ver.2
Home
|
Help
|
Advanced search
Previous release (v1)
2024-04-23 16:25:25, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001378493 3319 bp mRNA linear PRI 21-SEP-2023 DEFINITION Homo sapiens claudin 16 (CLDN16), transcript variant 3, mRNA. ACCESSION NM_001378493 VERSION NM_001378493.1 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 3319) 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 3319) 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 3319) 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 3319) 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 3319) 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 3319) 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 3319) 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 3319) 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 3319) 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 3319) 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 :: SRR1163658.250694.1 [ECO:0000332] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-231 AC080006.11 103833-104063 232-340 AC009520.16 75882-75990 341-416 AC009520.16 79517-79592 417-623 AC009520.16 93226-93432 624-726 AC009520.16 107326-107428 727-891 AC009520.16 109751-109915 892-1083 AC009520.16 113303-113494 1084-3319 AC009520.16 114892-117127 FEATURES Location/Qualifiers source 1..3319 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="3" /map="3q28" gene 1..3319 /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..340 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /inference="alignment:Splign:2.1.0" variation 232 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1718126081" variation 233 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1384248039" variation 236..237 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="tt" /replace="ttt" /db_xref="dbSNP:1404428245" variation 239 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:934159661" variation 241 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1718126290" variation 243 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1718126352" variation 244 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1047653867" variation 246 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:1718126434" variation 251 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1718126494" variation 253 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:751484225" variation 254 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1046208332" variation 258 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1173803435" variation 260 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1474178959" variation 262 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1308936510" variation 269 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:1005775848" variation 270 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1718126928" variation 271 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:564349242" variation 272 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1241076051" variation 273 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:2108647157" variation 277 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1718127032" variation 278 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:1718127086" variation 285 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:1718127143" variation 305 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:577049211" variation 306 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:545747527" variation 310 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:2108647168" variation 312 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:2108647171" variation 313 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:1269626680" variation 315 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1212880285" variation 320 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1718127483" variation 323 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1002320841" variation 327 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1271267543" variation 330 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1230293885" variation 333 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:1380949822" variation 339 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:918249540" variation 340 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1718127911" exon 341..416 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /inference="alignment:Splign:2.1.0" variation 343 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:1718208595" variation 344..354 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="tg" /replace="tgaactcgttg" /db_xref="dbSNP:1718208636" variation 351 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:571519012" variation 356 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1718208732" variation 359 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1019126167" variation 362 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:965754322" variation 364 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:527615251" variation 369 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:538626867" variation 371 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1718209317" variation 375 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:952314797" variation 377 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:756805072" variation 381 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1372215930" variation 387 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:547599368" variation 391 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1448013613" variation 392 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:915944062" variation 393 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:1274305968" variation 394 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:2108649376" misc_feature 396..398 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /note="upstream in-frame stop codon" variation 398 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:2108649378" variation 401 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1235702857" variation 403 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1371659538" variation 406 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:762574419" variation 407 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1577415037" variation 410 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="t" /db_xref="dbSNP:1373538182" variation 412 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1718210057" variation 415 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1332957276" variation 416 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1045709310" exon 417..623 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /inference="alignment:Splign:2.1.0" variation 417 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1388166379" variation 418 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:767080609" variation 420 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1375482100" variation 426 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:752540574" variation 428 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:756048104" variation 439 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:1577421257" variation 440 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1339149925" variation 441 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:777620076" variation 442 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:749083950" variation 443 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:757186184" variation 444 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:200400125" variation 445 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:558573665" variation 447 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1390469433" variation 448 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1458256618" variation 449 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1718556761" variation 452 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /db_xref="dbSNP:747245603" variation 455 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:768569589" variation 457 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:781362926" variation 460..461 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="cc" /replace="ccc" /db_xref="dbSNP:553547888" variation 460 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1006196806" variation 460 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="tcttccgatct" /db_xref="dbSNP:1553807669" variation 461 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1560093790" variation 463..465 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="" /replace="ggg" /db_xref="dbSNP:760754693" variation 463..465 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="gg" /replace="ggg" /replace="gggg" /db_xref="dbSNP:368234054" variation 463 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:201380153" variation 464..465 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="gg" /db_xref="dbSNP:386669518" variation 464 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:748213791" variation 465..466 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="" /replace="ac" /db_xref="dbSNP:763695473" variation 465 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:3214506" variation 467 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1718558327" variation 468 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:773763573" variation 469 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:149955797" variation 470 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1718558651" variation 472 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:771301899" variation 473..474 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="" /replace="agga" /db_xref="dbSNP:1718558849" variation 475 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:773947198" variation 477 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="gatct" /db_xref="dbSNP:866648881" variation 478 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="g" /db_xref="dbSNP:1718559086" variation 481 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:759268862" variation 484 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:767846686" variation 485 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:767119879" variation 486 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1277041944" variation 487 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:752230428" variation 489 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:760160835" variation 490 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:2108658208" variation 491..492 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="" /replace="tg" /db_xref="dbSNP:865841365" variation 491 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:2108658210" variation 492 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1210662953" variation 493 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:764125350" variation 494 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:1718560730" variation 498 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="c" /replace="t" /db_xref="dbSNP:753832878" variation 500 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="g" /replace="t" /db_xref="dbSNP:1277797748" variation 507 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /replace="a" /replace="g" /db_xref="dbSNP:1321220823" CDS 510..1217 /gene="CLDN16" /gene_synonym="HOMG3; PCLN1" /note="paracellin-1; hypomagnesemia 3, with hypercalciuria and nephrocalcinosis" /codon_start=1 /product="claudin-16" /protein_id="NP_001365422.1" /db_xref="CCDS:CCDS3296.2" /db_xref="GeneID:10686" /db_xref="HGNC:HGNC:2037" /db_xref="MIM:603959" /translation="
MRDLLQYIACFFAFFSAGFLIVATWTDCWMVNADDSLEVSTKCRGLWWECVTNAFDGIRTCDEYDSILAEHPLKLVVTRALMITADILAGFGFLTLLLGLDCVKFLPDEPYIKVRICFVAGATLLIAGTPGIIGSVWYAVDVYVERSTLVLHNIFLGIQYKFGWSCWLGMAGSLGCFLAGAVLTCCLYLFKDVGPERNYPYSLRKAYSAAGVSMAKSYSAPRTETAKMYAVDTRV"
misc_feature 519..581
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/note="propagated from UniProtKB/Swiss-Prot (Q9Y5I7.2);
transmembrane region"
misc_feature 540..1058
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/note="PMP-22/EMP/MP20/Claudin family; Region:
PMP22_Claudin; cl21598"
/db_xref="CDD:451326"
misc_feature 747..809
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/note="propagated from UniProtKB/Swiss-Prot (Q9Y5I7.2);
transmembrane region"
misc_feature 855..917
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/note="propagated from UniProtKB/Swiss-Prot (Q9Y5I7.2);
transmembrane region"
misc_feature 1017..1079
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/note="propagated from UniProtKB/Swiss-Prot (Q9Y5I7.2);
transmembrane region"
variation 510
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318788506"
variation 511
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:104893724"
variation 512
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1718561243"
variation 513
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:372525072"
