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Previous release (v1)
2024-04-26 02:51:34, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_152353 974 bp mRNA linear PRI 17-DEC-2022 DEFINITION Homo sapiens claudin domain containing 2 (CLDND2), mRNA. ACCESSION NM_152353 VERSION NM_152353.3 KEYWORDS RefSeq; MANE Select. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. REFERENCE 1 (bases 1 to 974) AUTHORS Luck K, Kim DK, Lambourne L, Spirohn K, Begg BE, Bian W, Brignall R, Cafarelli T, Campos-Laborie FJ, Charloteaux B, Choi D, Cote AG, Daley M, Deimling S, Desbuleux A, Dricot A, Gebbia M, Hardy MF, Kishore N, Knapp JJ, Kovacs IA, Lemmens I, Mee MW, Mellor JC, Pollis C, Pons C, Richardson AD, Schlabach S, Teeking B, Yadav A, Babor M, Balcha D, Basha O, Bowman-Colin C, Chin SF, Choi SG, Colabella C, Coppin G, D'Amata C, De Ridder D, De Rouck S, Duran-Frigola M, Ennajdaoui H, Goebels F, Goehring L, Gopal A, Haddad G, Hatchi E, Helmy M, Jacob Y, Kassa Y, Landini S, Li R, van Lieshout N, MacWilliams A, Markey D, Paulson JN, Rangarajan S, Rasla J, Rayhan A, Rolland T, San-Miguel A, Shen Y, Sheykhkarimli D, Sheynkman GM, Simonovsky E, Tasan M, Tejeda A, Tropepe V, Twizere JC, Wang Y, Weatheritt RJ, Weile J, Xia Y, Yang X, Yeger-Lotem E, Zhong Q, Aloy P, Bader GD, De Las Rivas J, Gaudet S, Hao T, Rak J, Tavernier J, Hill DE, Vidal M, Roth FP and Calderwood MA. TITLE A reference map of the human binary protein interactome JOURNAL Nature 580 (7803), 402-408 (2020) PUBMED 32296183 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AC008750.9 and BC029518.1. On May 17, 2019 this sequence version replaced NM_152353.2. ##Evidence-Data-START## Transcript exon combination :: BC029518.1, AI337031.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA2148874 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000291715.5/ ENSP00000291715.1 RefSeq Select criteria :: based on conservation, expression ##RefSeq-Attributes-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-348 AC008750.9 41606-41953 c 349-974 BC029518.1 349-974 FEATURES Location/Qualifiers source 1..974 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="19" /map="19q13.41" gene 1..974 /gene="CLDND2" /note="claudin domain containing 2" /db_xref="GeneID:125875" /db_xref="HGNC:HGNC:28511" exon 1..595 /gene="CLDND2" /inference="alignment:Splign:2.1.0" variation 1 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:914526138" variation 2 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1986559581" variation 4 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1394702753" variation 10 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1391173834" variation 12..15 /gene="CLDND2" /replace="ct" /replace="ctct" /db_xref="dbSNP:887267045" variation 12 /gene="CLDND2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1419305633" variation 15..19 /gene="CLDND2" /replace="tgt" /replace="tgtgt" /db_xref="dbSNP:1188234260" variation 17 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1352543403" variation 20 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1292709796" variation 23 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:989802041" variation 28 /gene="CLDND2" /replace="a" /replace="c" /db_xref="dbSNP:1223595861" variation 31 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:995281097" variation 36 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1986558519" variation 42 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1480223490" variation 48 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1986558195" variation 50 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:953045985" variation 52 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1986557983" variation 54 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:749488865" variation 56 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1986557750" variation 57 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1474003560" variation 58 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1599853775" variation 59 /gene="CLDND2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1179370989" variation 62 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1986557314" variation 65 /gene="CLDND2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1986557167" variation 72..75 /gene="CLDND2" /replace="ggg" /replace="gggg" /db_xref="dbSNP:1186639884" variation 72 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1568474861" variation 73 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1986556983" variation 75 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:2123635365" variation 78 /gene="CLDND2" /replace="a" /replace="t" /db_xref="dbSNP:1986556760" variation 83 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:2123635343" variation 84 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:78557740" variation 86 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:912517289" variation 88 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:2087982719" variation 90 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1167611555" variation 91 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:2123635283" variation 98 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1986556318" variation 100 /gene="CLDND2" /replace="a" /replace="c" /db_xref="dbSNP:1986556136" variation 104 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1353257625" variation 106 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1429573240" variation 110 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1308988552" variation 111 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1986555722" variation 112 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1986555620" variation 113 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1052338964" variation 114 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1413114226" variation 115 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:935184645" variation 116 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1337063897" variation 118 /gene="CLDND2" /replace="" /replace="c" /db_xref="dbSNP:925156454" variation 118 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1986554949" variation 119 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:975868654" variation 121 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:965893646" variation 125 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:527679034" variation 126 /gene="CLDND2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:560454877" variation 127 /gene="CLDND2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1232750837" variation 133 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:778206354" variation 134 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1599853701" variation 135 /gene="CLDND2" /replace="a" /replace="c" /db_xref="dbSNP:1800754604" variation 147 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1484497785" variation 152 