| 8586581 | CV121185 | single nucleotide variant | NM_021810.4(CDH26):c.294+514G>A | Lung cancer [RCV000101705] | uncertain significance | 20 | 60007301 | 60007301 | Human | | name |
| 8637411 | CV92637 | single nucleotide variant | NM_177980.2(CDH26):c.27C>T (p.Pro9=) | Malignant melanoma [RCV000072735] | not provided | 20 | 59958753 | 59958753 | Human | | name |
| 401860592 | CV2758536 | single nucleotide variant | NM_177980.4(CDH26):c.16G>A (p.Gly6Arg) | not specified [RCV004337628] | likely benign | 20 | 59958742 | 59958742 | Human | | name |
| 598169135 | CV3947429 | single nucleotide variant | NM_177980.4(CDH26):c.26C>T (p.Pro9Leu) | not specified [RCV005308363] | uncertain significance | 20 | 59958752 | 59958752 | Human | | name |
| 155932707 | CV2400077 | single nucleotide variant | NM_177980.4(CDH26):c.43C>G (p.Leu15Val) | not specified [RCV004246991] | uncertain significance | 20 | 59958769 | 59958769 | Human | | name |
| 597795449 | CV3641891 | single nucleotide variant | NM_177980.4(CDH26):c.58T>C (p.Trp20Arg) | not specified [RCV004903678] | uncertain significance | 20 | 59958784 | 59958784 | Human | | name |
| 156395988 | CV2326041 | single nucleotide variant | NM_177980.4(CDH26):c.148C>G (p.Arg50Gly) | not specified [RCV004176246] | uncertain significance | 20 | 59970103 | 59970103 | Human | | name |
| 329399772 | CV2467641 | single nucleotide variant | NM_177980.4(CDH26):c.109C>A (p.Leu37Ile) | not specified [RCV004287493] | uncertain significance | 20 | 59969006 | 59969006 | Human | | name |
| 401767922 | CV2678062 | single nucleotide variant | NM_177980.4(CDH26):c.256A>G (p.Met86Val) | not specified [RCV004296583] | uncertain significance | 20 | 59971986 | 59971986 | Human | | name |
| 405720746 | CV3296554 | single nucleotide variant | NM_177980.4(CDH26):c.133A>G (p.Ile45Val) | not specified [RCV004428103] | uncertain significance | 20 | 59970088 | 59970088 | Human | | name |
| 405720812 | CV3296563 | single nucleotide variant | NM_177980.4(CDH26):c.232C>G (p.Leu78Val) | not specified [RCV004428112] | uncertain significance | 20 | 59971962 | 59971962 | Human | | name |
| 407454998 | CV3422309 | single nucleotide variant | NM_177980.4(CDH26):c.135C>G (p.Ile45Met) | not specified [RCV004610100] | uncertain significance | 20 | 59970090 | 59970090 | Human | | name |
| 597795469 | CV3641898 | single nucleotide variant | NM_177980.4(CDH26):c.139C>G (p.Gln47Glu) | not specified [RCV004903685] | uncertain significance | 20 | 59970094 | 59970094 | Human | | name |
| 156232040 | CV2227649 | single nucleotide variant | NM_177980.4(CDH26):c.307A>T (p.Ile103Phe) | not specified [RCV004094053] | uncertain significance | 20 | 59972037 | 59972037 | Human | | name |
| 156023517 | CV2233461 | single nucleotide variant | NM_177980.4(CDH26):c.655C>T (p.Arg219Trp) | not specified [RCV004106085] | uncertain significance | 20 | 59984752 | 59984752 | Human | | name |
| 156276323 | CV2276777 | single nucleotide variant | NM_177980.4(CDH26):c.877G>C (p.Val293Leu) | not specified [RCV004140141] | uncertain significance | 20 | 59987492 | 59987492 | Human | | name |
| 401730890 | CV2686767 | single nucleotide variant | NM_177980.4(CDH26):c.359G>A (p.Arg120His) | not specified [RCV004301955] | uncertain significance | 20 | 59972089 | 59972089 | Human | | name |
| 401717586 | CV2714066 | single nucleotide variant | NM_177980.4(CDH26):c.877G>A (p.Val293Met) | not specified [RCV004315465] | uncertain significance | 20 | 59987492 | 59987492 | Human | | name |
| 401781997 | CV2719128 | single nucleotide variant | NM_177980.4(CDH26):c.332A>G (p.His111Arg) | not specified [RCV004324796] | uncertain significance | 20 | 59972062 | 59972062 | Human | | name |
