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Previous release (v1)
2024-04-19 04:42:05, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_199328 2092 bp mRNA linear PRI 14-MAR-2023 DEFINITION Homo sapiens claudin 8 (CLDN8), mRNA. ACCESSION NM_199328 VERSION NM_199328.3 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 2092) 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 2 (bases 1 to 2092) AUTHORS Nattramilarasu PK, Bucker R, Lobo de Sa FD, Fromm A, Nagel O, Lee IM, Butkevych E, Mousavi S, Genger C, Klove S, Heimesaat MM, Bereswill S, Schweiger MR, Nielsen HL, Troeger H and Schulzke JD. TITLE Campylobacter concisus Impairs Sodium Absorption in Colonic Epithelium via ENaC Dysfunction and Claudin-8 Disruption JOURNAL Int J Mol Sci 21 (2), 373 (2020) PUBMED 31936044 REMARK GeneRIF: Campylobacter concisus Impairs Sodium Absorption in Colonic Epithelium via ENaC Dysfunction and Claudin-8 Disruption. Publication Status: Online-Only REFERENCE 3 (bases 1 to 2092) AUTHORS Wang Z, Zhu J, Liu C and Ma L. TITLE Identification of key genes and pathways associated with Crohn's disease by bioinformatics analysis JOURNAL Scand J Gastroenterol 54 (10), 1205-1213 (2019) PUBMED 31526198 REMARK GeneRIF: MMP1 and CLDN8 were two key genes screened from the differentially expressed genes involved in the pathogenesis of Crohn's disease. REFERENCE 4 (bases 1 to 2092) AUTHORS Liu B, Lu B, Wang X, Jiang H and Kuang W. TITLE MiR-361-5p inhibits cell proliferation and induces cell apoptosis in retinoblastoma by negatively regulating CLDN8 JOURNAL Childs Nerv Syst 35 (8), 1303-1311 (2019) PUBMED 31161266 REMARK GeneRIF: MiR-361-5p inhibits cell proliferation and induces cell apoptosis in retinoblastoma by negatively regulating CLDN8. REFERENCE 5 (bases 1 to 2092) AUTHORS Zhou S, Piao X, Wang C, Wang R and Song Z. TITLE Identification of claudin-1, -3, -7 and -8 as prognostic markers in human laryngeal carcinoma JOURNAL Mol Med Rep 20 (1), 393-400 (2019) PUBMED 31115553 REMARK GeneRIF: the findings of the present study demonstrated that the expression levels of CLDN1, 3, 7 and 8 varied between laryngeal squamous carcinoma tissues and nonneoplastic tissues REFERENCE 6 (bases 1 to 2092) 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 7 (bases 1 to 2092) 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 8 (bases 1 to 2092) 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 REFERENCE 9 (bases 1 to 2092) AUTHORS Itoh M, Furuse M, Morita K, Kubota K, Saitou M and Tsukita S. TITLE Direct binding of three tight junction-associated MAGUKs, ZO-1, ZO-2, and ZO-3, with the COOH termini of claudins JOURNAL J Cell Biol 147 (6), 1351-1363 (1999) PUBMED 10601346 REFERENCE 10 (bases 1 to 2092) AUTHORS Morita K, Furuse M, Fujimoto K and Tsukita S. TITLE Claudin multigene family encoding four-transmembrane domain protein components of tight junction strands JOURNAL Proc Natl Acad Sci U S A 96 (2), 511-516 (1999) PUBMED 9892664 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DA629490.1, AY358707.1, AL049977.1 and AW235670.1. This sequence is a reference standard in the RefSeqGene project. On May 17, 2019 this sequence version replaced NM_199328.2. 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 protein plays important roles in the paracellular cation barrier of the distal renal tubule, and in the paracellular barrier to prevent sodium back-leakage in distal colon. Differential expression of this gene has been observed in colorectal carcinoma and renal cell tumors, and along with claudin-7, is an immunohistochemical marker for the differential diagnosis of chromophobe renal cell carcinoma and renal oncocytoma.[provided by RefSeq, May 2010]. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript is intronless :: AY358707.1, BC058004.1 [ECO:0000345] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000399899.2/ ENSP00000382783.1 RefSeq Select criteria :: based on single protein-coding transcript ##RefSeq-Attributes-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-76 DA629490.1 55-130 77-1532 AY358707.1 1-1456 1533-2081 AL049977.1 522-1070 2082-2092 AW235670.1 2-12 c FEATURES Location/Qualifiers source 1..2092 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="21" /map="21q22.11" gene 1..2092 /gene="CLDN8" /gene_synonym="HEL-S-79" /note="claudin 8" /db_xref="GeneID:9073" /db_xref="HGNC:HGNC:2050" /db_xref="MIM:611231" exon 1..2092 /gene="CLDN8" /gene_synonym="HEL-S-79" /inference="alignment:Splign:2.1.0" variation 2 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:1557297" variation 3 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="t" /db_xref="dbSNP:905936907" variation 11 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:1978977494" variation 14 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:901383837" variation 15 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:1978977287" variation 16 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="g" /replace="t" /db_xref="dbSNP:1978977191" variation 18 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:1428390580" variation 20 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1283508956" variation 23 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="g" /replace="t" /db_xref="dbSNP:1448305655" variation 25 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:1215928921" variation 26 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="g" /replace="t" /db_xref="dbSNP:571969620" variation 30 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:1978976543" variation 31 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:1978976454" variation 34 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:1009798865" variation 35 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="c" /db_xref="dbSNP:1195471948" variation 38 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="g" /replace="t" /db_xref="dbSNP:1395612686" variation 39 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="t" /db_xref="dbSNP:1978976061" variation 49..53 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="ac" /replace="accac" /db_xref="dbSNP:1156553098" variation 49 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:188042888" variation 50 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:1978975827" variation 