nucleotide variant | NM_153813.3(ZFPM1):c.931A>G (p.Met311Val) | not specified [RCV004108942] | uncertain significance | 16 | 88532220 | 88532220 | Human | | name |
| 156113682 | CV2263854 | single nucleotide variant | NM_153813.3(ZFPM1):c.757G>A (p.Glu253Lys) | not specified [RCV004137911] | uncertain significance | 16 | 88532046 | 88532046 | Human | | name |
| 156156510 | CV2266222 | single nucleotide variant | NM_153813.3(ZFPM1):c.452C>T (p.Thr151Met) | not specified [RCV004128790] | uncertain significance | 16 | 88526863 | 88526863 | Human | | name |
| 156103312 | CV2291598 | single nucleotide variant | NM_153813.3(ZFPM1):c.544G>A (p.Ala182Thr) | not specified [RCV004155894] | uncertain significance | 16 | 88528070 | 88528070 | Human | | name |
| 156341061 | CV2348151 | single nucleotide variant | NM_153813.3(ZFPM1):c.884C>A (p.Pro295His) | not specified [RCV004197824] | uncertain significance | 16 | 88532173 | 88532173 | Human | | name |
| 156281526 | CV2348783 | single nucleotide variant | NM_153813.3(ZFPM1):c.829G>A (p.Ala277Thr) | not specified [RCV004203230] | uncertain significance | 16 | 88532118 | 88532118 | Human | | name |
| 156131013 | CV2358175 | single nucleotide variant | NM_153813.3(ZFPM1):c.898A>G (p.Ser300Gly) | not specified [RCV004211975] | uncertain significance | 16 | 88532187 | 88532187 | Human | | name |
| 156303844 | CV2359448 | single nucleotide variant | NM_153813.3(ZFPM1):c.577G>A (p.Glu193Lys) | not specified [RCV004214770] | uncertain significance | 16 | 88528103 | 88528103 | Human | | name |
| 155965909 | CV2396010 | single nucleotide variant | NM_153813.3(ZFPM1):c.893G>A (p.Arg298His) | not specified [RCV004237557] | uncertain significance | 16 | 88532182 | 88532182 | Human | | name |
| 329356247 | CV2442542 | single nucleotide variant | NM_153813.3(ZFPM1):c.610A>G (p.Lys204Glu) | not specified [RCV004266769] | uncertain significance | 16 | 88528136 | 88528136 | Human | | name |
| 329391301 | CV2452224 | single nucleotide variant | NM_153813.3(ZFPM1):c.620C>A (p.Ala207Glu) | not specified [RCV004278923] | uncertain significance | 16 | 88528146 | 88528146 | Human | | name |
| 401748573 | CV2712987 | single nucleotide variant | NM_153813.3(ZFPM1):c.562G>A (p.Val188Met) | not specified [RCV004314693] | uncertain significance | 16 | 88528088 | 88528088 | Human | | name |
| 401878942 | CV2754892 | single nucleotide variant | NM_153813.3(ZFPM1):c.811G>A (p.Gly271Ser) | not specified [RCV004341366] | uncertain significance | 16 | 88532100 | 88532100 | Human | | name |
| 405669515 | CV3360387 | single nucleotide variant | NM_153813.3(ZFPM1):c.511G>A (p.Ala171Thr) | not specified [RCV004486194] | uncertain significance | 16 | 88528037 | 88528037 | Human | | name |
| 405669520 | CV3360388 | single nucleotide variant | NM_153813.3(ZFPM1):c.800G>A (p.Arg267His) | not specified [RCV004486195] | uncertain significance | 16 | 88532089 | 88532089 | Human | | name |
| 405669524 | CV3360389 | single nucleotide variant | NM_153813.3(ZFPM1):c.827C>T (p.Ala276Val) | not specified [RCV004486196] | uncertain significance | 16 | 88532116 | 88532116 | Human | | name |
| 407458076 | CV3490185 | single nucleotide variant | NM_153813.3(ZFPM1):c.572C>T (p.Thr191Met) | not specified [RCV004686564] | uncertain significance | 16 | 88528098 | 88528098 | Human | | name |
| 407458080 | CV3490186 | single nucleotide variant | NM_153813.3(ZFPM1):c.706A>G (p.Ile236Val) | not specified [RCV004686565] | likely benign | 16 | 88528232 | 88528232 | Human | | name |
| 407458096 | CV3490190 | single nucleotide variant | NM_153813.3(ZFPM1):c.565C>T (p.Leu189Phe) | not specified [RCV004686569] | uncertain significance | 16 | 88528091 | 88528091 | Human | | name |
| 597726317 | CV3624750 | single nucleotide variant | NM_153813.3(ZFPM1):c.544G>T (p.Ala182Ser) | not specified [RCV004888388] | uncertain significance | 16 | 88528070 | 88528070 | Human | | name |
| 598259739 | CV3937751 | single nucleotide variant | NM_153813.3(ZFPM1):c.625C>T (p.Pro209Ser) | not specified [RCV005300287] | uncertain significance | 16 | 88528151 | 88528151 | Human | | name |
| 598259778 | CV3937761 | single nucleotide variant | NM_153813.3(ZFPM1):c.704T>C (p.Val235Ala) | not specified [RCV005300294] | uncertain significance | 16 | 88528230 | 88528230 | Human | | name |
| 598259790 | CV3937765 | single nucleotide variant | NM_153813.3(ZFPM1):c.829G>T (p.Ala277Ser) | not specified [RCV005300296] | uncertain significance | 16 | 88532118 | 88532118 | Human | | name |