| 401892456 | CV2781978 | single nucleotide variant | NM_177980.4(CDH26):c.922G>T (p.Ala308Ser) | not specified [RCV004357208] | uncertain significance | 20 | 59987537 | 59987537 | Human | | name |
| 405720844 | CV3296567 | single nucleotide variant | NM_177980.4(CDH26):c.416G>T (p.Arg139Leu) | not specified [RCV004428116] | uncertain significance | 20 | 59982945 | 59982945 | Human | | name |
| 405720854 | CV3296568 | single nucleotide variant | NM_177980.4(CDH26):c.550A>G (p.Ile184Val) | not specified [RCV004428117] | uncertain significance | 20 | 59984647 | 59984647 | Human | | name |
| 405720863 | CV3296569 | single nucleotide variant | NM_177980.4(CDH26):c.764T>C (p.Leu255Pro) | not specified [RCV004428118] | uncertain significance | 20 | 59985056 | 59985056 | Human | | name |
| 405720873 | CV3296570 | single nucleotide variant | NM_177980.4(CDH26):c.944T>C (p.Ile315Thr) | not specified [RCV004428119] | uncertain significance | 20 | 59987559 | 59987559 | Human | | name |
| 405720879 | CV3296571 | single nucleotide variant | NM_177980.4(CDH26):c.998A>G (p.Asn333Ser) | not specified [RCV004428120] | uncertain significance | 20 | 59987613 | 59987613 | Human | | name |
| 407454988 | CV3422304 | single nucleotide variant | NM_177980.4(CDH26):c.326A>G (p.Glu109Gly) | not specified [RCV004610095] | uncertain significance | 20 | 59972056 | 59972056 | Human | | name |
| 407454996 | CV3422308 | single nucleotide variant | NM_177980.4(CDH26):c.831G>C (p.Gln277His) | not specified [RCV004610099] | uncertain significance | 20 | 59985123 | 59985123 | Human | | name |
| 407455000 | CV3422310 | single nucleotide variant | NM_177980.4(CDH26):c.389T>C (p.Phe130Ser) | not specified [RCV004610101] | uncertain significance | 20 | 59972119 | 59972119 | Human | | name |
| 407455007 | CV3422313 | single nucleotide variant | NM_177980.4(CDH26):c.373G>C (p.Glu125Gln) | not specified [RCV004610104] | uncertain significance | 20 | 59972103 | 59972103 | Human | | name |
| 597795446 | CV3641890 | single nucleotide variant | NM_177980.4(CDH26):c.758C>T (p.Pro253Leu) | not specified [RCV004903677] | uncertain significance | 20 | 59985050 | 59985050 | Human | | name |
| 598169025 | CV3947412 | single nucleotide variant | NM_177980.4(CDH26):c.863G>A (p.Arg288Gln) | not specified [RCV005308348] | likely benign | 20 | 59987478 | 59987478 | Human | | name |
| 598169035 | CV3947413 | single nucleotide variant | NM_177980.4(CDH26):c.733A>G (p.Ile245Val) | not specified [RCV005308349] | uncertain significance | 20 | 59985025 | 59985025 | Human | | name |
| 598169060 | CV3947418 | single nucleotide variant | NM_177980.4(CDH26):c.378G>A (p.Met126Ile) | not specified [RCV005308352] | uncertain significance | 20 | 59972108 | 59972108 | Human | | name |
| 598169079 | CV3947421 | single nucleotide variant | NM_177980.4(CDH26):c.744G>C (p.Arg248Ser) | not specified [RCV005308355] | uncertain significance | 20 | 59985036 | 59985036 | Human | | name |
| 598169103 | CV3947424 | single nucleotide variant | NM_177980.4(CDH26):c.533A>C (p.Gln178Pro) | not specified [RCV005308358] | uncertain significance | 20 | 59983062 | 59983062 | Human | | name |
| 598169125 | CV3947427 | single nucleotide variant | NM_177980.4(CDH26):c.347T>C (p.Ile116Thr) | not specified [RCV005308361] | uncertain significance | 20 | 59972077 | 59972077 | Human | | name |
| 156374442 | CV2198457 | single nucleotide variant | NM_177980.4(CDH26):c.1284A>C (p.Arg428Ser) | not specified [RCV004081985] | uncertain significance | 20 | 59992378 | 59992378 | Human | | name |