56 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1056386448" variation 57 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="g" /replace="t" /db_xref="dbSNP:1054418544" variation 61 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:938034635" variation 62 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1438764241" variation 63 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:1978975221" variation 67 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="g" /db_xref="dbSNP:926579756" variation 74 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:1978974976" variation 78 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="g" /replace="t" /db_xref="dbSNP:929879554" variation 83 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:1978974849" variation 84 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="c" /db_xref="dbSNP:1978974713" variation 85..87 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="t" /replace="tgt" /db_xref="dbSNP:1446523028" variation 85 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:1372344890" variation 86 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="g" /db_xref="dbSNP:1716053983" variation 88 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:897019809" variation 91 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1557296" variation 95 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:1978974116" variation 99 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:1978973923" variation 101 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="t" /db_xref="dbSNP:1046516728" variation 103 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:1224042201" variation 104 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:1978973537" variation 106 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:1288663513" variation 108 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:1978973287" variation 110 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="c" /db_xref="dbSNP:1038592332" variation 111 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="g" /db_xref="dbSNP:1557295" variation 114 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:949442466" variation 116 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:910987992" variation 120 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:2146515586" variation 121 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:2146515584" variation 124 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="g" /db_xref="dbSNP:756496110" variation 128 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="t" /db_xref="dbSNP:2146515579" variation 130 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:1978972589" variation 131 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1462999826" variation 132 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="c" /db_xref="dbSNP:751297214" variation 133 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /db_xref="dbSNP:766105942" variation 135 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:2146515551" variation 136 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:762573797" variation 137 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:772806127" variation 138 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:765222585" variation 141 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1361534869" variation 143 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:761593161" variation 144 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:776614655" variation 146 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1407016936" variation 147 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="g" /db_xref="dbSNP:373769301" variation 148 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:1167121491" misc_feature 152..154 /gene="CLDN8" /gene_synonym="HEL-S-79" /note="upstream in-frame stop codon" variation 156 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="c" /db_xref="dbSNP:760500803" variation 158 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:2146515522" variation 159 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:775714753" variation 160 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1172306425" variation 161 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="t" /db_xref="dbSNP:1428670484" variation 162 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="c" /replace="t" /db_xref="dbSNP:1389181552" variation 164 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="c" /db_xref="dbSNP:1978970291" variation 170 /gene="CLDN8" /gene_synonym="HEL-S-79" /replace="a" /replace="t" /db_xref="dbSNP:772244445" CDS 173..850 /gene="CLDN8" /gene_synonym="HEL-S-79" /note="epididymis secretory protein Li 79" /codon_start=1 /product="claudin-8" /protein_id="NP_955360.1" /db_xref="CCDS:CCDS13587.1" /db_xref="GeneID:9073" /db_xref="HGNC:HGNC:2050" /db_xref="MIM:611231" /translation="
MATHALEIAGLFLGGVGMVGTVAVTVMPQWRVSAFIENNIVVFENFWEGLWMNCVRQANIRMQCKIYDSLLALSPDLQAARGLMCAASVMSFLAFMMAILGMKCTRCTGDNEKVKAHILLTAGIIFIITGMVVLIPVSWVANAIIRDFYNSIVNVAQKRELGEALYLGWTTALVLIVGGALFCCVFCCNEKSSSYRYSIPSHRTTQKSYHTGKKSPSVYSRSQYV"
misc_feature 185..718
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/note="PMP-22/EMP/MP20/Claudin family; Region:
PMP22_Claudin; cl21598"
/db_xref="CDD:451326"
misc_feature 194..256
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/note="propagated from UniProtKB/Swiss-Prot (P56748.1);
transmembrane region"
misc_feature 416..478
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/note="propagated from UniProtKB/Swiss-Prot (P56748.1);
transmembrane region"
misc_feature 524..586
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/note="propagated from UniProtKB/Swiss-Prot (P56748.1);
transmembrane region"
misc_feature 671..733
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/note="propagated from UniProtKB/Swiss-Prot (P56748.1);
transmembrane region"
misc_feature 788..847
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/note="propagated from UniProtKB/Swiss-Prot (P56748.1);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 842..847
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/note="propagated from UniProtKB/Swiss-Prot (P56748.1);
Region: Interactions with TJP1, TJP2 and TJP3.
