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Previous release (v1)
2024-04-25 22:24:32, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001123395 3584 bp mRNA linear PRI 16-SEP-2023 DEFINITION Homo sapiens claudin 19 (CLDN19), transcript variant 2, mRNA. ACCESSION NM_001123395 VERSION NM_001123395.2 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 3584) AUTHORS Vall-Palomar M, Burballa C, Claverie-Martin F, Meseguer A and Ariceta G. TITLE Heterogeneity is a common ground in familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN19 gene mutations JOURNAL J Nephrol 34 (6), 2053-2062 (2021) PUBMED 33929692 REMARK GeneRIF: Heterogeneity is a common ground in familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN19 gene mutations. REFERENCE 2 (bases 1 to 3584) AUTHORS Liu F, Peng S, Adelman RA and Rizzolo LJ. TITLE Knockdown of Claudin-19 in the Retinal Pigment Epithelium Is Accompanied by Slowed Phagocytosis and Increased Expression of SQSTM1 JOURNAL Invest Ophthalmol Vis Sci 62 (2), 14 (2021) PUBMED 33591357 REMARK GeneRIF: Knockdown of Claudin-19 in the Retinal Pigment Epithelium Is Accompanied by Slowed Phagocytosis and Increased Expression of SQSTM1. REFERENCE 3 (bases 1 to 3584) AUTHORS Wang SB, Xu T, Peng S, Singh D, Ghiassi-Nejad M, Adelman RA and Rizzolo LJ. TITLE Disease-associated mutations of claudin-19 disrupt retinal neurogenesis and visual function JOURNAL Commun Biol 2, 113 (2019) PUBMED 30937396 REMARK GeneRIF: Mutated claudin-19 affects multiple stages of RPE and retinal differentiation through its effects on multiple functions of the RPE. Publication Status: Online-Only REFERENCE 4 (bases 1 to 3584) 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 5 (bases 1 to 3584) 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 3584) AUTHORS Gonzalez-Mariscal L, Betanzos A, Nava P and Jaramillo BE. TITLE Tight junction proteins JOURNAL Prog Biophys Mol Biol 81 (1), 1-44 (2003) PUBMED 12475568 REMARK Review article REFERENCE 7 (bases 1 to 3584) AUTHORS Tsukita S and Furuse M. TITLE Claudin-based barrier in simple and stratified cellular sheets JOURNAL Curr Opin Cell Biol 14 (5), 531-536 (2002) PUBMED 12231346 REMARK Review article REFERENCE 8 (bases 1 to 3584) AUTHORS Tsukita S, Furuse M and Itoh M. TITLE Multifunctional strands in tight junctions JOURNAL Nat Rev Mol Cell Biol 2 (4), 285-293 (2001) PUBMED 11283726 REMARK Review article REFERENCE 9 (bases 1 to 3584) AUTHORS Heiskala M, Peterson PA and Yang Y. TITLE The roles of claudin superfamily proteins in paracellular transport JOURNAL Traffic 2 (2), 93-98 (2001) PUBMED 11247307 REMARK Review article REFERENCE 10 (bases 1 to 3584) AUTHORS Kniesel U and Wolburg H. TITLE Tight junctions of the blood-brain barrier JOURNAL Cell Mol Neurobiol 20 (1), 57-76 (2000) PUBMED 10690502 REMARK Review article COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK096063.1, BC030524.1, AC098484.2 and BM681600.1. On May 31, 2019 this sequence version replaced NM_001123395.1. Summary: The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2010]. Transcript Variant: This variant (2) contains an additional segment in the coding region compared to variant 1. The resulting isoform (b) contains a shorter and distinct C-terminus compared to isoform a. 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 :: BC030524.1, AK291197.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1970526, SAMEA2142853 [ECO:0000348] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-309 AK096063.1 19-327 310-799 BC030524.1 214-703 800-1132 AC098484.2 83523-83855 c 1133-1542 BM681600.1 157-566 c 1543-1821 AK096063.1 818-1096 1822-1822 AC098484.2 82833-82833 c 1823-3584 AK096063.1 1098-2859 FEATURES Location/Qualifiers source 1..3584 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="1" /map="1p34.2" gene 1..3584 /gene="CLDN19" /gene_synonym="HOMG5" /note="claudin 19" /db_xref="GeneID:149461" /db_xref="HGNC:HGNC:2040" /db_xref="MIM:610036" exon 1..396 /gene="CLDN19" /gene_synonym="HOMG5" /inference="alignment:Splign:2.1.0" variation 3 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:529124083" variation 5 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1375607481" variation 7 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:897833054" variation 10 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="g" /db_xref="dbSNP:1249277796" variation 14 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1451899101" variation 16 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="g" /db_xref="dbSNP:1651508238" variation 18 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1651508158" variation 19 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="g" /db_xref="dbSNP:1038078008" variation 24 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:941943594" variation 25 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="g" /db_xref="dbSNP:560412100" variation 27 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:540012484" variation 28 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="g" /db_xref="dbSNP:144607541" variation 29 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1057515569" variation 30 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="c" /db_xref="dbSNP:1570446902" variation 32..34 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="cac" /db_xref="dbSNP:1651507405" variation 33 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="c" /db_xref="dbSNP:1570446896" variation 35 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:557561953" variation 37..65 /gene="CLDN19" /gene_synonym="HOMG5" /replace="ctccttctctgcctctgaccctccttctc" /replace="ctccttctctgcctctgaccctccttctctgcctctgaccctccttct c" /db_xref="dbSNP:1553139529" variation 37 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="g" /db_xref="dbSNP:1390908905" variation 39 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1651507077" variation 49 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1651506916" variation 55..57 /gene="CLDN19" /gene_synonym="HOMG5" /replace="cc" /replace="ccc" /db_xref="dbSNP:1651506685" variation 55 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="g" /db_xref="dbSNP:1651506837" variation 56 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1177750369" variation 59 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:908963748" variation 60..64 /gene="CLDN19" /gene_synonym="HOMG5" /replace="ct" /replace="cttct" /db_xref="dbSNP:1557553092" variation 60 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1314257979" variation 61 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1651506432" variation 65 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1380373520" variation 66..67 /gene="CLDN19" /gene_synonym="HOMG5" /replace="" /replace="taggaaga" /db_xref="dbSNP:1651506129" variation 71 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="t" /db_xref="dbSNP:1472412552" variation 74 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1651505964" variation 75..93 /gene="CLDN19" /gene_synonym="HOMG5" /replace="cctgcccagctgctcctcc" /replace="cctgcccagctgctcctcctgcccagctgctcctcc" /db_xref="dbSNP:1553139527" variation 75 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="c" /db_xref="dbSNP:1284530542" variation 76 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1055662634" variation 78..94 /gene="CLDN19" /gene_synonym="HOMG5" /replace="gcccagctgctcctccc" /replace="gcccagctgctcctcccgcccagctgctcctccc" /db_xref="dbSNP:1651505323" variation 83 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1651505707" variation 85 /gene="CLDN19" /gene_synonym="HOMG5" /replace="g" /replace="t" /db_xref="dbSNP:1651505630" variation 87 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1212746156" variation 90 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1651505482" variation 95 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="t" /db_xref="dbSNP:2124051197" variation 96 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="g" /db_xref="dbSNP:1651505254" variation 97 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:938486454" variation 100 /gene="CLDN19" /gene_synonym="HOMG5" /replace="g" /replace="t" /db_xref="dbSNP:1209953268" variation 103 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="g" /db_xref="dbSNP:1243092648" variation 104 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1285502726" variation 107 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1651504851" variation 113 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1214567441" variation 115 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:928410898" variation 123 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1651504564" variation 125 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="c" /db_xref="dbSNP:985328862" variation 130 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:977202893" variation 136 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1651504284" variation 138 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="g" /db_xref="dbSNP:1480537395" variation 142 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="g" /db_xref="dbSNP:1378884318" variation 147 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="g" /db_xref="dbSNP:1178964842" variation 148 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="g" /db_xref="dbSNP:1417995351" variation 150 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="c" /db_xref="dbSNP:1651503869" variation 151..173 /gene="CLDN19" /gene_synonym="HOMG5" /replace="ccctcggtcctctctcctgggcc" /replace="ccctcggtcctctctcctgggcccctcggtcctctctcctgggcc" /db_xref="dbSNP:1651502619" variation 152 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:958934446" variation 155 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:544361225" variation 156 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:372459481" variation 157 /gene="CLDN19" /gene_synonym="HOMG5" /replace="g" /replace="t" /db_xref="dbSNP:1651503324" variation 159 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:989751115" variation 160..166 /gene="CLDN19" /gene_synonym="HOMG5" /replace="ctctc" /replace="ctctctc" /db_xref="dbSNP:1651502897" variation 160 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:760579671" variation 162 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1651502967" variation 168 /gene="CLDN19" /gene_synonym="HOMG5" /replace="a" /replace="t" /db_xref="dbSNP:776610684" variation 171 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="g" /db_xref="dbSNP:112712288" variation 172 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1203294619" variation 173 /gene="CLDN19" /gene_synonym="HOMG5" /replace="c" /replace="t" /db_xref="dbSNP:1403858643" CDS 174..809 /gene="CLDN19" /gene_synonym="HOMG5" /note="isoform b is encoded by transcript variant 2" /codon_start=1 /product="claudin-19 isoform b" /protein_id="NP_001116867.1" /db_xref="CCDS:CCDS44125.1" /db_xref="GeneID:149461" /db_xref="HGNC:HGNC:2040" /db_xref="MIM:610036" /translation="
MANSGLQLLGYFLALGGWVGIIASTALPQWKQSSYAGDAIITAVGLYEGLWMSCASQSTGQVQCKLYDSLLALDGHIQSARALMVVAVLLGFVAMVLSVVGMKCTRVGDSNPIAKGRVAIAGGALFILAGLCTLTAVSWYATLVTQEFFNPSTPVNARYEFGPALFVGWASAGLAVLGGSFLCCTCPEPERPNSSPQPYRPGPSAAAREYV"
misc_feature 183..719
/gene="CLDN19"
/gene_synonym="HOMG5"
/note="PMP-22/EMP/MP20/Claudin family; Region:
PMP22_Claudin; cl21598"
/db_xref="CDD:451326"
misc_feature 195..257
/gene="CLDN19"
/gene_synonym="HOMG5"
/note="propagated from UniProtKB/Swiss-Prot (Q8N6F1.2);
transmembrane region"
misc_feature 417..479
/gene="CLDN19"
/gene_synonym="HOMG5"
/note="propagated from UniProtKB/Swiss-Prot (Q8N6F1.2);
transmembrane region"
misc_feature 525..587
/gene="CLDN19"
/gene_synonym="HOMG5"
/note="propagated from UniProtKB/Swiss-Prot (Q8N6F1.2);
transmembrane region"
misc_feature 654..716
/gene="CLDN19"
/gene_synonym="HOMG5"
/note="propagated from UniProtKB/Swiss-Prot (Q8N6F1.2);
transmembrane region"
variation 181
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2124050883"
variation 187
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007717189"
variation 188
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:763498750"
variation 191
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651500994"
variation 195
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1030881254"
variation 197
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651500767"
variation 200
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:748664372"
variation 203
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124050794"
variation 204
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:755733650"
variation 206
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651500390"
variation 207
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:368192028"
variation 209
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1334937552"
variation 211
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:767519642"
variation 212