| 598259797 | CV3937766 | single nucleotide variant | NM_153813.3(ZFPM1):c.700G>A (p.Ala234Thr) | not specified [RCV005300297] | uncertain significance | 16 | 88528226 | 88528226 | Human | | name |
| 598259811 | CV3937771 | single nucleotide variant | NM_153813.3(ZFPM1):c.376G>A (p.Ala126Thr) | not specified [RCV005300300] | uncertain significance | 16 | 88514494 | 88514494 | Human | | name |
| 155959712 | CV2193990 | single nucleotide variant | NM_153813.3(ZFPM1):c.2423C>A (p.Ala808Asp) | not specified [RCV004074713] | uncertain significance | 16 | 88534381 | 88534381 | Human | | name |
| 156151501 | CV2209288 | single nucleotide variant | NM_153813.3(ZFPM1):c.1957A>C (p.Thr653Pro) | not specified [RCV004091688] | uncertain significance | 16 | 88533915 | 88533915 | Human | | name |
| 156045133 | CV2215985 | single nucleotide variant | NM_153813.3(ZFPM1):c.1039A>T (p.Ser347Cys) | not specified [RCV004097040] | uncertain significance | 16 | 88532706 | 88532706 | Human | | name |
| 156331120 | CV2220482 | single nucleotide variant | NM_153813.3(ZFPM1):c.2375A>C (p.Asp792Ala) | not specified [RCV004097712] | uncertain significance | 16 | 88534333 | 88534333 | Human | | name |
| 156055463 | CV2243196 | single nucleotide variant | NM_153813.3(ZFPM1):c.1285G>T (p.Asp429Tyr) | not specified [RCV004110090] | uncertain significance | 16 | 88533243 | 88533243 | Human | | name |
| 156057051 | CV2243364 | single nucleotide variant | NM_153813.3(ZFPM1):c.2921G>A (p.Arg974Gln) | not specified [RCV004112055] | uncertain significance | 16 | 88534879 | 88534879 | Human | | name |
| 156202828 | CV2256271 | single nucleotide variant | NM_153813.3(ZFPM1):c.2645G>A (p.Gly882Asp) | not specified [RCV004116520] | uncertain significance | 16 | 88534603 | 88534603 | Human | | name |
| 156092638 | CV2256689 | single nucleotide variant | NM_153813.3(ZFPM1):c.1889C>T (p.Ala630Val) | not specified [RCV004118863] | uncertain significance | 16 | 88533847 | 88533847 | Human | | name |
| 156240821 | CV2265603 | single nucleotide variant | NM_153813.3(ZFPM1):c.2660G>C (p.Gly887Ala) | not specified [RCV004124338] | uncertain significance | 16 | 88534618 | 88534618 | Human | | name |
| 156016246 | CV2266302 | single nucleotide variant | NM_153813.3(ZFPM1):c.1690G>T (p.Gly564Cys) | not specified [RCV004129129] | uncertain significance | 16 | 88533648 | 88533648 | Human | | name |
| 156025281 | CV2273961 | single nucleotide variant | NM_153813.3(ZFPM1):c.2110T>C (p.Tyr704His) | not specified [RCV004134361] | uncertain significance | 16 | 88534068 | 88534068 | Human | | name |
| 155940787 | CV2294140 | single nucleotide variant | NM_153813.3(ZFPM1):c.1262C>T (p.Ala421Val) | not specified [RCV004149509] | uncertain significance | 16 | 88533220 | 88533220 | Human | | name |
| 156087089 | CV2295392 | single nucleotide variant | NM_153813.3(ZFPM1):c.2966T>A (p.Phe989Tyr) | not specified [RCV004158736] | uncertain significance | 16 | 88534924 | 88534924 | Human | | name |
| 156176715 | CV2299910 | single nucleotide variant | NM_153813.3(ZFPM1):c.1538C>A (p.Pro513Gln) | not specified [RCV004149047] | uncertain significance | 16 | 88533496 | 88533496 | Human | | name |
| 156191694 | CV2301831 | single nucleotide variant | NM_153813.3(ZFPM1):c.1685C>G (p.Ala562Gly) | not specified [RCV004156627] | uncertain significance | 16 | 88533643 | 88533643 | Human | | name |
| 155953506 | CV2303065 | single nucleotide variant | NM_153813.3(ZFPM1):c.1283T>A (p.Leu428Gln) | not specified [RCV004156853] | uncertain significance | 16 | 88533241 | 88533241 | Human | | name |
| 156265709 | CV2312252 | single nucleotide variant | NM_153813.3(ZFPM1):c.1243T>C (p.Ser415Pro) | not specified [RCV004166967] | uncertain significance | 16 | 88533201 | 88533201 | Human | | name |
| 156281843 | CV2317340 | single nucleotide variant | NM_153813.3(ZFPM1):c.2143C>G (p.Arg715Gly) | not specified [RCV004178822] | uncertain significance | 16 | 88534101 | 88534101 | Human | | name |
| 156281853 | CV2317341 | single nucleotide variant | NM_153813.3(ZFPM1):c.2206G>T (p.Ala736Ser) | not specified [RCV004178823] | uncertain significance | 16 | 88534164 | 88534164 | Human | | name |
| 156044499 | CV2322399 | single nucleotide variant | NM_153813.3(ZFPM1):c.2449C>G (p.His817Asp) | not specified [RCV004176146] | uncertain significance | 16 | 88534407 | 88534407 | Human | | name |
