| 156032329 | CV2259571 | single nucleotide variant | NM_024669.3(ANKRD55):c.23A>T (p.Asp8Val) | not specified [RCV004116619] | uncertain significance | 5 | 56232891 | 56232891 | Human | | name |
| 155988443 | CV2259572 | single nucleotide variant | NM_024669.3(ANKRD55):c.24T>A (p.Asp8Glu) | not specified [RCV004116620] | uncertain significance | 5 | 56232890 | 56232890 | Human | | name |
| 156028099 | CV2278496 | single nucleotide variant | NM_024669.3(ANKRD55):c.27C>A (p.Phe9Leu) | not specified [RCV004132937] | uncertain significance | 5 | 56232887 | 56232887 | Human | | name |
| 405683868 | CV3282299 | single nucleotide variant | NM_024669.3(ANKRD55):c.20T>G (p.Met7Arg) | not specified [RCV004422278] | uncertain significance | 5 | 56232894 | 56232894 | Human | | name |
| 156195794 | CV2251889 | single nucleotide variant | NM_024669.3(ANKRD55):c.89T>C (p.Met30Thr) | not specified [RCV004119865] | uncertain significance | 5 | 56183604 | 56183604 | Human | | name |
| 597638848 | CV3564302 | single nucleotide variant | NM_024669.3(ANKRD55):c.77T>C (p.Val26Ala) | not specified [RCV004825005] | uncertain significance | 5 | 56183616 | 56183616 | Human | | name |
| 15161641 | CV709951 | single nucleotide variant | NM_024669.3(ANKRD55):c.723G>A (p.Ala241=) | not provided [RCV000970125] | benign | 5 | 56126996 | 56126996 | Human | | name |
| 15130009 | CV749534 | single nucleotide variant | NM_024669.3(ANKRD55):c.474G>A (p.Gln158=) | not provided [RCV000919929] | likely benign | 5 | 56159842 | 56159842 | Human | | name |
| 155930510 | CV2296933 | single nucleotide variant | NM_024669.3(ANKRD55):c.296G>A (p.Cys99Tyr) | not specified [RCV004149080] | uncertain significance | 5 | 56176168 | 56176168 | Human | | name |
| 156288750 | CV2332966 | single nucleotide variant | NM_024669.3(ANKRD55):c.214C>T (p.Arg72Cys) | not specified [RCV004194267] | uncertain significance | 5 | 56176250 | 56176250 | Human | | name |
| 155983601 | CV2367792 | single nucleotide variant | NM_024669.3(ANKRD55):c.236T>C (p.Leu79Pro) | not specified [RCV004222909] | uncertain significance | 5 | 56176228 | 56176228 | Human | | name |
| 596946451 | CV3548271 | single nucleotide variant | NM_024669.3(ANKRD55):c.1617T>C (p.His539=) | not provided [RCV004810096] | likely benign | 5 | 56111131 | 56111131 | Human | | name |
| 597638857 | CV3564313 | single nucleotide variant | NM_024669.3(ANKRD55):c.104C>G (p.Ala35Gly) | not specified [RCV004825007] | uncertain significance | 5 | 56183589 | 56183589 | Human | | name |
| 156300672 | CV2244959 | single nucleotide variant | NM_024669.3(ANKRD55):c.958G>A (p.Glu320Lys) | not specified [RCV004104698] | uncertain significance | 5 | 56116622 | 56116622 | Human | | name |
| 156216015 | CV2257625 | single nucleotide variant | NM_024669.3(ANKRD55):c.568C>T (p.Leu190Phe) | not specified [RCV004127450] | uncertain significance | 5 | 56143845 | 56143845 | Human | | name |
| 156032058 | CV2274985 | single nucleotide variant | NM_024669.3(ANKRD55):c.415G>A (p.Asp139Asn) | not specified [RCV004135030] | uncertain significance | 5 | 56170701 | 56170701 | Human | | name |