/evidence=ECO:0000250|UniProtKB:Q9Z260"
variation 180
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:745952339"
variation 182
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395895887"
variation 184
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:2146515498"
variation 194
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223529777"
variation 195
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1901445778"
variation 196
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1978969552"
variation 197
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:778908212"
variation 198
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1200335966"
variation 202
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1337945344"
variation 203
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:771030877"
variation 206
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978968882"
variation 208
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482581522"
variation 210
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978968563"
variation 213
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1253380647"
variation 215
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:749828592"
variation 219
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978968099"
variation 222
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1978967846"
variation 226..227
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1978967427"
variation 226
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778312220"
variation 229
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:756482500"
variation 230
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:963177454"
variation 231
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:138394812"
variation 233
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978966634"
variation 235
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978966461"
variation 239
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:370248819"
variation 240
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:150078407"
variation 241
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:749962253"
variation 243
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:764708430"
variation 245
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557294"
variation 246
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1299610160"
variation 247
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978965206"
variation 248
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:2146515430"
variation 250
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:761359261"
variation 252
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1317239997"
variation 254
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:753772677"
variation 255
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:764047012"
variation 259
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1601034150"
variation 266
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:531956336"
variation 267
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:986413133"
variation 270
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568787209"
variation 271
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:775201255"
variation 272
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:772297302"
variation 279..307
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="ttgaaaacaacatcgtggtttttgaaaac"
/replace="ttgaaaacaacatcgtggtttttgaaaacaacatcgtggtttttgaaa
ac"
/db_xref="dbSNP:1978961069"
variation 279
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:759813417"
variation 280
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:774553337"
variation 285
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:953112188"
variation 288
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:770955180"
variation 290
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978962824"
variation 291
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978962653"
variation 292
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:375641409"
variation 293
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:778164419"
variation 294
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:770295035"
variation 295
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:748525098"
variation 297..301
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:750983909"
variation 298
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:781640763"
variation 301
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:755377935"
variation 304
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:141620647"
variation 306
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:778608955"
variation 307..311
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="ct"
/replace="cttct"
/db_xref="dbSNP:1978960533"
variation 307
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978960902"
variation 310
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1309050702"
variation 312
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756745321"
variation 315
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:2146515342"
variation 317
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:2038642248"
variation 319
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:753350719"
variation 327
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:763946058"
variation 332
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:978915979"
variation 333
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:760549552"
variation 334
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:387907424"
variation 335
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:752619315"
variation 336
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:796717455"
variation 337
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410894507"
variation 339
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1333849282"
variation 340
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:769169043"
variation 346
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1455933252"
variation 348
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:767367630"
variation 351
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1978958039"
variation 357
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:528758738"
variation 358
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:774484538"
variation 360
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1030402102"
variation 361
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1978957284"
variation 363
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1978957128"
variation 365..368
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1339321889"
variation 371..373
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="t"
/replace="tat"
/db_xref="dbSNP:1202043822"
variation 371
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250010351"
variation 372
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:766571800"
variation 375
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:79452452"
variation 378
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:762973038"
variation 379
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978955956"
variation 380
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978955788"
variation 381
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770434883"
variation 385
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:748719176"
variation 388..394
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="tct"
/replace="tctttct"
/db_xref="dbSNP:1486871622"
variation 391
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978955197"
variation 393
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271915484"
variation 394
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:967083664"
variation 397
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:567735724"
variation 398
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1339929374"
variation 402
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978954129"
variation 403
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1158680003"
variation 404
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:201177228"
variation 405
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:747333331"
variation 406
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:778463287"
variation 409
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1225104961"
variation 410
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:201941862"
variation 416..417
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="gg"
/db_xref="dbSNP:767844489"
variation 416
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1258484616"
variation 419
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:200097700"
variation 420..426
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="tg"
/replace="tgatgtg"
/db_xref="dbSNP:1457110788"
variation 421
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:748763576"
variation 423
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:777401334"
variation 424
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:755617586"
variation 428
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:752672377"
variation 430..434
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="t"
/replace="tgctt"
/db_xref="dbSNP:1978951021"
variation 432
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1179280467"
variation 434
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1686509198"
variation 436
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:372970119"
variation 437
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:893943148"
variation 439
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377461224"
variation 440
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1172380123"
variation 445
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1032600168"
variation 448
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978950197"
variation 453
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:61743791"
variation 454
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1448978168"
variation 456
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:751327021"
variation 458
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:994122095"
variation 462
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:55884670"
variation 463
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:763174117"
variation 464
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:561390736"
variation 469
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:868192260"
variation 473
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:765475207"
variation 475
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1978948241"
variation 486
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274054946"
variation 487
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978947881"
variation 494
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978947702"
variation 495
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1230558463"
variation 496
