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Previous release (v1)
2024-04-25 14:57:40, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_012131 1241 bp mRNA linear PRI 18-DEC-2022 DEFINITION Homo sapiens claudin 17 (CLDN17), mRNA. ACCESSION NM_012131 VERSION NM_012131.3 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 1241) AUTHORS Xu YN, Deng MS, Liu YF, Yao J and Xiao ZY. TITLE Tight junction protein CLDN17 serves as a tumor suppressor to reduce the invasion and migration of oral cancer cells by inhibiting epithelial-mesenchymal transition JOURNAL Arch Oral Biol 133, 105301 (2022) PUBMED 34781072 REMARK GeneRIF: Tight junction protein CLDN17 serves as a tumor suppressor to reduce the invasion and migration of oral cancer cells by inhibiting epithelial-mesenchymal transition. REFERENCE 2 (bases 1 to 1241) AUTHORS Sun L, Feng L and Cui J. TITLE Increased expression of claudin-17 promotes a malignant phenotype in hepatocyte via Tyk2/Stat3 signaling and is associated with poor prognosis in patients with hepatocellular carcinoma JOURNAL Diagn Pathol 13 (1), 72 (2018) PUBMED 30219077 REMARK GeneRIF: that the upregulated expression of CLDN17 significantly enhances the migration ability of hepatocytes in vitro and we found that the activation of the Stat3 pathway by Tyk2 may an important mechanism by which CLDN17 promotes aggressiveness in hepatocytes Publication Status: Online-Only REFERENCE 3 (bases 1 to 1241) AUTHORS Conrad MP, Piontek J, Gunzel D, Fromm M and Krug SM. TITLE Molecular basis of claudin-17 anion selectivity JOURNAL Cell Mol Life Sci 73 (1), 185-200 (2016) PUBMED 26194246 REMARK GeneRIF: The structural features of Cldn17 contributing to anion channel formation are presented in this work. REFERENCE 4 (bases 1 to 1241) AUTHORS Gao M, Li W, Wang H and Wang G. TITLE The distinct expression patterns of claudin-10, -14, -17 and E-cadherin between adjacent non-neoplastic tissues and gastric cancer tissues JOURNAL Diagn Pathol 8, 205 (2013) PUBMED 24325792 REMARK GeneRIF: Claudin 17 expression was down-regulated in gastric cancer. Publication Status: Online-Only REFERENCE 5 (bases 1 to 1241) AUTHORS Harris HJ, Davis C, Mullins JG, Hu K, Goodall M, Farquhar MJ, Mee CJ, McCaffrey K, Young S, Drummer H, Balfe P and McKeating JA. TITLE Claudin association with CD81 defines hepatitis C virus entry JOURNAL J Biol Chem 285 (27), 21092-21102 (2010) PUBMED 20375010 REFERENCE 6 (bases 1 to 1241) AUTHORS Tsukita S and Furuse M. TITLE Claudin-based barrier in simple and stratified cellular sheets JOURNAL Curr Opin Cell Biol 14 (5), 531-536 (2002) PUBMED 12231346 REMARK Review article REFERENCE 7 (bases 1 to 1241) AUTHORS Brandner JM, Kief S, Grund C, Rendl M, Houdek P, Kuhn C, Tschachler E, Franke WW and Moll I. TITLE Organization and formation of the tight junction system in human epidermis and cultured keratinocytes JOURNAL Eur J Cell Biol 81 (5), 253-263 (2002) PUBMED 12067061 REFERENCE 8 (bases 1 to 1241) AUTHORS Tsukita S, Furuse M and Itoh M. TITLE Multifunctional strands in tight junctions JOURNAL Nat Rev Mol Cell Biol 2 (4), 285-293 (2001) PUBMED 11283726 REMARK Review article REFERENCE 9 (bases 1 to 1241) AUTHORS Heiskala M, Peterson PA and Yang Y. TITLE The roles of claudin superfamily proteins in paracellular transport JOURNAL Traffic 2 (2), 93-98 (2001) PUBMED 11247307 REMARK Review article REFERENCE 10 (bases 1 to 1241) AUTHORS Kniesel U and Wolburg H. TITLE Tight junctions of the blood-brain barrier JOURNAL Cell Mol Neurobiol 20 (1), 57-76 (2000) PUBMED 10690502 REMARK Review article COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AP000884.1 and BC101503.1. On May 17, 2019 this sequence version replaced NM_012131.2. Summary: This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. This gene is intronless and is clustered with CLDN8 on chromosome 21q22.11. [provided by RefSeq, Jun 2010]. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript is intronless :: SRR1803617.500281.1, AY358094.1 [ECO:0000345] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000286808.5/ ENSP00000286808.3 RefSeq Select criteria :: based on single protein-coding transcript ##RefSeq-Attributes-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-152 AP000884.1 8990-9141 c 153-883 BC101503.1 1-731 884-1241 AP000884.1 7901-8258 c FEATURES Location/Qualifiers source 1..1241 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="21" /map="21q21.3" gene 1..1241 /gene="CLDN17" /note="claudin 17" /db_xref="GeneID:26285" /db_xref="HGNC:HGNC:2038" /db_xref="MIM:617005" exon 1..1241 /gene="CLDN17" /inference="alignment:Splign:2.1.0" variation 2 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:776055722" variation 3 /gene="CLDN17" /replace="" /replace="g" /db_xref="dbSNP:1195437924" variation 3 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:902963652" variation 4 /gene="CLDN17" /replace="a" /replace="c" /db_xref="dbSNP:1601012826" variation 5 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:1484058399" variation 10 /gene="CLDN17" /replace="c" /replace="g" /db_xref="dbSNP:1041854896" variation 11 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:1980861295" variation 13 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:556518952" variation 14 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:868345847" variation 15 /gene="CLDN17" /replace="g" /replace="t" /db_xref="dbSNP:1346572580" variation 22 /gene="CLDN17" /replace="a" /replace="c" /db_xref="dbSNP:1318249727" variation 24 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:538331933" variation 25 /gene="CLDN17" /replace="c" /replace="g" /db_xref="dbSNP:1980861006" variation 31 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:1980860950" variation 32 /gene="CLDN17" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1980860887" variation 35 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:892631751" variation 38 /gene="CLDN17" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1055423260" variation 40 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:1980860783" variation 41 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:770297573" variation 42 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:1980860688" variation 46 /gene="CLDN17" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:11910029" variation 47 /gene="CLDN17" /replace="a" /replace="c" /db_xref="dbSNP:1980860462" variation 49 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:2146493370" variation 50 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:904083790" misc_feature 51..53 /gene="CLDN17" /note="upstream in-frame stop codon" variation 51 /gene="CLDN17" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1325779530" variation 53 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:1980860276" variation 55 