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:756248535" variation 153 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:2123634936" variation 155 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1209627552" variation 159 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1237692854" variation 164 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:183741190" variation 165 /gene="CLDND2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1184237993" misc_feature 172..174 /gene="CLDND2" /note="upstream in-frame stop codon" variation 173 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1035928118" variation 176 /gene="CLDND2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1392939049" variation 179 /gene="CLDND2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:894495147" variation 186 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1986551931" variation 188 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1599853662" variation 197 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1986551579" variation 199 /gene="CLDND2" /replace="a" /replace="c" /db_xref="dbSNP:1373734055" variation 200 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1986551237" variation 202 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1986551130" variation 203 /gene="CLDND2" /replace="a" /replace="t" /db_xref="dbSNP:1986551027" variation 205 /gene="CLDND2" /replace="a" /replace="c" /db_xref="dbSNP:529156434" variation 212 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1986550837" variation 213 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1986550723" variation 216 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:772256043" variation 219 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:114233846" variation 221 /gene="CLDND2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1568474784" variation 222 /gene="CLDND2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1002963012" variation 224 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:2123634574" variation 225 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:907319472" variation 226 /gene="CLDND2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1359948198" variation 227 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1396578076" variation 230 /gene="CLDND2" /replace="a" /replace="t" /db_xref="dbSNP:1287156659" variation 236 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:2123634531" variation 238 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:543629154" variation 239 /gene="CLDND2" /replace="a" /replace="t" /db_xref="dbSNP:951688193" variation 244 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1299559506" variation 245 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1986549049" variation 251 /gene="CLDND2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1345551068" variation 252 /gene="CLDND2" /replace="a" /replace="t" /db_xref="dbSNP:1233275940" variation 256 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1278956994" variation 263 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1165096823" variation 264..270 /gene="CLDND2" /replace="gttg" /replace="gttgttg" /db_xref="dbSNP:1415243617" variation 264 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1986548432" variation 265 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1460447522" variation 273 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:2123634429" variation 275 /gene="CLDND2" /replace="a" /replace="aa" /db_xref="dbSNP:550914400" variation 276..281 /gene="CLDND2" /replace="ggggg" /replace="gggggg" /replace="ggggggg" /db_xref="dbSNP:1240967001" variation 276 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1986547710" variation 278 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:576247614" variation 280 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1986547386" variation 281 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1986547022" variation 282 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1599853582" variation 285 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:2123634355" variation 291 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1986546783" variation 304 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1041543903" variation 305..322 /gene="CLDND2" /replace="acc" /replace="acctcaggcaggagtacc" /db_xref="dbSNP:2123634250" variation 306 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:945899193" variation 307 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1189695496" variation 311..312 /gene="CLDND2" /replace="g" /replace="gg" /db_xref="dbSNP:529509563" variation 313 /gene="CLDND2" /replace="a" /replace="c" /db_xref="dbSNP:564170911" variation 316 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:914473059" variation 317 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1172333103" variation 318 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1986545867" variation 319 /gene="CLDND2" /replace="a" /replace="t" /db_xref="dbSNP:1986545763" variation 325 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1054389133" variation 330 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1416340246" variation 331 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1986545453" variation 332 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1986545359" variation 333 /gene="CLDND2" /replace="a" /replace="t" /db_xref="dbSNP:1599853550" variation 334 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:931606255" variation 337 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1387923844" variation 339..346 /gene="CLDND2" /replace="gg" /replace="ggaagcgg" /db_xref="dbSNP:1986544622" variation 339 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1986545066" variation 340 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1986544965" variation 341 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1986544870" variation 344 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:367589080" variation 345 /gene="CLDND2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:73934365" variation 348 /gene="CLDND2" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:944465421" variation 349 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1986544517" variation 352 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1986544411" variation 354 /gene="CLDND2" /replace="a" /replace="t" /db_xref="dbSNP:1986544323" variation 359 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1368673045" variation 360 /gene="CLDND2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:890777176" variation 361 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1275182248" variation 362 /gene="CLDND2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1369315745" variation 363 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1262743374" variation 366 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1221663309" variation 367 /gene="CLDND2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:781672317" variation 369 