| 155960411 | CV2204206 | single nucleotide variant | NM_177980.4(CDH26):c.2221G>C (p.Ala741Pro) | not specified [RCV004077002] | uncertain significance | 20 | 60006713 | 60006713 | Human | | name |
| 156224300 | CV2219323 | single nucleotide variant | NM_177980.4(CDH26):c.2090G>C (p.Gly697Ala) | not specified [RCV004095170] | uncertain significance | 20 | 59999656 | 59999656 | Human | | name |
| 156382846 | CV2223660 | single nucleotide variant | NM_177980.4(CDH26):c.1705C>T (p.Arg569Cys) | not specified [RCV004093783] | uncertain significance | 20 | 59995871 | 59995871 | Human | | name |
| 156188706 | CV2226786 | single nucleotide variant | NM_177980.4(CDH26):c.2480A>G (p.Glu827Gly) | not specified [RCV004102000] | uncertain significance | 20 | 60012711 | 60012711 | Human | | name |
| 156244893 | CV2231640 | single nucleotide variant | NM_177980.4(CDH26):c.2276T>C (p.Met759Thr) | not specified [RCV004098211] | uncertain significance | 20 | 60006768 | 60006768 | Human | | name |
| 156184419 | CV2239193 | single nucleotide variant | NM_177980.4(CDH26):c.1874T>C (p.Phe625Ser) | not specified [RCV004112175] | uncertain significance | 20 | 59996040 | 59996040 | Human | | name |
| 155919531 | CV2279436 | single nucleotide variant | NM_177980.4(CDH26):c.1996G>A (p.Glu666Lys) | not specified [RCV004141976] | uncertain significance | 20 | 59996738 | 59996738 | Human | | name |
| 155992580 | CV2281225 | single nucleotide variant | NM_177980.4(CDH26):c.1193C>T (p.Pro398Leu) | not specified [RCV004147474] | uncertain significance | 20 | 59989073 | 59989073 | Human | | name |
| 156075090 | CV2281494 | single nucleotide variant | NM_177980.4(CDH26):c.1157A>G (p.Gln386Arg) | not specified [RCV004153811] | uncertain significance | 20 | 59989037 | 59989037 | Human | | name |
| 156278936 | CV2285008 | single nucleotide variant | NM_177980.4(CDH26):c.1654G>A (p.Gly552Arg) | not specified [RCV004143437] | uncertain significance | 20 | 59994477 | 59994477 | Human | | name |
| 155940388 | CV2294070 | single nucleotide variant | NM_177980.4(CDH26):c.1340T>C (p.Val447Ala) | not specified [RCV004149449] | likely benign | 20 | 59992434 | 59992434 | Human | | name |
| 155999404 | CV2296192 | single nucleotide variant | NM_177980.4(CDH26):c.1397A>G (p.Tyr466Cys) | not specified [RCV004154112] | uncertain significance | 20 | 59992491 | 59992491 | Human | | name |
| 156083514 | CV2298995 | single nucleotide variant | NM_177980.4(CDH26):c.1999A>G (p.Ser667Gly) | not specified [RCV004158520] | uncertain significance | 20 | 59996741 | 59996741 | Human | | name |
| 156039024 | CV2313698 | single nucleotide variant | NM_177980.4(CDH26):c.2069C>G (p.Ala690Gly) | not specified [RCV004157615] | uncertain significance | 20 | 59999635 | 59999635 | Human | | name |
| 156283361 | CV2318846 | single nucleotide variant | NM_177980.4(CDH26):c.2444G>T (p.Gly815Val) | not specified [RCV004175755] | uncertain significance | 20 | 60012675 | 60012675 | Human | | name |
| 156066936 | CV2356573 | single nucleotide variant | NM_177980.4(CDH26):c.2422C>T (p.Pro808Ser) | not specified [RCV004201940] | uncertain significance | 20 | 60012653 | 60012653 | Human | | name |
| 156286725 | CV2360949 | single nucleotide variant | NM_177980.4(CDH26):c.1168G>A (p.Ala390Thr) | not specified [RCV004215760] | uncertain significance | 20 | 59989048 | 59989048 | Human | | name |
| 156085695 | CV2366219 | single nucleotide variant | NM_177980.4(CDH26):c.1207G>T (p.Val403Phe) | not specified [RCV004210237] | uncertain significance | 20 | 59989087 | 59989087 | Human | | name |