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:928841262" variation 62..65 /gene="CLDN17" /replace="aaa" /replace="aaaa" /db_xref="dbSNP:1372417580" variation 66 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:981636632" variation 67 /gene="CLDN17" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:549464674" variation 72 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:1980859918" variation 73 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:1045115552" variation 78 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:948069687" variation 82 /gene="CLDN17" /replace="a" /replace="c" /db_xref="dbSNP:1980859784" variation 85 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:1240037127" variation 86 /gene="CLDN17" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:907994592" variation 87 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:1980859666" variation 88 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:533904496" variation 91..98 /gene="CLDN17" /replace="catca" /replace="catcatca" /db_xref="dbSNP:1980859437" variation 91 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:1466961206" variation 95 /gene="CLDN17" /replace="a" /replace="t" /db_xref="dbSNP:1215405893" variation 97 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:985275053" variation 101 /gene="CLDN17" /replace="c" /replace="g" /db_xref="dbSNP:781027242" variation 103 /gene="CLDN17" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1396651734" variation 108 /gene="CLDN17" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1381642028" variation 118 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:11910218" variation 121 /gene="CLDN17" /replace="c" /replace="g" /db_xref="dbSNP:1469626748" variation 122 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:1980858925" variation 126 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:532918289" variation 128 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:1762196101" variation 129 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:974692167" variation 135 /gene="CLDN17" /replace="a" /replace="c" /db_xref="dbSNP:1980858729" variation 137 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:2146493334" variation 142 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:1980858669" variation 143 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:1980858616" variation 145 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:2146493330" variation 147 /gene="CLDN17" /replace="c" /replace="g" /db_xref="dbSNP:773196101" variation 148 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:907710361" variation 152 /gene="CLDN17" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:533297655" variation 153 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:1980858461" variation 155 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:984561558" variation 156 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:371321255" variation 157 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:776738707" variation 158 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:1980858214" variation 159..161 /gene="CLDN17" /replace="" /replace="cga" /db_xref="dbSNP:1980857980" variation 159 /gene="CLDN17" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:768824126" variation 160 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:747107338" variation 162..163 /gene="CLDN17" /replace="" /replace="ct" /db_xref="dbSNP:1980857923" variation 167 /gene="CLDN17" /replace="a" /replace="c" /db_xref="dbSNP:35890247" variation 169 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:778262997" variation 170 /gene="CLDN17" /replace="" /replace="a" /db_xref="dbSNP:1228765817" variation 172 /gene="CLDN17" /replace="c" /replace="t" /db_xref="dbSNP:1980857689" variation 173..174 /gene="CLDN17" /replace="" /replace="cagcaat" /db_xref="dbSNP:1980857619" variation 175..176 /gene="CLDN17" /replace="" /replace="g" /db_xref="dbSNP:1980857564" variation 175..176 /gene="CLDN17" /replace="" /replace="tc" /db_xref="dbSNP:1296459207" variation 179 /gene="CLDN17" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:780169273" variation 180..181 /gene="CLDN17" /replace="" /replace="ga" /db_xref="dbSNP:1980857446" variation 181 /gene="CLDN17" /replace="a" /replace="t" /db_xref="dbSNP:772138103" variation 182 /gene="CLDN17" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1028847041" variation 184..188 /gene="CLDN17" /replace="a" /replace="aggca" /db_xref="dbSNP:1980857245" variation 186 /gene="CLDN17" /replace="a" /replace="g" /db_xref="dbSNP:746406957" CDS 189..863 /gene="CLDN17" /note="human CLDN17 gene for claudin-17" /codon_start=1 /product="claudin-17" /protein_id="NP_036263.1" /db_xref="CCDS:CCDS13586.1" /db_xref="GeneID:26285" /db_xref="HGNC:HGNC:2038" /db_xref="MIM:617005" /translation="
MAFYPLQIAGLVLGFLGMVGTLATTLLPQWRVSAFVGSNIIVFERLWEGLWMNCIRQARVRLQCKFYSSLLALPPALETARALMCVAVALSLIALLIGICGMKQVQCTGSNERAKAYLLGTSGVLFILTGIFVLIPVSWTANIIIRDFYNPAIHIGQKRELGAALFLGWASAAVLFIGGGLLCGFCCCNRKKQGYRYPVPGYRVPHTDKRRNTTMLSKTSTSYV"
misc_feature 204..734
/gene="CLDN17"
/note="PMP-22/EMP/MP20/Claudin family; Region:
PMP22_Claudin; cl21598"
/db_xref="CDD:451326"
misc_feature 210..272
/gene="CLDN17"
/note="propagated from UniProtKB/Swiss-Prot (P56750.1);
transmembrane region"
misc_feature 432..494
/gene="CLDN17"
/note="propagated from UniProtKB/Swiss-Prot (P56750.1);
transmembrane region"
misc_feature 561..623
/gene="CLDN17"
/note="propagated from UniProtKB/Swiss-Prot (P56750.1);
transmembrane region"
misc_feature 681..743
/gene="CLDN17"
/note="propagated from UniProtKB/Swiss-Prot (P56750.1);
transmembrane region"
variation 192
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:377630320"
variation 193
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456785808"
variation 196
/gene="CLDN17"
/replace="t"
/replace="tgcct"
/db_xref="dbSNP:1980856981"
variation 200..201
/gene="CLDN17"
/replace=""
/replace="tc"
/db_xref="dbSNP:1980856917"
variation 202
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1391451306"
variation 203
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980856785"
variation 204
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1463567637"
variation 207
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757585314"
variation 216
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2146493278"
variation 217
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1234879410"
variation 218
/gene="CLDN17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1472453051"
variation 220
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1401846740"
variation 221
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1980856405"
variation 222
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1410281492"
variation 225
