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Previous release (v1)
2024-04-20 14:38:34, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001185072 3533 bp mRNA linear PRI 18-DEC-2022 DEFINITION Homo sapiens claudin 12 (CLDN12), transcript variant 1, mRNA. ACCESSION NM_001185072 VERSION NM_001185072.3 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 3533) AUTHORS Kolchakova D, Moten D, Batsalova T and Dzhambazov B. TITLE Tight Junction Protein Claudin-12 Is Involved in Cell Migration during Metastasis JOURNAL Biomolecules 11 (5), 636 (2021) PUBMED 33922921 REMARK GeneRIF: Tight Junction Protein Claudin-12 Is Involved in Cell Migration during Metastasis. Publication Status: Online-Only REFERENCE 2 (bases 1 to 3533) AUTHORS Rahman A, Kobayashi M, Sugimoto K, Endo Y, Kojima M, Furukawa S, Watanabe T, Soeda S, Hashimoto Y, Fujimori K and Chiba H. TITLE Reduced Claudin-12 Expression Predicts Poor Prognosis in Cervical Cancer JOURNAL Int J Mol Sci 22 (7), 3774 (2021) PUBMED 33917356 REMARK GeneRIF: Reduced Claudin-12 Expression Predicts Poor Prognosis in Cervical Cancer. Publication Status: Online-Only REFERENCE 3 (bases 1 to 3533) 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 REFERENCE 4 (bases 1 to 3533) AUTHORS Huang J, Yin P and Zhang L. TITLE COPII cargo claudin-12 promotes hepatitis C virus entry JOURNAL J Viral Hepat 26 (2), 308-312 (2019) PUBMED 30339745 REMARK GeneRIF: We found that COPII cargo CLDN12 is important for Hepatitis C Virus entry. REFERENCE 5 (bases 1 to 3533) AUTHORS Sweeney MD, Zhao Z, Montagne A, Nelson AR and Zlokovic BV. TITLE Blood-Brain Barrier: From Physiology to Disease and Back JOURNAL Physiol Rev 99 (1), 21-78 (2019) PUBMED 30280653 REMARK Review article REFERENCE 6 (bases 1 to 3533) AUTHORS Kiuchi-Saishin Y, Gotoh S, Furuse M, Takasuga A, Tano Y and Tsukita S. TITLE Differential expression patterns of claudins, tight junction membrane proteins, in mouse nephron segments JOURNAL J Am Soc Nephrol 13 (4), 875-886 (2002) PUBMED 11912246 REFERENCE 7 (bases 1 to 3533) AUTHORS Niimi T, Nagashima K, Ward JM, Minoo P, Zimonjic DB, Popescu NC and Kimura S. TITLE claudin-18, a novel downstream target gene for the T/EBP/NKX2.1 homeodomain transcription factor, encodes lung- and stomach-specific isoforms through alternative splicing JOURNAL Mol Cell Biol 21 (21), 7380-7390 (2001) PUBMED 11585919 REFERENCE 8 (bases 1 to 3533) 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 3533) 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 3533) 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 AC006153.2. On Nov 24, 2018 this sequence version replaced NM_001185072.2. 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 expressed in the inner ear and bladder epithelium, and it is over-expressed in colorectal carcinomas. This protein and claudin 2 are critical for vitamin D-dependent Ca2+ absorption between enterocytes. Multiple alternatively spliced transcript variants encoding the same protein have been found.[provided by RefSeq, Sep 2011]. Transcript Variant: This variant (1) is the longest transcript. Variants 1-3 encode the same protein. 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 exon combination :: SRR1660805.253211.1, SRR1660809.15320.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1968540, SAMEA1968832 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000496677.6/ ENSP00000419053.1 RefSeq Select criteria :: based on conservation, expression, longest protein ##RefSeq-Attributes-END## COMPLETENESS: full length. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-89 AC006153.2 39720-39808 90-179 AC006153.2 41778-41867 180-222 AC006153.2 48266-48308 223-3533 AC006153.2 48903-52213 FEATURES Location/Qualifiers source 1..3533 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="7" /map="7q21.13" gene 1..3533 /gene="CLDN12" /note="claudin 12" /db_xref="GeneID:9069" /db_xref="HGNC:HGNC:2034" /db_xref="MIM:611232" exon 1..89 /gene="CLDN12" /inference="alignment:Splign:2.1.0" variation 1 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:2115852648" variation 4..6 /gene="CLDN12" /replace="aac" /replace="aacaac" /db_xref="dbSNP:1796774149" variation 6 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:765746790" variation 7 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796774304" variation 8 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1796774373" variation 9 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:896219909" variation 10 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1796774534" variation 12 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:1796774614" variation 15 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1796774687" variation 17 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:370765493" variation 18 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1222423857" variation 20 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1011927155" variation 21 /gene="CLDN12" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:751279674" variation 22 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1385384287" variation 24 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796775480" variation 25 /gene="CLDN12" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1398100775" variation 29 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796775676" variation 30..33 /gene="CLDN12" /replace="gaga" /replace="gagagaga" /db_xref="dbSNP:1407169883" variation 30 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796775754" variation 32 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796775914" variation 34 /gene="CLDN12" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:143733597" variation 35 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1425856010" variation 36 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1168508452" variation 38 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1796776262" variation 39 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:2115852942" variation 40 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1475702583" variation 42 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:980932371" variation 44 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1190789610" variation 45 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796776471" variation 47 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:1227182688" variation 48 /gene="CLDN12" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1272088946" variation 49 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1459639556" variation 50 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:1796776658" variation 53 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:926736878" variation 57 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:544870413" variation 61 /gene="CLDN12" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1195806368" variation 63 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:2115853113" variation 65 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1322992370" variation 66 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796776863" variation 70 /gene="CLDN12" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:552258236" variation 71 /gene="CLDN12" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1247490960" variation 73 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1796777009" variation 76 /gene="CLDN12" /replace="a" /replace="c" /db_xref="dbSNP:931405359" variation 77 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796777129" variation 78 /gene="CLDN12" /replace="t" /replace="tt" /db_xref="dbSNP:1796777188" variation 80 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:1264722319" variation 81 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1450737590" variation 84 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796777328" variation 85 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796777380" variation 86 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:1796777438" variation 87 /gene="CLDN12" /replace="a" /replace="c" /db_xref="dbSNP:1048901650" variation 88 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:1796777552" exon 90..179 /gene="CLDN12" /inference="alignment:Splign:2.1.0" variation 91 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1248400932" variation 93 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1796817645" variation 95 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:963982658" variation 98 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:1796817809" variation 104 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:972278194" variation 106 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:116804658" variation 107 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:1796818109" variation 108 /gene="CLDN12" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1368552758" variation 109..111 /gene="CLDN12" /replace="t" /replace="tgt" /db_xref="dbSNP:773152966" variation 110 /gene="CLDN12" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:954322006" variation 124 /gene="CLDN12" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:987257325" variation 125 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:910285876" variation 130 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:2115863292" variation 133..134 /gene="CLDN12" /replace="t" /replace="tt" /db_xref="dbSNP:1796818542" variation 133 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:1796818489" variation 135 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1206373165" variation 139 /gene="CLDN12" /replace="" /replace="g" /db_xref="dbSNP:1796818649" variation 141 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:1796818701" variation 148 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:911440597" variation 149 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:755004916" variation 151 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1796818776" variation 153 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:551241265" variation 162 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1372481614" variation 165 /gene="CLDN12" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1430548490" variation 168 /gene="CLDN12" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1357263224" variation 169 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:781426929" variation 170 /gene="CLDN12" /replace="a" /replace="aa" /db_xref="dbSNP:1796819264" variation 171 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:925780228" variation 172 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1242659231" variation 174 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:185475099" variation 178 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1394975547" variation 179 /gene="CLDN12" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:934587691" exon 180..222 /gene="CLDN12" /inference="alignment:Splign:2.1.0" variation 180 /gene="CLDN12" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1796973498" variation 183 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796973569" variation 184 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:1383429449" variation 190 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:975399496" variation 191 /gene="CLDN12" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1310741550" variation 194 /gene="CLDN12" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1288830018" variation 197 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1429202221" variation 198..211 /gene="CLDN12" /replace="a" /replace="agggaagttctgaa" /db_xref="dbSNP:1796973919" variation 201 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:568368853" variation 204 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:925253464" variation 205 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1796974264" variation 208 /gene="CLDN12" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1177589459" variation 211 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1469546064" variation 214 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1427471526" variation 215 /gene="CLDN12" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:545400197" variation 218 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:535700024" variation 219 /gene="CLDN12" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1457015165" variation 220 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1429228385" exon 223..3533 /gene="CLDN12" /inference="alignment:Splign:2.1.0" misc_feature 229..231 /gene="CLDN12" /note="upstream in-frame stop codon" variation 231 /gene="CLDN12" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:942749126" variation 232 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:777642503" variation 234 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796990526" variation 235 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:2115896242" variation 236 /gene="CLDN12" /replace="a" /replace="c" /db_xref="dbSNP:1584668248" variation 239 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:914599269" variation 242 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1329882679" variation 246 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1210708993" variation 249 /gene="CLDN12" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:946000977" variation 252 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:749239357" variation 254 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1796990980" CDS 256..990 /gene="CLDN12" /codon_start=1 /product="claudin-12" /protein_id="NP_001172001.1" /db_xref="CCDS:CCDS5618.1" /db_xref="GeneID:9069" /db_xref="HGNC:HGNC:2034" /db_xref="MIM:611232" /translation="