| 156387357 | CV2372720 | single nucleotide variant | NM_177980.4(CDH26):c.1790G>T (p.Cys597Phe) | not specified [RCV004221912] | uncertain significance | 20 | 59995956 | 59995956 | Human | | name |
| 156140551 | CV2383624 | single nucleotide variant | NM_177980.4(CDH26):c.1815G>C (p.Glu605Asp) | not specified [RCV004229515] | uncertain significance | 20 | 59995981 | 59995981 | Human | | name |
| 329368403 | CV2428007 | single nucleotide variant | NM_177980.4(CDH26):c.2332G>A (p.Gly778Ser) | not specified [RCV004254386] | likely benign | 20 | 60012563 | 60012563 | Human | | name |
| 401741892 | CV2676549 | single nucleotide variant | NM_177980.4(CDH26):c.2133G>T (p.Gln711His) | not specified [RCV004288737] | uncertain significance | 20 | 60001378 | 60001378 | Human | | name |
| 401742995 | CV2694029 | single nucleotide variant | NM_177980.4(CDH26):c.1118C>T (p.Pro373Leu) | not specified [RCV004302472] | uncertain significance | 20 | 59988998 | 59988998 | Human | | name |
| 401735106 | CV2699165 | single nucleotide variant | NM_177980.4(CDH26):c.1488C>A (p.Asn496Lys) | not specified [RCV004303665] | uncertain significance | 20 | 59994311 | 59994311 | Human | | name |
| 401777675 | CV2718296 | single nucleotide variant | NM_177980.4(CDH26):c.2356G>A (p.Glu786Lys) | not specified [RCV004318136] | uncertain significance | 20 | 60012587 | 60012587 | Human | | name |
| 401880563 | CV2763089 | single nucleotide variant | NM_177980.4(CDH26):c.2410C>G (p.Gln804Glu) | not specified [RCV004336139] | uncertain significance | 20 | 60012641 | 60012641 | Human | | name |
| 401861217 | CV2769580 | single nucleotide variant | NM_177980.4(CDH26):c.1894C>G (p.Leu632Val) | not specified [RCV004351227] | uncertain significance | 20 | 59996636 | 59996636 | Human | | name |
| 401870111 | CV2772621 | single nucleotide variant | NM_177980.4(CDH26):c.1879G>A (p.Ala627Thr) | not specified [RCV004355371] | uncertain significance | 20 | 59996045 | 59996045 | Human | | name |
| 405720713 | CV3296550 | single nucleotide variant | NM_177980.4(CDH26):c.1024C>G (p.Pro342Ala) | not specified [RCV004428099] | uncertain significance | 20 | 59988904 | 59988904 | Human | | name |
| 405720723 | CV3296551 | single nucleotide variant | NM_177980.4(CDH26):c.1049C>T (p.Ala350Val) | not specified [RCV004428100] | likely benign | 20 | 59988929 | 59988929 | Human | | name |
| 405720728 | CV3296552 | single nucleotide variant | NM_177980.4(CDH26):c.1204A>T (p.Ile402Phe) | not specified [RCV004428101] | uncertain significance | 20 | 59989084 | 59989084 | Human | | name |
| 405720739 | CV3296553 | single nucleotide variant | NM_177980.4(CDH26):c.1216G>A (p.Glu406Lys) | not specified [RCV004428102] | likely benign | 20 | 59989096 | 59989096 | Human | | name |
| 405720752 | CV3296555 | single nucleotide variant | NM_177980.4(CDH26):c.1351G>A (p.Val451Met) | not specified [RCV004428104] | uncertain significance | 20 | 59992445 | 59992445 | Human | | name |
| 405720760 | CV3296556 | single nucleotide variant | NM_177980.4(CDH26):c.1369G>A (p.Glu457Lys) | not specified [RCV004428105] | uncertain significance | 20 | 59992463 | 59992463 | Human | | name |
| 405720767 | CV3296557 | single nucleotide variant | NM_177980.4(CDH26):c.1372T>A (p.Ser458Thr) | not specified [RCV004428106] | uncertain significance | 20 | 59992466 | 59992466 | Human | | name |
| 405720774 | CV3296558 | single nucleotide variant | NM_177980.4(CDH26):c.1652T>C (p.Leu551Ser) | not specified [RCV004428107] | uncertain significance | 20 | 59994475 | 59994475 | Human | | name |
| 405720782 | CV3296559 | single nucleotide variant | NM_177980.4(CDH26):c.1675G>C (p.Val559Leu) | not specified [RCV004428108] | uncertain significance | 20 | 59995841 | 59995841 | Human | | name |