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980856223"
variation 232
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:754192578"
variation 238
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:374657719"
variation 240
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307738325"
variation 242
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:965732164"
variation 243
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1434018029"
variation 244
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:780998613"
variation 246
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1202359916"
variation 248
/gene="CLDN17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1208150567"
variation 249
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1234053053"
variation 258
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1480663917"
variation 259
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:200995273"
variation 263
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:751242174"
variation 267
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367082329"
variation 270..271
/gene="CLDN17"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2146493239"
variation 271
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:766052962"
variation 274
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:762493404"
variation 277
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:750372043"
variation 280
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1277585739"
variation 283
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777564829"
variation 284
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:374816376"
variation 287
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424781934"
variation 288
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:550551260"
variation 289
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1384558716"
variation 290
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1980854417"
variation 295
/gene="CLDN17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:768429059"
variation 298
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1980854212"
variation 301
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:760956416"
variation 302
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1457202172"
variation 304
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356860122"
variation 305
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:775661818"
variation 306..307
/gene="CLDN17"
/replace=""
/replace="cct"
/db_xref="dbSNP:778957643"
variation 306
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:369334352"
variation 307
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1569280063"
variation 309
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:745911511"
variation 310
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:779320036"
variation 311
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:771403322"
variation 313
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:142016231"
variation 314
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:778337547"
variation 318
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1293606831"
variation 319
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1980853188"
variation 320
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1980853096"
variation 321
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:756540854"
variation 323
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980852948"
variation 324
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1464388735"
variation 330
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1275017545"
variation 332
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:746697944"
variation 333
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:779830873"
variation 334
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1569280056"
variation 335
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:757865028"
variation 336
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:749905276"
variation 338
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1308061231"
variation 345
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:201950581"
variation 347
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:561590635"
variation 350
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:376245503"
variation 351
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:753774028"
variation 353..354
/gene="CLDN17"
/replace="c"
/replace="cc"
/db_xref="dbSNP:755229364"
variation 353
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980852183"
variation 354
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:148594408"
variation 355
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:139360624"
variation 357
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:760445191"
variation 358
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:908046007"
variation 360
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:778611772"
variation 362
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:767740588"
variation 364
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1980851466"
variation 365
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1431894881"
variation 366
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:759541120"
variation 368
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:369668256"
variation 369
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:112285554"
variation 370
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:773823219"
variation 371
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:375142545"
variation 374
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2146493141"
variation 378
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980850925"
variation 384
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2146493140"
variation 386
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:563625822"
variation 388
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:748470055"
variation 389
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1313695921"
variation 392
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:779880091"
variation 396
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:757998649"
variation 397
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:745381698"
variation 398
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2146493127"
variation 399
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980850561"
variation 400
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274659949"
variation 405
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:778555407"
variation 406
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:572478746"
variation 407
/gene="CLDN17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:940799889"