| 156069877 | CV2325026 | single nucleotide variant | NM_153813.3(ZFPM1):c.2582C>G (p.Pro861Arg) | not specified [RCV004175573] | uncertain significance | 16 | 88534540 | 88534540 | Human | | name |
| 156336293 | CV2333650 | single nucleotide variant | NM_153813.3(ZFPM1):c.1584G>C (p.Gln528His) | not specified [RCV004192490] | uncertain significance | 16 | 88533542 | 88533542 | Human | | name |
| 155917331 | CV2336311 | single nucleotide variant | NM_153813.3(ZFPM1):c.1438G>A (p.Glu480Lys) | not specified [RCV004192060] | uncertain significance | 16 | 88533396 | 88533396 | Human | | name |
| 156064206 | CV2352928 | single nucleotide variant | NM_153813.3(ZFPM1):c.2299G>C (p.Glu767Gln) | not specified [RCV004200973] | uncertain significance | 16 | 88534257 | 88534257 | Human | | name |
| 156236680 | CV2356131 | single nucleotide variant | NM_153813.3(ZFPM1):c.1101G>C (p.Leu367Phe) | not specified [RCV004203939] | uncertain significance | 16 | 88532847 | 88532847 | Human | | name |
| 156067810 | CV2356737 | single nucleotide variant | NM_153813.3(ZFPM1):c.1720C>T (p.Pro574Ser) | not specified [RCV004202084] | uncertain significance | 16 | 88533678 | 88533678 | Human | | name |
| 155929636 | CV2356947 | single nucleotide variant | NM_153813.3(ZFPM1):c.1273T>C (p.Ser425Pro) | not specified [RCV004204317] | uncertain significance | 16 | 88533231 | 88533231 | Human | | name |
| 156136960 | CV2365082 | single nucleotide variant | NM_153813.3(ZFPM1):c.2143C>T (p.Arg715Cys) | not specified [RCV004224238] | uncertain significance | 16 | 88534101 | 88534101 | Human | | name |
| 156196812 | CV2367266 | single nucleotide variant | NM_153813.3(ZFPM1):c.1919G>A (p.Gly640Asp) | not specified [RCV004215687] | uncertain significance | 16 | 88533877 | 88533877 | Human | | name |
| 156050779 | CV2367603 | single nucleotide variant | NM_153813.3(ZFPM1):c.2878C>T (p.Pro960Ser) | not specified [RCV004211529] | uncertain significance | 16 | 88534836 | 88534836 | Human | | name |
| 156154514 | CV2369511 | single nucleotide variant | NM_153813.3(ZFPM1):c.2131G>A (p.Asp711Asn) | not specified [RCV004210446] | uncertain significance | 16 | 88534089 | 88534089 | Human | | name |
| 156307351 | CV2369686 | single nucleotide variant | NM_153813.3(ZFPM1):c.1495A>G (p.Arg499Gly) | not specified [RCV004215086] | uncertain significance | 16 | 88533453 | 88533453 | Human | | name |
| 156258506 | CV2383789 | single nucleotide variant | NM_153813.3(ZFPM1):c.1877C>G (p.Pro626Arg) | not specified [RCV004603393] | uncertain significance | 16 | 88533835 | 88533835 | Human | | name |
| 156192120 | CV2388628 | single nucleotide variant | NM_153813.3(ZFPM1):c.1415C>T (p.Ala472Val) | not specified [RCV004239509] | uncertain significance | 16 | 88533373 | 88533373 | Human | | name |
| 155928879 | CV2389009 | single nucleotide variant | NM_153813.3(ZFPM1):c.2111A>G (p.Tyr704Cys) | not specified [RCV004242002] | uncertain significance | 16 | 88534069 | 88534069 | Human | | name |
| 155933289 | CV2399294 | single nucleotide variant | NM_153813.3(ZFPM1):c.1665G>C (p.Gln555His) | not specified [RCV004242588] | uncertain significance | 16 | 88533623 | 88533623 | Human | | name |
| 155930768 | CV2399719 | single nucleotide variant | NM_153813.3(ZFPM1):c.1565G>C (p.Gly522Ala) | not specified [RCV004245537] | uncertain significance | 16 | 88533523 | 88533523 | Human | | name |
| 329376474 | CV2428456 | single nucleotide variant | NM_153813.3(ZFPM1):c.1400T>C (p.Val467Ala) | not specified [RCV004253249] | likely benign | 16 | 88533358 | 88533358 | Human | | name |
| 329375699 | CV2431613 | single nucleotide variant | NM_153813.3(ZFPM1):c.1874C>T (p.Pro625Leu) | not specified [RCV004254759] | uncertain significance | 16 | 88533832 | 88533832 | Human | | name |
| 329377964 | CV2436093 | single nucleotide variant | NM_153813.3(ZFPM1):c.2377G>C (p.Gly793Arg) | not specified [RCV004255309] | uncertain significance | 16 | 88534335 | 88534335 | Human | | name |
| 329380048 | CV2444163 | single nucleotide variant | NM_153813.3(ZFPM1):c.1807C>G (p.Arg603Gly) | not specified [RCV004260898] | uncertain significance | 16 | 88533765 | 88533765 | Human | | name |
| 329358145 | CV2453909 | single nucleotide variant | NM_153813.3(ZFPM1):c.1481G>A (p.Ser494Asn) | not specified [RCV004271297] | uncertain significance | 16 | 88533439 | 88533439 | Human | | name |