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:12065961"
variation 213
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1381084957"
variation 214
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:751251811"
variation 216
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469998876"
variation 218
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:139675253"
variation 220
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651499300"
variation 221
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570446700"
variation 222
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:555427014"
variation 224
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1452486962"
variation 226
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1363837773"
variation 227
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1180463718"
variation 232
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:118203979"
variation 236
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242311210"
variation 237
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:773544283"
variation 238
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:140913043"
variation 243
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:761923272"
variation 244
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1057515456"
variation 247
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124050531"
variation 249
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:866406931"
variation 252
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:776725990"
variation 253
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:769104160"
variation 256
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:553635114"
variation 257
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124050460"
variation 258
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1357851582"
variation 260
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1375501298"
variation 262
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1314960755"
variation 265
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:780216494"
variation 266
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1342611487"
variation 269
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315830730"
variation 274
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:867223625"
variation 275
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381262078"
variation 278
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:760544476"
variation 279
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1033106967"
variation 280
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422671061"
variation 282
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442564894"
variation 284
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:748869909"
variation 285
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:777520292"
variation 287
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:755860892"
variation 288
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1240115369"
variation 289
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1191344664"
variation 291
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651495650"
variation 295
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:752202900"
variation 301
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:387907421"
variation 302
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780859720"
variation 303
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:751576939"
variation 305
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1407788763"
variation 312..314
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="t"
/replace="tat"
/db_xref="dbSNP:1229360131"
variation 313
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1291749652"
variation 319
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358943115"
variation 321
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:762859529"
variation 323
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:750581981"
variation 326
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:387907418"
variation 329
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:762045827"
variation 331
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402626520"
variation 332
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:776635994"
variation 335
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303732063"
variation 336
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:768727872"
variation 341
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:907045006"
variation 342
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:118203980"
variation 343
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:761073623"
variation 344
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651493539"
variation 345
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1475211264"
variation 349
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339250013"
variation 350
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124049938"
variation 351..353
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="ggg"
/db_xref="dbSNP:1159781653"
variation 351
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1347509413"
variation 355
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1439229751"
variation 362
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:776112203"
variation 365
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:772291750"
variation 374
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:746201648"
variation 375
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:779164813"
variation 376
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1434953393"
variation 378
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1222974414"
variation 379
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:373645751"
variation 380
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:539643806"
variation 386
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780841156"
variation 387
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:571067526"
variation 395
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1279756315"
variation 396
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:780082160"
exon 397..561
/gene="CLDN19"
/gene_synonym="HOMG5"
/inference="alignment:Splign:2.1.0"
variation 397
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1355679787"
variation 402..409
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="atccaatc"
/replace="atccaatccaatc"
/db_xref="dbSNP:1557551861"
variation 402
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:140190002"
variation 407
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451717579"
variation 408
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1227282179"
variation 412
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:768309387"
variation 413
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:896880334"
variation 414
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450421453"
variation 415
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:901442993"
variation 416
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1299357363"
variation 421
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651447341"
variation 422
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651447252"
variation 423
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1439120120"
variation 430
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651447047"
variation 432
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1158407262"
variation 434
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:746656339"
variation 435
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:538666680"
variation 438
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:771549550"
variation 440
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1444446063"
variation 442
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:118203981"
variation 443
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651446362"
variation 444
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1553139268"
variation 449
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:778861111"
variation 450
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:34374110"
variation 451
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557551799"
variation 454
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651445702"
variation 456
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749031151"
variation 466
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:777556169"
variation 467
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:756289810"
variation 468
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:752926836"
variation 474
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:387907419"
variation 475
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651444990"
variation 480..481
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1651444883"
variation 482
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:748824249"
variation 485
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1289562292"
variation 486
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1466588520"
variation 487
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200640147"
variation 488
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201994736"
variation 489
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:752086015"
variation 490
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:766957259"
variation 492
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651443997"
variation 498
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651443863"
variation 503
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2124045042"
variation 506
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1349368590"
variation 507
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651443699"
variation 508
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:867064302"
variation 509
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:763579075"
variation 510
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:755364712"
variation 511
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:948617979"
variation 514
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:989252379"
variation 522
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:765527366"
variation 523
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:377319583"
variation 527
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124044916"
variation 530
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651442786"
variation 533
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:763138436"
variation 534
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:750311451"
variation 535
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570444933"
variation 536
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:771578996"
variation 537..541
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1288612884"
variation 537
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:759006357"
variation 538
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651441969"
variation 539
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:773871683"
variation 543
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1478541411"
variation 544
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1266106532"
variation 549
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:770796801"
variation 553
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1488735388"
variation 559
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:143479131"
variation 561
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557551678"
exon 562..646
/gene="CLDN19"
/gene_synonym="HOMG5"
/inference="alignment:Splign:2.1.0"
variation 562
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:769597140"
variation 568
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378831110"
variation 572
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1474323316"
variation 574..579
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tg"
/replace="tgactg"
/db_xref="dbSNP:762736103"
variation 584
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:747861227"
variation 586
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781067170"
variation 587
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370124717"
variation 591
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557551562"
variation 593
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:200835353"
variation 595
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375722346"
variation 598..600
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2124044159"
variation 598
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:780278993"
variation 600
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:906095096"
variation 602
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746364980"