variation 409
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:753825399"
variation 410
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:907941446"
variation 415
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1340204928"
variation 416
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1311448786"
variation 418
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444488671"
variation 419
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980849806"
variation 420
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:150877940"
variation 421
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1980849718"
variation 425
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:372250139"
variation 426..435
/gene="CLDN17"
/replace="gccc"
/replace="gcccgggccc"
/db_xref="dbSNP:1980848700"
variation 426
/gene="CLDN17"
/replace=""
/replace="g"
/db_xref="dbSNP:2146493102"
variation 426
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:368477110"
variation 427
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427866955"
variation 429
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:767649088"
variation 430
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:141599246"
variation 431
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473105396"
variation 432
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:35531957"
variation 433
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1475987936"
variation 434
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980848783"
variation 436
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:763101580"
variation 437
/gene="CLDN17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773878264"
variation 438
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:770381395"
variation 439
/gene="CLDN17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1980848377"
variation 440
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980848313"
variation 442
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:199537354"
variation 443
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1435545806"
variation 446
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:139335071"
variation 451
/gene="CLDN17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:373800539"
variation 453
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:745577971"
variation 454
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:778411818"
variation 462
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:574192286"
variation 467
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:138854149"
variation 468
/gene="CLDN17"
/replace=""
/replace="g"
/db_xref="dbSNP:2146493063"
variation 468
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1287937474"
variation 470
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:755988454"
variation 471
/gene="CLDN17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781106045"
variation 472
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:756815104"
variation 474
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1234357109"
variation 477
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1980846906"
variation 479
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:754696185"
variation 480
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:751856689"
variation 481
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:555547939"
variation 483
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473432746"
variation 486
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1412503992"
variation 489
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:763152445"
variation 492
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045394066"
variation 497
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:534314602"
variation 499
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465617543"
variation 501
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1238838096"
variation 504
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247887366"
variation 505
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1198936408"
variation 506
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:761768920"
variation 508
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980845840"
variation 509
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980845767"
variation 510
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:762466073"
variation 511
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980845601"
variation 513
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:776974726"
variation 514
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:370125987"
variation 515
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1267925300"
variation 517
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:760903403"
variation 521
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1370019984"
variation 522
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:770504734"
variation 524
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1980845101"
variation 526
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980845044"
variation 527
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1460701896"
variation 531
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1435842459"
variation 532
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:2146493024"
variation 534
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980844831"
variation 536
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:116090819"
variation 539
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323786326"
variation 541
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1458774031"
variation 542
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1389017645"
variation 543
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980844431"
variation 545
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:777325561"
variation 547
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980844279"
variation 556
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1398794219"
variation 559
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:769292058"
variation 560
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1980844058"
variation 562
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:748121412"
variation 563
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:199725880"
variation 564
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980843831"
variation 565
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:780966488"
variation 566
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1191012730"
variation 573
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:751268131"
variation 574
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:371701865"
variation 575
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:750659084"