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1327832285"
variation 497
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:761949265"
variation 498
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1319642510"
variation 499
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1433691791"
variation 500
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:949339666"
variation 501
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace=""
/replace="a"
/db_xref="dbSNP:762203558"
variation 502
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1568786967"
variation 503
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1339229115"
variation 504
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1470616708"
variation 506
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1401883342"
variation 509
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1171190908"
variation 510
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978945776"
variation 511
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:543328603"
variation 515
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1670296639"
variation 516
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:185171814"
variation 519
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:772187336"
variation 521
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:769250676"
variation 526
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1447703508"
variation 528
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978944789"
variation 529
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978944622"
variation 530
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:370704016"
variation 534
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:376757104"
variation 535
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:749038670"
variation 545
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:200767039"
variation 551
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1277564715"
variation 552
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:141376936"
variation 555
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:747608175"
variation 557
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:685967"
variation 558..559
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace=""
/replace="a"
/db_xref="dbSNP:1978942288"
variation 558
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:555436710"
variation 559
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1370955789"
variation 561
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:146174025"
variation 563
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:931878628"
variation 564
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451124576"
variation 565
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1159916190"
variation 566
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:758122461"
variation 567
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:867441012"
variation 569
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1449346538"
variation 571
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978940450"
variation 572
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:373504217"
variation 576
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:975739466"
variation 577
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411997468"
variation 579
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397712019"
variation 580
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="t"
/replace="tt"
/db_xref="dbSNP:773835736"
variation 581
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:765509944"
variation 583
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:568681833"
variation 584
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201870752"
variation 585
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1428092263"
variation 586
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762018445"
variation 587
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:2146514967"
variation 590
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978938714"
variation 592
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753906623"
variation 593
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1601033747"
variation 594
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473050368"
variation 597
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:764714350"
variation 599
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:761303990"
variation 600
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:778285222"
variation 601
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1418113787"
variation 602
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978938352"
variation 604
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1439305643"
variation 605
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978938041"
variation 606
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1821959874"
variation 607
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:775856986"
variation 609
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:772528868"
variation 611
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978937572"
variation 614
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1339674778"
variation 619
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1293251655"
variation 622
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:759798441"
variation 623
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:686364"
variation 624
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:769259130"
variation 626
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:369970339"
variation 628
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978935823"
variation 630
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:768034106"
variation 633
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978935450"
variation 634
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:2146514892"
variation 635
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:747030038"
variation 636
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:779821920"
variation 640
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:539459302"
variation 642
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1978934806"
variation 643
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:145203913"
variation 648
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757500351"
variation 650
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:754103569"
variation 651..664
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="agct"
/replace="agcttggagaagct"
/db_xref="dbSNP:1270587840"
variation 651
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1161371713"
variation 652
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471133213"
variation 653
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1412385865"
variation 654
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1194687583"
variation 656
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1181194612"
variation 660
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978933364"
variation 663
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:764337784"
variation 665
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1726072469"
variation 669
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1221900156"
variation 674
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978932325"
variation 675
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1013598296"
variation 676
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:760640871"
variation 679
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:2146514839"
variation 682
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1287156351"
variation 684
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1225931644"
variation 686
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:753299149"
variation 689..690
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace=""
/replace="cgagcgtctactccagaagtcagtatgtgtagt"
/db_xref="dbSNP:768376789"
variation 690
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:377189703"
variation 692
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:759975493"
variation 694
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978930906"
variation 697
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978930747"
variation 699
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978930576"
variation 701
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978930431"
variation 705
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978930201"
variation 707
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:374413964"
variation 713
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:769449570"
variation 715
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:761508071"
variation 716
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:776257548"
variation 718
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:897788554"
variation 722
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:768250266"
variation 723
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1320405169"
variation 724
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:746476394"
variation 725
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:780074870"
variation 726..731
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="tttttt"
/replace="ttttttt"
/db_xref="dbSNP:762312465"
variation 726
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1162093742"
variation 730
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1158420893"
variation 732
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:771840194"
variation 733
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:745676590"
variation 736
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978927564"
variation 738
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1461854104"
variation 739
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:76413867"
variation 740
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:757114600"
variation 743
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1477507803"
variation 745
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:992906770"
variation 746
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244403010"
variation 747
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:754154573"
variation 748
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978926028"
variation 749
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1309492412"
variation 757
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978925722"
variation 762
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:777838492"
variation 765
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:756242497"
variation 766
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978925242"
variation 768
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1336516028"
variation 770
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978924913"
variation 771
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1978924742"
variation 772
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1207438653"