variation 518
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482253091"
variation 519
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1199775812"
variation 522
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:199839143"
variation 524
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1718561810"
variation 526
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:867514971"
variation 528
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375640819"
variation 529
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368215264"
variation 530
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428685975"
variation 531
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:145118503"
variation 533
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372129081"
variation 534
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:965435011"
variation 536
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1718562646"
variation 537
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769827846"
variation 538
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:778198632"
variation 539..544
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ctt"
/replace="cttctt"
/db_xref="dbSNP:866440005"
variation 540
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:749819466"
variation 541
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1297905947"
variation 542
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1362947273"
variation 545..559
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tgc"
/replace="tgcctttttctctgc"
/db_xref="dbSNP:1560093930"
variation 546
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:977137021"
variation 547
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1020861027"
variation 554
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:149116671"
variation 556
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1718563800"
variation 560
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:967573821"
variation 562
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1181105329"
variation 563
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:774670118"
variation 569
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:759868163"
variation 571
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:771742472"
variation 573
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2108658311"
variation 576
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1293775732"
variation 584..585
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="caatgtgaaaat"
/db_xref="dbSNP:1718564412"
variation 585
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1254188095"
variation 587
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1718564576"
variation 589
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1718564664"
variation 590
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:775073665"
variation 596
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1064795763"
variation 597
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:545693736"
variation 605
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1718565564"
variation 608
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201545856"
variation 609
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:753777323"
variation 610
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108658338"
variation 612
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108658339"
variation 615
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:761873372"
variation 617
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765304853"
variation 618
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1560093977"
variation 619
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268061294"
exon 624..726
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/inference="alignment:Splign:2.1.0"
variation 624
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1278876951"
variation 625
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190419654"
variation 626
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:528344809"
variation 628
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:142152395"
variation 629
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1264612767"
variation 631
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:764353770"
variation 635
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1321219881"
variation 639
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:753901053"
variation 640
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:757395583"
variation 641
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274557149"
variation 644
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1219996621"
variation 645
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1718984196"
variation 646
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108670592"
variation 647
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1718984264"
variation 648
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:146727044"
variation 649
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:104893732"
variation 657
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1430185772"
variation 658
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149965853"
variation 659
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:370592530"
variation 660
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:920823997"
variation 665
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:573024259"
variation 669
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:758739389"
variation 670
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:61752083"
variation 671
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:780312463"
variation 672
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:747440607"
variation 674
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:144105475"
variation 677
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1055737562"
variation 678
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:747654138"
variation 680
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:56147287"
variation 683
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:773141087"
variation 684
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444245867"
variation 685
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:762831659"
variation 686
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:766383362"
variation 693
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1233586538"
variation 695
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1294742863"
variation 696
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773999256"
variation 697
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:759388455"
variation 698
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577429403"
variation 701
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199651054"
variation 702
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:761824865"
variation 703
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1208605810"
variation 704
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:950141430"
variation 710
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1257324344"
variation 711
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1474818508"
variation 714
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1718986912"
variation 715
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:765256758"
variation 716
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:137882210"
variation 719
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:758799163"
variation 722
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1718987282"
variation 724
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1477588982"
variation 725
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1718987423"
exon 727..891
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/inference="alignment:Splign:2.1.0"
variation 728
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:778765191"
variation 732
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719048031"
variation 733
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:104893731"
variation 734..747
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="ggtggtaactcgag"
/db_xref="dbSNP:1719048217"
variation 739
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1350393472"
variation 741
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:771816868"
variation 743
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:775232251"
variation 744
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:104893720"
variation 745
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:968906940"
variation 748
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769893284"
variation 749
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:373411163"
variation 751
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:104893730"
variation 752
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:104893729"
variation 754
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1195405538"
variation 756
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:774947384"
variation 757
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1452788815"
variation 760
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1158867345"
variation 763
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1386707552"
variation 766
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719050267"
variation 768
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403200551"
variation 769
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:911369572"
variation 770
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1371063500"
variation 773
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:760090790"
variation 774
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:527990106"
variation 778
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1577430719"
variation 783
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1335620169"
variation 785
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:753102053"
variation 787
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1326395870"
variation 790
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="ttggt"
/db_xref="dbSNP:1719051110"
variation 791
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:756572012"
variation 794
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354548248"
variation 795
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719051321"
variation 796
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:763587706"
variation 797
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1311824206"
variation 799
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:104893725"
variation 803
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:753542626"
variation 805
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1273948471"
variation 807
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1469870064"
variation 808
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:756674166"
variation 810
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:944275084"
variation 814
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719052138"
variation 815
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:547537371"
variation 816
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419689384"
variation 821
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719052386"
variation 822
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719052466"
variation 825
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:778427772"
variation 828
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719052758"
variation 829
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719052840"
variation 833
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:745420355"
variation 838
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140829596"
variation 839
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:898316282"
variation 840
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:567783618"
variation 842
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:746772676"
variation 843..847
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="attaa"
/replace="attaattaa"
/db_xref="dbSNP:1253995767"
variation 843
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462564694"
variation 845
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1275570743"
variation 846
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376431300"
variation 847
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370413403"
variation 850
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:536714046"
variation 851
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1308642000"
variation 852
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:929948127"
variation 853
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:556413628"
variation 854
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:759749571"
variation 857
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:768135151"