| 405720790 | CV3296560 | single nucleotide variant | NM_177980.4(CDH26):c.1786C>G (p.Pro596Ala) | not specified [RCV004428109] | uncertain significance | 20 | 59995952 | 59995952 | Human | | name |
| 405720796 | CV3296561 | single nucleotide variant | NM_177980.4(CDH26):c.1793C>G (p.Ala598Gly) | not specified [RCV004428110] | uncertain significance | 20 | 59995959 | 59995959 | Human | | name |
| 405720803 | CV3296562 | single nucleotide variant | NM_177980.4(CDH26):c.2263G>A (p.Val755Met) | not specified [RCV004428111] | uncertain significance | 20 | 60006755 | 60006755 | Human | | name |
| 405720820 | CV3296564 | single nucleotide variant | NM_177980.4(CDH26):c.2355C>A (p.Ser785Arg) | not specified [RCV004428113] | uncertain significance | 20 | 60012586 | 60012586 | Human | | name |
| 405720828 | CV3296565 | single nucleotide variant | NM_177980.4(CDH26):c.2407G>A (p.Glu803Lys) | not specified [RCV004428114] | uncertain significance | 20 | 60012638 | 60012638 | Human | | name |
| 405720836 | CV3296566 | single nucleotide variant | NM_177980.4(CDH26):c.2485G>A (p.Gly829Ser) | not specified [RCV004428115] | uncertain significance | 20 | 60012716 | 60012716 | Human | | name |
| 407454990 | CV3422305 | single nucleotide variant | NM_177980.4(CDH26):c.1321G>A (p.Val441Ile) | not specified [RCV004610096] | uncertain significance | 20 | 59992415 | 59992415 | Human | | name |
| 407454992 | CV3422306 | single nucleotide variant | NM_177980.4(CDH26):c.1153G>A (p.Val385Met) | not specified [RCV004610097] | uncertain significance | 20 | 59989033 | 59989033 | Human | | name |
| 407455002 | CV3422311 | single nucleotide variant | NM_177980.4(CDH26):c.2207T>C (p.Ile736Thr) | not specified [RCV004610102] | uncertain significance | 20 | 60002853 | 60002853 | Human | | name |
| 407455005 | CV3422312 | single nucleotide variant | NM_177980.4(CDH26):c.1982T>A (p.Val661Asp) | not specified [RCV004610103] | uncertain significance | 20 | 59996724 | 59996724 | Human | | name |
| 597795452 | CV3641892 | single nucleotide variant | NM_177980.4(CDH26):c.1622C>T (p.Thr541Ile) | not specified [RCV004903679] | uncertain significance | 20 | 59994445 | 59994445 | Human | | name |
| 597795455 | CV3641893 | single nucleotide variant | NM_177980.4(CDH26):c.2347G>A (p.Val783Ile) | not specified [RCV004903680] | uncertain significance | 20 | 60012578 | 60012578 | Human | | name |
| 597795458 | CV3641894 | single nucleotide variant | NM_177980.4(CDH26):c.1870G>T (p.Ala624Ser) | not specified [RCV004903681] | uncertain significance | 20 | 59996036 | 59996036 | Human | | name |
| 597795461 | CV3641895 | single nucleotide variant | NM_177980.4(CDH26):c.1128G>C (p.Lys376Asn) | not specified [RCV004903682] | uncertain significance | 20 | 59989008 | 59989008 | Human | | name |
| 597795467 | CV3641897 | single nucleotide variant | NM_177980.4(CDH26):c.2224T>A (p.Tyr742Asn) | not specified [RCV004903684] | uncertain significance | 20 | 60006716 | 60006716 | Human | | name |
| 597795472 | CV3641899 | single nucleotide variant | NM_177980.4(CDH26):c.1325A>G (p.Asp442Gly) | not specified [RCV004903686] | uncertain significance | 20 | 59992419 | 59992419 | Human | | name |
| 597795475 | CV3641900 | single nucleotide variant | NM_177980.4(CDH26):c.1103G>A (p.Arg368Lys) | not specified [RCV004903687] | uncertain significance | 20 | 59988983 | 59988983 | Human | | name |
| 597795478 | CV3641901 | single nucleotide variant | NM_177980.4(CDH26):c.1769T>C (p.Val590Ala) | not specified [RCV004903688] | uncertain significance | 20 | 59995935 | 59995935 | Human | | name |