variation 606
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:779246616"
variation 607
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1237543232"
variation 608
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651434298"
variation 609
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651434213"
variation 611
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651434118"
variation 612
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651434032"
variation 613
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386978279"
variation 617
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:11810617"
variation 618
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:757804403"
variation 619
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651433568"
variation 625
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1310630314"
variation 627
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242843559"
variation 628
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1442512269"
variation 633
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1381010022"
variation 634
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1333146300"
variation 635
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396212645"
variation 645
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651432829"
exon 647..3584
/gene="CLDN19"
/gene_synonym="HOMG5"
/inference="alignment:Splign:2.1.0"
variation 647
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651360381"
variation 649
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651360279"
variation 655
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651360194"
variation 659
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:962614350"
variation 663
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651359971"
variation 664..671
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="ccctgttc"
/db_xref="dbSNP:1651359589"
variation 665
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:762618011"
variation 666
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651359777"
variation 668
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1216799895"
variation 671
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:776225389"
variation 672
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163560341"
variation 674
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316432824"
variation 675
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1473655950"
variation 676
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:866174535"
variation 678
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570442822"
variation 679
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124036870"
variation 682
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768639835"
variation 683
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651358674"
variation 691
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:747223067"
variation 693
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570442807"
variation 696
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263949970"
variation 697
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124036796"
variation 698
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:138355552"
variation 699
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:772247940"
variation 701
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1289785127"
variation 702
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:867926864"
variation 703
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651357824"
variation 707
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:140842024"
variation 708
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:145591298"
variation 709
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1217588010"
variation 710
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:749872474"
variation 712
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201399564"
variation 713
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651357109"
variation 714
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035217156"
variation 715
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1003712779"
variation 716
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124036565"
variation 719
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1403033958"
variation 720
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1330521485"
variation 721
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1164602961"
variation 722
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324117597"
variation 723
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367075794"
variation 724
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124036479"
variation 726
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332219103"
variation 728
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:369184924"
variation 729
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1394029284"
variation 733
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:531931336"
variation 734
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:9660973"
variation 735
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1300085775"
variation 737
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1424431332"
variation 738
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1196017795"
variation 740..746
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="agaga"
/replace="agagaga"
/db_xref="dbSNP:1341096574"
variation 743
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651353668"
variation 744
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1477074057"
variation 745
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124036280"
variation 748
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1246687752"
variation 752
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:758094656"
variation 755
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1453711939"
variation 758
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651352981"
variation 759
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256503881"
variation 760
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:749847290"
variation 761
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651352001"
variation 764
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:764811412"
variation 765
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1259589527"
variation 766
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:549476247"
variation 769
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:114350566"
variation 771
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:763959764"
variation 772
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:116804195"
variation 774
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1333791679"
variation 775
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:775446633"
variation 778
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651350767"
variation 779
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651350663"
variation 780..782
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:772887123"
variation 782
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651350389"
variation 789
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1401372077"
variation 790
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:772360364"
variation 792
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1412877618"
variation 793
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424493671"
variation 795
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011136678"
variation 796
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:894082758"
variation 799
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:145157550"
variation 800
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:774289795"
variation 803
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376266757"
variation 804
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:373130417"
variation 808
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1188616660"
variation 813
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1207548434"
variation 814..816
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cgc"
/replace="tgt"
/db_xref="dbSNP:1557550020"
variation 814
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:4660658"
variation 815
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:866489456"
variation 816
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278656048"
variation 818
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:890540431"
variation 819
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1351503503"
variation 820
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:867345315"
variation 826
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:866665590"
variation 828
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:748466759"
variation 829
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1038523634"
variation 830..835
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cccccc"
/replace="ccccccc"
/replace="cccccccc"
/db_xref="dbSNP:1396440246"
variation 830
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378795834"
variation 831
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1300141317"
variation 832
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1301048287"
variation 833..840
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccca"
/replace="cccaccca"
/db_xref="dbSNP:1238469200"
variation 833
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446024618"
variation 834
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1358664309"
variation 835
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:948161573"
variation 836
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570442470"
variation 837
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416239266"
variation 839
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1379067335"
variation 841
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:781553369"
variation 846
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651346724"
variation 848
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1440746078"
variation 850
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570442455"
variation 852
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:757926348"
variation 853
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1179779575"
variation 855
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482692439"
variation 857
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1309461123"
variation 858
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:750160816"
variation 860
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:916659139"
variation 861..870
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccagcc"
/replace="ccagccagcc"
/db_xref="dbSNP:1651345724"
variation 861
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:778274875"
variation 862
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651345917"
variation 863
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1207362128"
variation 870
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1254784973"
variation 872
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756840769"
variation 873
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1285270660"
variation 874
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:199656937"
variation 875
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1355608797"
variation 877
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456719872"
variation 879
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381079432"
variation 880
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1310238805"
variation 882
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651344732"
variation 883
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651344659"
variation 885
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1226823680"
variation 889
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378806839"
variation 891
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284992714"
variation 896
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:866413020"
variation 898
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:778620439"
variation 899
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416757983"
variation 901
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1314103036"
variation 904
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1358672309"
variation 905
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1298153440"
variation 906
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:565025655"
variation 908
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1362861718"
variation 911
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:764084498"
variation 915
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:760700236"
variation 917