variation 858
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316949011"
variation 860
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719054426"
variation 864
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719054513"
variation 867
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1216704349"
variation 870
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:104893722"
variation 873
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108673379"
variation 875
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:150478692"
variation 876
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1048501191"
variation 877
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1480328199"
variation 878
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719055043"
variation 881
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:760895186"
variation 882
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:764545067"
variation 883..887
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="taata"
/replace="taataata"
/db_xref="dbSNP:1560098734"
variation 883
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1007522348"
variation 886
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719055460"
variation 887
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373189371"
variation 890
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:753395110"
variation 891
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1577430815"
exon 892..1083
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/inference="alignment:Splign:2.1.0"
variation 892
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:104893723"
variation 895..898
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1258535403"
variation 895
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1202664145"
variation 896
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1486834780"
variation 901
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:138308105"
variation 907
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261570205"
variation 911
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:762220084"
variation 913
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:570616277"
variation 917
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149645885"
variation 918
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:765895243"
variation 922
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:544158479"
variation 924
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1270704258"
variation 927
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1376923358"
variation 930
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719158559"
variation 932
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:754911596"
variation 935
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:781052097"
variation 937
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:752533102"
variation 939
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:753223645"
variation 942
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371258878"
variation 945
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:758946923"
variation 946
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:772241737"
variation 947
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1336299188"
variation 950
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719159332"
variation 951
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:780153615"
variation 952
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1281243864"
variation 956
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1453710173"
variation 958
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1302134732"
variation 961
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1408388959"
variation 962
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1577432849"
variation 963
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1329454729"
variation 967
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201367228"
variation 968
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719160156"
variation 969
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:769190460"
variation 971
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1260497925"
variation 975
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1170178042"
variation 976..977
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1553809654"
variation 979
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719160566"
variation 981
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719160649"
variation 983
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719160734"
variation 986
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:532245223"
variation 987
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298030528"
variation 994
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:104893726"
variation 996
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1577432872"
variation 997
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:104893727"
variation 998
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:762095241"
variation 1000
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1182563283"
variation 1003
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:104893728"
variation 1009
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1453219704"
variation 1011
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:543523352"
variation 1013
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772803074"
variation 1014
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:104893721"
variation 1015
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719162432"
variation 1024
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:751056950"
variation 1026
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1577432896"
variation 1027
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345543207"
variation 1028
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:368589513"
variation 1031
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:767423701"
variation 1034
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1053422587"
variation 1038..1042
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1273573190"
variation 1041
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143316426"
variation 1042
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:777745636"
variation 1044
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719163555"
variation 1048
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:139251569"
variation 1053
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201641346"
variation 1054
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719163916"
variation 1055
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:758673667"
variation 1060
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:780195981"
variation 1061
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1314203005"
variation 1062
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1317860117"
variation 1064
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719164345"
variation 1070
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:747105311"
variation 1071
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143097871"
variation 1072
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1312786315"
variation 1073
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719164774"
variation 1074
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1035298979"
variation 1078
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:781678462"
variation 1081
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1210040068"
exon 1084..3319
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/inference="alignment:Splign:2.1.0"
variation 1085
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:766553260"
variation 1087
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1416877202"
variation 1090
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:751740742"
variation 1091
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719228059"
variation 1093
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:755033066"
variation 1094
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:781161632"
variation 1097
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748266585"
variation 1099
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="g"
/db_xref="dbSNP:1577434022"
variation 1099
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:756589441"
variation 1105
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719228589"
variation 1110
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1404996591"
variation 1112
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355259272"
variation 1114
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1411885209"
variation 1120
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1641467526"
variation 1122
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:387906880"
variation 1125
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:539967883"
variation 1126
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1415814850"
variation 1129
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:35041121"
variation 1130
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:121908543"
variation 1132
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1338030534"
variation 1135
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:139846352"
variation 1136
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:745542693"
variation 1137
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:549642537"
variation 1138
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719230472"
variation 1139
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:775121017"
variation 1143
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:760321632"
variation 1144
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:764121096"
variation 1147..1148
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2108521351"
variation 1147
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:776710987"
variation 1148
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:761606829"
variation 1149
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1475042783"
variation 1164
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:764960055"
variation 1168
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371465699"
variation 1170
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1560100409"
variation 1171
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:141823638"
variation 1173
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200023201"
variation 1174
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:752758478"
variation 1177
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719231870"
variation 1179
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:756192568"
variation 1180
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1193820441"
variation 1181
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434084"
variation 1183
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374751726"
variation 1184
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1325118362"
variation 1185
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:749782586"
variation 1187
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482633360"
variation 1188..1191
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:755344639"
variation 1188
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1276759277"
variation 1189
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1366697751"
variation 1192
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231476372"
variation 1196
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:757602181"
variation 1197
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150621351"
variation 1199
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1201892517"
variation 1202
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719233474"
variation 1206
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:746297543"
variation 1207
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:121908542"
variation 1208
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:771613047"
variation 1210
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1193773094"
variation 1211
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719234034"
variation 1212
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1249854366"
variation 1214
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:779922888"
variation 1216
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719234295"
variation 1217
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1191842560"
variation 1220
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:746450356"
variation 1222
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719234541"
variation 1224
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1466740266"
variation 1225
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:768292566"
variation 1226
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1368443391"