MGCRDVHAATVLSFLCGIASVAGLFAGTLLPNWRKLRLITFNRNEKNLTVYTGLWVKCARYDGSSDCLMYDTTWYSSVDQLDLRVLQFALPLSMLIAMGALLLCLIGMCNTAFRSSVPNIKLAKCLVNSAGCHLVAGLLFFLAGTVSLSPSIWVIFYNIHLNKKFEPVFSFDYAVYVTIASAGGLFMTSLILFIWYCTCKSLPSPFWQPLYSHPPSMHTYSQPYSARSRLSAIEIDIPVVSHTT"
misc_feature 286..348
/gene="CLDN12"
/note="propagated from UniProtKB/Swiss-Prot (P56749.1);
transmembrane region"
misc_feature 517..579
/gene="CLDN12"
/note="propagated from UniProtKB/Swiss-Prot (P56749.1);
transmembrane region"
misc_feature 661..723
/gene="CLDN12"
/note="propagated from UniProtKB/Swiss-Prot (P56749.1);
transmembrane region"
misc_feature 778..840
/gene="CLDN12"
/note="propagated from UniProtKB/Swiss-Prot (P56749.1);
transmembrane region"
misc_feature 937..939
/gene="CLDN12"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P56749.1); phosphorylation site"
misc_feature 946..948
/gene="CLDN12"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:19690332,
ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P56749.1); phosphorylation site"
variation 256
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1341616884"
variation 263
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1796991072"
variation 264
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:757087056"
variation 265
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1796991212"
variation 266
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:200372770"
variation 267
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201163165"
variation 269
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1796991447"
variation 271
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:745619799"
variation 273
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1796991550"
variation 276
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1180615075"
variation 277
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:761164855"
variation 284
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:775261538"
variation 289
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1796991783"
variation 293
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115896574"
variation 294
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:746541829"
variation 298
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:902429408"
variation 299
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:768207460"
variation 308
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1796991990"
variation 309
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:374340236"
variation 312
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:762394956"
variation 328
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1796992187"
variation 336
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:765595005"
variation 339
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1796992247"
variation 343
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:563004910"
variation 348
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:763251187"
variation 349
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:766633842"
variation 350
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1230245825"
variation 351
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1796992501"
variation 360
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356210861"
variation 363
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1796992608"
variation 364
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056206386"
variation 365
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:894925508"
variation 370
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:530429481"
variation 371
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:755075227"
variation 372
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1421096252"
variation 374
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115896933"
variation 378
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:767652846"
variation 383
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:752656827"
variation 387
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:140108357"
variation 388
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1252002472"
variation 389..395
/gene="CLDN12"
/replace="agaa"
/replace="agaagaa"
/db_xref="dbSNP:1796993185"
variation 393
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1796993244"
variation 397
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1388876915"
variation 401
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1185916821"
variation 405
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:778948294"
variation 408
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1257994346"
variation 409
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1445655137"
variation 412
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1796993920"
variation 414
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:745707657"
variation 417
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:758236906"
variation 419
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208351338"
variation 420
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433317264"
variation 424
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:779918948"
variation 426
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017072069"
variation 427
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461239450"
variation 430
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1308429047"
variation 433
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:367561054"
variation 434
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1796994585"
variation 437
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:371660301"
variation 441
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:17862175"
variation 442
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:200164858"
variation 444
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1562969445"
variation 447
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:970838406"
variation 454..461
/gene="CLDN12"
/replace=""
/replace="tgcctgat"
/db_xref="dbSNP:761720130"
variation 458..476
/gene="CLDN12"
/replace="tg"
/replace="tgatgtacgacactacttg"
/db_xref="dbSNP:1796995132"
variation 464..468
/gene="CLDN12"
/replace="ac"
/replace="acgac"
/db_xref="dbSNP:1303999268"
variation 465
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:185427290"
variation 466
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:368401578"
variation 469
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1796995439"
variation 471..481
/gene="CLDN12"
/replace="tact"
/replace="tacttggtact"
/db_xref="dbSNP:1796995497"
variation 472
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1275779056"
variation 473
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1445448312"
variation 477..478
/gene="CLDN12"
/replace=""
/replace="ccc"
/db_xref="dbSNP:1796995702"
variation 479
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1484264687"
variation 480
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1219772042"
variation 481
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:763344432"
variation 482
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:372373015"
variation 483
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488499672"
variation 486
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:200281270"
variation 487
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:774643531"
variation 495
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:759812081"
variation 496
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1796996253"
variation 498
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:767596396"
variation 500
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1584668526"
variation 504
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:926814363"
variation 505
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422564484"
variation 506
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:756709778"
variation 508
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:964186372"
variation 510
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:868742300"
variation 513
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1796996690"
variation 522
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1349545698"
variation 525
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471326978"
variation 535
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1233688018"
variation 537
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:566157753"
variation 540
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1796997046"
variation 543
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:539978988"
variation 544
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:750382986"
variation 546
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:990256012"
variation 547
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:76988207"
variation 548
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:780008661"
variation 549
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1584668597"
variation 551
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244278168"
variation 553
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360064110"
variation 558
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1796997647"
variation 560
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1796997721"
variation 561
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751243867"
variation 564
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1796997877"
variation 565
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:754688920"
variation 570
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:79632494"
variation 572
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1239862137"
variation 573
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1796998129"
variation 581
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1485280228"
variation 582
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1189107272"
variation 583
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1249840221"
variation 589
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442500935"
variation 590
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1162698211"
variation 596
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1796998536"
variation 602
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:747740249"
variation 603
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:34378679"
variation 604
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:749812448"
variation 611
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:370065476"
variation 612
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:373294317"
variation 615..626
/gene="CLDN12"
/replace="caaactggccaa"
/replace="caaactggccaaactggccaa"
/db_xref="dbSNP:771967868"
variation 617
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1796999322"
variation 620
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:146056566"
variation 623
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409135371"
variation 624
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1321764678"
variation 626
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367983663"
variation 630
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450838716"
variation 633
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471726358"
variation 634
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:555785316"
variation 637
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:759773648"
variation 638
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:772387218"
variation 641
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1281762078"
variation 642
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797000329"
variation 646
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797000393"
variation 654
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1315755536"
variation 655
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1208839238"
variation 660..661
/gene="CLDN12"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:911772551"
variation 662
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775546156"
variation 666
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1200239537"
variation 669