| 329390679 | CV2455369 | single nucleotide variant | NM_153813.3(ZFPM1):c.1504G>A (p.Ala502Thr) | not specified [RCV004274868] | uncertain significance | 16 | 88533462 | 88533462 | Human | | name |
| 329357357 | CV2456739 | single nucleotide variant | NM_153813.3(ZFPM1):c.2072G>A (p.Arg691His) | not specified [RCV004270720] | uncertain significance | 16 | 88534030 | 88534030 | Human | | name |
| 329395880 | CV2463038 | single nucleotide variant | NM_153813.3(ZFPM1):c.1094G>A (p.Ser365Asn) | not specified [RCV004272854] | uncertain significance | 16 | 88532840 | 88532840 | Human | | name |
| 329397267 | CV2466004 | single nucleotide variant | NM_153813.3(ZFPM1):c.2293G>A (p.Ala765Thr) | not specified [RCV004277905] | uncertain significance | 16 | 88534251 | 88534251 | Human | | name |
| 329362101 | CV2466005 | single nucleotide variant | NM_153813.3(ZFPM1):c.2294C>A (p.Ala765Glu) | not specified [RCV004277906] | uncertain significance | 16 | 88534252 | 88534252 | Human | | name |
| 329381988 | CV2467451 | single nucleotide variant | NM_153813.3(ZFPM1):c.2723C>G (p.Ala908Gly) | not specified [RCV004287061] | uncertain significance | 16 | 88534681 | 88534681 | Human | | name |
| 329392191 | CV2470461 | single nucleotide variant | NM_153813.3(ZFPM1):c.2408G>A (p.Arg803His) | not specified [RCV004273486] | uncertain significance | 16 | 88534366 | 88534366 | Human | | name |
| 401739019 | CV2676420 | single nucleotide variant | NM_153813.3(ZFPM1):c.1835C>T (p.Ala612Val) | not specified [RCV004286441] | uncertain significance | 16 | 88533793 | 88533793 | Human | | name |
| 401740749 | CV2680469 | single nucleotide variant | NM_153813.3(ZFPM1):c.2191G>A (p.Ala731Thr) | not specified [RCV004291113] | uncertain significance | 16 | 88534149 | 88534149 | Human | | name |
| 401759695 | CV2701676 | single nucleotide variant | NM_153813.3(ZFPM1):c.2326G>A (p.Gly776Arg) | not specified [RCV004314088] | uncertain significance | 16 | 88534284 | 88534284 | Human | | name |
| 401779163 | CV2713041 | single nucleotide variant | NM_153813.3(ZFPM1):c.2386G>A (p.Asp796Asn) | not specified [RCV004316601] | uncertain significance | 16 | 88534344 | 88534344 | Human | | name |
| 401770342 | CV2715143 | single nucleotide variant | NM_153813.3(ZFPM1):c.1630G>A (p.Ala544Thr) | not specified [RCV004322713] | uncertain significance | 16 | 88533588 | 88533588 | Human | | name |
| 401879528 | CV2755183 | single nucleotide variant | NM_153813.3(ZFPM1):c.2261C>G (p.Ala754Gly) | not specified [RCV004337375] | uncertain significance | 16 | 88534219 | 88534219 | Human | | name |
| 401866889 | CV2759035 | single nucleotide variant | NM_153813.3(ZFPM1):c.2171C>G (p.Pro724Arg) | not specified [RCV004342342] | uncertain significance | 16 | 88534129 | 88534129 | Human | | name |
| 401867198 | CV2759126 | single nucleotide variant | NM_153813.3(ZFPM1):c.1193G>A (p.Ser398Asn) | not specified [RCV004342425] | uncertain significance | 16 | 88533151 | 88533151 | Human | | name |
| 401889709 | CV2763338 | single nucleotide variant | NM_153813.3(ZFPM1):c.2848C>T (p.Pro950Ser) | not specified [RCV004349234] | uncertain significance | 16 | 88534806 | 88534806 | Human | | name |
| 401870763 | CV2766335 | single nucleotide variant | NM_153813.3(ZFPM1):c.2557G>T (p.Ala853Ser) | not specified [RCV004342588] | uncertain significance | 16 | 88534515 | 88534515 | Human | | name |
| 401877149 | CV2769353 | single nucleotide variant | NM_153813.3(ZFPM1):c.2698C>T (p.Pro900Ser) | not specified [RCV004357347] | uncertain significance | 16 | 88534656 | 88534656 | Human | | name |
| 401887627 | CV2772056 | single nucleotide variant | NM_153813.3(ZFPM1):c.2257G>C (p.Gly753Arg) | not specified [RCV004344726] | uncertain significance | 16 | 88534215 | 88534215 | Human | | name |
| 401869515 | CV2772428 | single nucleotide variant | NM_153813.3(ZFPM1):c.1717G>A (p.Ala573Thr) | not specified [RCV004355216] | uncertain significance | 16 | 88533675 | 88533675 | Human | | name |
| 401897400 | CV2786980 | single nucleotide variant | NM_153813.3(ZFPM1):c.2791G>A (p.Gly931Ser) | not specified [RCV004366109] | uncertain significance | 16 | 88534749 | 88534749 | Human | | name |
| 401868112 | CV2787770 | single nucleotide variant | NM_153813.3(ZFPM1):c.2179G>C (p.Ala727Pro) | not specified [RCV004356676] | uncertain significance | 16 | 88534137 | 88534137 | Human | | name |