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:977990338"
variation 919
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1466485858"
variation 920
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:967912511"
variation 924
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1330499189"
variation 925
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:544937247"
variation 926
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651342944"
variation 929
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022106419"
variation 930
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772513053"
variation 932
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1366405529"
variation 944
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651342598"
variation 945
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:567128668"
variation 949
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:774741981"
variation 950
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651342298"
variation 953
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:759663769"
variation 954
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1018692736"
variation 956
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651342000"
variation 959
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651341512"
variation 975
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124034842"
variation 977
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1314531151"
variation 978
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="a"
/db_xref="dbSNP:1651341350"
variation 978
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1009023125"
variation 981
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651341219"
variation 986
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651341136"
variation 987
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651341089"
variation 991
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651341023"
variation 994
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651340952"
variation 996
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:950371999"
variation 1000
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651340773"
variation 1004
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456719913"
variation 1005
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1390669324"
variation 1008
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1320998903"
variation 1009
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1239070859"
variation 1010
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1025957490"
variation 1011
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:994439822"
variation 1013
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651340259"
variation 1014
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427342313"
variation 1016
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:555913979"
variation 1025
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651340035"
variation 1026
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1433791171"
variation 1027
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1169882297"
variation 1030
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570442247"
variation 1035
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:898731607"
variation 1036..1038
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cac"
/replace="cacac"
/db_xref="dbSNP:1331759851"
variation 1038
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1038973831"
variation 1039
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:550620549"
variation 1042
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651339377"
variation 1048
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:536058712"
variation 1049
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370684135"
variation 1050
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557549800"
variation 1051
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570442219"
variation 1052
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570442214"
variation 1055
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:573614349"
variation 1056
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651338833"
variation 1059
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651338767"
variation 1060
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570442209"
variation 1067
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1367710944"
variation 1070
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1167233205"
variation 1071
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1278153633"
variation 1073
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056556314"
variation 1074
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424598155"
variation 1076
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651336218"
variation 1077
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:958266587"
variation 1081
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651336052"
variation 1086
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651335943"
variation 1090
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274145956"
variation 1091
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1321411740"
variation 1094
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:140498057"
variation 1097
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651333329"
variation 1106
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:181776711"
variation 1107
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1490544441"
variation 1108
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1042348540"
variation 1109
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1192984336"
variation 1111
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1260998336"
variation 1112
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651332744"
variation 1114
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651332665"
variation 1115
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651332594"
variation 1116
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:571260727"
variation 1119
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:558473657"
variation 1120
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651332354"
variation 1122
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651332273"
variation 1126
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651332197"
variation 1131
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651332117"
variation 1132
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:12141833"
variation 1135
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403329333"
variation 1138
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:915151352"
variation 1142
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:993965686"
variation 1144
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:975020708"
variation 1145
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:964577864"
variation 1146
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:780389459"
variation 1147
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1487739799"
variation 1150
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651331169"
variation 1152
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1267596829"
variation 1153
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651331002"
variation 1154
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223403161"
variation 1155
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2124033931"
variation 1157
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651330831"
variation 1158..1168
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tagag"
/replace="tagagatagag"
/db_xref="dbSNP:1226928582"
variation 1158
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651330755"
variation 1160
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651330667"
variation 1164
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770205728"
variation 1165
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651330477"
variation 1166
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1378911877"
variation 1170
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1292323792"
variation 1174
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1360406686"
variation 1180
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1216029747"
variation 1181
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651330010"
variation 1182
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:745928043"
variation 1183
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651329838"
variation 1185
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651329757"
variation 1194
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651329673"
variation 1195
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570442088"
variation 1196
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651329531"
variation 1201
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570442086"
variation 1203
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:781433880"
variation 1205
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570442076"
variation 1206
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:941232493"
variation 1207
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651329153"
variation 1209
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651329078"
variation 1210
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651329000"
variation 1211
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651328911"
variation 1215..1217
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2124033603"
variation 1218
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651328824"
variation 1219
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:571548302"
variation 1223
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570442065"
variation 1224
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:950424439"
variation 1226
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:569593546"
variation 1228
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1054990359"
variation 1230
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:937667307"
variation 1232
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298289259"
variation 1233
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026009370"
variation 1238
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:927592582"
variation 1241
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2124033479"
variation 1243
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1414120405"
variation 1247
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651327829"
variation 1248..1251
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ca"
/replace="caca"
/db_xref="dbSNP:1651327691"
variation 1250
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1418710998"
variation 1253
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:994493897"
variation 1257
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:981821556"
variation 1258..1261
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="ccac"
/db_xref="dbSNP:913683166"
variation 1259
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:115864005"
variation 1264
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124033343"
variation 1267
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651327264"
variation 1269
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651327171"
variation 1273
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:189463551"
variation 1274
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295063346"
variation 1285
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:146829937"
variation 1286
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017856464"
variation 1287
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:895328399"
variation 1288
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205745945"
variation 1291
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1166828875"
variation 1301
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441990"
variation 1302
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1057009534"
variation 1303
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651326301"
variation 1305
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651326224"
variation 1307
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1431750471"
variation 1311
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212055901"
variation 1318
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651325985"
variation 1323
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441977"
variation 1329
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:547115625"
variation 1334
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651325743"
variation 1336
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651325660"
variation 1338
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:955001262"