variation 576
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:750242106"
variation 581
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1314381760"
variation 584
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:765477205"
variation 585
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:761963508"
variation 595
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:140821942"
variation 596
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:201580398"
variation 601
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1005273075"
variation 602
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210975339"
variation 604
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980842718"
variation 605
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1250514041"
variation 606
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:761110025"
variation 607
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1980842480"
variation 610
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:775662949"
variation 616
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:767858689"
variation 620
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:762664243"
variation 621
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980842094"
variation 623
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252784960"
variation 625
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1405243538"
variation 627
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1360729495"
variation 628
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:772817706"
variation 629
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980841730"
variation 634
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433746016"
variation 638
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980841592"
variation 639
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:769339338"
variation 643
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:747559662"
variation 647
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:768410360"
variation 651
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:746833230"
variation 652
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:780051728"
variation 654..655
/gene="CLDN17"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1238437785"
variation 654
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:367675205"
variation 663
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:202213185"
variation 664
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:779230372"
variation 668
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:757445066"
variation 670
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:753793642"
variation 672
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:764678957"
variation 673
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1294738941"
variation 674
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980840381"
variation 676
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:2146492931"
variation 678
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039242244"
variation 680
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2079774258"
variation 682
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1212753688"
variation 685
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:944651825"
variation 688
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:945965202"
variation 690
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1303212378"
variation 696
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:756641161"
variation 697
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1373228872"
variation 700
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:753246242"
variation 701
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:767911871"
variation 702
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:759868892"
variation 706
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:539744023"
variation 708
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:148072252"
variation 709
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1980839375"
variation 716
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:761386178"
variation 717
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:775945093"
variation 718
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:768198964"
variation 721
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:746985238"
variation 723
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1206198207"
variation 724
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1275482880"
variation 725
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775536316"
variation 726
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980838705"
variation 727
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1249719058"
variation 728
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:772016801"
variation 730
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:988525622"
variation 740
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:146427219"
variation 742
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1980838229"
variation 747
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1313427368"
variation 759
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1980838081"
variation 760
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:779281924"
variation 763
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1353376442"
variation 764
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1424170280"
variation 765
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:757367950"
variation 766
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:148930702"
variation 769
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2146492882"
variation 770
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:777785443"
variation 774
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1295951628"
variation 779
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:201369045"
variation 780
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:568268585"
variation 781
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:2146492878"
variation 786
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:182327550"
variation 788
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:755362951"
variation 793
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488123685"
variation 794
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:576177657"
variation 795
/gene="CLDN17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:143848087"
variation 796
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:563734261"
variation 800
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775601768"
variation 805
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:772069765"