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760904190"
variation 672
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1182972744"
variation 673
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1237832831"
variation 674
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1421803319"
variation 684
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:890079426"
variation 687
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1183769329"
variation 691
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1406103443"
variation 701
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456713791"
variation 702
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:764256390"
variation 703
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753910760"
variation 704
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762986952"
variation 705
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:766378731"
variation 707
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:751390117"
variation 709
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1227469450"
variation 716
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797002010"
variation 717
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:754704274"
variation 719
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:774617903"
variation 720
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1008641536"
variation 725
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1349496355"
variation 726
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1228407374"
variation 728
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:139669349"
variation 729
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115899093"
variation 733
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1284739711"
variation 736
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797002541"
variation 741
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1562969631"
variation 742..747
/gene="CLDN12"
/replace="aag"
/replace="aagaag"
/db_xref="dbSNP:773058903"
variation 743
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1320879422"
variation 746
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:752284824"
variation 751
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:761520976"
variation 753
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:755709686"
variation 758
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:777274351"
variation 760
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797003096"
variation 768
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1366238040"
variation 773
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:748759222"
variation 776
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797003265"
variation 780
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797003319"
variation 786
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797003409"
variation 790
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:993873530"
variation 791
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1346219704"
variation 796
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:757786645"
variation 797
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:779267034"
variation 798
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:746285653"
variation 799
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1479528196"
variation 802
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115899421"
variation 803
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797003916"
variation 806
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797003989"
variation 807
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:574014370"
variation 808
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:149798695"
variation 810
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1416451842"
variation 815
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797004322"
variation 818
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:2115899527"
variation 819
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:747247531"
variation 822
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797004444"
variation 828
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797004504"
variation 831
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:779705246"
variation 834
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:768932001"
variation 837
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:776879207"
variation 847
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:761934562"
variation 849
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:148668482"
variation 850
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1191786166"
variation 852
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:759438469"
variation 853
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797005046"
variation 855
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:142157384"
variation 857
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:767199576"
variation 858
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:955988159"
variation 861
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1375782905"
variation 868
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:752426881"
variation 869
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1486801818"
variation 872
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1584668952"
variation 873
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797005569"
variation 876
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:755799542"
variation 877
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:763690839"
variation 879
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:753398499"
variation 882
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1206115664"
variation 883
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:756729926"
variation 884
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:779542822"
variation 885
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1198251095"
variation 888
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008503268"
variation 890..892
/gene="CLDN12"
/replace="ccc"
/replace="ccccc"
/db_xref="dbSNP:1223711404"
variation 891
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:746347780"
variation 894
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1166728057"
variation 895
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1389906667"
variation 896
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:758882760"
variation 897
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797006493"
variation 898
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1170053675"
variation 900
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:780285790"
variation 901
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797006667"
variation 902
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:376598671"
variation 904
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:747335564"
variation 905
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797006893"
variation 906
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332390514"
variation 907
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:970708263"
variation 909
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428520245"
variation 912
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797007228"
variation 914..919
/gene="CLDN12"
/replace="ac"
/replace="actcac"
/db_xref="dbSNP:760654070"
variation 915
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:769020005"
variation 917
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797007490"
variation 918
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1230381453"
variation 922
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:189780617"
variation 924
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748275826"
variation 926
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:769754148"
variation 929
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268142593"
variation 931
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:147857522"
variation 933
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:759400199"
variation 934
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:141430153"
variation 935
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:865961955"
variation 936
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:775287956"
variation 938
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760443285"
variation 940
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:747014345"
variation 941
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:763777074"
variation 943
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429133550"
variation 949
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756850579"
variation 952
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398470804"
variation 954
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1187804658"
variation 955
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:764668076"
variation 956
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:749880828"
variation 962
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:967846329"
variation 964
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1271494883"
variation 965
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1436940870"
variation 966
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:758860405"
variation 969
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:780560088"
variation 981
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:752018635"
variation 982
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797010396"
variation 984
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1266312378"
variation 991
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1562969817"
variation 992..995
/gene="CLDN12"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:977418221"
variation 994
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:928650226"
variation 995
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:2115900827"
variation 998
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:374720515"
variation 999
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1206908768"
variation 1001
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1267989651"
variation 1008
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1465732406"
variation 1010..1106
/gene="CLDN12"
/replace=""
/replace="taaagaaaacttcttgtagcctcacattccccttgtgcaaagagctct
tttggacctacatacattttcctttgtttttgaccaatcaatgaagcca"
/db_xref="dbSNP:1797011251"
variation 1013
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:375989620"
variation 1014
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797011398"
variation 1020
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:769996911"
variation 1022
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:182726869"
variation 1024
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797011748"
variation 1025
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1187748511"
variation 1029..1030
/gene="CLDN12"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1226803013"
variation 1030
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:147269114"
variation 1031
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316158945"
variation 1038
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:866289679"
variation 1039
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1584669245"
variation 1040
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395737979"
variation 1043
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797013768"
variation 1045
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377257671"
variation 1046
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797013910"
variation 1048
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:900273326"
variation 1051
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797014053"
variation 1060
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1179310503"
variation 1062
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:947945946"
variation 1064
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797014312"
variation 1066
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:999866390"
variation 1068
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:898274718"
variation 1069
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797014547"
variation 1070
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797014627"
variation 1072
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:140861444"
variation 1073
/gene="CLDN12"
/replace=""
/replace="a"
/db_xref="dbSNP:1797014858"
variation 1073
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:891619549"
variation 1089
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115901329"
variation 1090
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1427727674"
variation 1091
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797015010"