variation 1227
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108521448"
variation 1229..1271
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ca"
/replace="cagggtgtgtttgcatatgatttaatcaatcagtatggttaca"
/db_xref="dbSNP:1189438200"
variation 1229
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:776656418"
variation 1230
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756756376"
variation 1231
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:772860827"
variation 1232
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2108521458"
variation 1233
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:368827991"
variation 1234
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1162057598"
variation 1236
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:752931762"
variation 1242
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:993342773"
variation 1243
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331896797"
variation 1244
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719235955"
variation 1249
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719236025"
variation 1252
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108521476"
variation 1253
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302060265"
variation 1254
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719236167"
variation 1257
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1179623863"
variation 1258..1262
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tcagt"
/db_xref="dbSNP:1719236391"
variation 1258
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482602961"
variation 1259
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252342533"
variation 1263
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1207049107"
variation 1268
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372140161"
variation 1270
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1289465976"
variation 1272
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210456095"
variation 1275..1282
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ata"
/replace="ataaaata"
/db_xref="dbSNP:1719236908"
variation 1277
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1358627083"
variation 1282..1288
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="agt"
/replace="agtaagt"
/db_xref="dbSNP:1278266886"
variation 1283
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1364319377"
variation 1290
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434165"
variation 1291
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:886058245"
variation 1292
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1719237393"
variation 1293
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1351477777"
variation 1295
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719237542"
variation 1297
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1290535138"
variation 1298
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719237845"
variation 1299
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719237920"
variation 1301
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719237992"
variation 1303
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719238060"
variation 1305
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1432770137"
variation 1306
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719238933"
variation 1309
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1347716809"
variation 1310
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1322503307"
variation 1315
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719239131"
variation 1316
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1405410283"
variation 1319
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1392338624"
variation 1320
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:766995290"
variation 1322..1332
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aattaaattaa"
/replace="aattaaattaaattaa"
/db_xref="dbSNP:1719239415"
variation 1331
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:892300472"
variation 1333
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1412623271"
variation 1335
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="g"
/db_xref="dbSNP:1184028451"
variation 1335
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1476930089"
variation 1336
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243512298"
variation 1338
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010771548"
variation 1339
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719239926"
variation 1340
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719239992"
variation 1347
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719240061"
variation 1357
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:868026523"
variation 1360
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719240224"
variation 1363
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719240296"
variation 1369..1373
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1719240361"
variation 1371..1379
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tttct"
/replace="tttctttct"
/db_xref="dbSNP:1358040277"
variation 1374
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210770141"
variation 1375
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1453400955"
variation 1376
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1282323481"
variation 1378
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1267864594"
variation 1380
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1463863570"
variation 1381
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719240902"
variation 1382
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1208201800"
variation 1383
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1191046955"
variation 1387
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:984582606"
variation 1389
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330345743"
variation 1390
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1270611227"
variation 1391
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719241349"
variation 1392
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1249265644"
variation 1397
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2108521603"
variation 1398
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145675747"
variation 1399
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:571524553"
variation 1405
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108521613"
variation 1409
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:969808380"
variation 1410
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719241796"
variation 1414
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:755751630"
variation 1416
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1034332544"
variation 1417
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:960031461"
variation 1420
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719242146"
variation 1421
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:73053979"
variation 1422
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149191729"
variation 1426
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1158756925"
variation 1428
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161343286"
variation 1429
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1412515275"
variation 1430
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424286620"
variation 1431
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719242608"
variation 1432
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1387607568"
variation 1434
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719242760"
variation 1436
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1479096605"
variation 1440..1442
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1719242896"
variation 1444
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1455495704"
variation 1450
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1246433837"
variation 1452
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719243230"
variation 1454
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:191200989"
variation 1456
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719243389"
variation 1457
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:865808205"
variation 1460
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:142380851"
variation 1466
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:886058246"
variation 1467
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719243762"
variation 1469
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="t"
/db_xref="dbSNP:1719243840"
variation 1472
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465420183"
variation 1476
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1250425802"
variation 1478
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719244329"
variation 1480
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1202399429"
variation 1486
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1311958057"
variation 1491
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1279706403"
variation 1495
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1221295875"
variation 1497
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:962606383"
variation 1499
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719244830"
variation 1500
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1341791237"
variation 1502
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1294973811"
variation 1508
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719245015"
variation 1509
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1577434287"
variation 1515
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1433682157"
variation 1516
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:181803078"
variation 1517
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1287399767"
variation 1518
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719245583"
variation 1519
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108521724"
variation 1520
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:973593024"
variation 1522
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719245732"
variation 1525
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176441679"
variation 1526
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719245874"
variation 1537
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:947362511"
variation 1538
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1577434299"
variation 1539
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1049720745"
variation 1542
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1168253607"
variation 1543
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450160660"
variation 1549
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386093996"
variation 1553
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719246241"
variation 1555
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719246309"
variation 1556
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1392162749"
variation 1558
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1180204001"
variation 1559
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719246517"
variation 1561
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719246577"
variation 1563
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2108521763"
variation 1565
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434306"
variation 1567
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719246700"
variation 1570
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1483169407"
variation 1573
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="a"
/db_xref="dbSNP:1269257985"
variation 1573
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719246844"
variation 1574
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1483222776"
variation 1575
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434314"
variation 1577
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212626622"
variation 1580
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719247239"
variation 1582
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:889886848"
variation 1590
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1482306246"
variation 1591
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108521787"
variation 1594
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2108521790"
variation 1595
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1272000961"
variation 1596
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1227301370"
variation 1600
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:575561257"
variation 1604
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1198760198"
variation 1606
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719247693"
variation 1617
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1299106403"
variation 1621
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719247843"
variation 1626..1627
