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Previous release (v1)
2024-04-20 10:59:29, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001378492 3486 bp mRNA linear PRI 22-SEP-2023 DEFINITION Homo sapiens claudin 16 (CLDN16), transcript variant 2, mRNA. ACCESSION NM_001378492 VERSION NM_001378492.1 KEYWORDS RefSeq. 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 3486) AUTHORS Malakoutian T, Madadi B and Saber S. TITLE A Novel Mutation in CLDN16 Gene Causing Familial Hypomagnesemia, Hypercalciuria, Nephrocalcinosis in An Iranian Family JOURNAL Iran J Kidney Dis 16 (3), 209-213 (2022) PUBMED 35714216 REMARK GeneRIF: A Novel Mutation in CLDN16 Gene Causing Familial Hypomagnesemia, Hypercalciuria, Nephrocalcinosis in An Iranian Family. REFERENCE 2 (bases 1 to 3486) AUTHORS Rouka E, Liakopoulos V, Gourgoulianis KI, Hatzoglou C and Zarogiannis SG. TITLE In-Depth Bioinformatic Study of the CLDN16 Gene and Protein: Prediction of Subcellular Localization to Mitochondria JOURNAL Medicina (Kaunas) 55 (8), 409 (2019) PUBMED 31357502 REMARK GeneRIF: To gain more understanding about the mechanisms by which CLDN16 mutations can induce FHHNC, we performed an in-depth computational analysis of the CLDN16 gene and protein, focusing specifically on the prediction of the latter's subcellular localization. Publication Status: Online-Only REFERENCE 3 (bases 1 to 3486) AUTHORS Perdomo-Ramirez A, Aguirre M, Davitaia T, Ariceta G, Ramos-Trujillo E and Claverie-Martin F. CONSRTM RenalTube Group TITLE Characterization of two novel mutations in the claudin-16 and claudin-19 genes that cause familial hypomagnesemia with hypercalciuria and nephrocalcinosis JOURNAL Gene 689, 227-234 (2019) PUBMED 30576809 REMARK GeneRIF: Results show that CLDN16 mutation c.602G>A had no effect on pre-mRNA splicing in familial hypomagnesemia with hypercalciuria and nephrocalcinosis. This study expands the genotypic classification of this rare disease and provides the first report of a CLDN19 mutation affecting splicing. REFERENCE 4 (bases 1 to 3486) AUTHORS Perdomo-Ramirez A, de Armas-Ortiz M, Ramos-Trujillo E, Suarez-Artiles L and Claverie-Martin F. TITLE Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations JOURNAL BMC Med Genet 20 (1), 6 (2019) PUBMED 30621608 REMARK GeneRIF: Mutations in CLDN16 that encodes claudin-16, a tight-junction protein involved in paracellular reabsorption of magnesium and calcium in the renal tubule. Publication Status: Online-Only REFERENCE 5 (bases 1 to 3486) AUTHORS Arcidiacono T, Simonini M, Lanzani C, Citterio L, Salvi E, Barlassina C, Spotti D, Cusi D, Manunta P and Vezzoli G. TITLE Claudin-14 Gene Polymorphisms and Urine Calcium Excretion JOURNAL Clin J Am Soc Nephrol 13 (10), 1542-1549 (2018) PUBMED 30232134 REMARK GeneRIF: No significant associations were found among claudin-16 and claudin-19 single-nucleotide polymorphisms and calcium excretion and between claudin-14, claudin-16, and claudin-19 single-nucleotide polymorphisms and stones. REFERENCE 6 (bases 1 to 3486) 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 7 (bases 1 to 3486) AUTHORS Weber S, Hoffmann K, Jeck N, Saar K, Boeswald M, Kuwertz-Broeking E, Meij II, Knoers NV, Cochat P, Sulakova T, Bonzel KE, Soergel M, Manz F, Schaerer K, Seyberth HW, Reis A and Konrad M. TITLE Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene JOURNAL Eur J Hum Genet 8 (6), 414-422 (2000) PUBMED 10878661 REFERENCE 8 (bases 1 to 3486) 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 3486) AUTHORS Simon DB, Lu Y, Choate KA, Velazquez H, Al-Sabban E, Praga M, Casari G, Bettinelli A, Colussi G, Rodriguez-Soriano J, McCredie D, Milford D, Sanjad S and Lifton RP. TITLE Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption JOURNAL Science 285 (5424), 103-106 (1999) PUBMED 10390358 REFERENCE 10 (bases 1 to 3486) AUTHORS Manz,F., Scharer,K., Janka,P. and Lombeck,J. TITLE Renal magnesium wasting, incomplete tubular acidosis, hypercalciuria and nephrocalcinosis in siblings JOURNAL Eur J Pediatr 128 (2), 67-79 (1978) PUBMED 668721 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AC080006.11 and AC009520.16. Summary: Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. It is found primarily in the kidneys, specifically in the thick ascending limb of Henle, where it acts as either an intercellular pore or ion concentration sensor to regulate the paracellular resorption of magnesium ions. Defects in this gene are a cause of primary hypomagnesemia, which is characterized by massive renal magnesium wasting with hypomagnesemia and hypercalciuria, resulting in nephrocalcinosis and renal failure. This gene and the CLDN1 gene are clustered on chromosome 3q28. [provided by RefSeq, Jun 2010]. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: SRR1163658.543679.1 [ECO:0000332] RNAseq introns :: partial sample support SAMEA1965299, SAMEA1966682 [ECO:0000350] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-231 AC080006.11 103833-104063 232-398 AC009520.16 19882-20048 399-507 AC009520.16 75882-75990 508-583 AC009520.16 79517-79592 584-790 AC009520.16 93226-93432 791-893 AC009520.16 107326-107428 894-1058 AC009520.16 109751-109915 1059-1250 AC009520.16 113303-113494 1251-3486 AC009520.16 114892-117127 FEATURES Location/Qualifiers source 1..3486 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="3" /map="3q28" gene 1..3486 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /note="claudin 16" /db_xref="GeneID:10686" /db_xref="HGNC:HGNC:2037" /db_xref="MIM:603959" exon 1..231 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /inference="alignment:Splign:2.1.0" variation 14 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:935391029" variation 19 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1716023026" variation 21 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1487832060" variation 23 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:9845911" variation 25 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1716023386" variation 28 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1348970264" variation 29 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1560068070" variation 32..35 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="aaa" /replace="aaaa" /db_xref="dbSNP:1212466900" variation 32 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:538425515" variation 33 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:893798471" variation 36 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:905320640" variation 38 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:2108594509" variation 41 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1294708631" variation 42 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:1716023838" variation 43 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1716023899" variation 45 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1560068076" variation 47 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1716024007" variation 54 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:2108594520" variation 56 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1236489579" variation 58 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1716024104" variation 59 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1716024156" variation 63 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1716024211" variation 68 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1211245606" variation 73 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1716024360" variation 74 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:558116212" variation 75 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1392131510" variation 78 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:2108594534" variation 79 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:1034168824" variation 86 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1716024568" variation 87 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1012231148" variation 88 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1461994295" variation 90 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:571668927" variation 97 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:1157027422" variation 101..102 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="t" /replace="tt" /db_xref="dbSNP:751155384" variation 104 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:1481815299" variation 109 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:960129619" variation 116 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:575060988" variation 119 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:1232914527" variation 121 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:1477671157" variation 122 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:1716025249" variation 123 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:534037059" variation 124 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:140853994" variation 125 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1716025455" variation 126 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1025729389" variation 132 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:573722463" variation 134 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1716025637" variation 135 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:967070087" variation 138..139 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="" /replace="ctaattcaaaaaaaa" /db_xref="dbSNP:1454539306" variation 138 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:1716025747" variation 141..142 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="" /replace="gg" /db_xref="dbSNP:1168251084" variation 143..150 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="aaaaaaa" /replace="aaaaaaaa" /replace="aaaaaaaaa" /db_xref="dbSNP:951674292" variation 143 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1716025920" variation 146 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:143076902" variation 150 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:78397525" variation 151 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:1411824187" variation 152 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:925608891" variation 154 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1373274847" variation 156 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1349317248" variation 157 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1716026482" variation 164 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:1434956642" variation 168 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1328515574" variation 172 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:963814481" variation 173 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:963727480" variation 177 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1372259423" variation 178 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:191970548" variation 182 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1433211144" variation 190 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1716026888" variation 193 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:975049653" variation 195 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:544344862" variation 196 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1456016083" variation 198 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:1240870556" variation 215 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1190322887" variation 217 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:564132719" variation 224 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1716027646" variation 230 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="" /replace="a" /db_xref="dbSNP:1560068111" exon 232..398 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /inference="alignment:Splign:2.1.0" variation 235 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:558419491" variation 247 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1716725364" variation 251 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:924871818" variation 253 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1485533531" variation 257 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1156599898" variation 259 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:1716725716" variation 268 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:577953502" variation 273 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1202639320" variation 276 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:900244147" variation 277 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1381875372" variation 283 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:1454507116" variation 284 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1716726304" variation 288 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1340794956" variation 291 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1279663008" variation 294 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:745484122" variation 298 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1172172719" variation 302 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1716726698" variation 310 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:57746373" variation 312 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1051897920" variation 317 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:1054728979" variation 320 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1716727033" variation 324 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1716727108" variation 327 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1716727187" variation 328 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:1416035350" variation 330 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:1394464778" variation 335 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:2108610579" variation 336 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:2108610583" variation 337 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1716727415" variation 338 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1577390112" variation 339 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:886706757" variation 340 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1577390119" variation 348 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:1577390123" variation 352 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1716727815" variation 354 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1716727889" variation 356 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:186334465" variation 358 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:1716728053" variation 361 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1005165832" variation 365 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1577390133" variation 