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1210037645" variation 370 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1239946895" variation 375 /gene="CLDND2" /replace="a" /replace="t" /db_xref="dbSNP:1363990302" variation 378 /gene="CLDND2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1319444065" variation 384 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1384240552" variation 385 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:1467500955" variation 386 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:369227307" variation 387 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1247603782" variation 389 /gene="CLDND2" /replace="a" /replace="c" /db_xref="dbSNP:774296274" variation 391 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:2123633864" variation 392 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:766265260" variation 393 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1986542420" variation 394 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:763026622" variation 395 /gene="CLDND2" /replace="a" /replace="c" /db_xref="dbSNP:773327552" variation 396 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1986542085" variation 398 /gene="CLDND2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:769977271" variation 401 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1373837783" variation 403 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:951570323" variation 404..408 /gene="CLDND2" /replace="cccc" /replace="ccccc" /db_xref="dbSNP:1161424977" variation 404 /gene="CLDND2" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:748368381" variation 405 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:138507210" variation 406 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1472987837" variation 408 /gene="CLDND2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:575060013" variation 409 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:751899966" variation 410 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:747335411" variation 413 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1986540699" variation 417 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:376369107" variation 419 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1367870523" variation 421 /gene="CLDND2" /replace="a" /replace="aa" /db_xref="dbSNP:1986540370" variation 423 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1986540253" variation 425 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1392241759" CDS 427..930 /gene="CLDND2" /codon_start=1 /product="claudin domain-containing protein 2" /protein_id="NP_689566.1" /db_xref="CCDS:CCDS12829.1" /db_xref="GeneID:125875" /db_xref="HGNC:HGNC:28511" /translation="
MGVKRSLQSGGILLSLVANVLMVLSTATNYWTRQQEGHSGLWQECNHGICSSIPCQTTLAVTVACMVLAVGVGVVGMVMGLRIRCDEGESLRGQTTSAFLFLGGLLLLTALIGYTVKNAWKNNVFFSWSYFSGWLALPFSILAGFCFLLADMIMQSTDAISGFPVCL"
misc_feature 445..507
/gene="CLDND2"
/note="propagated from UniProtKB/Swiss-Prot (Q8NHS1.1);
transmembrane region"
misc_feature 454..858
/gene="CLDND2"
/note="PMP-22/EMP/MP20/Claudin family; Region:
PMP22_Claudin; cl21598"
/db_xref="CDD:451326"
misc_feature 601..663
/gene="CLDND2"
/note="propagated from UniProtKB/Swiss-Prot (Q8NHS1.1);
transmembrane region"
misc_feature 712..774
/gene="CLDND2"
/note="propagated from UniProtKB/Swiss-Prot (Q8NHS1.1);
transmembrane region"
misc_feature 826..888
/gene="CLDND2"
/note="propagated from UniProtKB/Swiss-Prot (Q8NHS1.1);
transmembrane region"
variation 429..433
/gene="CLDND2"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1437433976"
variation 429
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:758921395"
variation 430
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1986539816"
variation 431
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200312007"
variation 432
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:538045785"
variation 433
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1351339775"
variation 436
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2123633567"
variation 437
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:777335261"
variation 438
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1230101024"
variation 439
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371550969"
variation 440
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:143028916"
variation 442
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:754799498"
variation 443
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:751289647"
variation 445
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369800546"
variation 446
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762873455"
variation 448..449
/gene="CLDND2"
/replace=""
/replace="ca"
/db_xref="dbSNP:753083530"
variation 449
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397526552"
variation 453
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1181982791"
variation 453
/gene="CLDND2"
/replace="t"
/replace="tt"
/db_xref="dbSNP:765717056"
variation 454
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568474544"
variation 455
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:765336897"
variation 456
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1366435982"
variation 457
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1229737224"
variation 458
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:141927207"
variation 459
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354887417"
variation 462
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986535878"
variation 464
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1986535732"
variation 466
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986535614"
variation 468
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1756564974"
variation 471
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986535481"
variation 474
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1475521451"
variation 475
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1986535216"
variation 477
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1986535084"
variation 478
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:150482801"
variation 479
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:907270970"
variation 482
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1291041024"
variation 483
/gene="CLDND2"
/replace=""
/replace="c"
/db_xref="dbSNP:1986534455"
variation 484
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1453747054"
variation 485
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:137890141"
variation 488
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:747388530"
variation 489
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1490479401"
variation 490
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1473019042"
variation 491
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273287505"
variation 496
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:766705239"