variation 1339
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:752275663"
variation 1344
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570441964"
variation 1345
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651325274"
variation 1346
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1470222436"
variation 1349..1353
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ggggg"
/replace="gggggg"
/db_xref="dbSNP:1171463827"
variation 1349
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1557549605"
variation 1354
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1425128711"
variation 1356
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651324772"
variation 1358
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651324655"
variation 1361
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1269922455"
variation 1363
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441948"
variation 1364
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651324363"
variation 1373..1400
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gg"
/replace="ggtcggaccatggcgcccctgcccccgg"
/db_xref="dbSNP:1220887984"
variation 1376
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:533160815"
variation 1377
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:993520421"
variation 1383
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407311555"
variation 1385
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:902591128"
variation 1386
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:564169958"
variation 1387..1494
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gcccctgcccccg"
/replace="gcccctgcccccgggaatgggccccaggcagggctgctgtgagggcca
aggtctggccacgctggccagtacccatgtccgggcctgaatgcacagcccctgcccc
cg"
/db_xref="dbSNP:1651318199"
variation 1387
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1042403857"
variation 1388
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1005324205"
variation 1390
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:766985702"
variation 1394
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:867072861"
variation 1395
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1160256565"
variation 1398
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:544224952"
variation 1399..1401
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1263612424"
variation 1399
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:531471001"
variation 1404
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2124032758"
variation 1411
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651322461"
variation 1415
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651322377"
variation 1416
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557549561"
variation 1417
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651322226"
variation 1418
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1038958519"
variation 1419
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:937904168"
variation 1420
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:751482708"
variation 1424
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651321885"
variation 1428
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124032667"
variation 1431
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651321814"
variation 1436
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1310295582"
variation 1438
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651321238"
variation 1445
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:911748345"
variation 1446
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:562452279"
variation 1447
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:143708479"
variation 1448
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:573827426"
variation 1449
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:553575963"
variation 1450
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651320439"
variation 1453
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651320363"
variation 1459
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387097409"
variation 1460
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:919004200"
variation 1461
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:868235687"
variation 1465..1468
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="ccgg"
/db_xref="dbSNP:989256170"
variation 1466
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376759002"
variation 1467
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:913634313"
variation 1469
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1398992220"
variation 1471
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651319662"
variation 1474
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:963044897"
variation 1478
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:577543955"
variation 1479
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:910699717"
variation 1480
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651319288"
variation 1483..1486
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1030616687"
variation 1483
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:372581520"
variation 1484
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:955095486"
variation 1489..1493
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cccc"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:376221466"
variation 1489
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:184994488"
variation 1490
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:972471763"
variation 1492
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651318655"
variation 1493..1494
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="t"
/db_xref="dbSNP:1557549490"
variation 1493
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:74885359"
variation 1494
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:569528348"
variation 1497
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:763045798"
variation 1498
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:773299018"
variation 1499
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1220634133"
variation 1502
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:770230972"
variation 1506
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1290915035"
variation 1507
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:528764011"
variation 1507
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235329729"
variation 1509
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748661119"
variation 1510
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:781537112"
variation 1511
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1477762274"
variation 1513
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1364784331"
variation 1518
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:769126862"
variation 1520
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441741"
variation 1521..1530
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ctctctctct"
/replace="ctctctctctctctctct"
/db_xref="dbSNP:1651316147"
variation 1523
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:374216538"
variation 1526
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778667951"
variation 1533
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651316071"
variation 1534
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1166673287"
variation 1537
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651315898"
variation 1544
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:756892751"
variation 1547
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651315741"
variation 1549
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422290318"
variation 1551
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651315592"
variation 1555
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1193831713"
variation 1557
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:753338977"
variation 1561
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777425105"
variation 1562
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147528059"
variation 1564
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651315070"
variation 1567
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:752738519"
variation 1568
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:535667246"
variation 1573
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1215803586"
variation 1574
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:200491942"
variation 1575
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1257662822"
variation 1576
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1219376620"
variation 1577
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1279949075"
variation 1578
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1309299294"
variation 1579
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:371686331"
variation 1586
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:766571498"
variation 1587
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:387907420"
variation 1588
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:764858690"
variation 1590
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:773211263"
variation 1592
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328261253"
variation 1593
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:769931882"
variation 1598
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:762297703"
variation 1600
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:777172207"
variation 1601
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:768871931"
variation 1602
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:747361042"
variation 1605
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:775740656"
variation 1608
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:770548857"
variation 1609
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:367910861"
variation 1610
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:777408812"
variation 1611
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:546757402"
variation 1616
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:755733771"
variation 1617
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:748064968"
variation 1619
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1177658979"
variation 1621
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:781140631"
variation 1623
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651312522"
variation 1624
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429507975"
variation 1625
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:373755403"
variation 1629
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:750026527"
variation 1632
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651312175"
variation 1636
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200471599"
variation 1637
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1313365002"
variation 1638
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039423338"
variation 1645
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651311814"
variation 1646
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651311737"
variation 1647
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:910316814"
variation 1648..1654
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:1351281461"
variation 1649
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230470801"
variation 1654
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651311406"
variation 1658
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:943323880"
variation 1660
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651311245"
variation 1662
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1290591903"
variation 1670..1677
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="catccagc"
/db_xref="dbSNP:369052611"
variation 1670
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1312372093"
variation 1673
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:890355984"
variation 1674
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:796219031"
variation 1676
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651310688"
variation 1677..1680
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1310273077"
variation 1677
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051634158"
polyA_site 1682
/gene="CLDN19"
/gene_synonym="HOMG5"
/note="major polyA site"
variation 1682
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:77236131"
variation 1685
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651309054"
variation 1686
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:919054603"
variation 1691
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651308898"
variation 1694
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651308816"
variation 1696
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:765909170"
variation 1697