variation 811
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:759417826"
variation 812
/gene="CLDN17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770759302"
variation 813..819
/gene="CLDN17"
/replace="aagcgaa"
/replace="aagcgaaaagcgaa"
/db_xref="dbSNP:749537388"
variation 813
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1980836568"
variation 814
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1314331108"
variation 815
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213048178"
variation 816
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:377679902"
variation 817
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:778036499"
variation 820
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1569279796"
variation 824
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:138251734"
variation 825
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:748182900"
variation 826
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:781665299"
variation 827
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1027901826"
variation 828
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1012807011"
variation 834
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:755415911"
variation 838
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1460363484"
variation 840
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1391203464"
variation 841
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1406164256"
variation 844
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:752048768"
variation 847
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:188114857"
variation 850
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1569279783"
variation 851
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1980835196"
variation 852
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:146572430"
variation 853
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1178558405"
variation 858
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1980834977"
variation 863
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980834836"
variation 864
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:776149659"
variation 866
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753480841"
variation 867
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:763764272"
variation 870
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:563005963"
variation 873..874
/gene="CLDN17"
/replace=""
/replace="a"
/db_xref="dbSNP:1980834289"
variation 876
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1249604476"
variation 878
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:183838947"
variation 882
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:767126875"
variation 885
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:574128183"
variation 893
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:774403452"
variation 894
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2146492821"
variation 900..905
/gene="CLDN17"
/replace="t"
/replace="tgtttt"
/db_xref="dbSNP:780091585"
variation 901
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1569279766"
variation 902..907
/gene="CLDN17"
/replace="tttttt"
/replace="ttttttt"
/db_xref="dbSNP:756233700"
variation 908
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1189126342"
variation 909
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:890509905"
variation 910
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1367954156"
variation 913
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:770683030"
variation 920
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:528102692"
variation 927..929
/gene="CLDN17"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1980832839"
variation 928
/gene="CLDN17"
/replace=""
/replace="g"
/db_xref="dbSNP:1980833051"
variation 928
/gene="CLDN17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1175029061"
variation 934
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:143710208"
variation 935
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1452648316"
variation 941
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980832508"
variation 945
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288588359"
variation 947
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1980832334"
variation 950
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980832256"
variation 952
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1479312077"
variation 955
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1980832083"
variation 958
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1384331399"
variation 959
/gene="CLDN17"
/replace=""
/replace="t"
/db_xref="dbSNP:1980831894"
variation 959
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1321802161"
variation 965
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1370959044"
variation 970
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1305742180"
variation 971
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:57014707"
variation 973
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:373695346"
variation 975
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1352572415"
variation 977
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:935884228"
variation 979
/gene="CLDN17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:148953477"
variation 980
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:545915811"
variation 982
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213690776"
variation 987
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980830783"
variation 988
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1601012015"
variation 991
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980830597"
variation 997
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446685694"
variation 998
/gene="CLDN17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1980830371"
variation 999
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980830308"
variation 1001
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279535839"
variation 1003
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980830116"
variation 1020
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980830041"
variation 1025
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1980829964"
variation 1029
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:979910608"
variation 1030
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2146492757"
variation 1034
/gene="CLDN17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1156474569"
variation 1036
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:994886905"
variation 1037
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1980829582"
variation 1045
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1321765503"
variation 1046