variation 774
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:752677704"
variation 775
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271306785"
variation 776
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1344775322"
variation 777
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1254727142"
variation 779
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:367879638"
variation 780
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1251241097"
variation 781
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:780559017"
variation 782
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:756602075"
variation 784
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295018297"
variation 785
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:766793245"
variation 786
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:139251282"
variation 788
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:776312674"
variation 789..794
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="aaaaa"
/replace="aaaaaa"
/replace="aaaaaaa"
/db_xref="dbSNP:769497921"
variation 789
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1978922317"
variation 792
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:538422021"
variation 793
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1455595082"
variation 794
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:760239486"
variation 795
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:774807900"
variation 796
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:146073584"
variation 798
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:774399838"
variation 799
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace=""
/replace="t"
/db_xref="dbSNP:1978920366"
variation 799
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:375605292"
variation 800
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:945719662"
variation 801
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1397519312"
variation 805
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:200705375"
variation 806
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:778089405"
variation 808
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1246936443"
variation 810
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748272009"
variation 811
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:577364229"
variation 812
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568786693"
variation 813
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:144192947"
variation 818
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:143649743"
variation 819
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:73900962"
variation 820
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:758781407"
variation 821
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:750722864"
variation 822
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:763824206"
variation 823
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:760307552"
variation 824..827
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="gtct"
/replace="gtctgtct"
/db_xref="dbSNP:1568786663"
variation 824
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1364482689"
variation 826
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295534740"
variation 827
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:745990197"
variation 828
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:775207820"
variation 830
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1432723593"
variation 831
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978915959"
variation 836
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978915799"
variation 838
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:766976823"
variation 839
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1381264197"
variation 840
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:759095576"
variation 844
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1447014900"
variation 844
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1208335368"
variation 845
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:199918464"
variation 847..851
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="gtagt"
/replace="gtagtagt"
/db_xref="dbSNP:745789079"
variation 847
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:756882658"
variation 853
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:770953799"
variation 855
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:2146514577"
variation 856
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1052842601"
variation 857
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:749098404"
variation 858
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1476620884"
variation 859
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace=""
/replace="g"
/db_xref="dbSNP:1978913928"
variation 859
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:199764335"
variation 860..866
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="tttttt"
/replace="ttttttt"
/db_xref="dbSNP:776761841"
variation 860
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:373609628"
variation 862
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978913582"
variation 866
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:781440822"
variation 868
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1482468050"
variation 869
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:981358616"
variation 876
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1254444178"
variation 877
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:755095093"
variation 879
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:747039686"
variation 881
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:370521194"
variation 882
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1248241005"
variation 883
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:758848634"
variation 885
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="t"
/replace="tt"
/db_xref="dbSNP:770821048"
variation 886
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:750931771"
variation 887
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1313310056"
variation 888
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1395437369"
variation 891
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:779215999"
variation 898..899
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace=""
/replace="t"
/db_xref="dbSNP:542408205"
variation 900
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409987622"
variation 901
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:139320130"
variation 903
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:992975523"
variation 904
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1014920319"
variation 908
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1978911096"
variation 915
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752342346"
variation 916
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1279002627"
variation 917
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1368589577"
variation 919
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:767231069"
variation 920
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1006329503"
variation 921
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:533171817"
variation 922
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:751048099"
variation 924
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:766430229"
variation 925
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482964478"
variation 929
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:763040182"
variation 930
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978909763"
variation 931
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:751059004"
variation 935
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1050504984"
variation 937
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978909354"
variation 939
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:961806236"
variation 940
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:562419430"
variation 947
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:996420500"
variation 950
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978908855"
variation 961
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978908721"
variation 964
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1339122383"
variation 967
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:763638044"
variation 972
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978908309"
variation 974
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978908209"
variation 978
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978908099"
variation 979
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1601033225"
variation 986
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1252282832"
variation 988
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1452357111"
variation 991
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1175211996"
variation 999
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397152956"
variation 1000
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978907387"
variation 1003
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568786554"
variation 1004
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016267178"
variation 1010
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace=""
/replace="a"
/db_xref="dbSNP:1158631612"
variation 1017
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1978907010"
variation 1020
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1343556498"
variation 1023
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978906795"
variation 1025
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1978906696"
variation 1026
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978906604"
variation 1028
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978906495"
variation 1031..1033
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:2146514454"
variation 1034
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:9647055"
variation 1035
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978906098"
variation 1039
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978905997"
variation 1041
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1300773060"
variation 1043..1049
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="ttg"
/replace="ttgattg"
/db_xref="dbSNP:1978905528"
variation 1047
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400670300"
variation 1049
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978905414"
variation 1056
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978905313"
variation 1060
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1439160204"
variation 1061
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1040309768"
variation 1062..1066
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="ta"
/replace="tagta"
/db_xref="dbSNP:1222899871"
variation 1062
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:192870760"