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:550521995"
variation 1700
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:958751979"
variation 1702
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441516"
variation 1704
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486463471"
variation 1710
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376052803"
variation 1711
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:915602099"
variation 1713
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651306549"
variation 1718
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:991547265"
variation 1721
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1412202056"
variation 1722
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1184440731"
variation 1725
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002446383"
variation 1726
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1437925300"
variation 1730
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2124031042"
variation 1735
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651305332"
variation 1738
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651305260"
variation 1740
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:959681582"
variation 1744
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651305109"
variation 1745
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:530817596"
variation 1747
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1035678117"
variation 1749
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:140105842"
variation 1751
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:966857083"
variation 1752
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1408035464"
variation 1753
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651304418"
variation 1754
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:372780855"
variation 1756
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330294458"
variation 1760
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651304187"
variation 1761
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374175709"
variation 1762
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651304043"
variation 1766
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1225012393"
variation 1768
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:371735000"
variation 1769
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="a"
/db_xref="dbSNP:1651303556"
variation 1770
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441448"
variation 1774
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651303395"
variation 1777
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651303321"
variation 1778
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651303242"
variation 1787
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651303183"
variation 1788
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:762336108"
variation 1790
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651303028"
variation 1793
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651302955"
variation 1794
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1017633734"
variation 1795
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651302791"
variation 1796
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1233170783"
variation 1798
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007966109"
variation 1804
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1266027309"
variation 1806
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210312530"
variation 1810
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204652754"
variation 1812
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651302185"
variation 1814
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:890420008"
variation 1821
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="t"
/db_xref="dbSNP:1237852963"
variation 1822
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:912075"
variation 1823
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651301614"
variation 1825
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1179091682"
variation 1826
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124030579"
variation 1827
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441403"
variation 1830
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:936351398"
variation 1837
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651301325"
variation 1838
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651301258"
variation 1841
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651301175"
variation 1845
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651301086"
variation 1848
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:796637327"
variation 1849
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1173907268"
variation 1851
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1431290070"
variation 1852
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557549135"
variation 1853..1855
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1470171925"
variation 1855..1857
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="t"
/replace="tct"
/db_xref="dbSNP:1651300214"
variation 1856
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169660133"
variation 1862
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651300144"
variation 1863..1868
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccccc"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:532996510"
variation 1863
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1397759529"
variation 1866
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651299939"
variation 1867
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557549123"
variation 1870
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:374721300"
variation 1876
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:897677267"
variation 1878..1893
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tggccttggccttggc"
/replace="tggccttggccttggccttggc"
/db_xref="dbSNP:1382161816"
variation 1880
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651299417"
variation 1886
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:769241790"
variation 1887
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1037519071"
variation 1888
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1313526522"
variation 1894
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1651298963"
variation 1901
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1224550639"
variation 1902
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1257815975"
variation 1904
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306041428"
variation 1906..1907
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1387012858"
variation 1907
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651298546"
variation 1910
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:560322698"
variation 1913
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:923428502"
variation 1915..1916
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="tt"
/db_xref="dbSNP:1651298185"
variation 1915
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441330"
variation 1918
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651298103"
variation 1920
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1488210994"
variation 1922
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651297939"
variation 1923
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651297853"
variation 1930
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189528235"
variation 1931
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:972643328"
variation 1932
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651297622"
variation 1940
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:940921614"
variation 1946
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651297444"
variation 1947
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:915635301"
variation 1948
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651297274"
variation 1955
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192750059"
variation 1957
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651297101"
variation 1958
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:909480057"
variation 1965
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651296925"
variation 1966
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1411376424"
variation 1967
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1170743499"
variation 1968
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651296740"
variation 1972
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348885607"
variation 1973
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651296606"
variation 1977
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:540075482"
variation 1978
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1458132860"
variation 1982
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1304397001"
variation 1984
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651296322"
variation 1986
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1348005048"
variation 1990
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406074500"
variation 1993
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:991208270"
variation 1994
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1360351404"
variation 1995
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651295905"
variation 1998
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1216643137"
variation 2002
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:938348889"
variation 2006
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651295666"
variation 2011
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651295584"
variation 2012..2013
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1557549040"
variation 2012
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:958740672"
variation 2013
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:577777997"
variation 2014
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557549032"
variation 2021
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1220436490"
variation 2026
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651295069"
variation 2027
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651294954"
variation 2029..2030
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="ct"
/db_xref="dbSNP:1651294861"
variation 2036
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651294764"
variation 2043
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441257"
variation 2048
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:927363928"
variation 2049
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651294479"
variation 2051
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1490516616"
variation 2053
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1215809504"
variation 2059
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651294239"
variation 2061
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1240247833"
variation 2063
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651294088"
variation 2066
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651294006"
variation 2068
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1476285590"
variation 2080
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557549013"
variation 2082
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762244030"
variation 2092
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651293632"
variation 2099
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:971891724"
variation 2100
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:982342001"
variation 2103
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1421685531"
variation 2105
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2124029487"
variation 2106
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651293273"
variation 2107
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:966911128"
variation 2110
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="a"
/db_xref="dbSNP:1651293052"
variation 2112
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651292928"
variation 2113
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570441205"
variation 2114
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:776804215"
variation 2121
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="c"
/db_xref="dbSNP:138777333"
variation 2121
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570441195"
variation 2121
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2124029388"
variation 2123
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651292465"
variation 2127
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1057515528"
variation 2129
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1433378024"
variation 2129
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124029327"