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1365250433"
variation 1052
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262898789"
variation 1060
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:971152051"
variation 1061
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1394321887"
variation 1065
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:558288902"
variation 1067
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1439377538"
variation 1068
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1980829184"
variation 1070
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:539806328"
variation 1074
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295295206"
variation 1075
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1980828907"
variation 1079
/gene="CLDN17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1980828808"
variation 1080
/gene="CLDN17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:145028739"
variation 1082
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:150345746"
variation 1083
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:944526321"
variation 1084
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:911848024"
variation 1085
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1272354148"
variation 1086
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1980828287"
variation 1089
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:535769380"
variation 1091
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1980828081"
variation 1094
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1215503025"
variation 1102
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1340732017"
variation 1109
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1980827836"
variation 1115
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:568148029"
variation 1117
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980827649"
variation 1119
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1468051935"
variation 1122
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1017741612"
variation 1128
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1472725199"
variation 1133
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:925618400"
variation 1134
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2146492715"
variation 1136
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1009006361"
variation 1139
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2146492710"
variation 1140
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1356138711"
variation 1141
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1417595176"
variation 1142
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:890562482"
variation 1143
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1171116720"
variation 1146
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1351020999"
variation 1147
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:978395150"
variation 1149
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980826713"
variation 1150
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1980826623"
variation 1153
/gene="CLDN17"
/replace=""
/replace="a"
/db_xref="dbSNP:1980826549"
variation 1154
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:140434145"
variation 1155
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1352518713"
variation 1158
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:893816261"
variation 1164
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980826174"
variation 1166
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1054157575"
variation 1169
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:146762160"
variation 1170
/gene="CLDN17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1234978521"
variation 1171
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:570171520"
variation 1172
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2146492694"
variation 1174
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980825658"
variation 1182
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980825584"
variation 1189
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1980825510"
variation 1194
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980825417"
variation 1195
/gene="CLDN17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1980825337"
variation 1196
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:991031674"
variation 1197
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:143449409"
variation 1201
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1980825130"
variation 1204
/gene="CLDN17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1035317417"
variation 1209
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:917035438"
variation 1211
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:983227416"
variation 1212
/gene="CLDN17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1569279706"
variation 1213
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309810082"
regulatory 1217..1222
/regulatory_class="polyA_signal_sequence"
/gene="CLDN17"
/note="hexamer: AATAAA"
variation 1228
/gene="CLDN17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271455933"
variation 1231
/gene="CLDN17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1255048567"
variation 1236
/gene="CLDN17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:950478234"
polyA_site 1241
/gene="CLDN17"
/note="major polyA site"
ORIGIN
atgcatttacaacaggtacttctagttaggccaagttcagtcacagctactgatttggactaaaacgttatgggcagcagccaaggagaacatcatcaaagacttctctagactcaaaaggcttccacgttctacatcttgagcatcttctaccactccgaattgaaccagtcttcaaagtaaaggcaatggcattttatcccttgcaaattgctgggctggttcttgggttccttggcatggtggggactcttgccacaacccttctgcctcagtggagagtatcagcttttgttggcagcaacattattgtctttgagaggctctgggaagggctctggatgaattgcatccgacaagccagggtccggttgcaatgcaagttctatagctccttgttggctctcccgcctgccctggaaacagcccgggccctcatgtgtgtggctgttgctctctccttgatcgccctgcttattggcatctgtggcatgaagcaggtccagtgcacaggctctaacgagagggccaaagcataccttctgggaacttcaggagtcctcttcatcctgacgggcatcttcgttctgattccggtgagctggacagccaatataatcatcagagatttctacaacccagccatccacataggtcagaaacgagagctgggagcagcacttttccttggctgggcaagcgctgctgtcctcttcattggagggggtctgctttgtggattttgctgctgcaacagaaagaagcaagggtacagatatccagtgcctggctaccgtgtgccacacacagataagcgaagaaatacgacaatgcttagtaagacctccaccagttatgtctaatgcctccttttggctccaagtatggactatggtcaatgttttttataaagtcctgctagaaactgtaagtatgtgaggcaggagaacttgctttatgtctagatttacattgatacgaaagtttcaatttgttactggtggtaggaatgaaaatgacttacttggacattctgacttcaggtgtattaaatgcattgactattgttggacccaatcgctgctccaattttcatattctaaattcaagtatacccataatcattagcaagtgtacaatgatggactacttattactttttgaccatcatgtattatctgataagaatctaaagttgaaattgatattctataacaataaaacatatacctattctaaaa
//
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.
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