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1719247993"
variation 1626
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719247912"
variation 1627
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:931732278"
variation 1628
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719248252"
variation 1634
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303384959"
variation 1637
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719248349"
variation 1641
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719248428"
variation 1642
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1449930758"
variation 1647
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:544538250"
variation 1651..1653
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="gtg"
/db_xref="dbSNP:1719248608"
variation 1659
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:557949152"
variation 1664
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1430576814"
variation 1668
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719248855"
variation 1677
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:911549923"
variation 1678
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:944354002"
variation 1681
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2068245906"
variation 1682
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1423343452"
variation 1683
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1415128978"
variation 1687
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199716341"
variation 1688
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719249316"
variation 1695
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719249376"
variation 1706
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1052521743"
variation 1708
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1251623797"
variation 1709
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108521867"
variation 1710
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719249633"
variation 1712
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:901678187"
variation 1717
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719249804"
variation 1720
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:946605671"
variation 1721
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043568318"
variation 1722
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:993416555"
variation 1723
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1026173159"
variation 1738
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1577434359"
variation 1740
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719250303"
variation 1741
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108521890"
variation 1742
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:905013137"
variation 1745
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434366"
variation 1746
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:887482525"
variation 1747
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1001578693"
variation 1750
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471447498"
variation 1751
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719250798"
variation 1752
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434377"
variation 1756
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719250928"
variation 1757..1762
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aac"
/replace="aacaac"
/db_xref="dbSNP:778070121"
variation 1758
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:186108585"
variation 1761
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1577434385"
variation 1765
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006316565"
variation 1766
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434393"
variation 1770
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:540301575"
variation 1771
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719251449"
variation 1772
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719251521"
variation 1779
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1372588646"
variation 1780
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:970217940"
variation 1783
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345662272"
variation 1785
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719251933"
variation 1798
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:981206118"
variation 1803
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:560036875"
variation 1804..1810
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="cccccc"
/replace="ccccccc"
/replace="cccccccc"
/db_xref="dbSNP:895882395"
variation 1804
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411881940"
variation 1805
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:956173827"
variation 1806
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719253034"
variation 1807
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:115611104"
variation 1808
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:542212640"
variation 1809
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:953486547"
variation 1810
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749108552"
variation 1811
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1719253479"
variation 1812..1816
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:758965630"
variation 1813
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:911677788"
variation 1815
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1326939252"
variation 1821
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719253755"
variation 1830
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1348257306"
variation 1832
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1230569810"
variation 1833
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719253988"
variation 1840
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719254080"
variation 1844..1869
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tac"
/replace="tactggagctcgtggtgactttctac"
/db_xref="dbSNP:1719254164"
variation 1845
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:966182367"
variation 1848
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1228755363"
variation 1849
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719254374"
variation 1850
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2108521997"
variation 1851
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:985868711"
variation 1853
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1299459579"
variation 1856
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719254548"
variation 1861
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:911192374"
variation 1862
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="c"
/db_xref="dbSNP:779878146"
variation 1862
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1289408389"
variation 1866
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719254812"
variation 1867
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1312017393"
variation 1868
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719254957"
variation 1874
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:987846768"
variation 1877
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719255101"
variation 1887
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112253194"
variation 1890
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522028"
variation 1896
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1433028193"
variation 1902
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1258346631"
variation 1903
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1560100716"
variation 1904
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1388491456"
variation 1908
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483616922"
variation 1911
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1204525682"
variation 1914
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:754896663"
variation 1923
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1376354921"
variation 1924
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719255794"
variation 1925
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719255858"
variation 1927
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:531851017"
variation 1934
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1249814822"
variation 1935
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1484170679"
variation 1937
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1577434483"
variation 1939
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719256310"
variation 1940
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1267646593"
variation 1941
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:886058247"
variation 1942
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1184029948"
variation 1946
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463199087"
variation 1952
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719256645"
variation 1953
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1560100743"
variation 1955
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:778985429"
variation 1960
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:946655268"
variation 1962
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352554358"
variation 1973
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043586027"
variation 1975
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719257142"
variation 1977
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719257210"
variation 1978
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:886058248"
variation 1982
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:551693948"
variation 1983
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719257411"
variation 1985
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="g"
/db_xref="dbSNP:886058249"
variation 1986
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719257555"
variation 1991
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1312954012"
variation 2000
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719257660"
variation 2006
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:901710762"
variation 2008
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719257792"
variation 2011
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2293532"
variation 2012
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719258031"
variation 2013
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1432968420"
variation 2014
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719258194"
variation 2018
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719258283"
variation 2020
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1364604379"
variation 2022
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719258443"
variation 2023
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719258497"
variation 2026
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:558543277"
variation 2028
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719258617"
variation 2030
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432445325"
variation 2031
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719258788"
variation 2033
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:937883108"
variation 2036
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1379307938"
variation 2039
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1384483860"
variation 2040
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:771018706"
variation 2046
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400692450"
variation 2047
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1047528788"
variation 2050
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719259307"
variation 2052
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1434739508"
variation 2053
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:377075907"
variation 2055
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1006101929"
variation 2059
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:77656241"
variation 2065
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:746066027"
variation 2066
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719259819"
variation 2069..2070
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1719259880"
variation 2070
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:895925213"
variation 2071
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1175169218"
variation 2079
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719260112"
variation 2085
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1447125696"
variation 2088
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:769934589"
variation 2103
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1188654028"
variation 2106
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1448597711"
variation 2107
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719261472"
variation 2108
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719261560"
variation 2115