variation 1093
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1386933821"
variation 1095
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1188004664"
variation 1097..1102
/gene="CLDN12"
/replace="aa"
/replace="aatgaa"
/db_xref="dbSNP:2115901396"
variation 1098
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:532905007"
variation 1099
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:890800093"
variation 1100
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1178538518"
variation 1114
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483121516"
variation 1121
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1584669303"
variation 1122
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:3810874"
variation 1124
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1414265200"
variation 1129
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:187870115"
variation 1135
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797015989"
variation 1138
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:560572122"
variation 1139
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1331745815"
variation 1140
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797016195"
variation 1142
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1272440914"
variation 1147
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:906557611"
variation 1153
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1244540414"
variation 1155..1166
/gene="CLDN12"
/replace="tatatta"
/replace="tatattatatta"
/db_xref="dbSNP:1797016509"
variation 1157
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115901668"
variation 1162
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1378691088"
variation 1166
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797016620"
variation 1170
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1447132010"
variation 1180
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:774645854"
variation 1181
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1033653763"
variation 1184
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:959452294"
variation 1188
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797016909"
variation 1193
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797016968"
variation 1194
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:973856566"
variation 1196
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1562969901"
variation 1197
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:900083050"
variation 1199
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306254029"
variation 1200
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1236327058"
variation 1201
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:2115901874"
variation 1202
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797017290"
variation 1204
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1011768718"
variation 1212
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163722599"
variation 1214..1215
/gene="CLDN12"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1797017629"
variation 1214
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256518254"
variation 1215
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797017692"
variation 1216
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797017748"
variation 1219
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1027862498"
variation 1220
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473129326"
variation 1222
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797017943"
variation 1223
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797017993"
variation 1226
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1251638835"
variation 1232
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1180638747"
variation 1241
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797018142"
variation 1243..1244
/gene="CLDN12"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1797018186"
variation 1244
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1490998943"
variation 1248
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1267404539"
variation 1249
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1343977226"
variation 1255
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:191882778"
variation 1257
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797018457"
variation 1260
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:967541357"
variation 1266
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797018614"
variation 1267
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:547780944"
variation 1274
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797018812"
variation 1277
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:2115902195"
variation 1283
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797018888"
variation 1286..1334
/gene="CLDN12"
/replace="catgttaaagaatgatggttagcagaagctgttgtatacaatcttcat
g"
/replace="catgttaaagaatgatggttagcagaagctgttgtatacaatcttcat
gttaaagaatgatggttagcagaagctgttgtatacaatcttcatg"
/db_xref="dbSNP:1797018963"
variation 1287
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1198534959"
variation 1288
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:759662047"
variation 1292
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:2115902237"
variation 1294
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:559947062"
variation 1297
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797019216"
variation 1300
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797019297"
variation 1301
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797019376"
variation 1305
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:983742931"
variation 1308
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115902293"
variation 1316
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:998912183"
variation 1318
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1328221542"
variation 1320
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797019659"
variation 1322
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797019714"
variation 1323
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1459234257"
variation 1324
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:912147725"
variation 1326
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:533404402"
variation 1338
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797020021"
variation 1339..1341
/gene="CLDN12"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1797020107"
variation 1344
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1584669443"
variation 1346
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115902441"
variation 1348
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:944930760"
variation 1349
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797020354"
variation 1350
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1035697540"
variation 1351..1355
/gene="CLDN12"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1341622967"
variation 1356
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1324237708"
variation 1361
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:183250663"
variation 1364
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201561756"
variation 1366
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:921560776"
variation 1367
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:17865130"
variation 1370
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797021149"
variation 1371
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:775800641"
variation 1373
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1171166572"
variation 1375
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:916540737"
variation 1377
/gene="CLDN12"
/replace=""
/replace="c"
/db_xref="dbSNP:1411668520"
variation 1377
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402960380"
variation 1378
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797021627"
variation 1381
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797021699"
variation 1383
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:761220112"
variation 1403
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797021861"
variation 1410
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:969698079"
variation 1411
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378745647"
variation 1413
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465816431"
variation 1416
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1449383814"
variation 1420
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797022284"
variation 1423
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263307715"
variation 1425
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208952414"
variation 1431
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:973988290"
variation 1445
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:2115902887"
variation 1447
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017104"
variation 1449
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:891653604"
variation 1452
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1345566892"
variation 1460
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797022778"
variation 1463
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274194047"
variation 1465
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797022886"
variation 1468
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797022933"
variation 1469..1472
/gene="CLDN12"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1232533722"
variation 1473
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1329410221"
variation 1475
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115903074"
variation 1476
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:945853582"
variation 1478
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:549473969"
variation 1479
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:533121034"
variation 1481
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:760268284"
variation 1482
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1330426305"
variation 1489
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471169901"
variation 1491
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231028407"
variation 1493
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797023526"
variation 1498
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797023593"
variation 1499
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:567681750"
variation 1507
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115903256"
variation 1509
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1172501538"
variation 1514
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1477360361"
variation 1521
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374271262"
variation 1523
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797023880"
variation 1524
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1188685236"
variation 1527
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797023965"
variation 1536
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:550000862"
variation 1542
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797024060"
variation 1546
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318404977"
variation 1547
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651805770"
variation 1548
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1336291604"
variation 1549
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797024205"
variation 1552
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1562970064"
variation 1553
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:2115903425"
variation 1558
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1245839054"
variation 1563
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1205265446"
variation 1566
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442790804"
variation 1569
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1017105"
variation 1570
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1012253900"
variation 1571
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797024663"
variation 1572
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797024716"
variation 1579
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1017106"
variation 1581
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:895147073"
variation 1584
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797024838"
variation 1585
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797024924"
variation 1586..1594
/gene="CLDN12"
/replace="aga"
/replace="agaataaga"
/db_xref="dbSNP:552639099"
variation 1587
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797025017"
variation 1591
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797025067"
variation 1598
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1295686881"
variation 1603