variation 2130
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000530698"
variation 2137
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441171"
variation 2138
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:549719300"
variation 2140
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1378789687"
variation 2142
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:529459531"
variation 2152
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1317340602"
variation 2153
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1050521162"
variation 2155
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:958183930"
variation 2156
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651291501"
variation 2158
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124029210"
variation 2159
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557548969"
variation 2160
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651291298"
variation 2161
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:901605896"
variation 2164
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651291140"
variation 2166
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1036501699"
variation 2167
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:746091783"
variation 2168
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1465219512"
variation 2171
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651290809"
variation 2172
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651290725"
variation 2177
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651290639"
variation 2178
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651290539"
variation 2179
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="c"
/db_xref="dbSNP:2124029075"
variation 2179
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236668999"
variation 2182
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651290394"
variation 2187
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288859510"
variation 2188
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1018104979"
variation 2189
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651290159"
variation 2193
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1570441109"
variation 2196
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651290016"
variation 2198
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651289946"
variation 2201
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1208353733"
variation 2202
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1358653297"
variation 2204
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1007604392"
variation 2208
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1266123585"
variation 2209
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1227696453"
variation 2212
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:940889035"
variation 2213..2217
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:551118125"
variation 2213
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441086"
variation 2215
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:761260010"
variation 2217
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1406509120"
variation 2220
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:909468672"
variation 2227
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:954884639"
variation 2228
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570441069"
variation 2229
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651288831"
variation 2230
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030310070"
variation 2232
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:563880269"
variation 2233
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:781380872"
variation 2235
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651288511"
variation 2237
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:993435665"
variation 2242
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651288359"
variation 2243
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450854555"
variation 2251
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:927279008"
variation 2255
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570441044"
variation 2256
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1383775010"
variation 2258
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:981869447"
variation 2259
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:897729862"
variation 2260
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651287512"
variation 2261
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651287434"
variation 2263
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651287367"
variation 2264
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651287302"
variation 2265
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441028"
variation 2274
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651287140"
variation 2277
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:544178185"
variation 2282
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376179882"
variation 2285
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:770893678"
variation 2294..2300
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gaggtcc"
/replace="gaggtccgaggtcc"
/db_xref="dbSNP:1224286686"
variation 2301
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651286686"
variation 2302
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:894268522"
variation 2304
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651286537"
variation 2305..2309
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tcttt"
/replace="tctttcttt"
/db_xref="dbSNP:1651286378"
variation 2306
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1055959077"
variation 2326
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:142957479"
variation 2328
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557548866"
variation 2331
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651286100"
variation 2333
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651285812"
variation 2334
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163371071"
variation 2336
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:956565410"
variation 2339
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205305296"
variation 2343
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124028436"
variation 2345
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651285410"
variation 2346
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651285325"
variation 2348
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651285222"
variation 2352
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1032252022"
variation 2358..2361
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1651284899"
variation 2360
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1457037795"
variation 2363
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1179119133"
variation 2372
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570440973"
variation 2374
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651284640"
variation 2375
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651284567"
variation 2383
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428584044"
variation 2384
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000749435"
variation 2385
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651284324"
variation 2391
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777568849"
variation 2392
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1041346817"
variation 2402
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1028632951"
variation 2403
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1245915070"
variation 2404
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1429147609"
variation 2405
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651283714"
variation 2409
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651283626"
variation 2410..2411
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1651283478"
variation 2410
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651283551"
variation 2411
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:368436876"
variation 2419
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651283324"
variation 2422..2423
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="cccctt"
/db_xref="dbSNP:1651283244"
variation 2425..2428
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="gtac"
/db_xref="dbSNP:1651282989"
variation 2425
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651283164"
variation 2427
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196406854"
variation 2432..2437
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:1049224758"
variation 2433
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:181070200"
variation 2434
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:914148776"
variation 2435
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268267008"
variation 2436
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:377585440"
variation 2437
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:887914551"
variation 2441
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1225184734"
variation 2444
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651282146"
variation 2446
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651282052"
variation 2451
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263511720"
variation 2454
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651281877"
variation 2455
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124027921"
variation 2456
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651281784"
variation 2458
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:796839004"
variation 2460
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651281593"
variation 2461
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1274622493"
variation 2463
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651281450"
variation 2464
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370331996"
variation 2467
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1273470824"
variation 2469
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651281232"
variation 2471
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268854758"
variation 2480
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1045719913"
variation 2482
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="g"
/db_xref="dbSNP:1651280966"
variation 2485
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:910688779"
variation 2487
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1332005923"
variation 2492
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:375306800"
variation 2495
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:913313445"
variation 2497
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:988929125"
variation 2498..2506
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ag"
/replace="aggccagag"
/db_xref="dbSNP:2124027665"
variation 2499
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:758420361"
variation 2501
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124027693"
variation 2503
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302621983"
variation 2506
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:148594631"
variation 2509
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651280180"
variation 2512
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1368236439"
variation 2513
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:954754714"
variation 2515
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651279898"
variation 2516
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:369724376"
variation 2519
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124027562"
variation 2520
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1406709368"
variation 2527
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:925067368"
variation 2530
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1030363830"
variation 2531
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124027513"
variation 2532
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1224900327"
variation 2534
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651279231"
variation 2540
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410475059"
variation 2546..2549
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1651278770"
variation 2548
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424315949"
variation 2549
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651278627"
variation 2552
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:570565492"
variation 2553
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651278296"
variation 2554
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:550710062"
variation 2555
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:961993377"