| 156152804 | CV2328463 | single nucleotide variant | NM_024669.3(ANKRD55):c.659G>C (p.Gly220Ala) | not specified [RCV004175848] | uncertain significance | 5 | 56127060 | 56127060 | Human | | name |
| 156274152 | CV2334087 | single nucleotide variant | NM_024669.3(ANKRD55):c.931A>G (p.Thr311Ala) | not specified [RCV004183602] | uncertain significance | 5 | 56116649 | 56116649 | Human | | name |
| 156063803 | CV2352834 | single nucleotide variant | NM_024669.3(ANKRD55):c.377A>G (p.Asn126Ser) | not specified [RCV004198841] | uncertain significance | 5 | 56170739 | 56170739 | Human | | name |
| 156135677 | CV2357001 | single nucleotide variant | NM_024669.3(ANKRD55):c.382C>T (p.Arg128Cys) | not specified [RCV004206808] | uncertain significance | 5 | 56170734 | 56170734 | Human | | name |
| 155936214 | CV2380341 | single nucleotide variant | NM_024669.3(ANKRD55):c.572T>C (p.Val191Ala) | not specified [RCV004217956] | uncertain significance | 5 | 56143841 | 56143841 | Human | | name |
| 329366194 | CV2438216 | single nucleotide variant | NM_024669.3(ANKRD55):c.740T>C (p.Ile247Thr) | not specified [RCV004256983] | uncertain significance | 5 | 56126979 | 56126979 | Human | | name |
| 401759342 | CV2690869 | single nucleotide variant | NM_024669.3(ANKRD55):c.911A>G (p.Tyr304Cys) | not specified [RCV004298572] | uncertain significance | 5 | 56116669 | 56116669 | Human | | name |
| 401869538 | CV2772436 | single nucleotide variant | NM_024669.3(ANKRD55):c.478A>G (p.Asn160Asp) | not specified [RCV004355223] | uncertain significance | 5 | 56159838 | 56159838 | Human | | name |
| 405683871 | CV3282300 | single nucleotide variant | NM_024669.3(ANKRD55):c.667A>T (p.Ile223Leu) | not specified [RCV004422279] | uncertain significance | 5 | 56127052 | 56127052 | Human | | name |
| 405683875 | CV3282301 | single nucleotide variant | NM_024669.3(ANKRD55):c.838T>G (p.Cys280Gly) | not specified [RCV004422280] | uncertain significance | 5 | 56116742 | 56116742 | Human | | name |
| 405683883 | CV3282302 | single nucleotide variant | NM_024669.3(ANKRD55):c.859T>G (p.Leu287Val) | not specified [RCV004422281] | uncertain significance | 5 | 56116721 | 56116721 | Human | | name |
| 597648111 | CV3564270 | single nucleotide variant | NM_024669.3(ANKRD55):c.431C>T (p.Thr144Met) | not specified [RCV004833327] | uncertain significance | 5 | 56159885 | 56159885 | Human | | name |
| 597648154 | CV3564280 | single nucleotide variant | NM_024669.3(ANKRD55):c.530A>G (p.His177Arg) | not specified [RCV004833333] | uncertain significance | 5 | 56143883 | 56143883 | Human | | name |
| 597638836 | CV3564290 | single nucleotide variant | NM_024669.3(ANKRD55):c.653A>G (p.His218Arg) | not specified [RCV004825003] | uncertain significance | 5 | 56127066 | 56127066 | Human | | name |
| 597638878 | CV3564333 | single nucleotide variant | NM_024669.3(ANKRD55):c.424C>A (p.Leu142Ile) | not specified [RCV004825011] | uncertain significance | 5 | 56159892 | 56159892 | Human | | name |
| 598167631 | CV3986147 | single nucleotide variant | NM_024669.3(ANKRD55):c.764A>T (p.Glu255Val) | not specified [RCV005369558] | uncertain significance | 5 | 56126955 | 56126955 | Human | | name |