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1268208384"
variation 1607
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797025225"
variation 1620
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:994966682"
variation 1629..1630
/gene="CLDN12"
/replace=""
/replace="at"
/db_xref="dbSNP:903352549"
variation 1629
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:2115903714"
variation 1634
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1413233891"
variation 1635
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797025472"
variation 1639
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797025521"
variation 1644
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797025594"
variation 1648
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1399297577"
variation 1649
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:374000239"
variation 1652
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115903807"
variation 1653
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797025797"
variation 1655
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1428553214"
variation 1658
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451510157"
variation 1661
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1584669652"
variation 1667
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1028134579"
variation 1670
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1387862871"
variation 1676
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115903888"
variation 1683
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797026258"
variation 1689
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797026336"
variation 1691
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1185042417"
variation 1694
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1472953732"
variation 1697
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1236655377"
variation 1698
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797026622"
variation 1707
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797026687"
variation 1708
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:950806358"
variation 1714
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797026821"
variation 1724
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797028208"
variation 1725
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115904009"
variation 1727..1732
/gene="CLDN12"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1562970120"
variation 1731
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:984038424"
variation 1733
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797028421"
variation 1737
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797028511"
variation 1739
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1439444036"
variation 1740
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1275284469"
variation 1743
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797028756"
variation 1748
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:998944770"
variation 1753
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797028929"
variation 1755
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797028992"
variation 1757
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797029074"
variation 1759
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1019037247"
variation 1760
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:966267349"
variation 1767
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1478353974"
variation 1769
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797029420"
variation 1771
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797029491"
variation 1778
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797029560"
variation 1781
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1283932650"
variation 1782
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446308788"
variation 1788
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1480633045"
variation 1795
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1584669723"
variation 1798
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797029921"
variation 1800
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797029989"
variation 1804
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584669725"
variation 1806
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:376739855"
variation 1807
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1584669740"
variation 1809
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:567106439"
variation 1821..1825
/gene="CLDN12"
/replace="tct"
/replace="tctct"
/db_xref="dbSNP:1409819331"
variation 1822
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1584669759"
variation 1824
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:534834365"
variation 1831
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:754923918"
variation 1833
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797030748"
variation 1834
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368142857"
variation 1841
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:963389194"
variation 1845
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1421044873"
variation 1846
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:974400768"
variation 1849
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:974961464"
variation 1854
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:921635723"
variation 1857
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797031478"
variation 1865
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:935650705"
variation 1866
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797031637"
variation 1867
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471043531"
variation 1869
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797031714"
variation 1871
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797031786"
variation 1873
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1293571453"
variation 1875
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1252356341"
variation 1879
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:750152497"
variation 1883..1885
/gene="CLDN12"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1384990512"
variation 1888
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1249674258"
variation 1892
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797032334"
variation 1893
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:912992887"
variation 1893
/gene="CLDN12"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1797032473"
variation 1900
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:982612622"
variation 1907
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797032618"
variation 1911
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1289445533"
variation 1913
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1226894064"
variation 1916
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1331653911"
variation 1917..1918
/gene="CLDN12"
/replace="a"
/replace="aa"
/db_xref="dbSNP:140787647"
variation 1923
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1217821009"
variation 1924
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1349222438"
variation 1926
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:945789489"
variation 1931
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797033299"
variation 1935
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797033352"
variation 1936
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1436593969"
variation 1937
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1348873072"
variation 1939..1940
/gene="CLDN12"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1321175332"
variation 1941..1967
/gene="CLDN12"
/replace="ccttgattcatt"
/replace="ccttgattcattcacccttgattcatt"
/db_xref="dbSNP:932326055"
variation 1941
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797033649"
variation 1942
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:193147106"
variation 1949
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1584669868"
variation 1950
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1158199722"
variation 1954
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1247314127"
variation 1955
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471546613"
variation 1964
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:906996301"
variation 1971
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:920946811"
variation 1972
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:937281533"
variation 1973..1977
/gene="CLDN12"
/replace="cccc"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:947032141"
variation 1973
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1466456646"
variation 1974
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:778741633"
variation 1975
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:895178364"
variation 1976
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797034687"
variation 1977
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:995263893"
variation 1978
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797034822"
variation 1979
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797034880"
variation 1984
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1049027514"
variation 1985
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797035028"
variation 1992
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1266011398"
variation 1993
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:903426027"
variation 1995
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193362122"
variation 2000..2005
/gene="CLDN12"
/replace="atatat"
/replace="atatatat"
/db_xref="dbSNP:1261530209"
variation 2000
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:886530167"
variation 2002
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:934869590"
variation 2003
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1057210209"
variation 2006
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1436790996"
variation 2014
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:547044063"
variation 2021
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:571569072"
variation 2023
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1019108615"
variation 2026
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797035643"
variation 2030
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:556714945"
variation 2031
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115905351"
variation 2032
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797035747"
variation 2033
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1455939440"
variation 2040
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:996411871"
variation 2043
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:575067068"
variation 2044
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1029180653"
variation 2048
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:538983399"
variation 2050
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:957622732"
variation 2052
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797036301"
variation 2062
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797036351"
variation 2064
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115905499"
variation 2067
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797036400"
variation 2069
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424520538"
variation 2071
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797036501"
variation 2076
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:899170131"
variation 2079
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451513203"
variation 2081
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797036674"
variation 2085
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:754778051"
variation 2088
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1361115269"
variation 2093
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797036824"
variation 2100
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797036877"
variation 2101
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797036932"
variation 2103
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797036982"
variation 2105..2121
/gene="CLDN12"
/replace="a"
/replace="acctggcagttggggaa"
/db_xref="dbSNP:1399382784"
variation 2114
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797037077"
variation 2116
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1188257270"
variation 2117
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1463822025"
variation 2118
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797037228"
variation 2119
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797037279"
variation 2130
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:142246998"
variation 2133
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1027358393"
variation 2134
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:11563542"