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719265975"
variation 2118
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:879005444"
variation 2121
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719266118"
variation 2124
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:116488781"
variation 2127
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719266321"
variation 2129
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1199615871"
variation 2130
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1035424989"
variation 2135
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1282707603"
variation 2136
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:955745713"
variation 2137
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108522215"
variation 2140
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719266744"
variation 2142
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1411238482"
variation 2146..2151
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aaaaaa"
/replace="aaaaaaa"
/db_xref="dbSNP:1719266918"
variation 2153
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719266981"
variation 2156
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1298437823"
variation 2157
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367325239"
variation 2159
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719267223"
variation 2161
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010428271"
variation 2162
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1021763433"
variation 2165
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:763316001"
variation 2166
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339171481"
variation 2171
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:969384621"
variation 2172
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1272611410"
variation 2175
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719267913"
variation 2178
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="t"
/db_xref="dbSNP:1719267980"
variation 2179
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1344473010"
variation 2181
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1314315969"
variation 2182
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:769075597"
variation 2185
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719268328"
variation 2191
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1246414280"
variation 2194
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:953602137"
variation 2195
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:911254109"
variation 2197
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1577434607"
variation 2198
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007768932"
variation 2201
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1577434614"
variation 2205
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719268901"
variation 2206
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1019510874"
variation 2210
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1189267271"
variation 2213
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719269169"
variation 2214
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259425513"
variation 2215
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:774827215"
variation 2218
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1269320130"
variation 2225
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1454682905"
variation 2226
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1275645982"
variation 2227
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:965848414"
variation 2228
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:965390858"
variation 2229
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719270203"
variation 2233
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:567611922"
variation 2234
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719270436"
variation 2236
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719270504"
variation 2238
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:536751926"
variation 2239
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:556567304"
variation 2240
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1286773850"
variation 2242
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719270879"
variation 2244
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:976835789"
variation 2245
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:767025229"
variation 2247
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1431161797"
variation 2248..2271
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="cctg"
/replace="cctggctaacatggtgaaaccctg"
/db_xref="dbSNP:1719271312"
variation 2248
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:930021289"
variation 2249
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1047559982"
variation 2251
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719271868"
variation 2253..2254
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="ct"
/db_xref="dbSNP:1719271952"
variation 2254
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1388038369"
variation 2259
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:909037215"
variation 2262
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:967655512"
variation 2263
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:979061004"
variation 2264
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:941979192"
variation 2266
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1577434658"
variation 2267
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1179683712"
variation 2268
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252767381"
variation 2270
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="t"
/db_xref="dbSNP:1184329836"
variation 2270
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044300619"
variation 2272
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1259042040"
variation 2274
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719272892"
variation 2275
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:937912506"
variation 2284
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201642794"
variation 2288
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719273124"
variation 2291
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1266809940"
variation 2292..2295
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="atta"
/replace="attatta"
/db_xref="dbSNP:1337535456"
variation 2298
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:570080234"
variation 2299
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330293904"
variation 2303
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1279769818"
variation 2304
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:992035157"
variation 2305
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719273726"
variation 2306
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:905554893"
variation 2310
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1002552972"
variation 2311
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056795067"
variation 2314
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1441027710"
variation 2318
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1396564635"
variation 2321
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719274941"
variation 2324
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:375704078"
variation 2327
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1156902117"
variation 2328
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522380"
variation 2330
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719275268"
variation 2332
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719275351"
variation 2333
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719275437"
variation 2334
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:10470534"
variation 2337
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1289358804"
variation 2339
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1408513000"
variation 2340
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1160098826"
variation 2344
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577434721"
variation 2348
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719276337"
variation 2352
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1477124170"
variation 2354
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719276491"
variation 2355
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719276557"
variation 2356
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1009956782"
variation 2357..2359
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:1719276818"
variation 2357
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1577434726"
variation 2358
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719276917"
variation 2362
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1022246328"
variation 2363
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:968913173"
variation 2365
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719277087"
variation 2366
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719277169"
variation 2371..2373
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="gtg"
/db_xref="dbSNP:1719277240"
variation 2372
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:558111287"
variation 2373
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719277419"
variation 2374
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719277493"
variation 2377
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:577763881"
variation 2378
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:950181288"
variation 2379
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1217842329"
variation 2383
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1342372385"
variation 2384
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719278006"
variation 2386
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1007578934"
variation 2387
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:886058250"
variation 2388
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:760316748"
variation 2389
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1018517588"
variation 2393
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318443756"
variation 2395
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:533709248"
variation 2396
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:765950941"
variation 2398
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1319993573"
variation 2402
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522470"
variation 2404
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1450715663"
variation 2406
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719278900"
variation 2411
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1424698372"
variation 2412
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719279028"
variation 2413
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1577434770"
variation 2414
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1186606932"
variation 2418
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:190527986"
variation 2419
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108522482"
variation 2426
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:140801126"
variation 2427
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:889392676"
variation 2429
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1560100924"
variation 2430
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719279680"
variation 2431
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007799900"
variation 2436
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1019124017"
variation 2437
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1577434786"
variation 2438
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1208428510"
variation 2440
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1442242355"
variation 2441
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1277470359"
variation 2444
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:879585750"
variation 2449..2469
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aaataaataaataaata"
/replace="aaataaataaataaataaata"
/replace="aaataaataaataaataaataaata"
/db_xref="dbSNP:901970657"
variation 2451
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:144651280"
variation 2459
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719280534"
variation 2462
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:984165827"
variation 2465
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:183599112"
variation 2469
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719280819"
variation 2473
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1457107753"
variation 2475
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:909061450"
variation 2483
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021159365"
variation 2484
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719281137"
variation 2486
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1271908394"