| 598200804 | CV3986167 | single nucleotide variant | NM_024669.3(ANKRD55):c.566C>T (p.Thr189Ile) | not specified [RCV005375918] | uncertain significance | 5 | 56143847 | 56143847 | Human | | name |
| 15149397 | CV709950 | single nucleotide variant | NM_024669.3(ANKRD55):c.835G>A (p.Glu279Lys) | not provided [RCV000967746] | benign|likely benign | 5 | 56116745 | 56116745 | Human | | name |
| 8626038 | CV81182 | single nucleotide variant | NM_024669.2(ANKRD55):c.372T>A (p.Asp124Glu) | Malignant melanoma [RCV000061260] | not provided | 5 | 56170744 | 56170744 | Human | | name |
| 156132625 | CV2206648 | single nucleotide variant | NM_024669.3(ANKRD55):c.1106G>A (p.Arg369Gln) | not specified [RCV004080986] | likely benign | 5 | 56111642 | 56111642 | Human | | name |
| 156049104 | CV2241852 | single nucleotide variant | NM_024669.3(ANKRD55):c.1399G>A (p.Ala467Thr) | not specified [RCV004106775] | uncertain significance | 5 | 56111349 | 56111349 | Human | | name |
| 156180635 | CV2258459 | single nucleotide variant | NM_024669.3(ANKRD55):c.1042C>G (p.Gln348Glu) | not specified [RCV004115651] | uncertain significance | 5 | 56111706 | 56111706 | Human | | name |
| 155921744 | CV2276366 | single nucleotide variant | NM_024669.3(ANKRD55):c.1000A>G (p.Ser334Gly) | not specified [RCV004144106] | uncertain significance | 5 | 56111748 | 56111748 | Human | | name |
| 156304083 | CV2308550 | single nucleotide variant | NM_024669.3(ANKRD55):c.1234G>A (p.Asp412Asn) | not specified [RCV004166826] | uncertain significance | 5 | 56111514 | 56111514 | Human | | name |
| 156270501 | CV2312186 | single nucleotide variant | NM_024669.3(ANKRD55):c.1384G>C (p.Ala462Pro) | not specified [RCV004165085] | uncertain significance | 5 | 56111364 | 56111364 | Human | | name |
| 156265731 | CV2312255 | single nucleotide variant | NM_024669.3(ANKRD55):c.1833T>A (p.Ser611Arg) | not specified [RCV004166969] | uncertain significance | 5 | 56100195 | 56100195 | Human | | name |
| 156050106 | CV2336572 | single nucleotide variant | NM_024669.3(ANKRD55):c.1585G>T (p.Val529Phe) | not specified [RCV004196820] | uncertain significance | 5 | 56111163 | 56111163 | Human | | name |
| 156213594 | CV2385859 | single nucleotide variant | NM_024669.3(ANKRD55):c.1294A>G (p.Ile432Val) | not specified [RCV004226904] | uncertain significance | 5 | 56111454 | 56111454 | Human | | name |
| 156223792 | CV2399222 | single nucleotide variant | NM_024669.3(ANKRD55):c.1078G>A (p.Ala360Thr) | not specified [RCV004247012] | uncertain significance | 5 | 56111670 | 56111670 | Human | | name |
| 156004090 | CV2400950 | single nucleotide variant | NM_024669.3(ANKRD55):c.1745G>A (p.Arg582Gln) | not specified [RCV004244238] | uncertain significance | 5 | 56100283 | 56100283 | Human | | name |
| 329357330 | CV2431342 | single nucleotide variant | NM_024669.3(ANKRD55):c.1307G>A (p.Ser436Asn) | not specified [RCV004252461] | uncertain significance | 5 | 56111441 | 56111441 | Human | | name |
| 329389542 | CV2445112 | single nucleotide variant | NM_024669.3(ANKRD55):c.1195G>A (p.Asp399Asn) | not specified [RCV004263760] | uncertain significance | 5 | 56111553 | 56111553 | Human | | name |