variation 2135
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1230005617"
variation 2145
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797037616"
variation 2146
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748038842"
variation 2155
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1296423810"
variation 2156
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432532566"
variation 2158
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797037885"
variation 2160
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:928487682"
variation 2162
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:572751121"
variation 2164
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1465452920"
variation 2166
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:975568982"
variation 2171
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:576056629"
variation 2173
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797038407"
variation 2176
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:2115905908"
variation 2178
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1321153174"
variation 2180
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1168187142"
variation 2181..2182
/gene="CLDN12"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1427013136"
variation 2181
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670066"
variation 2183
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243896507"
variation 2189
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258669180"
variation 2190
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:947073657"
variation 2192
/gene="CLDN12"
/replace=""
/replace="c"
/db_xref="dbSNP:1797039089"
variation 2192
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1483181859"
variation 2194
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797039174"
variation 2206
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1256038868"
variation 2210
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797039308"
variation 2211
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797039388"
variation 2213
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797039454"
variation 2216
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1206594484"
variation 2217
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670098"
variation 2225
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:540218408"
variation 2227
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1273357484"
variation 2228
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288305075"
variation 2229
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797039917"
variation 2232
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:536938497"
variation 2236
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:151249770"
variation 2237
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:934927186"
variation 2239
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797040238"
variation 2240
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:2115906196"
variation 2242
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:555238649"
variation 2245
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797040431"
variation 2247
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1376806671"
variation 2251
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797040563"
variation 2253
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:895991227"
variation 2258
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:948855688"
variation 2261..2267
/gene="CLDN12"
/replace="ca"
/replace="cagtcca"
/db_xref="dbSNP:1044911159"
variation 2262
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1049534377"
variation 2263
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:886436147"
variation 2266
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1168084725"
variation 2269
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797041120"
variation 2270
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1182013421"
variation 2272
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370441770"
variation 2274
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1562970326"
variation 2276
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1255085510"
variation 2285
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1005408928"
variation 2288
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1165859003"
variation 2300
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670166"
variation 2301
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423601634"
variation 2308
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797041609"
variation 2312
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1562970332"
variation 2313
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797041698"
variation 2314
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:772162884"
variation 2319
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1040420941"
variation 2323
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1483696092"
variation 2325
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797041912"
variation 2326
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115906514"
variation 2328
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:533659745"
variation 2330
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797042009"
variation 2332
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:781394155"
variation 2337
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1489227199"
variation 2345
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:996320503"
variation 2348
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1421494035"
variation 2350
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797042249"
variation 2351
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775641475"
variation 2352
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:899246704"
variation 2355
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797042455"
variation 2356
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797042500"
variation 2361
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115906685"
variation 2365
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:995272217"
variation 2374
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797042607"
variation 2379
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1290038988"
variation 2385
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797042707"
variation 2388
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1179948472"
variation 2395
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1380422565"
variation 2397
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026303981"
variation 2399
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:747407397"
variation 2403
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1584670238"
variation 2409
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1029090662"
variation 2413
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:17861306"
variation 2415
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:886408648"
variation 2417..2419
/gene="CLDN12"
/replace="t"
/replace="tct"
/db_xref="dbSNP:1797043169"
variation 2424
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1004148918"
variation 2427
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:34833025"
variation 2432
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670253"
variation 2437
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1019502395"
variation 2442
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1294333584"
variation 2445
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1457646450"
variation 2446
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:2115906955"
variation 2448
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797043495"
variation 2452
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:957866681"
variation 2456
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1360627967"
variation 2457
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:965213810"
variation 2460
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011794834"
variation 2468
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:745904312"
variation 2477
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:552033731"
variation 2479..2480
/gene="CLDN12"
/replace=""
/replace="tctttagccttat"
/db_xref="dbSNP:1797043926"
variation 2479
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797043882"
variation 2481
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1020409995"
variation 2482
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797044070"
variation 2483
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:758483645"
variation 2484
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1178971100"
variation 2494
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1434396237"
variation 2497
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1267511875"
variation 2508
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:967063239"
variation 2517
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208852565"
variation 2524
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797044582"
variation 2526
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797044640"
variation 2527
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797044697"
variation 2528
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:769881194"
variation 2529
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797044787"
variation 2530
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1378687437"
variation 2531
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1562970407"
variation 2534
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797044921"
variation 2538
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1269744016"
variation 2540
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797045019"
variation 2546
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1209145387"
variation 2549
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328320779"
variation 2550
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450772647"
variation 2556
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:563896573"
variation 2557
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:531095413"
variation 2568
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386395021"
variation 2570
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797045442"
variation 2577
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670348"
variation 2585
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797045540"
variation 2588
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:17867644"
variation 2595..2600
/gene="CLDN12"
/replace="ag"
/replace="agctag"
/db_xref="dbSNP:1797045671"
variation 2596
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797045730"
variation 2599
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:928352216"
variation 2604
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458105363"
variation 2606
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:978863706"
variation 2614
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:762216364"
variation 2617
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1715026992"
variation 2620
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1468077747"
variation 2622
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:924298842"
variation 2626
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797046266"
variation 2629
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797046336"
variation 2632
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797046394"
variation 2634
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:934288696"
variation 2642
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797046575"
variation 2644
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:991328066"
variation 2651
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1452131616"
variation 2655
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1249523650"
variation 2661
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797046858"
variation 2663
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797046932"
variation 2664
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1188892883"
variation 2666..2685
/gene="CLDN12"
/replace=""
/replace="tgtatttggtactttttccc"
/db_xref="dbSNP:1464268800"
variation 2666
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797047096"
variation 2667
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:919730924"
variation 2668
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:931262369"
variation 2674
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1211293525"
variation 2675
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797047354"
variation 2683
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:764872441"
variation 2684
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1202086053"
variation 2693