| 401894514 | CV2788292 | single nucleotide variant | NM_153813.3(ZFPM1):c.1067T>G (p.Ile356Ser) | not specified [RCV004352879] | uncertain significance | 16 | 88532813 | 88532813 | Human | | name |
| 401892700 | CV2791684 | single nucleotide variant | NM_153813.3(ZFPM1):c.2359C>G (p.Pro787Ala) | not specified [RCV004353024] | uncertain significance | 16 | 88534317 | 88534317 | Human | | name |
| 401870045 | CV2792260 | single nucleotide variant | NM_153813.3(ZFPM1):c.1310C>T (p.Thr437Ile) | not specified [RCV004361451] | uncertain significance | 16 | 88533268 | 88533268 | Human | | name |
| 405270047 | CV3187596 | single nucleotide variant | NM_153813.3(ZFPM1):c.2738G>A (p.Gly913Glu) | not provided [RCV003887680] | uncertain significance | 16 | 88534696 | 88534696 | Human | | name |
| 405669351 | CV3360354 | single nucleotide variant | NM_153813.3(ZFPM1):c.1054A>G (p.Ser352Gly) | not specified [RCV004486161] | uncertain significance | 16 | 88532800 | 88532800 | Human | | name |
| 405669361 | CV3360356 | single nucleotide variant | NM_153813.3(ZFPM1):c.1162G>A (p.Gly388Arg) | not specified [RCV004486163] | uncertain significance | 16 | 88532908 | 88532908 | Human | | name |
| 405669365 | CV3360357 | single nucleotide variant | NM_153813.3(ZFPM1):c.1261G>A (p.Ala421Thr) | not specified [RCV004486164] | uncertain significance | 16 | 88533219 | 88533219 | Human | | name |
| 405669382 | CV3360360 | single nucleotide variant | NM_153813.3(ZFPM1):c.1379G>A (p.Arg460Lys) | not specified [RCV004486167] | uncertain significance | 16 | 88533337 | 88533337 | Human | | name |
| 405669385 | CV3360361 | single nucleotide variant | NM_153813.3(ZFPM1):c.1651C>T (p.His551Tyr) | not specified [RCV004486168] | uncertain significance | 16 | 88533609 | 88533609 | Human | | name |
| 405669391 | CV3360362 | single nucleotide variant | NM_153813.3(ZFPM1):c.1792C>T (p.Leu598Phe) | not specified [RCV004486169] | uncertain significance | 16 | 88533750 | 88533750 | Human | | name |
| 405669394 | CV3360363 | single nucleotide variant | NM_153813.3(ZFPM1):c.1852C>T (p.Pro618Ser) | not specified [RCV004486170] | uncertain significance | 16 | 88533810 | 88533810 | Human | | name |
| 405669401 | CV3360364 | single nucleotide variant | NM_153813.3(ZFPM1):c.2044C>T (p.Arg682Cys) | not specified [RCV004486171] | uncertain significance | 16 | 88534002 | 88534002 | Human | | name |
| 405669404 | CV3360365 | single nucleotide variant | NM_153813.3(ZFPM1):c.2134C>G (p.Pro712Ala) | not specified [RCV004486172] | uncertain significance | 16 | 88534092 | 88534092 | Human | | name |
| 405669409 | CV3360366 | single nucleotide variant | NM_153813.3(ZFPM1):c.2155G>A (p.Ala719Thr) | not specified [RCV004486173] | uncertain significance | 16 | 88534113 | 88534113 | Human | | name |
| 405669414 | CV3360367 | single nucleotide variant | NM_153813.3(ZFPM1):c.2176C>T (p.Pro726Ser) | not specified [RCV004486174] | uncertain significance | 16 | 88534134 | 88534134 | Human | | name |
| 405669424 | CV3360369 | single nucleotide variant | NM_153813.3(ZFPM1):c.2246T>C (p.Leu749Pro) | not specified [RCV004486176] | uncertain significance | 16 | 88534204 | 88534204 | Human | | name |
| 405669429 | CV3360370 | single nucleotide variant | NM_153813.3(ZFPM1):c.2260G>A (p.Ala754Thr) | not specified [RCV004486177] | uncertain significance | 16 | 88534218 | 88534218 | Human | | name |
| 405669434 | CV3360371 | single nucleotide variant | NM_153813.3(ZFPM1):c.2273C>T (p.Pro758Leu) | not specified [RCV004486178] | uncertain significance | 16 | 88534231 | 88534231 | Human | | name |
| 405669439 | CV3360372 | single nucleotide variant | NM_153813.3(ZFPM1):c.2332G>C (p.Gly778Arg) | not specified [RCV004486179] | uncertain significance | 16 | 88534290 | 88534290 | Human | | name |
| 405669444 | CV3360373 | single nucleotide variant | NM_153813.3(ZFPM1):c.2357C>G (p.Ser786Trp) | not specified [RCV004486180] | uncertain significance | 16 | 88534315 | 88534315 | Human | | name |
| 405669449 | CV3360374 | single nucleotide variant | NM_153813.3(ZFPM1):c.2360C>T (p.Pro787Leu) | not specified [RCV004486181] | uncertain significance | 16 | 88534318 | 88534318 | Human | | name |
| 405669454 | CV3360375 | single nucleotide variant | NM_153813.3(ZFPM1):c.2401C>G (p.Pro801Ala) | not specified [RCV004486182] | uncertain significance | 16 | 88534359 | 88534359 | Human | | name |