variation 1063
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:77291057"
variation 1066..1067
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1372476178"
variation 1066
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1028218207"
variation 1073
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:912930804"
variation 1078
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1318260238"
variation 1079
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1215810245"
variation 1080
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:561690725"
variation 1081
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:2146514414"
variation 1083
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:540423635"
variation 1088
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:2146514406"
variation 1090
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:188819091"
variation 1091
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:183221587"
variation 1094
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1253448849"
variation 1095
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978903497"
variation 1097
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978903393"
variation 1099
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:555343681"
variation 1107
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:76319527"
variation 1108
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1601033099"
variation 1109
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978902958"
variation 1113
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:927041356"
variation 1121
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978902683"
variation 1122
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402534497"
variation 1124
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461064387"
variation 1125
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:979835895"
variation 1127
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1949529068"
variation 1131
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978902175"
variation 1134
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1200968408"
variation 1136
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:78984798"
variation 1139
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1042691392"
variation 1140
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978901538"
variation 1144
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:546105661"
variation 1148
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1277424248"
variation 1149
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374978808"
variation 1150
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:2146514366"
variation 1152
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1223882223"
variation 1153
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:992438671"
variation 1157
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978900905"
variation 1160
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1244861272"
variation 1161
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:962270612"
variation 1166
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1015160976"
variation 1167
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:556894101"
variation 1168
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace=""
/replace="a"
/db_xref="dbSNP:1437071518"
variation 1170
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1006647979"
variation 1171
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978899957"
variation 1173
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1309956688"
variation 1175
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1978899667"
variation 1178
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1057283260"
variation 1184
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1231404985"
variation 1185
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978899377"
variation 1193
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:952046885"
variation 1194
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:938852215"
variation 1195
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451408357"
variation 1197
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:13048274"
variation 1198
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1029495195"
variation 1200
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978898669"
variation 1203
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1333085839"
variation 1205
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1444390908"
variation 1207
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:2146514319"
variation 1211
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:996274559"
variation 1212..1214
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="ata"
/db_xref="dbSNP:1392007826"
variation 1213
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1167823031"
variation 1214..1218
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="aga"
/replace="agaga"
/db_xref="dbSNP:1978897471"
variation 1214
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1601033003"
variation 1215
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:972594220"
variation 1218
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1978897335"
variation 1219
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327220074"
variation 1221
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1601032988"
variation 1223
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:901720597"
variation 1224..1225
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="t"
/replace="tt"
/db_xref="dbSNP:138941503"
variation 1224
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978896887"
variation 1225
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1601032972"
variation 1228
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978896405"
variation 1229
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978896238"
variation 1236
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978896112"
variation 1237
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978895984"
variation 1238
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1978895839"
variation 1252
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1978895717"
variation 1254
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:2146514270"
variation 1255
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978895598"
variation 1256
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1978895460"
variation 1275
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163712451"
variation 1278
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:909238822"
variation 1283
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1978895071"
variation 1289
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1040172129"
variation 1295
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978894818"
variation 1296..1298
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1978894673"
variation 1298
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1459385586"
variation 1299
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1311863322"
variation 1306
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:537346475"
variation 1308
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:986146479"
variation 1313
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:2146514243"
variation 1315
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1284727729"
variation 1322
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1370227758"
variation 1323
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:953328629"
variation 1324..1325
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1978893284"
variation 1324
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:757179655"
variation 1327
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1212623591"
variation 1329
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1161777794"
variation 1331
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010134843"
variation 1336
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438165460"
variation 1345
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1257073785"
variation 1347
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1601032918"
variation 1348
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1484765717"
variation 1352
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1978892095"
variation 1355..1360
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="at"
/replace="attaat"
/db_xref="dbSNP:1978891868"
variation 1356
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1190075234"
variation 1361
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:891735011"
variation 1362
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978891600"
variation 1363
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1475345148"
variation 1364
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:374048151"
variation 1366
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978891260"
variation 1368
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1978891133"
variation 1373
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1601032891"
variation 1375
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978890873"
variation 1376
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:753603834"
variation 1378
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:538200782"
variation 1381
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1028249458"
variation 1382
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1180893944"
variation 1388
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:976656038"
variation 1392
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373176760"
variation 1393
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1978889902"
variation 1404
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:2146514188"
variation 1409
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978889774"
variation 1410
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978889664"
variation 1411
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1416099188"
variation 1417
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:751570741"
variation 1420
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:767726368"
variation 1421
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1978889079"
variation 1423
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1325810972"
variation 1428
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044570989"
variation 1431
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568786385"
variation 1432
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978888372"
variation 1434
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271827384"
variation 1435
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1342695559"
variation 1436
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:949816117"
variation 1440
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1601032834"
variation 1441..1446
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="tttttt"
/replace="ttttttt"