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:540782667"
variation 2694
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:907894060"
variation 2698
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:940676159"
variation 2700
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797047650"
variation 2701
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1256619712"
variation 2704..2713
/gene="CLDN12"
/replace="tata"
/replace="tatatatata"
/replace="tatatatatata"
/db_xref="dbSNP:1233683720"
variation 2705
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1300096104"
variation 2707
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1040328332"
variation 2709
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:901949934"
variation 2710
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:917492584"
variation 2712
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797048071"
variation 2715
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:932036114"
variation 2716
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:559357320"
variation 2720..2722
/gene="CLDN12"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1797048243"
variation 2726
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403567804"
variation 2727
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:893301629"
variation 2732
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797048395"
variation 2734
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:766157192"
variation 2738
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1171425269"
variation 2739
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797048523"
variation 2747
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:534758357"
variation 2748
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:777199816"
variation 2749
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:930760045"
variation 2752..2756
/gene="CLDN12"
/replace="ag"
/replace="agtag"
/db_xref="dbSNP:1047817247"
variation 2757
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:886441156"
variation 2760
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1448550405"
variation 2762
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1240112127"
variation 2765
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1189399121"
variation 2767
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:902873098"
variation 2769
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1002551520"
variation 2772
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670467"
variation 2773
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1442880662"
variation 2774
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797049566"
variation 2775
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1255396559"
variation 2776..2782
/gene="CLDN12"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:1562970505"
variation 2777
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176630485"
variation 2781
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035319829"
variation 2782
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1008866447"
variation 2783
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:958446477"
variation 2784
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797050127"
variation 2786
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:546965228"
variation 2791
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1027265526"
variation 2792
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797050282"
variation 2797
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797050326"
variation 2800
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1175047169"
variation 2808
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1584670514"
variation 2809
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:952560771"
variation 2816
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:571487034"
variation 2819
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1468418122"
variation 2822
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:397759219"
variation 2823
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:397829267"
variation 2824
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1333632831"
variation 2829
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797050729"
variation 2833
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797050768"
variation 2834
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1584670545"
variation 2835
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797050880"
variation 2836
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1401034875"
variation 2843
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1268738832"
variation 2846
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:901086369"
variation 2848
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797051063"
variation 2849
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1341525427"
variation 2851
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:2115908811"
variation 2852
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:577566452"
variation 2854
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1312801622"
variation 2855
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797051232"
variation 2857
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797051282"
variation 2858
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446170006"
variation 2864
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:184613376"
variation 2865
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:943930679"
variation 2866
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:769109092"
variation 2869
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:751187006"
variation 2872
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1164716133"
variation 2882
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797051611"
variation 2883
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:932109832"
variation 2894
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:999951759"
variation 2895..2898
/gene="CLDN12"
/replace=""
/replace="tttt"
/db_xref="dbSNP:1370335953"
variation 2900
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1050526265"
variation 2901
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797051819"
variation 2902
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797051879"
variation 2907
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1048883"
variation 2909
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797052050"
variation 2917
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:893323586"
variation 2919
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797052208"
variation 2921
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301013251"
variation 2922
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1031349699"
variation 2926
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797052448"
variation 2930
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:770889312"
variation 2933
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1042255724"
variation 2942
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797052620"
variation 2944
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797052671"
variation 2953
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:556800887"
variation 2956
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1205988867"
variation 2961
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797052814"
variation 2967
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1437404656"
variation 2970
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1220031653"
variation 2973
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797052954"
variation 2974
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:754831345"
variation 2979..2980
/gene="CLDN12"
/replace=""
/replace="tata"
/db_xref="dbSNP:1797053046"
variation 2981
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:992452555"
variation 2983
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258313188"
variation 2984
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797053172"
variation 2995
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:767405026"
variation 2996
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:774762433"
variation 3004
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797053359"
variation 3009
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:970325178"
variation 3010
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115909450"
variation 3011
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1035394292"
variation 3017
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797053515"
variation 3018
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352898945"
variation 3019
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670657"
variation 3023
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115909510"
variation 3024
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797053669"
variation 3025..3030
/gene="CLDN12"
/replace="ag"
/replace="agacag"
/db_xref="dbSNP:1288375953"
variation 3025
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797053723"
variation 3026
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797053824"
variation 3028
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:894138443"
variation 3031..3037
/gene="CLDN12"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:1797053927"
variation 3037
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:781641197"
variation 3040
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797054028"
variation 3043
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797054079"
variation 3046
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1247987207"
variation 3052
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1012698606"
variation 3056
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:568718729"
variation 3057..3064
/gene="CLDN12"
/replace="at"
/replace="ataaacat"
/db_xref="dbSNP:1797054344"
variation 3057
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797054298"
variation 3058
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797054403"
variation 3061
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026715065"
variation 3066
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797054515"
variation 3067
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115909795"
variation 3068
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1352335014"
variation 3075
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:186714887"
variation 3076
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1405647009"
variation 3077
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:982647638"
variation 3081
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1478681950"
variation 3083
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1162570148"
variation 3084
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797054998"
variation 3087
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:558116406"
variation 3090
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:572884216"
variation 3100
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:930764716"
variation 3103
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:191175070"
variation 3115
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797055506"
variation 3121
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1182906250"
variation 3124
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1469690049"
variation 3126
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797055664"
variation 3128
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:370567033"
variation 3131
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1465346932"
variation 3135
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1224019264"
variation 3138
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797055868"
variation 3139
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797055922"
variation 3146
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:976635967"
variation 3147
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115910133"
variation 3149
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797056014"
variation 3153..3157
/gene="CLDN12"
/replace="tt"
/replace="ttatt"
/db_xref="dbSNP:1797056080"
variation 3154
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:923308201"
variation 3155
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:755973015"
variation 3156
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1047849387"
variation 3159
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:745517196"
variation 3160
/gene="CLDN12"
/replace=""
/replace="c"
/db_xref="dbSNP:1797056453"
variation 3162
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797056532"
variation 3163..3170
/gene="CLDN12"
/replace="ttt"
/replace="ttttcttt"
/db_xref="dbSNP:1272900117"
variation 3170
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:931973835"