| 405669460 | CV3360376 | single nucleotide variant | NM_153813.3(ZFPM1):c.2441C>T (p.Ala814Val) | not specified [RCV004486183] | uncertain significance | 16 | 88534399 | 88534399 | Human | | name |
| 405669465 | CV3360377 | single nucleotide variant | NM_153813.3(ZFPM1):c.2453A>C (p.Glu818Ala) | not specified [RCV004486184] | uncertain significance | 16 | 88534411 | 88534411 | Human | | name |
| 405669472 | CV3360378 | single nucleotide variant | NM_153813.3(ZFPM1):c.2479C>T (p.His827Tyr) | not specified [RCV004486185] | uncertain significance | 16 | 88534437 | 88534437 | Human | | name |
| 405669475 | CV3360379 | single nucleotide variant | NM_153813.3(ZFPM1):c.2492C>T (p.Ala831Val) | not specified [RCV004486186] | uncertain significance | 16 | 88534450 | 88534450 | Human | | name |
| 405669481 | CV3360380 | single nucleotide variant | NM_153813.3(ZFPM1):c.2560G>A (p.Ala854Thr) | not specified [RCV004486187] | uncertain significance | 16 | 88534518 | 88534518 | Human | | name |
| 405669485 | CV3360381 | single nucleotide variant | NM_153813.3(ZFPM1):c.2663C>T (p.Pro888Leu) | not specified [RCV004486188] | uncertain significance | 16 | 88534621 | 88534621 | Human | | name |
| 405669490 | CV3360382 | single nucleotide variant | NM_153813.3(ZFPM1):c.2704C>T (p.Pro902Ser) | not specified [RCV004486189] | uncertain significance | 16 | 88534662 | 88534662 | Human | | name |
| 405669495 | CV3360383 | single nucleotide variant | NM_153813.3(ZFPM1):c.2768C>G (p.Pro923Arg) | not specified [RCV004486190] | uncertain significance | 16 | 88534726 | 88534726 | Human | | name |
| 405669499 | CV3360384 | single nucleotide variant | NM_153813.3(ZFPM1):c.2815G>T (p.Ala939Ser) | not specified [RCV004486191] | uncertain significance | 16 | 88534773 | 88534773 | Human | | name |
| 405669505 | CV3360385 | single nucleotide variant | NM_153813.3(ZFPM1):c.2836C>T (p.Pro946Ser) | not specified [RCV004486192] | uncertain significance | 16 | 88534794 | 88534794 | Human | | name |
| 405669510 | CV3360386 | single nucleotide variant | NM_153813.3(ZFPM1):c.2849C>G (p.Pro950Arg) | not specified [RCV004486193] | uncertain significance | 16 | 88534807 | 88534807 | Human | | name |
| 407458067 | CV3490183 | single nucleotide variant | NM_153813.3(ZFPM1):c.2855A>G (p.Tyr952Cys) | not specified [RCV004686562] | uncertain significance | 16 | 88534813 | 88534813 | Human | | name |
| 407458072 | CV3490184 | single nucleotide variant | NM_153813.3(ZFPM1):c.1877C>T (p.Pro626Leu) | not specified [RCV004686563] | uncertain significance | 16 | 88533835 | 88533835 | Human | | name |
| 407458089 | CV3490188 | single nucleotide variant | NM_153813.3(ZFPM1):c.1551G>C (p.Glu517Asp) | not specified [RCV004686567] | uncertain significance | 16 | 88533509 | 88533509 | Human | | name |
| 407458093 | CV3490189 | single nucleotide variant | NM_153813.3(ZFPM1):c.2747G>A (p.Gly916Asp) | not specified [RCV004686568] | uncertain significance | 16 | 88534705 | 88534705 | Human | | name |
| 407459175 | CV3490191 | single nucleotide variant | NM_153813.3(ZFPM1):c.2641C>T (p.Leu881Phe) | not specified [RCV004687064] | uncertain significance | 16 | 88534599 | 88534599 | Human | | name |
| 407459178 | CV3490192 | single nucleotide variant | NM_153813.3(ZFPM1):c.2005C>T (p.Pro669Ser) | not specified [RCV004687065] | uncertain significance | 16 | 88533963 | 88533963 | Human | | name |
| 407459181 | CV3490193 | single nucleotide variant | NM_153813.3(ZFPM1):c.1825G>C (p.Ala609Pro) | not specified [RCV004687066] | uncertain significance | 16 | 88533783 | 88533783 | Human | | name |
| 407459184 | CV3490194 | single nucleotide variant | NM_153813.3(ZFPM1):c.2489A>T (p.Glu830Val) | not specified [RCV004687067] | uncertain significance | 16 | 88534447 | 88534447 | Human | | name |
| 407459189 | CV3490196 | single nucleotide variant | NM_153813.3(ZFPM1):c.1694C>T (p.Ala565Val) | not specified [RCV004687069] | uncertain significance | 16 | 88533652 | 88533652 | Human | | name |
| 407459192 | CV3490197 | single nucleotide variant | NM_153813.3(ZFPM1):c.1202G>C (p.Ser401Thr) | not specified [RCV004687070] | uncertain significance | 16 | 88533160 | 88533160 | Human | | name |
| 597800267 | CV3624739 | single nucleotide variant | NM_153813.3(ZFPM1):c.2410C>G (p.Pro804Ala) | not specified [RCV004880152] | uncertain significance | 16 | 88534368 | 88534368 | Human | | name |