variation 2487
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1445499496"
variation 2491
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:967771615"
variation 2492
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:188089990"
variation 2493
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1033294124"
variation 2496
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1368957747"
variation 2500
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1167998468"
variation 2501
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:959296706"
variation 2502
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:372146584"
variation 2511
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1422227758"
variation 2514
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1180691398"
variation 2515
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1044594052"
variation 2520
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719282071"
variation 2521
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:927251239"
variation 2523
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771484743"
variation 2524
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1258586230"
variation 2529
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213470685"
variation 2530
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:565421878"
variation 2532
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:891461218"
variation 2535
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272070280"
variation 2546
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203182396"
variation 2549
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522562"
variation 2550
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:886058251"
variation 2551..2552
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1719282840"
variation 2553
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:939815267"
variation 2554
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1226594338"
variation 2556
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719283037"
variation 2562
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378370140"
variation 2563
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719283160"
variation 2565
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:753612393"
variation 2566
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416428859"
variation 2569
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719283488"
variation 2573..2579
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tttt"
/replace="tttttt"
/replace="ttttttt"
/db_xref="dbSNP:1719283630"
variation 2573
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1230219728"
variation 2581
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1348808536"
variation 2583
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1294194615"
variation 2588
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:545295861"
variation 2589
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:919380095"
variation 2592
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719284042"
variation 2594
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:886058252"
variation 2595
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719284172"
variation 2596
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:565280429"
variation 2607
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719284318"
variation 2622
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719284402"
variation 2623
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719284469"
variation 2624
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1356410000"
variation 2630
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1042795499"
variation 2631
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1162783200"
variation 2633
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1405218490"
variation 2636
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335227985"
variation 2637..2644
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="gtca"
/replace="gtcagtca"
/db_xref="dbSNP:1719284944"
variation 2641
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719285018"
variation 2644
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:191406701"
variation 2645
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049117498"
variation 2649
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1577434877"
variation 2654
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:778897400"
variation 2656
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007074574"
variation 2657
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176333881"
variation 2662
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522630"
variation 2664..2666
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:2108522632"
variation 2667
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1480667202"
variation 2668
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1560101014"
variation 2669
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108522638"
variation 2670
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:13076274"
variation 2673..2675
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1719286019"
variation 2680
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:901439215"
variation 2683..2718
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="acctgaaaagaatatcaac"
/replace="acctgaaaagaatatcaacctgaaaagaatatcaac"
/replace="acctgaaaagaatatcaacctgaaaagaatatcaacctgaaaagaata
tcaac"
/db_xref="dbSNP:372414927"
variation 2684
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:902087850"
variation 2694
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:998383710"
variation 2703
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025637829"
variation 2707
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1287946981"
variation 2708
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:113286536"
variation 2709
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719286719"
variation 2710
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1375804964"
variation 2714
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719286861"
variation 2717
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719286927"
variation 2725
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="a"
/db_xref="dbSNP:1291816668"
variation 2733
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1000542507"
variation 2735
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522673"
variation 2736
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:984647483"
variation 2737
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2108522683"
variation 2739
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1157436007"
variation 2741..2748
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/replace="aaaaaaaaa"
/db_xref="dbSNP:958990554"
variation 2747
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419235717"
variation 2748
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719287507"
variation 2749
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719287573"
variation 2752
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719287626"
variation 2758
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:530102213"
variation 2769
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:577574442"
variation 2770
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1660340440"
variation 2773
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719287923"
variation 2775
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334144623"
variation 2776
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:886058253"
variation 2782
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108522725"
variation 2786..2789
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="gt"
/replace="gtgt"
/db_xref="dbSNP:1719288240"
variation 2786
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1467681744"
variation 2788
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1686386626"
variation 2790
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719288317"
variation 2794
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1253540410"
variation 2796
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719288463"
variation 2797
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719288544"
variation 2798
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719288620"
variation 2804
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1215543100"
variation 2808
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719288753"
variation 2809
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463498861"
variation 2813
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719288905"
variation 2814
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:961315668"
variation 2815
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719289054"
variation 2826
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719289131"
variation 2828
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719289198"
variation 2836
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:979977937"
variation 2839
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:537088739"
variation 2840
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719289436"
variation 2843
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1350111456"
variation 2844
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108522765"
variation 2845
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522766"
variation 2852
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:781286477"
variation 2853
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719289649"
variation 2854
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1371905149"
variation 2859
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1328502693"
variation 2861
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108522779"
variation 2865
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719289864"
variation 2866
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719289945"
variation 2871
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:927083429"
variation 2876
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719290052"
variation 2881
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:938608167"
variation 2883
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:919743196"
variation 2892
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719290314"
variation 2892
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tcat"
/db_xref="dbSNP:1719290376"
variation 2894
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719290455"
variation 2898
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268175655"
variation 2899
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719290527"
variation 2902
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1227503577"
variation 2904
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719290683"
variation 2905
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719290766"
variation 2911
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2108522821"
variation 2915..2916
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1719290830"
variation 2921
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719290918"
variation 2923
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719291008"
variation 2927
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1365163558"
variation 2929
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719291137"
variation 2930
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719291191"
variation 2932
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1286260666"
variation 2934
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1173596286"
variation 2937
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719291418"
variation 2938
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:114902531"
variation 2941
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1395096569"
variation 2946..2948
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1719291671"
variation 2950
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:886058254"
variation 2952..2954
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tat"
/db_xref="dbSNP:1560101073"
variation 2953
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1194958915"
variation 2957
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719291945"
variation 2958..2966
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="att"
/replace="atttttatt"
/db_xref="dbSNP:1447536540"
variation 2961
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1260983275"
variation 2962
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719292167"
variation 2970..2972
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1205481827"
variation 2972
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:912939643"
variation 2975
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1486748019"
variation 2977
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2108522852"
variation 2980
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:9844654"