373 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:573445801" variation 376 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:1716728396" variation 378 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1426100652" variation 380 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:1716728587" variation 382 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:190689655" variation 385 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:899213205" variation 390 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:758392821" variation 391 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1716728921" variation 393 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1716728997" variation 398 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1238339772" exon 399..507 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /inference="alignment:Splign:2.1.0" variation 399 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1718126081" variation 400 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1384248039" variation 403..404 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="tt" /replace="ttt" /db_xref="dbSNP:1404428245" variation 406 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:934159661" variation 408 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1718126290" variation 410 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1718126352" variation 411 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1047653867" variation 413 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:1718126434" variation 418 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1718126494" variation 420 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:751484225" variation 421 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1046208332" variation 425 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1173803435" variation 427 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1474178959" variation 429 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1308936510" variation 436 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:1005775848" variation 437 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1718126928" variation 438 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:564349242" variation 439 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1241076051" variation 440 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:2108647157" variation 444 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1718127032" variation 445 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:1718127086" variation 452 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:1718127143" variation 472 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:577049211" variation 473 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:545747527" variation 477 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:2108647168" variation 479 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:2108647171" variation 480 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:1269626680" variation 482 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1212880285" variation 487 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1718127483" variation 490 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1002320841" variation 494 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1271267543" variation 497 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1230293885" variation 500 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:1380949822" variation 506 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:918249540" variation 507 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1718127911" exon 508..583 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /inference="alignment:Splign:2.1.0" variation 510 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:1718208595" variation 511..521 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="tg" /replace="tgaactcgttg" /db_xref="dbSNP:1718208636" variation 518 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:571519012" variation 523 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1718208732" variation 526 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1019126167" variation 529 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:965754322" variation 531 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:527615251" variation 536 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:538626867" variation 538 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1718209317" variation 542 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:952314797" variation 544 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:756805072" variation 548 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1372215930" variation 554 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:547599368" variation 558 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1448013613" variation 559 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:915944062" variation 560 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:1274305968" variation 561 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:2108649376" misc_feature 563..565 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /note="upstream in-frame stop codon" variation 565 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:2108649378" variation 568 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1235702857" variation 570 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1371659538" variation 573 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:762574419" variation 574 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1577415037" variation 577 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:1373538182" variation 579 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1718210057" variation 582 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1332957276" variation 583 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1045709310" exon 584..790 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /inference="alignment:Splign:2.1.0" variation 584 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1388166379" variation 585 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:767080609" variation 587 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1375482100" variation 593 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:752540574" variation 595 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:756048104" variation 606 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:1577421257" variation 607 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1339149925" variation 608 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:777620076" variation 609 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:749083950" variation 610 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:757186184" variation 611 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:200400125" variation 612 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:558573665" variation 614 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1390469433" variation 615 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1458256618" variation 616 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1718556761" variation 619 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:747245603" variation 622 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:768569589" variation 624 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:781362926" variation 627..628 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="cc" /replace="ccc" /db_xref="dbSNP:553547888" variation 627 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1006196806" variation 627 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="tcttccgatct" /db_xref="dbSNP:1553807669" variation 628 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1560093790" variation 630..632 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="" /replace="ggg" /db_xref="dbSNP:760754693" variation 630..632 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="gg" /replace="ggg" /replace="gggg" /db_xref="dbSNP:368234054" variation 630 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:201380153" variation 631..632 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="gg" /db_xref="dbSNP:386669518" variation 631 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:748213791" variation 632..633 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="" /replace="ac" /db_xref="dbSNP:763695473" variation 632 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:3214506" variation 634 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1718558327" variation 635 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:773763573" variation 636 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:149955797" variation 637 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1718558651" variation 639 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:771301899" variation 640..641 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="" /replace="agga" /db_xref="dbSNP:1718558849" variation 642 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:773947198" variation 644 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="gatct" /db_xref="dbSNP:866648881" variation 645 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:1718559086" variation 648 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:759268862" variation 651 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:767846686" variation 652 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:767119879" variation 653 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1277041944" variation 654 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:752230428" variation 656 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:760160835" variation 657 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:2108658208" variation 658..659 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="" /replace="tg" /db_xref="dbSNP:865841365" variation 658 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:2108658210" variation 659 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1210662953" variation 660 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:764125350" variation 661 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1718560730" variation 665 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:753832878" variation 667 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1277797748" variation 674 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1321220823" CDS 677..1384 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /note="paracellin-1; hypomagnesemia 3, with hypercalciuria and nephrocalcinosis" /codon_start=1 /product="claudin-16" /protein_id="NP_001365421.1" /db_xref="CCDS:CCDS3296.2" /db_xref="GeneID:10686" /db_xref="HGNC:HGNC:2037" /db_xref="MIM:603959" /translation="
MRDLLQYIACFFAFFSAGFLIVATWTDCWMVNADDSLEVSTKCRGLWWECVTNAFDGIRTCDEYDSILAEHPLKLVVTRALMITADILAGFGFLTLLLGLDCVKFLPDEPYIKVRICFVAGATLLIAGTPGIIGSVWYAVDVYVERSTLVLHNIFLGIQYKFGWSCWLGMAGSLGCFLAGAVLTCCLYLFKDVGPERNYPYSLRKAYSAAGVSMAKSYSAPRTETAKMYAVDTRV"
misc_feature 686..748
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/note="propagated from UniProtKB/Swiss-Prot (Q9Y5I7.2);
transmembrane region"
misc_feature 707..1225
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/note="PMP-22/EMP/MP20/Claudin family; Region:
PMP22_Claudin; cl21598"
/db_xref="CDD:451326"
misc_feature 914..976
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/note="propagated from UniProtKB/Swiss-Prot (Q9Y5I7.2);
transmembrane region"
misc_feature 1022..1084
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/note="propagated from UniProtKB/Swiss-Prot (Q9Y5I7.2);
transmembrane region"
misc_feature 1184..1246
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/note="propagated from UniProtKB/Swiss-Prot (Q9Y5I7.2);
transmembrane region"
variation 677
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318788506"
variation 678
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:104893724"
variation 679
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1718561243"
variation 680
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:372525072"
variation 685
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482253091"
variation 686
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1199775812"
variation 689
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:199839143"
variation 691
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1718561810"
variation 693
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:867514971"
variation 695
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375640819"
variation 696
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368215264"
variation 697
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428685975"
variation 698
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:145118503"
variation 700
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372129081"
variation 701
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:965435011"
variation 703
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1718562646"
variation 704
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769827846"
variation 705
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:778198632"
variation 706..711
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ctt"
/replace="cttctt"
/db_xref="dbSNP:866440005"
variation 707
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:749819466"
variation 708
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1297905947"
variation 709
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1362947273"
variation 712..726
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tgc"
/replace="tgcctttttctctgc"
/db_xref="dbSNP:1560093930"
variation 713
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:977137021"
variation 714
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1020861027"
variation 721
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:149116671"
variation 723
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1718563800"
variation 727
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:967573821"
variation 729
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1181105329"
variation 730
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:774670118"
variation 736
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:759868163"
variation 738
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:771742472"
variation 740
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2108658311"
variation 743
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1293775732"
variation 751..752
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="caatgtgaaaat"
/db_xref="dbSNP:1718564412"
variation 752