| 597800268 | CV3624740 | single nucleotide variant | NM_153813.3(ZFPM1):c.2183C>T (p.Ala728Val) | not specified [RCV004880153] | uncertain significance | 16 | 88534141 | 88534141 | Human | | name |
| 597800271 | CV3624742 | single nucleotide variant | NM_153813.3(ZFPM1):c.2279C>T (p.Pro760Leu) | not specified [RCV004880154] | uncertain significance | 16 | 88534237 | 88534237 | Human | | name |
| 597726285 | CV3624743 | single nucleotide variant | NM_153813.3(ZFPM1):c.1946G>C (p.Gly649Ala) | not specified [RCV004888384] | uncertain significance | 16 | 88533904 | 88533904 | Human | | name |
| 597726293 | CV3624744 | single nucleotide variant | NM_153813.3(ZFPM1):c.1949G>A (p.Gly650Asp) | not specified [RCV004888385] | uncertain significance | 16 | 88533907 | 88533907 | Human | | name |
| 597726300 | CV3624745 | single nucleotide variant | NM_153813.3(ZFPM1):c.1924G>A (p.Gly642Arg) | not specified [RCV004888386] | uncertain significance | 16 | 88533882 | 88533882 | Human | | name |
| 597800273 | CV3624746 | single nucleotide variant | NM_153813.3(ZFPM1):c.1861C>G (p.Pro621Ala) | not specified [RCV004880155] | uncertain significance | 16 | 88533819 | 88533819 | Human | | name |
| 597726308 | CV3624747 | single nucleotide variant | NM_153813.3(ZFPM1):c.1420C>A (p.Pro474Thr) | not specified [RCV004888387] | uncertain significance | 16 | 88533378 | 88533378 | Human | | name |
| 597800275 | CV3624748 | single nucleotide variant | NM_153813.3(ZFPM1):c.2368G>A (p.Ala790Thr) | not specified [RCV004880156] | uncertain significance | 16 | 88534326 | 88534326 | Human | | name |
| 597800277 | CV3624749 | single nucleotide variant | NM_153813.3(ZFPM1):c.2576G>A (p.Cys859Tyr) | not specified [RCV004880157] | uncertain significance | 16 | 88534534 | 88534534 | Human | | name |
| 597800279 | CV3624751 | single nucleotide variant | NM_153813.3(ZFPM1):c.1478G>A (p.Arg493His) | not specified [RCV004880158] | uncertain significance | 16 | 88533436 | 88533436 | Human | | name |
| 597800243 | CV3628183 | single nucleotide variant | NM_153813.3(ZFPM1):c.2548G>T (p.Gly850Cys) | not specified [RCV004880139] | uncertain significance | 16 | 88534506 | 88534506 | Human | | name |
| 597800244 | CV3628184 | single nucleotide variant | NM_153813.3(ZFPM1):c.1635G>C (p.Lys545Asn) | not specified [RCV004880140] | uncertain significance | 16 | 88533593 | 88533593 | Human | | name |
| 597800246 | CV3628185 | single nucleotide variant | NM_153813.3(ZFPM1):c.2043C>G (p.Ser681Arg) | not specified [RCV004880141] | uncertain significance | 16 | 88534001 | 88534001 | Human | | name |
| 597800248 | CV3628186 | single nucleotide variant | NM_153813.3(ZFPM1):c.1268C>T (p.Thr423Ile) | not specified [RCV004880142] | uncertain significance | 16 | 88533226 | 88533226 | Human | | name |
| 597800252 | CV3628188 | single nucleotide variant | NM_153813.3(ZFPM1):c.2521C>T (p.Pro841Ser) | not specified [RCV004880144] | uncertain significance | 16 | 88534479 | 88534479 | Human | | name |
| 597800254 | CV3628189 | single nucleotide variant | NM_153813.3(ZFPM1):c.1546G>A (p.Gly516Ser) | not specified [RCV004880145] | uncertain significance | 16 | 88533504 | 88533504 | Human | | name |
| 597800255 | CV3628190 | single nucleotide variant | NM_153813.3(ZFPM1):c.1231G>A (p.Gly411Ser) | not specified [RCV004880146] | uncertain significance | 16 | 88533189 | 88533189 | Human | | name |
| 597800257 | CV3628192 | single nucleotide variant | NM_153813.3(ZFPM1):c.1348G>A (p.Gly450Arg) | not specified [RCV004880147] | uncertain significance | 16 | 88533306 | 88533306 | Human | | name |
| 597726270 | CV3628193 | single nucleotide variant | NM_153813.3(ZFPM1):c.1715G>C (p.Gly572Ala) | not specified [RCV004888382] | uncertain significance | 16 | 88533673 | 88533673 | Human | | name |
| 597800259 | CV3628194 | single nucleotide variant | NM_153813.3(ZFPM1):c.1834G>T (p.Ala612Ser) | not specified [RCV004880148] | uncertain significance | 16 | 88533792 | 88533792 | Human | | name |
| 597800261 | CV3628195 | single nucleotide variant | NM_153813.3(ZFPM1):c.1702G>A (p.Gly568Arg) | not specified [RCV004880149] | uncertain significance | 16 | 88533660 | 88533660 | Human | | name |
| 597800263 | CV3628196 | single nucleotide variant | NM_153813.3(ZFPM1):c.2728C>T (p.Pro910Ser) | not specified [RCV004880150] | uncertain significance | 16 | 88534686 | 88534686 | Human | | name |
| 597800480 | CV3628197 | single nucleotide variant | NM_153813.3(ZFPM1):c.2399A>G (p.Lys800Arg) | not specified [RCV004880151] | uncertain significance | 16 | 88534357 | 88534357 | Human | | name |