| 329401892 | CV2457499 | single nucleotide variant | NM_024669.3(ANKRD55):c.1048T>C (p.Phe350Leu) | not specified [RCV004267312] | uncertain significance | 5 | 56111700 | 56111700 | Human | | name |
| 401738520 | CV2676311 | single nucleotide variant | NM_024669.3(ANKRD55):c.1301C>T (p.Thr434Met) | not specified [RCV004286346] | uncertain significance | 5 | 56111447 | 56111447 | Human | | name |
| 401747208 | CV2692095 | single nucleotide variant | NM_024669.3(ANKRD55):c.1529C>T (p.Ser510Phe) | not specified [RCV004301807] | uncertain significance | 5 | 56111219 | 56111219 | Human | | name |
| 405683838 | CV3282292 | single nucleotide variant | NM_024669.3(ANKRD55):c.1276C>T (p.Arg426Cys) | not specified [RCV004422271] | uncertain significance | 5 | 56111472 | 56111472 | Human | | name |
| 405683847 | CV3282294 | single nucleotide variant | NM_024669.3(ANKRD55):c.1421G>T (p.Arg474Leu) | not specified [RCV004422273] | uncertain significance | 5 | 56111327 | 56111327 | Human | | name |
| 405683851 | CV3282295 | single nucleotide variant | NM_024669.3(ANKRD55):c.1582G>C (p.Glu528Gln) | not specified [RCV004422274] | uncertain significance | 5 | 56111166 | 56111166 | Human | | name |
| 405683854 | CV3282296 | single nucleotide variant | NM_024669.3(ANKRD55):c.1687A>G (p.Thr563Ala) | not specified [RCV004422275] | uncertain significance | 5 | 56102530 | 56102530 | Human | | name |
| 405683858 | CV3282297 | single nucleotide variant | NM_024669.3(ANKRD55):c.1722A>T (p.Lys574Asn) | not specified [RCV004422276] | uncertain significance | 5 | 56102495 | 56102495 | Human | | name |
| 407515728 | CV3450934 | single nucleotide variant | NM_024669.3(ANKRD55):c.1411C>G (p.Gln471Glu) | not specified [RCV004650004] | uncertain significance | 5 | 56111337 | 56111337 | Human | | name |
| 597648235 | CV3564249 | single nucleotide variant | NM_024669.3(ANKRD55):c.1586T>C (p.Val529Ala) | not specified [RCV004833310] | uncertain significance | 5 | 56111162 | 56111162 | Human | | name |
| 597648058 | CV3564259 | single nucleotide variant | NM_024669.3(ANKRD55):c.1744C>T (p.Arg582Trp) | not specified [RCV004833319] | uncertain significance | 5 | 56100284 | 56100284 | Human | | name |
| 597648580 | CV3564324 | single nucleotide variant | NM_024669.3(ANKRD55):c.1787A>G (p.His596Arg) | not specified [RCV004833368] | uncertain significance | 5 | 56100241 | 56100241 | Human | | name |
| 598167653 | CV3986159 | single nucleotide variant | NM_024669.3(ANKRD55):c.1663C>T (p.His555Tyr) | not specified [RCV005369562] | uncertain significance | 5 | 56102554 | 56102554 | Human | | name |
| 598200829 | CV3986174 | single nucleotide variant | NM_024669.3(ANKRD55):c.1810G>A (p.Glu604Lys) | not specified [RCV005375922] | uncertain significance | 5 | 56100218 | 56100218 | Human | | name |
| 15103992 | CV721485 | single nucleotide variant | NM_024669.3(ANKRD55):c.1126T>C (p.Ser376Pro) | not provided [RCV000892794] | likely benign | 5 | 56111622 | 56111622 | Human | | name |
| 15119718 | CV749533 | single nucleotide variant | NM_024669.3(ANKRD55):c.1052G>A (p.Cys351Tyr) | not provided [RCV000918188] | likely benign | 5 | 56111696 | 56111696 | Human | | name |