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1254188095"
variation 754
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1718564576"
variation 756
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1718564664"
variation 757
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:775073665"
variation 763
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1064795763"
variation 764
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:545693736"
variation 772
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1718565564"
variation 775
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201545856"
variation 776
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:753777323"
variation 777
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108658338"
variation 779
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108658339"
variation 782
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:761873372"
variation 784
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765304853"
variation 785
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1560093977"
variation 786
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268061294"
exon 791..893
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/inference="alignment:Splign:2.1.0"
variation 791
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1278876951"
variation 792
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190419654"
variation 793
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:528344809"
variation 795
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:142152395"
variation 796
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1264612767"
variation 798
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:764353770"
variation 802
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1321219881"
variation 806
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:753901053"
variation 807
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:757395583"
variation 808
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274557149"
variation 811
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1219996621"
variation 812
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1718984196"
variation 813
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108670592"
variation 814
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1718984264"
variation 815
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:146727044"
variation 816
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:104893732"
variation 824
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1430185772"
variation 825
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149965853"
variation 826
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:370592530"
variation 827
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:920823997"
variation 832
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:573024259"
variation 836
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:758739389"
variation 837
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:61752083"
variation 838
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:780312463"
variation 839
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:747440607"
variation 841
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:144105475"
variation 844
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1055737562"
variation 845
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:747654138"
variation 847
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:56147287"
variation 850
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:773141087"
variation 851
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444245867"
variation 852
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:762831659"
variation 853
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:766383362"
variation 860
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1233586538"
variation 862
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1294742863"
variation 863
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773999256"
variation 864
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:759388455"
variation 865
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577429403"
variation 868
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199651054"
variation 869
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:761824865"
variation 870
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1208605810"
variation 871
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:950141430"
variation 877
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1257324344"
variation 878
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1474818508"
variation 881
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1718986912"
variation 882
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:765256758"
variation 883
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:137882210"
variation 886
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:758799163"
variation 889
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1718987282"
variation 891
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1477588982"
variation 892
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1718987423"
exon 894..1058
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/inference="alignment:Splign:2.1.0"
variation 895
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:778765191"
variation 899
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719048031"
variation 900
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:104893731"
variation 901..914
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="ggtggtaactcgag"
/db_xref="dbSNP:1719048217"
variation 906
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1350393472"
variation 908
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:771816868"
variation 910
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:775232251"
variation 911
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:104893720"
variation 912
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:968906940"
variation 915
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769893284"
variation 916
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:373411163"
variation 918
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:104893730"
variation 919
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:104893729"
variation 921
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1195405538"
variation 923
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:774947384"
variation 924
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1452788815"
variation 927
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1158867345"
variation 930
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1386707552"
variation 933
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719050267"
variation 935
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403200551"
variation 936
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:911369572"
variation 937
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1371063500"
variation 940
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:760090790"
variation 941
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:527990106"
variation 945
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1577430719"
variation 950
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1335620169"
variation 952
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:753102053"
variation 954
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1326395870"
variation 957
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="ttggt"
/db_xref="dbSNP:1719051110"
variation 958
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:756572012"
variation 961
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354548248"
variation 962
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719051321"
variation 963
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:763587706"
variation 964
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1311824206"
variation 966
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:104893725"
variation 970
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:753542626"
variation 972
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1273948471"
variation 974
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1469870064"
variation 975
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:756674166"
variation 977
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:944275084"
variation 981
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719052138"
variation 982
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:547537371"
variation 983
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419689384"
variation 988
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719052386"
variation 989
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719052466"
variation 992
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:778427772"
variation 995
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719052758"
variation 996
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719052840"
variation 1000
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:745420355"
variation 1005
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140829596"
variation 1006
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:898316282"
variation 1007
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:567783618"
variation 1009
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:746772676"
variation 1010..1014
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="attaa"
/replace="attaattaa"
/db_xref="dbSNP:1253995767"
variation 1010
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462564694"
variation 1012
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1275570743"
variation 1013
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376431300"
variation 1014
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370413403"
variation 1017
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:536714046"
variation 1018
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1308642000"
variation 1019
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:929948127"
variation 1020
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:556413628"
variation 1021
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:759749571"
variation 1024
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:768135151"
variation 1025
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316949011"
variation 1027
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719054426"
variation 1031
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719054513"
variation 1034
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1216704349"
variation 1037
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:104893722"
variation 1040
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108673379"
variation 1042
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:150478692"
variation 1043
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1048501191"
variation 1044
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1480328199"
variation 1045
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719055043"
variation 1048
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:760895186"
variation 1049
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:764545067"
variation 1050..1054
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="taata"
/replace="taataata"
/db_xref="dbSNP:1560098734"
variation 1050
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1007522348"
variation 1053
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719055460"
variation 1054
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373189371"
variation 1057
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:753395110"
variation 1058
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1577430815"
exon 1059..1250
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/inference="alignment:Splign:2.1.0"
variation 1059
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:104893723"
variation 1062..1065
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1258535403"
variation 1062
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1202664145"
variation 1063
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1486834780"
variation 1068
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:138308105"
variation 1074
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261570205"
variation 1078
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:762220084"
variation 1080
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:570616277"
variation 1084
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149645885"
variation 1085
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:765895243"
variation 1089
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:544158479"
variation 1091
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1270704258"
variation 1094
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1376923358"
variation 1097
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719158559"
variation 1099
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:754911596"
variation 1102
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:781052097"
variation 1104
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:752533102"
variation 1106
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:753223645"
variation 1109
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371258878"
variation 1112
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:758946923"
variation 1113
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:772241737"
variation 1114
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1336299188"
variation 1117
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719159332"
variation 1118
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:780153615"
variation 1119
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1281243864"
variation 1123
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1453710173"
variation 1125
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1302134732"
variation 1128
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1408388959"
variation 1129
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1577432849"
variation 1130
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1329454729"
variation 1134
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201367228"
variation 1135
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719160156"
variation 1136
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:769190460"
variation 1138
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1260497925"
variation 1142
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1170178042"