variation 501
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:892985932"
variation 503
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1163841957"
variation 504..519
/gene="CLDND2"
/replace="gg"
/replace="ggccaccaactactgg"
/db_xref="dbSNP:1286962093"
variation 504
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368172559"
variation 505
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265286290"
variation 508
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1986532815"
variation 510..513
/gene="CLDND2"
/replace="caac"
/replace="caacaac"
/db_xref="dbSNP:1986532411"
variation 510
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1234260170"
variation 512
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:931887664"
variation 514
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1307144896"
variation 517
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986532297"
variation 519
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:746357149"
variation 520
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1310555112"
variation 521
/gene="CLDND2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:34633086"
variation 523
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370928932"
variation 524
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:199591571"
variation 528
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1331139384"
variation 533
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:780828288"
variation 535
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:944395544"
variation 536
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375294321"
variation 537
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:141435818"
variation 538
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:779793613"
variation 540
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1156786260"
variation 542
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:758314796"
variation 543
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568474407"
variation 544
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:566771736"
variation 546
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1183337530"
variation 547
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201357238"
variation 550
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1986529600"
variation 552
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1432886304"
variation 555
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1986529320"
variation 557
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:765042158"
variation 559
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:761954347"
variation 560
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1337348640"
variation 561
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:753908258"
variation 563
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1254335351"
variation 567
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:145587573"
variation 568
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352030933"
variation 571
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1239174330"
variation 575
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:776039544"
variation 576
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1231115650"
variation 578
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:772546495"
variation 581
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326767106"
variation 582
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1167750554"
variation 583
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1986527530"
variation 585
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1441380989"
variation 586
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1387872499"
variation 587
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396317297"
variation 588
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1347860377"
variation 589
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1431258664"
variation 590
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:149708978"
exon 596..736
/gene="CLDND2"
/inference="alignment:Splign:2.1.0"
variation 596
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1435993047"
variation 598
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1310043039"
variation 599
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1208844685"
variation 600..605
/gene="CLDND2"
/replace="gc"
/replace="gctggc"
/db_xref="dbSNP:766420239"
variation 601
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:746481949"
variation 604
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1169234910"
variation 606
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:199854670"
variation 609
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:771562132"
variation 611
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:558697101"
variation 612..615
/gene="CLDND2"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:760657397"
variation 613
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:778565175"
variation 616
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568473823"
variation 617
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986494403"
variation 618
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:374413392"
variation 621
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:181014895"
variation 623
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:749220517"
variation 626
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1449292548"
variation 628
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:777808790"
variation 630
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1207141951"
variation 631
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1421949058"
variation 632
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:756295215"
variation 635
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1343062109"
variation 638
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:752758697"
variation 639
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:767795968"
variation 640
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274929937"
variation 646
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231206904"
variation 647..660
/gene="CLDND2"
/replace="tggtgggcatggtg"
/replace="tggtgggcatggtgggcatggtg"
/db_xref="dbSNP:773407298"
variation 647
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:140994018"
variation 648
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318528069"
variation 650
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1364344485"
variation 652
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1986491266"
variation 654
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:751993787"
variation 657
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:766628417"
variation 660
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2123629995"
variation 662
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:763254992"
variation 664