| 597795481 | CV3641902 | single nucleotide variant | NM_177980.4(CDH26):c.1972C>A (p.Gln658Lys) | not specified [RCV004903689] | uncertain significance | 20 | 59996714 | 59996714 | Human | | name |
| 597795484 | CV3641903 | single nucleotide variant | NM_177980.4(CDH26):c.1285T>C (p.Tyr429His) | not specified [RCV004903690] | uncertain significance | 20 | 59992379 | 59992379 | Human | | name |
| 597795487 | CV3641904 | single nucleotide variant | NM_177980.4(CDH26):c.1298A>C (p.His433Pro) | not specified [RCV004903691] | uncertain significance | 20 | 59992392 | 59992392 | Human | | name |
| 598168994 | CV3947407 | single nucleotide variant | NM_177980.4(CDH26):c.1513C>T (p.Arg505Cys) | not specified [RCV005308343] | uncertain significance | 20 | 59994336 | 59994336 | Human | | name |
| 598169001 | CV3947408 | single nucleotide variant | NM_177980.4(CDH26):c.1994C>T (p.Ala665Val) | not specified [RCV005308344] | uncertain significance | 20 | 59996736 | 59996736 | Human | | name |
| 598169009 | CV3947409 | single nucleotide variant | NM_177980.4(CDH26):c.2084C>T (p.Thr695Met) | not specified [RCV005308345] | uncertain significance | 20 | 59999650 | 59999650 | Human | | name |
| 598169019 | CV3947411 | single nucleotide variant | NM_177980.4(CDH26):c.1418T>C (p.Val473Ala) | not specified [RCV005308347] | uncertain significance | 20 | 59992512 | 59992512 | Human | | name |
| 598229670 | CV3947414 | single nucleotide variant | NM_177980.4(CDH26):c.1246G>A (p.Gly416Arg) | not specified [RCV005319266] | uncertain significance | 20 | 59989126 | 59989126 | Human | | name |
| 598169042 | CV3947415 | single nucleotide variant | NM_177980.4(CDH26):c.1493C>G (p.Pro498Arg) | not specified [RCV005308350] | uncertain significance | 20 | 59994316 | 59994316 | Human | | name |
| 598229676 | CV3947416 | single nucleotide variant | NM_177980.4(CDH26):c.1867G>T (p.Ala623Ser) | not specified [RCV005319267] | uncertain significance | 20 | 59996033 | 59996033 | Human | | name |
| 598169051 | CV3947417 | single nucleotide variant | NM_177980.4(CDH26):c.1077T>G (p.Asn359Lys) | not specified [RCV005308351] | uncertain significance | 20 | 59988957 | 59988957 | Human | | name |
| 598169072 | CV3947420 | single nucleotide variant | NM_177980.4(CDH26):c.2398G>A (p.Ala800Thr) | not specified [RCV005308354] | likely benign | 20 | 60012629 | 60012629 | Human | | name |
| 598169088 | CV3947422 | single nucleotide variant | NM_177980.4(CDH26):c.1561G>A (p.Glu521Lys) | not specified [RCV005308356] | uncertain significance | 20 | 59994384 | 59994384 | Human | | name |
| 598169096 | CV3947423 | single nucleotide variant | NM_177980.4(CDH26):c.2119T>C (p.Ser707Pro) | not specified [RCV005308357] | uncertain significance | 20 | 60001364 | 60001364 | Human | | name |
| 598169112 | CV3947425 | single nucleotide variant | NM_177980.4(CDH26):c.1531G>A (p.Glu511Lys) | not specified [RCV005308359] | uncertain significance | 20 | 59994354 | 59994354 | Human | | name |
| 598169119 | CV3947426 | single nucleotide variant | NM_177980.4(CDH26):c.2326G>T (p.Asp776Tyr) | not specified [RCV005308360] | uncertain significance | 20 | 60012557 | 60012557 | Human | | name |
| 598169130 | CV3947428 | single nucleotide variant | NM_177980.4(CDH26):c.2278G>C (p.Ala760Pro) | not specified [RCV005308362] | uncertain significance | 20 | 60006770 | 60006770 | Human | | name |
| 598169146 | CV3947431 | single nucleotide variant | NM_177980.4(CDH26):c.1762C>G (p.Gln588Glu) | not specified [RCV005308365] | uncertain significance | 20 | 59995928 | 59995928 | Human | | name |