variation 1143..1144
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1553809654"
variation 1146
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719160566"
variation 1148
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719160649"
variation 1150
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719160734"
variation 1153
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:532245223"
variation 1154
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298030528"
variation 1161
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:104893726"
variation 1163
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1577432872"
variation 1164
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:104893727"
variation 1165
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:762095241"
variation 1167
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1182563283"
variation 1170
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:104893728"
variation 1176
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1453219704"
variation 1178
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:543523352"
variation 1180
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772803074"
variation 1181
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:104893721"
variation 1182
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719162432"
variation 1191
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:751056950"
variation 1193
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1577432896"
variation 1194
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345543207"
variation 1195
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:368589513"
variation 1198
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:767423701"
variation 1201
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1053422587"
variation 1205..1209
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1273573190"
variation 1208
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143316426"
variation 1209
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:777745636"
variation 1211
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719163555"
variation 1215
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:139251569"
variation 1220
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201641346"
variation 1221
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719163916"
variation 1222
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:758673667"
variation 1227
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:780195981"
variation 1228
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1314203005"
variation 1229
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1317860117"
variation 1231
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719164345"
variation 1237
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:747105311"
variation 1238
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143097871"
variation 1239
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1312786315"
variation 1240
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719164774"
variation 1241
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1035298979"
variation 1245
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:781678462"
variation 1248
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1210040068"
exon 1251..3486
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/inference="alignment:Splign:2.1.0"
variation 1252
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:766553260"
variation 1254
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1416877202"
variation 1257
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:751740742"
variation 1258
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719228059"
variation 1260
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:755033066"
variation 1261
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:781161632"
variation 1264
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748266585"
variation 1266
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="g"
/db_xref="dbSNP:1577434022"
variation 1266
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:756589441"
variation 1272
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719228589"
variation 1277
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1404996591"
variation 1279
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355259272"
variation 1281
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1411885209"
variation 1287
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1641467526"
variation 1289
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:387906880"
variation 1292
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:539967883"
variation 1293
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1415814850"
variation 1296
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:35041121"
variation 1297
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:121908543"
variation 1299
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1338030534"
variation 1302
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:139846352"
variation 1303
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:745542693"
variation 1304
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:549642537"
variation 1305
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719230472"
variation 1306
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:775121017"
variation 1310
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:760321632"
variation 1311
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:764121096"
variation 1314..1315
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2108521351"
variation 1314
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:776710987"
variation 1315
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:761606829"
variation 1316
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1475042783"
variation 1331
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:764960055"
variation 1335
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371465699"
variation 1337
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1560100409"
variation 1338
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:141823638"
variation 1340
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200023201"
variation 1341
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:752758478"
variation 1344
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719231870"
variation 1346
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:756192568"
variation 1347
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1193820441"
variation 1348
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434084"
variation 1350
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374751726"
variation 1351
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1325118362"
variation 1352
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:749782586"
variation 1354
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482633360"
variation 1355..1358
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:755344639"
variation 1355
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1276759277"
variation 1356
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1366697751"
variation 1359
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231476372"
variation 1363
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:757602181"
variation 1364
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150621351"
variation 1366
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1201892517"
variation 1369
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719233474"
variation 1373
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:746297543"
variation 1374
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:121908542"
variation 1375
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:771613047"
variation 1377
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1193773094"
variation 1378
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719234034"
variation 1379
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1249854366"
variation 1381
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:779922888"
variation 1383
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719234295"
variation 1384
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1191842560"
variation 1387
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:746450356"
variation 1389
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719234541"
variation 1391
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1466740266"
variation 1392
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:768292566"
variation 1393
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1368443391"
variation 1394
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108521448"
variation 1396..1438
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ca"
/replace="cagggtgtgtttgcatatgatttaatcaatcagtatggttaca"
/db_xref="dbSNP:1189438200"
variation 1396
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:776656418"
variation 1397
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756756376"
variation 1398
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:772860827"
variation 1399
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2108521458"
variation 1400
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:368827991"
variation 1401
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1162057598"
variation 1403
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:752931762"
variation 1409
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:993342773"
variation 1410
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331896797"
variation 1411
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719235955"
variation 1416
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719236025"
variation 1419
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108521476"
variation 1420
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302060265"
variation 1421
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719236167"
variation 1424
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1179623863"
variation 1425..1429
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tcagt"
/db_xref="dbSNP:1719236391"
variation 1425
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482602961"
variation 1426
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252342533"
variation 1430
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1207049107"
variation 1435
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372140161"
variation 1437
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1289465976"
variation 1439
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210456095"
variation 1442..1449
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ata"
/replace="ataaaata"
/db_xref="dbSNP:1719236908"
variation 1444
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1358627083"
variation 1449..1455
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="agt"
/replace="agtaagt"
/db_xref="dbSNP:1278266886"
variation 1450
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1364319377"
variation 1457
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434165"
variation 1458
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:886058245"
variation 1459
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1719237393"
variation 1460
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1351477777"
variation 1462
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719237542"
variation 1464
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1290535138"
variation 1465
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719237845"
variation 1466
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719237920"
variation 1468
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719237992"
variation 1470
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719238060"
variation 1472
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1432770137"
variation 1473
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719238933"
variation 1476
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1347716809"
variation 1477
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1322503307"
variation 1482
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719239131"
variation 1483
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1405410283"
variation 1486
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1392338624"
variation 1487
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:766995290"
variation 1489..1499
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aattaaattaa"
/replace="aattaaattaaattaa"
/db_xref="dbSNP:1719239415"
variation 1498
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:892300472"
variation 1500
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1412623271"
variation 1502
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="g"
/db_xref="dbSNP:1184028451"
variation 1502
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1476930089"
variation 1503
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243512298"
variation 1505
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010771548"
variation 1506
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719239926"
variation 1507
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719239992"
variation 1514
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719240061"
variation 1524
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:868026523"
variation 1527
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719240224"
variation 1530
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719240296"
variation 1536..1540
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1719240361"
variation 1538..1546
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tttct"
/replace="tttctttct"
/db_xref="dbSNP:1358040277"
variation 1541
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210770141"
variation 1542
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1453400955"
variation 1543
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1282323481"
variation 1545
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1267864594"
variation 1547
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1463863570"
variation 1548
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719240902"
variation 1549
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1208201800"
variation 1550
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1191046955"
variation 1554
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:984582606"
variation 1556
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330345743"
variation 1557
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1270611227"