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:750065635"
variation 667
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:765661741"
variation 669
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163274581"
variation 670
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1461215602"
variation 672
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419236582"
variation 676
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:995987172"
variation 677
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1167661295"
variation 681
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:3745403"
variation 682
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:61736500"
variation 685
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2123629821"
variation 689
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1177841337"
variation 690
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:771821890"
variation 691
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:139548240"
variation 693
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1211608610"
variation 694
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986487715"
variation 695
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:756866627"
variation 696
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1467817776"
variation 697
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273741707"
variation 698
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:35337369"
variation 699
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1206256235"
variation 700
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:376652333"
variation 701
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:749054663"
variation 702
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:373643518"
variation 704
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756057433"
variation 707
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2123629581"
variation 708
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1323420932"
variation 709
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:748298147"
variation 710
/gene="CLDND2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1395591812"
variation 711
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:536390977"
variation 713
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1452333172"
variation 714
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:550109619"
variation 716
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143947857"
variation 717
/gene="CLDND2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1420901645"
variation 718
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:765786340"
variation 719
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:74538792"
variation 720
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469070489"
variation 723
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2123629356"
variation 725
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1253453283"
variation 726
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:775103545"
variation 727
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1986483492"
variation 732..733
/gene="CLDND2"
/replace=""
/replace="tt"
/db_xref="dbSNP:1568473600"
variation 733
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568473594"
variation 734
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1054818020"
variation 735
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986482685"
variation 736
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:766917605"
exon 737..856
/gene="CLDND2"
/inference="alignment:Splign:2.1.0"
variation 738
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:886252090"
variation 739..750
/gene="CLDND2"
/replace="ctgctgctg"
/replace="ctgctgctgctg"
/replace="ctgctgctgctgctg"
/db_xref="dbSNP:774085638"
variation 741
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1357375096"
variation 746
/gene="CLDND2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:762502780"
variation 747
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397458806"
variation 748
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:750129630"
variation 749
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:764916263"
variation 750
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1986454475"
variation 753
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761525613"
variation 754
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1164044064"
variation 756
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:776470517"
variation 757
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1369751601"
variation 761
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:764001121"
variation 763..764
/gene="CLDND2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1986452504"
variation 763
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:760627572"
variation 764
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:775592435"
variation 767
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1986452211"
variation 770
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:867796482"
variation 772
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:772164503"
variation 779
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1038380123"
variation 780
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1467373673"
variation 781
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:745910460"
variation 783
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1599851554"
variation 784
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1234509795"
variation 790..795
/gene="CLDND2"
/replace="aac"
/replace="aacaac"
/db_xref="dbSNP:1599851539"
variation 792
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1337569389"
variation 793
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1986450972"
variation 795..798
/gene="CLDND2"
/replace="c"
/replace="cgtc"
/db_xref="dbSNP:1051331535"
variation 795
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986450693"
variation 796
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:61737052"
variation 797..805
/gene="CLDND2"
/replace="tcttct"
/replace="tcttcttct"
/db_xref="dbSNP:768471991"
variation 797
/gene="CLDND2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1986450238"
variation 798
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1238386392"
variation 801
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986449786"
variation 803
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1331082939"
variation 806
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1229799125"
variation 809
/gene="CLDND2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771131130"
variation 815
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1986448995"
variation 816..820
/gene="CLDND2"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1273298552"
variation 816
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2123626658"
variation 819