/db_xref="dbSNP:1568786374"
variation 1441
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978887736"
variation 1450
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210886475"
variation 1454
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978887364"
variation 1456
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1359114586"
variation 1458
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345943491"
variation 1464
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:904262911"
variation 1465
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1288896242"
variation 1466
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1244659281"
variation 1469
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1978886711"
variation 1471
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978886576"
variation 1473
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:2146514127"
variation 1474
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446468030"
variation 1478
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1021300921"
variation 1479
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:918112280"
variation 1480
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978886227"
variation 1485
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1300709668"
variation 1493
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1450490221"
variation 1494
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1601032795"
variation 1495
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:992345295"
variation 1496..1504
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="tttttttt"
/replace="ttttttttt"
/replace="tttttttttt"
/db_xref="dbSNP:1012545248"
variation 1500
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1392917137"
variation 1505
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:894107527"
variation 1507
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978885108"
variation 1508
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1311074478"
variation 1509
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1003117593"
variation 1511
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568786329"
variation 1512
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1334887092"
variation 1517
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:574288165"
variation 1519
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1300921118"
variation 1520
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:141451662"
variation 1522
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1036511638"
variation 1523
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:908132677"
variation 1529..1533
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:2146514058"
variation 1529
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:942167760"
variation 1536
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:761985571"
variation 1537
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:2146514051"
variation 1538
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465268174"
variation 1539
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1050468433"
variation 1545
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978883129"
variation 1550
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:952182868"
variation 1553
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1193431799"
variation 1554
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1455833617"
variation 1559
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1199214465"
variation 1563
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:2146514023"
variation 1565
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1028987976"
variation 1568
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:975263251"
variation 1570
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1381132760"
variation 1571..1574
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1978882063"
variation 1578
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1766009510"
variation 1579
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1160620457"
variation 1580
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1468801054"
variation 1583
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:966083822"
variation 1589
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1323771144"
variation 1594
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1396497141"
variation 1599
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:534427526"
variation 1600
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:190899748"
variation 1601
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978880993"
variation 1602
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:977109253"
variation 1604
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:376173408"
variation 1608
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:768923544"
variation 1610
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1237018977"
variation 1612
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:891589381"
variation 1614
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1033379920"
variation 1623
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:2146513948"
variation 1631
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1000108779"
variation 1633
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213667770"
variation 1636
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1271825272"
variation 1637
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1489705848"
variation 1638
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1676567718"
variation 1650
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978879673"
variation 1652
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978879556"
variation 1653..1657
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1978879413"
variation 1656
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:2146513931"
variation 1660
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978879298"
variation 1662
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1221076866"
variation 1670
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:539444049"
variation 1673
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1978878877"
variation 1674
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1249388414"
variation 1677
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:968489047"
variation 1684
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1978878527"
variation 1685
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:568951343"
variation 1686
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1412116770"
variation 1687
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1978878089"
variation 1690
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1978877969"
variation 1691
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1474591394"
variation 1693
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044048130"
variation 1694
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:186485421"
variation 1695
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:958397608"
variation 1696..1704
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="tat"
/replace="tatatgtat"
/db_xref="dbSNP:1978876448"
variation 1697..1711
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="atatgtatggatata"
/replace="atatgtatggatataatatgtatggatata"
/db_xref="dbSNP:1978875929"
variation 1697
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1035348344"
variation 1698
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:529126627"
variation 1699
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1428998617"
variation 1700
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1275199818"
variation 1701
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:113129587"
variation 1706
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978876297"
variation 1708
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978876158"
variation 1709
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:895580982"
variation 1712
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978875811"
variation 1713
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1232737915"
variation 1719
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1036749108"
variation 1720
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:940842014"
variation 1722..1726
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="t"
/replace="tattt"
/db_xref="dbSNP:1978875177"
variation 1722
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978875317"
variation 1727
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1323959469"
variation 1731
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978874947"
variation 1737..1739
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1978874694"
variation 1737
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978874826"
variation 1739
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1036989859"
variation 1742
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978874437"
variation 1746
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:2146513856"
variation 1748
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1978874306"
variation 1752
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1251152749"
variation 1753
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1479844472"
variation 1758
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1601032581"
variation 1760
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:908034006"
variation 1763
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1006404238"
variation 1764
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1978873531"
variation 1766
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978873397"
variation 1767
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1282622264"
variation 1768
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:985481043"
variation 1769
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:763538896"
variation 1770
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415909004"
variation 1774
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1978872865"
variation 1778
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:887907723"
variation 1779
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978872630"
variation 1780
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1050540448"
variation 1783
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:932047907"
variation 1785
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:921952954"
variation 1788
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:765211580"
variation 1791
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:2146513809"
variation 1793
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:974792048"
variation 1795
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978871808"
variation 1798
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:546442183"
variation 1799
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400546339"
variation 1800
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978871399"
variation 1801..1807