variation 1558
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719241349"
variation 1559
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1249265644"
variation 1564
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2108521603"
variation 1565
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145675747"
variation 1566
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:571524553"
variation 1572
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108521613"
variation 1576
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:969808380"
variation 1577
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719241796"
variation 1581
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:755751630"
variation 1583
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1034332544"
variation 1584
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:960031461"
variation 1587
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719242146"
variation 1588
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:73053979"
variation 1589
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149191729"
variation 1593
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1158756925"
variation 1595
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161343286"
variation 1596
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1412515275"
variation 1597
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424286620"
variation 1598
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719242608"
variation 1599
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1387607568"
variation 1601
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719242760"
variation 1603
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1479096605"
variation 1607..1609
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1719242896"
variation 1611
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1455495704"
variation 1617
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1246433837"
variation 1619
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719243230"
variation 1621
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:191200989"
variation 1623
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719243389"
variation 1624
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:865808205"
variation 1627
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:142380851"
variation 1633
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:886058246"
variation 1634
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719243762"
variation 1636
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="t"
/db_xref="dbSNP:1719243840"
variation 1639
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465420183"
variation 1643
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1250425802"
variation 1645
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719244329"
variation 1647
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1202399429"
variation 1653
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1311958057"
variation 1658
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1279706403"
variation 1662
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1221295875"
variation 1664
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:962606383"
variation 1666
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719244830"
variation 1667
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1341791237"
variation 1669
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1294973811"
variation 1675
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719245015"
variation 1676
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1577434287"
variation 1682
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1433682157"
variation 1683
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:181803078"
variation 1684
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1287399767"
variation 1685
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719245583"
variation 1686
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108521724"
variation 1687
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:973593024"
variation 1689
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719245732"
variation 1692
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176441679"
variation 1693
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719245874"
variation 1704
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:947362511"
variation 1705
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1577434299"
variation 1706
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1049720745"
variation 1709
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1168253607"
variation 1710
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450160660"
variation 1716
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386093996"
variation 1720
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719246241"
variation 1722
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719246309"
variation 1723
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1392162749"
variation 1725
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1180204001"
variation 1726
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719246517"
variation 1728
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719246577"
variation 1730
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2108521763"
variation 1732
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434306"
variation 1734
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719246700"
variation 1737
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1483169407"
variation 1740
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="a"
/db_xref="dbSNP:1269257985"
variation 1740
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719246844"
variation 1741
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1483222776"
variation 1742
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434314"
variation 1744
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212626622"
variation 1747
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719247239"
variation 1749
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:889886848"
variation 1757
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1482306246"
variation 1758
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108521787"
variation 1761
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2108521790"
variation 1762
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1272000961"
variation 1763
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1227301370"
variation 1767
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:575561257"
variation 1771
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1198760198"
variation 1773
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719247693"
variation 1784
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1299106403"
variation 1788
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719247843"
variation 1793..1794
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1719247993"
variation 1793
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719247912"
variation 1794
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:931732278"
variation 1795
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719248252"
variation 1801
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303384959"
variation 1804
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719248349"
variation 1808
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719248428"
variation 1809
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1449930758"
variation 1814
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:544538250"
variation 1818..1820
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="gtg"
/db_xref="dbSNP:1719248608"
variation 1826
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:557949152"
variation 1831
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1430576814"
variation 1835
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719248855"
variation 1844
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:911549923"
variation 1845
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:944354002"
variation 1848
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2068245906"
variation 1849
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1423343452"
variation 1850
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1415128978"
variation 1854
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199716341"
variation 1855
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719249316"
variation 1862
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719249376"
variation 1873
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1052521743"
variation 1875
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1251623797"
variation 1876
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108521867"
variation 1877
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719249633"
variation 1879
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:901678187"
variation 1884
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719249804"
variation 1887
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:946605671"
variation 1888
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043568318"
variation 1889
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:993416555"
variation 1890
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1026173159"
variation 1905
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1577434359"
variation 1907
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719250303"
variation 1908
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108521890"
variation 1909
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:905013137"
variation 1912
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434366"
variation 1913
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:887482525"
variation 1914
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1001578693"
variation 1917
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471447498"
variation 1918
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719250798"
variation 1919
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434377"
variation 1923
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719250928"
variation 1924..1929
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aac"
/replace="aacaac"
/db_xref="dbSNP:778070121"
variation 1925
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:186108585"
variation 1928
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1577434385"
variation 1932
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006316565"
variation 1933
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434393"
variation 1937
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:540301575"
variation 1938
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719251449"
variation 1939
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719251521"
variation 1946
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1372588646"
variation 1947
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:970217940"
variation 1950
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345662272"
variation 1952
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719251933"
variation 1965
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:981206118"
variation 1970
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:560036875"
variation 1971..1977
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="cccccc"
/replace="ccccccc"
/replace="cccccccc"
/db_xref="dbSNP:895882395"
variation 1971
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411881940"
variation 1972
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:956173827"
variation 1973
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719253034"
variation 1974
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:115611104"
variation 1975
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:542212640"
variation 1976
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:953486547"
variation 1977
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749108552"
variation 1978
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1719253479"
variation 1979..1983
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:758965630"
variation 1980
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:911677788"
variation 1982
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1326939252"
variation 1988
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719253755"
variation 1997
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1348257306"
variation 1999
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1230569810"
variation 2000
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719253988"
variation 2007
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719254080"
variation 2011..2036
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tac"
/replace="tactggagctcgtggtgactttctac"
/db_xref="dbSNP:1719254164"
variation 2012
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:966182367"
variation 2015
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1228755363"
variation 2016
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719254374"
variation 2017
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2108521997"
variation 2018
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:985868711"
variation 2020
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1299459579"
variation 2023
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719254548"
variation 2028
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:911192374"
variation 2029
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="c"
/db_xref="dbSNP:779878146"
variation 2029
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1289408389"
variation 2033
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719254812"
variation 2034
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1312017393"
variation 2035
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719254957"
variation 2041
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:987846768"
variation 2044
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719255101"
variation 2054
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112253194"
variation 2057
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522028"
variation 2063
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1433028193"
variation 2069
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1258346631"
variation 2070
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1560100716"
variation 2071
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1388491456"
variation 2075
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483616922"
variation 2078