variation 3171
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797056743"
variation 3172
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331761043"
variation 3174
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1293475661"
variation 3184
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:986645515"
variation 3185
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797056958"
variation 3188
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:544649141"
variation 3189
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797057066"
variation 3196
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797057140"
variation 3198
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115910364"
variation 3206
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:947424244"
variation 3207
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1289526240"
variation 3209
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1041890726"
variation 3210
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:9731"
variation 3211
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695614681"
variation 3212
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:938947137"
variation 3213
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:2115910499"
variation 3217
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446345598"
variation 3219
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:901114812"
variation 3220
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797057588"
variation 3224
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797057642"
variation 3230
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797057696"
variation 3231
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:576737071"
variation 3232
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:2115910604"
variation 3238
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797057792"
variation 3242
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1369822644"
variation 3246
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1323584028"
variation 3248..3251
/gene="CLDN12"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1797057932"
variation 3250
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797057981"
variation 3254
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:745956902"
variation 3259
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:2115910679"
variation 3274
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797058094"
variation 3280
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797058145"
variation 3281
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797058213"
variation 3282
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1389192782"
variation 3283
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797058352"
variation 3285
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797058424"
variation 3289
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1158273121"
variation 3291..3295
/gene="CLDN12"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1797058581"
variation 3304
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797058652"
variation 3307
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316883037"
variation 3308
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1405844726"
variation 3310
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:894169464"
variation 3315
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797059374"
variation 3316
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1192064772"
variation 3319
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1466524143"
variation 3323
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797059508"
variation 3325
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1012602241"
variation 3326
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1215674137"
variation 3332
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315698081"
variation 3333
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1280072272"
variation 3344
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:545732176"
variation 3345
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797059696"
variation 3347
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1346619779"
variation 3352
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1300801034"
variation 3356
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797059831"
variation 3360
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797059890"
variation 3361
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797059938"
variation 3362
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1436906132"
variation 3364
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1733723153"
variation 3365
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:17863096"
variation 3367
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:888211500"
variation 3369
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1004331449"
variation 3383
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1266722145"
variation 3384
/gene="CLDN12"
/replace=""
/replace="t"
/db_xref="dbSNP:1178254743"
variation 3385..3386
/gene="CLDN12"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1435418017"
variation 3385
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797060319"
variation 3386
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797060420"
variation 3391
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1023940250"
variation 3399
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797060544"
variation 3403
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797060581"
variation 3405..3407
/gene="CLDN12"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1451611393"
variation 3406
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1562970685"
variation 3412
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797060727"
variation 3417
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1584670878"
variation 3418
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797060823"
variation 3422
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:531134386"
variation 3423
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797060935"
variation 3424
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1584670890"
variation 3425
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797061029"
variation 3426
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:780262130"
variation 3431
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:980379733"
variation 3434
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:747178785"
variation 3435
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:920807704"
variation 3436
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1485051455"
variation 3446..3448
/gene="CLDN12"
/replace="ata"
/replace="atata"
/db_xref="dbSNP:1277638017"
variation 3448
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1230123160"
variation 3451
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1489120300"
variation 3454
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797061859"
variation 3459
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:965175977"
variation 3463
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797061965"
variation 3469
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1294523360"
variation 3471
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797062126"
variation 3472
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:530747526"
variation 3474
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797062284"
variation 3477
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:2115911443"
variation 3479
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:998090009"
variation 3480
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:543242983"
variation 3482
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:561267693"
variation 3483
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1028179618"
variation 3485
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:953942632"
variation 3491
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670950"
variation 3492
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:184005906"
variation 3493
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:914516784"
variation 3495
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797062749"
variation 3496
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797062801"
variation 3501
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1414150112"
variation 3505
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1475207043"
regulatory 3512..3517
/regulatory_class="polyA_signal_sequence"
/gene="CLDN12"
/note="hexamer: ATTAAA"
variation 3514
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797062957"
variation 3515..3518
/gene="CLDN12"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1797063002"
variation 3518
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:17866176"
variation 3519
/gene="CLDN12"
/replace=""
/replace="g"
/db_xref="dbSNP:1311180978"
variation 3519
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797063171"
variation 3520
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:776979988"
variation 3525..3529
/gene="CLDN12"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1797063331"
polyA_site 3533
/gene="CLDN12"
/note="major polyA site"
ORIGIN
gggaacgcacttcctgggacgctgagagggagacgctccaagaggctcctcagtgtgggcgagtaaaatgccctgcgtgtgagaagcaggctcagattattgctactctgtattcagatcttcatgtgtctcttctaagctgaataaagctgttttggaactgtcaggtacctcaaagcatgaagaaaacgaggcacagggaagttctgaatctggcccaagtctgactgacagtactccacaagcttgcctgccatgggctgtcgggatgtccacgcagccacagtcctttccttcctgtgtggaatcgcctcagtagcaggcctctttgcagggactctgcttcccaactggagaaaattacgattgatcacattcaacagaaacgagaagaacctgactgtttacacaggcctgtgggtgaaatgtgcccggtatgacgggagcagtgactgcctgatgtacgacactacttggtactcatcagttgaccagctggacctgcgtgtcctccagtttgccctacccctcagcatgctgatcgccatgggtgccctgctgctctgcctgattggaatgtgcaacactgccttcaggtcctcggtgcccaacatcaaactggccaagtgtctggtcaatagtgcaggttgccacctggtggctgggctgctatttttcctggcaggtactgtgagcctctccccatctatctgggtcatcttttataacatccatctgaacaagaagtttgagccagtcttttcatttgactatgcagtgtatgtcactattgctagtgctgggggcctgtttatgacttcccttatactatttatttggtattgtacatgcaaatctttgccttctcctttctggcaaccattgtactcccatccacccagtatgcatacttactcacagccctattcagcacgctctcgcctctctgccattgaaattgacattccagtagtttcacacaccacttaatggggaaatagttaattgttaaagaaaacttcttgtagcctcacattccccttgtgcaaagagctcttttggacctacatacattttcctttgtttttgaccaatcaatgaagccaaatttatatgtcctagtagaatgaagtgctgctagtttttatgagaagtatattatattaaatgtgaattttttaaattttgcttcttatactggaaggaattttagccttcatattgatatctaattaattatttaagtggaagaggcctgcatcacaattgaggtaatgtagagcaacatgttaaagaatgatggttagcagaagctgttgtatacaatcttcatgaaaatttcagtgtgtatttttctttttctataatacctttaactgcaaagaaaaggcagtttcaaatataagaaatttatttcaggtaagggtaatattttaatagtagtcaataatctagcttaaggctgtaactcttctatcggggctaattgtatgaataggtgtcagtatgttgaagattactttcttttgtgactttcttctacctcatgccactgtttaaaagtaaaacgtattttaacgatgttagaataagactaccattctaaatatcacctacttatgaataacatgtaataatttttaacattaatgattccataaattgtattattgggattagaatgtgctttatgacaggttagtgtttcctctgaggcagaaaactcttttttggagatatcttccatcaagcagtactcgtgcccatatacaatctcttagtggctaggagaaataaataaaagggccataatggtttgttctctttcagacataatttagtaggggacaagaagtctgttcttcagtgagtacactagagatttactctggtgactgccttttgagttatgggtgaagtaaggtatggctttaccataaccttgattcattcacccttgattcatttctcgcccccgtcactgattatttccttgagcatatatctctgcctaacactttagtaggtgctatagaggatacatgaaaagtatgagatctggttccatccagtaagacattttaatagagaagatcaaaatgttacctggcagttggggaataatctgacttcgttggcagttggccttaacttcttaatcattgatccaggaatatttcaaccagagacacaactttctggcagacagacaaattgtacaacaccaacaatatcctggaccttgaaattctgtttacttcagtccattgtatcctttaaggcacctgtgctagcctagattttgtaataacactgatttatgagaatggacaaaagtggtagggaaattgttccctctccacttctgaaagtatgatgatgtattaaggatggaggagttattaaaaatgtctcttctgatgaggtaacaattagatgaaaccatgttaaagctgagatgaacacttagaaattcagggatattgggtctttagccttatgaatttgagctgcttatttaattggtgtaatttactacatattagtactatattcgtaaggattttttattaaccattacagattttacaaacagctagttatatggtaaacagattattatgcctttttgcaattctgaatatgattctagtatttgtgtagatgtatttggtactttttcccctaattccaacactagtttatatatatagcgaataaatctagttgtataaatttttaaatgccgtcagtagaaagcacacaaggttatgatttttttaattactggcttctgatttctttcacttctgatccttttcctttttctcagatgtagctgagtcttgatcattttaagacaacgatgggtagaattttgagattaatgttaattttccctttttgttaatttcagtcccctctcactatgcttttgtccagaaggatcaagaattctaccatcccttgggtctttgtgtataaacaatgttaaataaaggtagactcagtctttaagatattagacagtttttttagtccatgggattgtaaatataaacattaactttcctataagaatattttggctttgtaatctatagcctcaaattggtatttattatggattcactagacaaacagctgtttccttattgtcttttttctttagtgtttctgatttgctatcagtagctgtttttaaagccgtccaaggaaaataattatttacagtttttgaagtcacttttgagccctcatcaagctctcattgtgatgggagggatacctttttgttgttaaaagcctattattgttaaaggccttttatggaaaccaacttggaaaacaaccttaaatgtggatgtatcagatttggtttatccagccatgggagagaaaacaaacctaagtttactttacttgtacatatacactacaatggatagtatatttgctgtaaactacaatgtaaaacctcaataaaagtgcgctgtacttcttaatgtttattaaaagatgtatttttacaa
//
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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