variation 2983..2987
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1719292721"
variation 2983
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1210510143"
variation 2986
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1348887751"
variation 2988
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="t"
/db_xref="dbSNP:1305636676"
variation 2993
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1226318922"
variation 2994
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719293011"
variation 2996
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:115514339"
variation 3000
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:904271785"
variation 3005
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:780250179"
variation 3006..3015
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="att"
/replace="attagttatt"
/db_xref="dbSNP:1312664517"
variation 3006..3009
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="atta"
/db_xref="dbSNP:1400583744"
variation 3006
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1433639526"
variation 3007..3013
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tta"
/replace="ttagtta"
/db_xref="dbSNP:1719293559"
variation 3008
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1257720033"
variation 3010
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:942417865"
variation 3015
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719293776"
variation 3020
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719293845"
variation 3021
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174917504"
variation 3029
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138543261"
variation 3030
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719294051"
variation 3031
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="g"
/db_xref="dbSNP:1719294114"
variation 3034
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:764222909"
variation 3042
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719294287"
variation 3044
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719294375"
variation 3045
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719294444"
variation 3050
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:116119310"
variation 3052
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719294614"
variation 3053..3054
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1719294752"
variation 3053
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719294687"
variation 3054
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:774739453"
variation 3057..3063
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="tc"
/replace="tcctctc"
/db_xref="dbSNP:1719294883"
variation 3061
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719294945"
variation 3065
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430069375"
variation 3072..3076
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1042547822"
variation 3072
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1159416126"
variation 3079
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:904007166"
variation 3084
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:534116529"
variation 3089
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:563600967"
variation 3100
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:573815116"
variation 3103
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719295583"
variation 3104
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1577435047"
variation 3106
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1338873341"
variation 3107
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1017325373"
variation 3109
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:969512543"
variation 3116
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719295904"
variation 3127
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1416183286"
variation 3131
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:182724933"
variation 3133
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:894886761"
variation 3134
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2108522965"
variation 3138
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719296474"
variation 3139
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2108522970"
variation 3140
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108522971"
variation 3142
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:981251021"
variation 3143
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719296627"
variation 3147
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:562280702"
variation 3149
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719296759"
variation 3150
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719296811"
variation 3157
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719296859"
variation 3163
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719296937"
variation 3169
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:555889249"
variation 3170
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:959856826"
variation 3175
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202000030"
variation 3177
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719297244"
variation 3178
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719297318"
variation 3180
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1719297375"
variation 3183
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1314373675"
variation 3185
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1407710410"
variation 3186
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1337294777"
variation 3189
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577435078"
variation 3192
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2108523015"
variation 3194
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:772469095"
variation 3196
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719297818"
variation 3197
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:961617423"
variation 3199
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719297974"
variation 3205
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719298041"
variation 3214..3215
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="acaag"
/db_xref="dbSNP:1719298109"
variation 3215
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719298173"
variation 3216
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:994054804"
variation 3218..3219
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace=""
/replace="gatagtt"
/db_xref="dbSNP:1719298336"
variation 3220
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1366681067"
variation 3221
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1560101157"
variation 3223
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1026836380"
variation 3224
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:913158756"
variation 3227
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719298666"
variation 3228
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1259840564"
variation 3230
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719298804"
variation 3231
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:945912441"
variation 3233
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719298962"
variation 3234
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374777475"
variation 3246
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719299118"
variation 3249
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:978466461"
variation 3252
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2108523053"
variation 3256
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1719299253"
variation 3260
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719299317"
variation 3261
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:925599595"
variation 3264
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1719299482"
variation 3265
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:910681740"
variation 3268
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:942490351"
variation 3269
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1719299687"
variation 3271
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403742814"
variation 3272
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577435102"
variation 3285
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1039859745"
variation 3286
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1719299981"
variation 3287
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:575625746"
variation 3289
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:976521023"
variation 3295
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1719300193"
regulatory 3299..3304
/regulatory_class="polyA_signal_sequence"
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/note="hexamer: ATTAAA"
variation 3299
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1294731034"
variation 3300
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:879203376"
variation 3302..3305
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1439497170"
variation 3306
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:923269080"
variation 3311
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1202574986"
variation 3312
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="a"
/replace="g"
/db_xref="dbSNP:945638320"
variation 3313
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="c"
/replace="t"
/db_xref="dbSNP:901385416"
variation 3315
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/replace="g"
/replace="t"
/db_xref="dbSNP:187708101"
polyA_site 3319
/gene="CLDN16"
/gene_synonym="HOMG3; PCLN1"
/note="major polyA site"
ORIGIN
gcattttagagagcttttgtctgtgaaggctaaaagaatggccacttgtagagtatacttgaaaaagaattaggtttagtctaaattgtatcatttgaccttcaggatctctttcagtcctaggtggaagacaattttaaggaaaaaaaacctactctttcatacctcaccattttcgtttccataaattgtcctcctttcatcagctcatctctgaaattctacaaggagatgattcctgccctcaaacatcggactccaagttcttgagttttgggactcagactggctttcttgctcctcagcttgcagatgaactactgtgggatcttgtgatcatgactgaactcgttgttggccacctgtttggaaaaccattctcttgtggttggatctaacacatacagcatgtgaaggtaccagaaacacagaagactgacacccgccacttaagtggggccagggctggtgtctgcccatgttgccatcctgatgggctgcttgccacaatgagggatcttcttcaatacatcgcttgcttctttgcctttttctctgctgggtttttgattgtggccacctggactgactgttggatggtgaatgctgatgactctctggaggtgagcacaaaatgccgaggcctctggtgggaatgcgtcacaaatgcttttgatgggattcgcacctgtgatgagtacgattccatacttgcggagcatcccttgaagctggtggtaactcgagcgttgatgattactgcagatattctagctgggtttggatttctcaccctgctccttggtcttgactgcgtgaaattcctccctgatgagccgtacattaaagtccgcatctgctttgttgctggagccacgttactaatagcaggtaccccaggaatcattggctctgtgtggtatgctgttgatgtgtatgtggaacgttctactttggttttgcacaatatatttcttggtatccaatataaatttggttggtcctgttggctcggaatggctgggtctctgggttgctttttggctggagctgttctcacctgctgcttatatctttttaaagatgttggacctgagagaaactatccttattccttgaggaaagcctattcagccgcgggtgtttccatggccaagtcatactcagcccctcgcacagagacggccaaaatgtatgctgtagacacaagggtgtaaaatgcacgtttcagggtgtgtttgcatatgatttaatcaatcagtatggttacattgataaaatagtaagtcaatccaggaacagttatttagaattcatattgaattaaattaattgctagcttaatcaaaatgtttgattctcctatactttttctttctattactcttatattttcccgtcattctctctgctaaccttccaccttatgcacacactttccctatattttaagataagtctgctaggatgtagaaatatttgtttgtgatttctatatagctattagagattatgacatagtaatattaaaatgaaatgatacttaaacagaaagcaatttccaaagaggccagggaccctaatctttgaagagatgaagaaacttacttttctccctggcttttggttcactttttgtacttttaacaagtgggtgaattatttgataattttgaggaagattattcttttaaattcaaactagtatgtcaatgcctaccattactctgattatattaaaacagaaaaaggaaataacaacttcgtataccagccactggtgagagttaaagacaagagctgcccccccacccccaaatgtcaaaggcaaatgctaaattgatactggagctcgtggtgactttctacctcactaacaacataagggatctccatattatttcaccactattctagctttgctgatatattgccaaatgattagactacagaatagttcaaccagagaatttactcatttattgattaaacatccaaatactattgtaatatactatgttaaaattcatcaattcaagtgcccacacaccactgaatcatcagcaccaagcaatatattagacatatggcaaaattcaacaaatatattttgatataaataaataaacgttcacgactttacttaaaaaatcaatgttgcggctgggcacggtagctcgcgtctgtaatccccgcactttgggaggccaaggcgggtggatcacgaggtcaagagacggagaccatcctggctaacatggtgaaaccctgtctctactaaaaatacaaaaattagccgggcgtggtggcggtgcctgtagtcccagctactcgggaggctgaggcaggagaatcgtttgaacccaggaggtggaggttgcagtgagcggagatcgcaccattgcactccagtctggcaacagagcgagactccatctcaaaaaacaaaaataaataaataaataaatattcttcataaaatgtgggttttggggaaaatatagaattacatatacatttaacgaagtcgctaatgacatttcattcatattcataatgtaaccatcttgaatttttttaattgtagcgattttaaaaatgtttgtaaaatttaatttccagttttctaattacttgtcagtcacattaataacattagtacctttatggtacccttgcagtacctgaaaagaatatcaacctgaaaagaatatcaactcacccagaaattagttctttgaaaaaaaagaaattaagttgtgaatttctaaagaccttgaaataagtgtttcaaatttaaagaacaaagaatgatgtgaaaatgagattatgattcctactacatgaattaacgtttcgagattgctgtttattacttcccagagtatctttaacagtattctctgaagcagttccaatctagttggagaattaacagcaattgatttaactatctcatttttattaactgtaatttactttaaaaatatttgcaaatcatactcattagttatttgatcattgttctatgcattttaaaattaattttgtgttgttcctctcaatatttgtttttaacatttattcccatttttattttatactattgtctgtcatgctttatgtattccaataagtgtcttgaaatccttgtggggaaaggcaggacaaaaataattagttaattagatttgaaaaatgtaatttttccattttaaatatttcatttgtataagaaaatatttcagagaaccatgatgataatggatatgtgtgactgttttgaatttttttctcaattaaaacattttgtatgtaa
//
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]