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1204525682"
variation 2081
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:754896663"
variation 2090
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1376354921"
variation 2091
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719255794"
variation 2092
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719255858"
variation 2094
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:531851017"
variation 2101
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1249814822"
variation 2102
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1484170679"
variation 2104
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1577434483"
variation 2106
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719256310"
variation 2107
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1267646593"
variation 2108
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:886058247"
variation 2109
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1184029948"
variation 2113
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463199087"
variation 2119
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719256645"
variation 2120
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1560100743"
variation 2122
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:778985429"
variation 2127
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:946655268"
variation 2129
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352554358"
variation 2140
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043586027"
variation 2142
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719257142"
variation 2144
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719257210"
variation 2145
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:886058248"
variation 2149
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:551693948"
variation 2150
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719257411"
variation 2152
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="g"
/db_xref="dbSNP:886058249"
variation 2153
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719257555"
variation 2158
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1312954012"
variation 2167
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719257660"
variation 2173
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:901710762"
variation 2175
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719257792"
variation 2178
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2293532"
variation 2179
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719258031"
variation 2180
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1432968420"
variation 2181
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719258194"
variation 2185
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719258283"
variation 2187
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1364604379"
variation 2189
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719258443"
variation 2190
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719258497"
variation 2193
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:558543277"
variation 2195
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719258617"
variation 2197
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432445325"
variation 2198
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719258788"
variation 2200
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:937883108"
variation 2203
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1379307938"
variation 2206
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1384483860"
variation 2207
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:771018706"
variation 2213
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400692450"
variation 2214
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1047528788"
variation 2217
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719259307"
variation 2219
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1434739508"
variation 2220
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:377075907"
variation 2222
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1006101929"
variation 2226
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:77656241"
variation 2232
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:746066027"
variation 2233
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719259819"
variation 2236..2237
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1719259880"
variation 2237
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:895925213"
variation 2238
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1175169218"
variation 2246
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719260112"
variation 2252
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1447125696"
variation 2255
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:769934589"
variation 2270
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1188654028"
variation 2273
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1448597711"
variation 2274
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719261472"
variation 2275
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719261560"
variation 2282
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719265975"
variation 2285
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:879005444"
variation 2288
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719266118"
variation 2291
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:116488781"
variation 2294
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719266321"
variation 2296
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1199615871"
variation 2297
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1035424989"
variation 2302
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1282707603"
variation 2303
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:955745713"
variation 2304
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108522215"
variation 2307
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719266744"
variation 2309
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1411238482"
variation 2313..2318
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aaaaaa"
/replace="aaaaaaa"
/db_xref="dbSNP:1719266918"
variation 2320
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719266981"
variation 2323
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1298437823"
variation 2324
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367325239"
variation 2326
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719267223"
variation 2328
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010428271"
variation 2329
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1021763433"
variation 2332
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:763316001"
variation 2333
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339171481"
variation 2338
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:969384621"
variation 2339
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1272611410"
variation 2342
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719267913"
variation 2345
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="t"
/db_xref="dbSNP:1719267980"
variation 2346
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1344473010"
variation 2348
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1314315969"
variation 2349
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:769075597"
variation 2352
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719268328"
variation 2358
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1246414280"
variation 2361
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:953602137"
variation 2362
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:911254109"
variation 2364
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1577434607"
variation 2365
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007768932"
variation 2368
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1577434614"
variation 2372
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719268901"
variation 2373
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1019510874"
variation 2377
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1189267271"
variation 2380
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719269169"
variation 2381
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259425513"
variation 2382
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:774827215"
variation 2385
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1269320130"
variation 2392
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1454682905"
variation 2393
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1275645982"
variation 2394
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:965848414"
variation 2395
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:965390858"
variation 2396
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719270203"
variation 2400
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:567611922"
variation 2401
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719270436"
variation 2403
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719270504"
variation 2405
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:536751926"
variation 2406
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:556567304"
variation 2407
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1286773850"
variation 2409
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719270879"
variation 2411
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:976835789"
variation 2412
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:767025229"
variation 2414
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1431161797"
variation 2415..2438
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="cctg"
/replace="cctggctaacatggtgaaaccctg"
/db_xref="dbSNP:1719271312"
variation 2415
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:930021289"
variation 2416
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1047559982"
variation 2418
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719271868"
variation 2420..2421
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="ct"
/db_xref="dbSNP:1719271952"
variation 2421
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1388038369"
variation 2426
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:909037215"
variation 2429
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:967655512"
variation 2430
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:979061004"
variation 2431
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:941979192"
variation 2433
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1577434658"
variation 2434
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1179683712"
variation 2435
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252767381"
variation 2437
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="t"
/db_xref="dbSNP:1184329836"
variation 2437
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044300619"
variation 2439
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1259042040"
variation 2441
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719272892"
variation 2442
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:937912506"
variation 2451
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201642794"
variation 2455
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719273124"
variation 2458
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1266809940"
variation 2459..2462
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="atta"
/replace="attatta"
/db_xref="dbSNP:1337535456"
variation 2465
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:570080234"
variation 2466
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330293904"
variation 2470
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1279769818"
variation 2471
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:992035157"
variation 2472
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719273726"
variation 2473
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:905554893"
variation 2477
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1002552972"
variation 2478
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056795067"
variation 2481
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1441027710"
variation 2485
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1396564635"
variation 2488
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719274941"
variation 2491
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:375704078"
variation 2494
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1156902117"
variation 2495
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522380"
variation 2497
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719275268"
variation 2499
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719275351"
variation 2500
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719275437"
variation 2501
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:10470534"
variation 2504
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1289358804"
variation 2506
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1408513000"
variation 2507
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1160098826"
variation 2511
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434721"
variation 2515
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719276337"
variation 2519
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1477124170"
variation 2521
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719276491"
variation 2522
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719276557"
variation 2523
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1009956782"
variation 2524..2526
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:1719276818"
variation 2524
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1577434726"
variation 2525
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719276917"
variation 2529
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1022246328"
variation 2530
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:968913173"
variation 2532
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719277087"
variation 2533
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719277169"
variation 2538..2540
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="gtg"
/db_xref="dbSNP:1719277240"
variation 2539
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:558111287"
variation 2540
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719277419"
variation 2541
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719277493"
variation 2544
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:577763881"