| 598259727 | CV3937748 | single nucleotide variant | NM_153813.3(ZFPM1):c.1597C>A (p.Pro533Thr) | not specified [RCV005300285] | uncertain significance | 16 | 88533555 | 88533555 | Human | | name |
| 598159028 | CV3937749 | single nucleotide variant | NM_153813.3(ZFPM1):c.2798C>A (p.Pro933His) | not specified [RCV005306471] | uncertain significance | 16 | 88534756 | 88534756 | Human | | name |
| 598259733 | CV3937750 | single nucleotide variant | NM_153813.3(ZFPM1):c.1762A>C (p.Asn588His) | not specified [RCV005300286] | uncertain significance | 16 | 88533720 | 88533720 | Human | | name |
| 598159033 | CV3937752 | single nucleotide variant | NM_153813.3(ZFPM1):c.2369C>T (p.Ala790Val) | not specified [RCV005306472] | uncertain significance | 16 | 88534327 | 88534327 | Human | | name |
| 598259750 | CV3937754 | single nucleotide variant | NM_153813.3(ZFPM1):c.2261C>T (p.Ala754Val) | not specified [RCV005300289] | uncertain significance | 16 | 88534219 | 88534219 | Human | | name |
| 598259755 | CV3937755 | single nucleotide variant | NM_153813.3(ZFPM1):c.1849G>A (p.Ala617Thr) | not specified [RCV005300290] | uncertain significance | 16 | 88533807 | 88533807 | Human | | name |
| 598259762 | CV3937756 | single nucleotide variant | NM_153813.3(ZFPM1):c.2149C>A (p.Pro717Thr) | not specified [RCV005300291] | uncertain significance | 16 | 88534107 | 88534107 | Human | | name |
| 598259767 | CV3937757 | single nucleotide variant | NM_153813.3(ZFPM1):c.1602C>G (p.Asp534Glu) | not specified [RCV005300292] | uncertain significance | 16 | 88533560 | 88533560 | Human | | name |
| 598259773 | CV3937758 | single nucleotide variant | NM_153813.3(ZFPM1):c.2351C>A (p.Ala784Glu) | not specified [RCV005300293] | uncertain significance | 16 | 88534309 | 88534309 | Human | | name |
| 598159037 | CV3937759 | single nucleotide variant | NM_153813.3(ZFPM1):c.1952C>T (p.Ala651Val) | not specified [RCV005306473] | uncertain significance | 16 | 88533910 | 88533910 | Human | | name |
| 598159047 | CV3937762 | single nucleotide variant | NM_153813.3(ZFPM1):c.2785C>G (p.Pro929Ala) | not specified [RCV005306475] | uncertain significance | 16 | 88534743 | 88534743 | Human | | name |
| 598159053 | CV3937763 | single nucleotide variant | NM_153813.3(ZFPM1):c.1721C>G (p.Pro574Arg) | not specified [RCV005306476] | uncertain significance | 16 | 88533679 | 88533679 | Human | | name |
| 598259783 | CV3937764 | single nucleotide variant | NM_153813.3(ZFPM1):c.1129G>C (p.Gly377Arg) | not specified [RCV005300295] | uncertain significance | 16 | 88532875 | 88532875 | Human | | name |
| 598159058 | CV3937767 | single nucleotide variant | NM_153813.3(ZFPM1):c.2603A>G (p.Asp868Gly) | not specified [RCV005306477] | uncertain significance | 16 | 88534561 | 88534561 | Human | | name |
| 598259802 | CV3937768 | single nucleotide variant | NM_153813.3(ZFPM1):c.1880G>A (p.Gly627Asp) | not specified [RCV005300298] | uncertain significance | 16 | 88533838 | 88533838 | Human | | name |
| 598259807 | CV3937769 | single nucleotide variant | NM_153813.3(ZFPM1):c.2423C>G (p.Ala808Gly) | not specified [RCV005300299] | uncertain significance | 16 | 88534381 | 88534381 | Human | | name |
| 598159063 | CV3937770 | single nucleotide variant | NM_153813.3(ZFPM1):c.2302T>C (p.Ser768Pro) | not specified [RCV005306478] | uncertain significance | 16 | 88534260 | 88534260 | Human | | name |
| 598259819 | CV3937772 | single nucleotide variant | NM_153813.3(ZFPM1):c.2803T>C (p.Ser935Pro) | not specified [RCV005300301] | uncertain significance | 16 | 88534761 | 88534761 | Human | | name |
| 15182489 | CV715164 | single nucleotide variant | NM_153813.3(ZFPM1):c.1332G>C (p.Glu444Asp) | not provided [RCV000974643] | benign | 16 | 88533290 | 88533290 | Human | | name |
| 401767673 | CV2729832 | single nucleotide variant | NM_153813.3(ZFPM1):c.3013G>A (p.Val1005Met) | not specified [RCV004332839] | uncertain significance | 16 | 88534971 | 88534971 | Human | | name |
| 598129083 | CV3886887 | deletion | NM_153813.3(ZFPM1):c.2165_2191del (p.Gly722_Pro730del) | not provided [RCV005244547] | likely benign | 16 | 88534107 | 88534133 | Human | | name |
| 40816190 | CV969186 | deletion | NM_153813.3(ZFPM1):c.1331_1333del (p.Glu444_Pro445delinsAla) | not specified [RCV001260310] | uncertain significance | 16 | 88533289 | 88533291 | Human | | name |