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="aaaaaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:935305443"
variation 1802
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1371338724"
variation 1805
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:528320810"
variation 1806..1816
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="aacaacaa"
/replace="aacaacaacaa"
/db_xref="dbSNP:1427658032"
variation 1807
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1300149809"
variation 1808
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace=""
/replace="c"
/db_xref="dbSNP:1399125034"
variation 1808
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:28454137"
variation 1810
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978870473"
variation 1811
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1978870343"
variation 1812
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:988851571"
variation 1814
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:564150210"
variation 1815..1821
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="aaaaa"
/replace="aaaaaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:1199244804"
variation 1815
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:968560491"
variation 1817
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1208124248"
variation 1818
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1238756165"
variation 1819
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483275065"
variation 1821
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1032831655"
variation 1832
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:914397965"
variation 1834
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1185929024"
variation 1837
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978868470"
variation 1845
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:73343574"
variation 1846
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1978868124"
variation 1847
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1978868016"
variation 1848..1849
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1188892963"
variation 1849
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:905798069"
variation 1851
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978867627"
variation 1853
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:958427843"
variation 1854
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035823032"
variation 1855
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:2146513741"
variation 1859
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002553525"
variation 1862
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978867063"
variation 1864
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978866938"
variation 1871
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:961983150"
variation 1872
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:368721226"
variation 1873
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978866573"
variation 1876
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278972224"
variation 1878
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201946473"
variation 1884
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:776080253"
variation 1895
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1013936522"
variation 1897
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:895444684"
variation 1899
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1036822687"
variation 1901
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:776677652"
variation 1907
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:575305190"
variation 1909
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1601032470"
variation 1912
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:939745689"
variation 1916
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978864996"
variation 1917
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978864870"
variation 1921
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978864658"
variation 1924
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1029154011"
variation 1926
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:770457160"
variation 1927..1930
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1978864131"
variation 1927
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:886636502"
variation 1931
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1370693078"
variation 1931
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:182250092"
variation 1936
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/db_xref="dbSNP:1690578737"
variation 1947
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace=""
/replace="a"
/db_xref="dbSNP:1282402326"
variation 1947
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231679449"
variation 1948
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1312327979"
variation 1949
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1214385614"
variation 1950
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978863470"
variation 1951
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:541812802"
variation 1956
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978863209"
variation 1957..1959
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="t"
/replace="tct"
/db_xref="dbSNP:1466167785"
variation 1960
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="g"
/db_xref="dbSNP:1049212286"
variation 1983
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978862813"
variation 1984
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:901945543"
variation 1986
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1452335500"
variation 1990
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978862406"
variation 1991
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978862280"
variation 1995
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:779787815"
variation 2002
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:2146513646"
variation 2003
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:2146513644"
variation 2004
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1342315228"
variation 2006
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978861877"
variation 2007
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1978861764"
variation 2009
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427457613"
variation 2010
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace=""
/replace="g"
/db_xref="dbSNP:1158424794"
variation 2010
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:569825465"
variation 2012
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1039229449"
variation 2013
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:542138581"
variation 2018
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1321778557"
variation 2020
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1978860946"
variation 2027..2034
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="aatg"
/replace="aatgaatg"
/db_xref="dbSNP:1335033571"
variation 2034
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:2146513610"
variation 2035
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:911882747"
variation 2036
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:2146513602"
variation 2041
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781459949"
variation 2043
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1978860479"
variation 2045
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1978860352"
variation 2046
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:13433507"
variation 2051
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1434750856"
variation 2053
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978860101"
variation 2054
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1404318867"
variation 2055
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="t"
/db_xref="dbSNP:1978859848"
variation 2056
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1978859744"
variation 2058
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:867745351"
regulatory 2063..2068
/regulatory_class="polyA_signal_sequence"
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/note="hexamer: AATAAA"
variation 2069
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="c"
/replace="t"
/db_xref="dbSNP:1276265891"
variation 2072
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176194947"
variation 2079
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:947291936"
variation 2083
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:1222740301"
variation 2084
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="a"
/replace="g"
/db_xref="dbSNP:956112679"
variation 2085
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:556041936"
variation 2089
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/replace="g"
/replace="t"
/db_xref="dbSNP:1426461889"
polyA_site 2092
/gene="CLDN8"
/gene_synonym="HEL-S-79"
/note="major polyA site"
ORIGIN
actggatactatctggccagaagtagcaaagcagctcttatttgaaaaaccactgggttccgagttcattactacaggaaaaactgttctcttctgtggcacagagaaccctgcttcaaagcagaagtagcagttccggagtccagctggctaaaactcatcccagaggataatggcaacccatgccttagaaatcgctgggctgtttcttggtggtgttggaatggtgggcacagtggctgtcactgtcatgcctcagtggagagtgtcggccttcattgaaaacaacatcgtggtttttgaaaacttctgggaaggactgtggatgaattgcgtgaggcaggctaacatcaggatgcagtgcaaaatctatgattccctgctggctctttctccggacctacaggcagccagaggactgatgtgtgctgcttccgtgatgtccttcttggctttcatgatggccatccttggcatgaaatgcaccaggtgcacgggggacaatgagaaggtgaaggctcacattctgctgacggctggaatcatcttcatcatcacgggcatggtggtgctcatccctgtgagctgggttgccaatgccatcatcagagatttctataactcaatagtgaatgttgcccaaaaacgtgagcttggagaagctctctacttaggatggaccacggcactggtgctgattgttggaggagctctgttctgctgcgttttttgttgcaacgaaaagagcagtagctacagatactcgataccttcccatcgcacaacccaaaaaagttatcacaccggaaagaagtcaccgagcgtctactccagaagtcagtatgtgtagttgtgtatgtttttttaactttactataaagccatgcaaatgacaaaaatctatattactttctcaaaatggaccccaaagaaactttgatttactgttcttaactgcctaatcttaattacaggaactgtgcatcagctatttatgattctataagctatttcagcagaatgagatattaaacccaatgctttgattgttctagaaagtatagtaatttgttttctaaggtggttcaagcatctactctttttatcatttacttcaaaatgacattgctaaagactgcattattttactactgtaatttctccacgacatagcattatgtacatagatgagtgtaacatttatatctcacatagagacatgcttatatggttttatttaaaatgaaatgccagtccattacactgaataaatagaactcaactattgcttttcagggaaatcatggatagggttgaagaaggttactattaattgtttaaaaacagcttagggattaatgtcctccatttataatgaagattaaaatgaaggctttaatcagcattgtaaaggaaattgaatggctttctgatatgctgttttttagcctaggagttagaaatcctaacttctttatcctcttctcccagaggctttttttttcttgtgtattaaattaacatttttaaaaagcagatattttgtcaaggggctttgcattcaaactgcttttccagggctatactcagaagaaagataaaagtgtgatctaagaaaaagtgatggttttaggaaagtgaaaatatttttgtttttgtatttgaagaagaatgatgcattttgacaagaaatcatatatgtatggatatattttaataagtatttgagtacagactttgaggtttcatcaatataaataaaagagcagaaaaatatgtcttggttttcatttgcttaccaaaaaaacaacaacaaaaaaagttgtcctttgagaacttcacctgctcctatgtgggtacctgagtcaaaattgtcatttttgttctgtgaaaaataaatttccttcttgtaccatttctgtttagttttactaaaatctgtaaatactgtatttttctgtttattccaaatttgatgaaactgacaatccaatttgaaagtttgtgtcgacgtctgtctagcttaaatgaatgtgttctatttgctttatacatttatattaataaattgtacatttttctaattatttga
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
[Full Text]