variation 2545
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:950181288"
variation 2546
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1217842329"
variation 2550
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1342372385"
variation 2551
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719278006"
variation 2553
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1007578934"
variation 2554
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:886058250"
variation 2555
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:760316748"
variation 2556
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1018517588"
variation 2560
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318443756"
variation 2562
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:533709248"
variation 2563
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:765950941"
variation 2565
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1319993573"
variation 2569
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522470"
variation 2571
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1450715663"
variation 2573
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719278900"
variation 2578
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1424698372"
variation 2579
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719279028"
variation 2580
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1577434770"
variation 2581
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1186606932"
variation 2585
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:190527986"
variation 2586
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108522482"
variation 2593
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:140801126"
variation 2594
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:889392676"
variation 2596
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1560100924"
variation 2597
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719279680"
variation 2598
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007799900"
variation 2603
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1019124017"
variation 2604
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1577434786"
variation 2605
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1208428510"
variation 2607
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1442242355"
variation 2608
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1277470359"
variation 2611
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:879585750"
variation 2616..2636
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aaataaataaataaata"
/replace="aaataaataaataaataaata"
/replace="aaataaataaataaataaataaata"
/db_xref="dbSNP:901970657"
variation 2618
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:144651280"
variation 2626
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719280534"
variation 2629
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:984165827"
variation 2632
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:183599112"
variation 2636
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719280819"
variation 2640
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1457107753"
variation 2642
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:909061450"
variation 2650
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021159365"
variation 2651
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719281137"
variation 2653
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1271908394"
variation 2654
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1445499496"
variation 2658
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:967771615"
variation 2659
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:188089990"
variation 2660
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1033294124"
variation 2663
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1368957747"
variation 2667
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1167998468"
variation 2668
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:959296706"
variation 2669
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:372146584"
variation 2678
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1422227758"
variation 2681
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1180691398"
variation 2682
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1044594052"
variation 2687
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719282071"
variation 2688
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:927251239"
variation 2690
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771484743"
variation 2691
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1258586230"
variation 2696
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213470685"
variation 2697
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:565421878"
variation 2699
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:891461218"
variation 2702
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272070280"
variation 2713
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203182396"
variation 2716
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522562"
variation 2717
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:886058251"
variation 2718..2719
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1719282840"
variation 2720
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:939815267"
variation 2721
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1226594338"
variation 2723
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719283037"
variation 2729
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378370140"
variation 2730
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719283160"
variation 2732
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:753612393"
variation 2733
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416428859"
variation 2736
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719283488"
variation 2740..2746
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tttt"
/replace="tttttt"
/replace="ttttttt"
/db_xref="dbSNP:1719283630"
variation 2740
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1230219728"
variation 2748
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1348808536"
variation 2750
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1294194615"
variation 2755
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:545295861"
variation 2756
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:919380095"
variation 2759
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719284042"
variation 2761
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:886058252"
variation 2762
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719284172"
variation 2763
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:565280429"
variation 2774
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719284318"
variation 2789
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719284402"
variation 2790
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719284469"
variation 2791
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1356410000"
variation 2797
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1042795499"
variation 2798
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1162783200"
variation 2800
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1405218490"
variation 2803
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335227985"
variation 2804..2811
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="gtca"
/replace="gtcagtca"
/db_xref="dbSNP:1719284944"
variation 2808
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719285018"
variation 2811
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:191406701"
variation 2812
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049117498"
variation 2816
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1577434877"
variation 2821
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:778897400"
variation 2823
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007074574"
variation 2824
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176333881"
variation 2829
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522630"
variation 2831..2833
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:2108522632"
variation 2834
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1480667202"
variation 2835
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1560101014"
variation 2836
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108522638"
variation 2837
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:13076274"
variation 2840..2842
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1719286019"
variation 2847
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:901439215"
variation 2850..2885
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="acctgaaaagaatatcaac"
/replace="acctgaaaagaatatcaacctgaaaagaatatcaac"
/replace="acctgaaaagaatatcaacctgaaaagaatatcaacctgaaaagaata
tcaac"
/db_xref="dbSNP:372414927"
variation 2851
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:902087850"
variation 2861
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:998383710"
variation 2870
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025637829"
variation 2874
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1287946981"
variation 2875
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:113286536"
variation 2876
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719286719"
variation 2877
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1375804964"
variation 2881
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719286861"
variation 2884
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719286927"
variation 2892
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="a"
/db_xref="dbSNP:1291816668"
variation 2900
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1000542507"
variation 2902
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522673"
variation 2903
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:984647483"
variation 2904
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2108522683"
variation 2906
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1157436007"
variation 2908..2915
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/replace="aaaaaaaaa"
/db_xref="dbSNP:958990554"
variation 2914
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419235717"
variation 2915
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719287507"
variation 2916
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719287573"
variation 2919
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719287626"
variation 2925
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:530102213"
variation 2936
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:577574442"
variation 2937
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1660340440"
variation 2940
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719287923"
variation 2942
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334144623"
variation 2943
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:886058253"
variation 2949
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108522725"
variation 2953..2956
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="gt"
/replace="gtgt"
/db_xref="dbSNP:1719288240"
variation 2953
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1467681744"
variation 2955
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1686386626"
variation 2957
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719288317"
variation 2961
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1253540410"
variation 2963
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719288463"
variation 2964
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719288544"
variation 2965
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719288620"
variation 2971
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1215543100"
variation 2975
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719288753"
variation 2976
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463498861"
variation 2980
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719288905"
variation 2981
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:961315668"
variation 2982
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719289054"
variation 2993
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719289131"
variation 2995
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719289198"
variation 3003
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:979977937"
variation 3006
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:537088739"
variation 3007
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719289436"
variation 3010
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1350111456"
variation 3011
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108522765"
variation 3012
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522766"
variation 3019
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:781286477"
variation 3020
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719289649"
variation 3021
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1371905149"
variation 3026
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1328502693"
variation 3028
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108522779"
variation 3032
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719289864"
variation 3033
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719289945"
variation 3038
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:927083429"
variation 3043
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719290052"
variation 3048
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:938608167"
variation 3050
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:919743196"
variation 3059
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719290314"
variation 3059
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tcat"
/db_xref="dbSNP:1719290376"
variation 3061
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719290455"
variation 3065
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268175655"
variation 3066
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719290527"
variation 3069
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1227503577"
variation 3071
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719290683"
variation 3072
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719290766"
variation 3078
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108522821"
variation 3082..3083
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1719290830"
variation 3088
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719290918"
variation 3090
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719291008"