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324972016"
variation 822
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461934179"
variation 823
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1392768297"
variation 824
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1156328694"
variation 825
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469147368"
variation 829
/gene="CLDND2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1986447921"
variation 829
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1364025183"
variation 830
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:150545272"
variation 832
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1452170652"
variation 833
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986447338"
variation 834
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986447186"
variation 838..840
/gene="CLDND2"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:749182476"
variation 838
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:778195808"
variation 843
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1986446586"
variation 848
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1986446362"
variation 849
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373919523"
variation 853
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1986445876"
variation 854
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:748645509"
variation 855
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143501994"
variation 856
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:114975292"
exon 857..974
/gene="CLDND2"
/inference="alignment:Splign:2.1.0"
variation 857
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:755754582"
variation 861
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:752559823"
variation 863
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1165758878"
variation 865..867
/gene="CLDND2"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1368913884"
variation 868..873
/gene="CLDND2"
/replace="ctg"
/replace="ctgctg"
/replace="ctgctgctg"
/db_xref="dbSNP:777453479"
variation 870
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1177936955"
variation 871
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:199756062"
variation 876
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1986426279"
variation 878
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:751539630"
variation 880..884
/gene="CLDND2"
/replace="at"
/replace="atgat"
/db_xref="dbSNP:1375455615"
variation 880
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298769311"
variation 881
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:766161552"
variation 888
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:185510103"
variation 889
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1223138752"
variation 890
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1986425063"
variation 892
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1314556151"
variation 894
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1311910677"
variation 896..897
/gene="CLDND2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1568472642"
variation 897
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1059344"
variation 900
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:141450057"
variation 902
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268759728"
variation 903
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1986423843"
variation 904
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:199917528"
variation 907
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1986423336"
variation 909
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301760024"
variation 910
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1440564055"
variation 915..918
/gene="CLDND2"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:765627231"
variation 917
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:777181361"
variation 918
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1204637370"
variation 919
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1986422183"
variation 920
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1337242900"
variation 921
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295730829"
variation 927
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:769162667"
variation 933..950
/gene="CLDND2"
/replace="g"
/replace="gcagcctgcctggggcag"
/db_xref="dbSNP:1191550743"
variation 934..942
/gene="CLDND2"
/replace=""
/replace="cagcctgcc"
/db_xref="dbSNP:1568472573"
variation 942
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:756560566"
variation 943
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568472568"
variation 944
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1159320301"
variation 945
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:761078378"
variation 946
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370612637"
variation 948
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368435588"
variation 950
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1481910306"
regulatory 951..956
/regulatory_class="polyA_signal_sequence"
/gene="CLDND2"
/note="hexamer: AATAAA"
variation 954
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:772403705"
variation 957..958
/gene="CLDND2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1267991046"
variation 961
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:904812810"
variation 962
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:748889646"
variation 964
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:777148133"
variation 965..971
/gene="CLDND2"
/replace="tttttt"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:5828475"
variation 970
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:769476219"
polyA_site 974
/gene="CLDND2"
/note="major polyA site"
variation 974
/gene="CLDND2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:112263850"
ORIGIN
gtctctctgggctctgtgtctaaggagccctagggcactgggtgtgagtcacttaggtgggcctgtgtggaggggtgtctggggaggacattgaacaggctgggctgaaagggcgttcggctgtcgggggaggtctctgggaagacaggttcctcacagcaaagcctgtggtgaaggtctcagaggcctctcaggggaagtctcaaggtctccagtaaggggaacgaggtctggagggaggaggttgtggatcctcaggcagggttgttgagggaggggggtctccaggtccccagaagcagggacctcaggcaggagtaccaggggaggagtgtggaggaagcgggctcctcagctgggggcctcggggtaggaaaggcctgggcccatcctgcccttgtggcccccggctgcagcctcagtggcatgggggtgaagcggagcctccagagtgggggcattctgctcagcctcgtggccaacgtcctcatggtgctctccacggccaccaactactggacccgccaacaagagggccacagtggcctgtggcaggaatgcaaccacggcatctgctccagcatcccctgccagaccacgctggcggtgactgtggcgtgcatggtgctggcggtgggtgtcggcgtggtgggcatggtgatgggactgcggattcggtgcgacgagggcgagtcgctgcggggccagaccacgagcgccttcctcttcctcggcggactgctgctgctgaccgccttgataggctacaccgtgaagaatgcgtggaagaacaacgtcttcttctcttggtcctatttttctgggtggctggccttacccttctcaattctcgcgggcttctgctttctgctggcagacatgatcatgcagagcaccgacgccatcagtggattccccgtgtgtctgtgactgcagcctgcctggggcagaataaaggaacggctttttttagc
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
[Full Text]