variation 3094
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1365163558"
variation 3096
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719291137"
variation 3097
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719291191"
variation 3099
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1286260666"
variation 3101
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1173596286"
variation 3104
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719291418"
variation 3105
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:114902531"
variation 3108
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1395096569"
variation 3113..3115
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1719291671"
variation 3117
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:886058254"
variation 3119..3121
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tat"
/db_xref="dbSNP:1560101073"
variation 3120
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1194958915"
variation 3124
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719291945"
variation 3125..3133
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="att"
/replace="atttttatt"
/db_xref="dbSNP:1447536540"
variation 3128
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1260983275"
variation 3129
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719292167"
variation 3137..3139
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1205481827"
variation 3139
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:912939643"
variation 3142
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1486748019"
variation 3144
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2108522852"
variation 3147
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:9844654"
variation 3150..3154
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1719292721"
variation 3150
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1210510143"
variation 3153
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1348887751"
variation 3155
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="t"
/db_xref="dbSNP:1305636676"
variation 3160
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1226318922"
variation 3161
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719293011"
variation 3163
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:115514339"
variation 3167
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:904271785"
variation 3172
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:780250179"
variation 3173..3182
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="att"
/replace="attagttatt"
/db_xref="dbSNP:1312664517"
variation 3173..3176
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="atta"
/db_xref="dbSNP:1400583744"
variation 3173
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1433639526"
variation 3174..3180
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tta"
/replace="ttagtta"
/db_xref="dbSNP:1719293559"
variation 3175
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1257720033"
variation 3177
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:942417865"
variation 3182
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719293776"
variation 3187
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719293845"
variation 3188
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174917504"
variation 3196
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138543261"
variation 3197
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719294051"
variation 3198
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="g"
/db_xref="dbSNP:1719294114"
variation 3201
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:764222909"
variation 3209
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719294287"
variation 3211
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719294375"
variation 3212
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719294444"
variation 3217
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:116119310"
variation 3219
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719294614"
variation 3220..3221
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1719294752"
variation 3220
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719294687"
variation 3221
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:774739453"
variation 3224..3230
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tc"
/replace="tcctctc"
/db_xref="dbSNP:1719294883"
variation 3228
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719294945"
variation 3232
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430069375"
variation 3239..3243
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1042547822"
variation 3239
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1159416126"
variation 3246
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:904007166"
variation 3251
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:534116529"
variation 3256
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:563600967"
variation 3267
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:573815116"
variation 3270
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719295583"
variation 3271
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1577435047"
variation 3273
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1338873341"
variation 3274
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1017325373"
variation 3276
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:969512543"
variation 3283
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719295904"
variation 3294
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1416183286"
variation 3298
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:182724933"
variation 3300
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:894886761"
variation 3301
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2108522965"
variation 3305
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719296474"
variation 3306
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2108522970"
variation 3307
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522971"
variation 3309
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:981251021"
variation 3310
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719296627"
variation 3314
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:562280702"
variation 3316
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719296759"
variation 3317
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719296811"
variation 3324
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719296859"
variation 3330
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719296937"
variation 3336
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:555889249"
variation 3337
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:959856826"
variation 3342
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202000030"
variation 3344
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719297244"
variation 3345
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719297318"
variation 3347
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719297375"
variation 3350
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1314373675"
variation 3352
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1407710410"
variation 3353
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1337294777"
variation 3356
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577435078"
variation 3359
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108523015"
variation 3361
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:772469095"
variation 3363
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719297818"
variation 3364
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:961617423"
variation 3366
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719297974"
variation 3372
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719298041"
variation 3381..3382
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="acaag"
/db_xref="dbSNP:1719298109"
variation 3382
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719298173"
variation 3383
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:994054804"
variation 3385..3386
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="gatagtt"
/db_xref="dbSNP:1719298336"
variation 3387
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1366681067"
variation 3388
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1560101157"
variation 3390
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1026836380"
variation 3391
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:913158756"
variation 3394
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719298666"
variation 3395
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1259840564"
variation 3397
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719298804"
variation 3398
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:945912441"
variation 3400
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719298962"
variation 3401
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374777475"
variation 3413
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719299118"
variation 3416
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:978466461"
variation 3419
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2108523053"
variation 3423
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719299253"
variation 3427
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719299317"
variation 3428
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:925599595"
variation 3431
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719299482"
variation 3432
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:910681740"
variation 3435
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:942490351"
variation 3436
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719299687"
variation 3438
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403742814"
variation 3439
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577435102"
variation 3452
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1039859745"
variation 3453
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719299981"
variation 3454
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:575625746"
variation 3456
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:976521023"
variation 3462
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719300193"
regulatory 3466..3471
/regulatory_class="polyA_signal_sequence"
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/note="hexamer: ATTAAA"
variation 3466
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1294731034"
variation 3467
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:879203376"
variation 3469..3472
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1439497170"
variation 3473
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:923269080"
variation 3478
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1202574986"
variation 3479
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:945638320"
variation 3480
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:901385416"
variation 3482
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:187708101"
polyA_site 3486
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/note="major polyA site"
ORIGIN
gcattttagagagcttttgtctgtgaaggctaaaagaatggccacttgtagagtatacttgaaaaagaattaggtttagtctaaattgtatcatttgaccttcaggatctctttcagtcctaggtggaagacaattttaaggaaaaaaaacctactctttcatacctcaccattttcgtttccataaattgtcctcctttcatcagctcatctctgaaattctacaaggagattccaggtggcagaggaactgctggatcaaaacacatgttccacggaccacaggtttaccaggaaggaactgaagctgcttgtaaggttattacacaactttttccttggaatcacaagccatactgtggtatgaagaggaaagtaccaagggctccatggttaagatgattcctgccctcaaacatcggactccaagttcttgagttttgggactcagactggctttcttgctcctcagcttgcagatgaactactgtgggatcttgtgatcatgactgaactcgttgttggccacctgtttggaaaaccattctcttgtggttggatctaacacatacagcatgtgaaggtaccagaaacacagaagactgacacccgccacttaagtggggccagggctggtgtctgcccatgttgccatcctgatgggctgcttgccacaatgagggatcttcttcaatacatcgcttgcttctttgcctttttctctgctgggtttttgattgtggccacctggactgactgttggatggtgaatgctgatgactctctggaggtgagcacaaaatgccgaggcctctggtgggaatgcgtcacaaatgcttttgatgggattcgcacctgtgatgagtacgattccatacttgcggagcatcccttgaagctggtggtaactcgagcgttgatgattactgcagatattctagctgggtttggatttctcaccctgctccttggtcttgactgcgtgaaattcctccctgatgagccgtacattaaagtccgcatctgctttgttgctggagccacgttactaatagcaggtaccccaggaatcattggctctgtgtggtatgctgttgatgtgtatgtggaacgttctactttggttttgcacaatatatttcttggtatccaatataaatttggttggtcctgttggctcggaatggctgggtctctgggttgctttttggctggagctgttctcacctgctgcttatatctttttaaagatgttggacctgagagaaactatccttattccttgaggaaagcctattcagccgcgggtgtttccatggccaagtcatactcagcccctcgcacagagacggccaaaatgtatgctgtagacacaagggtgtaaaatgcacgtttcagggtgtgtttgcatatgatttaatcaatcagtatggttacattgataaaatagtaagtcaatccaggaacagttatttagaattcatattgaattaaattaattgctagcttaatcaaaatgtttgattctcctatactttttctttctattactcttatattttcccgtcattctctctgctaaccttccaccttatgcacacactttccctatattttaagataagtctgctaggatgtagaaatatttgtttgtgatttctatatagctattagagattatgacatagtaatattaaaatgaaatgatacttaaacagaaagcaatttccaaagaggccagggaccctaatctttgaagagatgaagaaacttacttttctccctggcttttggttcactttttgtacttttaacaagtgggtgaattatttgataattttgaggaagattattcttttaaattcaaactagtatgtcaatgcctaccattactctgattatattaaaacagaaaaaggaaataacaacttcgtataccagccactggtgagagttaaagacaagagctgcccccccacccccaaatgtcaaaggcaaatgctaaattgatactggagctcgtggtgactttctacctcactaacaacataagggatctccatattatttcaccactattctagctttgctgatatattgccaaatgattagactacagaatagttcaaccagagaatttactcatttattgattaaacatccaaatactattgtaatatactatgttaaaattcatcaattcaagtgcccacacaccactgaatcatcagcaccaagcaatatattagacatatggcaaaattcaacaaatatattttgatataaataaataaacgttcacgactttacttaaaaaatcaatgttgcggctgggcacggtagctcgcgtctgtaatccccgcactttgggaggccaaggcgggtggatcacgaggtcaagagacggagaccatcctggctaacatggtgaaaccctgtctctactaaaaatacaaaaattagccgggcgtggtggcggtgcctgtagtcccagctactcgggaggctgaggcaggagaatcgtttgaacccaggaggtggaggttgcagtgagcggagatcgcaccattgcactccagtctggcaacagagcgagactccatctcaaaaaacaaaaataaataaataaataaatattcttcataaaatgtgggttttggggaaaatatagaattacatatacatttaacgaagtcgctaatgacatttcattcatattcataatgtaaccatcttgaatttttttaattgtagcgattttaaaaatgtttgtaaaatttaatttccagttttctaattacttgtcagtcacattaataacattagtacctttatggtacccttgcagtacctgaaaagaatatcaacctgaaaagaatatcaactcacccagaaattagttctttgaaaaaaaagaaattaagttgtgaatttctaaagaccttgaaataagtgtttcaaatttaaagaacaaagaatgatgtgaaaatgagattatgattcctactacatgaattaacgtttcgagattgctgtttattacttcccagagtatctttaacagtattctctgaagcagttccaatctagttggagaattaacagcaattgatttaactatctcatttttattaactgtaatttactttaaaaatatttgcaaatcatactcattagttatttgatcattgttctatgcattttaaaattaattttgtgttgttcctctcaatatttgtttttaacatttattcccatttttattttatactattgtctgtcatgctttatgtattccaataagtgtcttgaaatccttgtggggaaaggcaggacaaaaataattagttaattagatttgaaaaatgtaatttttccattttaaatatttcatttgtataagaaaatatttcagagaaccatgatgataatggatatgtgtgactgttttgaatttttttctcaattaaaacattttgtatgtaa
//
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]