variation 2565
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1016190439"
variation 2566
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006102105"
variation 2567
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:894312717"
variation 2576
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1055609220"
variation 2577
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1003059924"
variation 2580
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440821"
variation 2585
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1490681272"
variation 2586
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1377976423"
variation 2588
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651276774"
variation 2589
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:906949228"
variation 2590
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651276379"
variation 2595
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440801"
variation 2596
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:966138586"
variation 2599
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482159495"
variation 2602
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1191445002"
variation 2609
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:114944537"
variation 2610
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:568148786"
variation 2611
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:945714612"
variation 2613
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442385976"
variation 2622
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124027137"
variation 2630
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651272818"
variation 2635
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124027109"
variation 2636
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651272715"
variation 2638
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1277175863"
variation 2641
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1426580574"
variation 2645
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440761"
variation 2646
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303707822"
variation 2647
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651272059"
variation 2648
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:914201766"
variation 2651
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651271743"
variation 2652
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651271624"
variation 2662
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1380357646"
variation 2663
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:887547668"
variation 2664
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1057515527"
variation 2665
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1243631825"
variation 2665
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651271035"
variation 2666..2667
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="acctccccttcc"
/db_xref="dbSNP:1651270946"
variation 2668
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651270816"
variation 2676
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:548984051"
variation 2677
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124026869"
variation 2678
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1361015949"
variation 2680
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651270491"
variation 2685
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651270406"
variation 2686
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:189819580"
variation 2688..2694
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ctggcct"
/replace="ctggcctggcct"
/db_xref="dbSNP:1651269933"
variation 2689
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1002138865"
variation 2691
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651270061"
variation 2692..2699
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cctcc"
/replace="cctcctcc"
/db_xref="dbSNP:1651269737"
variation 2694
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1203815179"
variation 2699
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:906096762"
variation 2705
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124026713"
variation 2707
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:564714068"
variation 2708
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1227401183"
variation 2713
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348176800"
variation 2716
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651268960"
variation 2719
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:950072291"
variation 2726
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1363228211"
variation 2728
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1451529541"
variation 2729
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2124026616"
variation 2731
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:529158343"
variation 2732
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1391371008"
variation 2735
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651268246"
variation 2736
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651268154"
variation 2745..2746
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="gcttctccttcg"
/db_xref="dbSNP:1385411183"
variation 2750
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:891756677"
variation 2751
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332181117"
variation 2753
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:184596944"
variation 2763
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:796988312"
variation 2765
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651267544"
variation 2766
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651267448"
variation 2769
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406550607"
variation 2770
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:144430420"
variation 2773
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471748356"
variation 2776
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262971116"
variation 2777
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124026409"
variation 2778
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651266929"
variation 2780
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:910732047"
variation 2783
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1351873770"
variation 2796
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:778687377"
variation 2797
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:986301112"
variation 2804
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651266461"
variation 2809
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1241571392"
variation 2811
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651266301"
variation 2813
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651266207"
variation 2816
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:754589000"
variation 2820
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:926038941"
variation 2823
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1184356468"
variation 2826
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1472535414"
variation 2827
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1249928199"
variation 2831
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651264513"
variation 2833
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:753515106"
variation 2844
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:933422896"
variation 2850
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212936203"
variation 2853
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651264106"
variation 2854
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651264023"
variation 2861
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651263951"
variation 2863
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651263878"
variation 2871
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651263788"
variation 2875
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:976373319"
variation 2877
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:766100803"
variation 2880
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:546730630"
variation 2881
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:965993611"
variation 2884
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1321561594"
variation 2887
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1470006770"
variation 2888
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651263108"
variation 2892
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651263025"
variation 2893..2894
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="ac"
/db_xref="dbSNP:1297176277"
variation 2893
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440619"
variation 2894
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651262799"
variation 2896
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651262709"
variation 2899
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440610"
variation 2900
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:923346842"
variation 2901
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1014521584"
variation 2902
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1351603683"
variation 2903
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:972101560"
variation 2904
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651262102"
variation 2905
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651262021"
variation 2906
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1326675459"
variation 2908
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651261851"
variation 2910
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1204553607"
variation 2913
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1289876170"
variation 2914
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:760068656"
variation 2915
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1479712621"
variation 2916
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:962046453"
variation 2917
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124025830"
variation 2918
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:76855155"
variation 2920
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651261007"
variation 2922..2940
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gcaca"
/replace="gcacatccaccggggcaca"
/db_xref="dbSNP:1169331973"
variation 2922
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570440564"
variation 2923
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1480061117"
variation 2924
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1281856305"
variation 2926
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1197119795"
variation 2927
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651260597"
variation 2928
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651260497"
variation 2929
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:985131155"
variation 2930
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440550"
variation 2932
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:958630245"
variation 2933
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651260155"
variation 2934
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651260083"
variation 2936
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651260006"
variation 2942
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651259846"
variation 2944
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:745884385"
variation 2948
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200527665"
variation 2950..2953
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tgtc"
/replace="tgtctgtc"
/db_xref="dbSNP:1001707873"
variation 2952
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440539"
variation 2953
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651259427"
variation 2957
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651259312"
variation 2967
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651259241"
variation 2968
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:567823099"
variation 2969
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651259065"
variation 2970
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1024484460"
variation 2971
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651258894"
variation 2974
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651258809"
variation 2988
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281860320"
variation 2992
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:544361263"
variation 2994
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1014880889"
variation 2998..3001
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1651257735"
variation 3000
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651257827"
variation 3001
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:373188579"
variation 3005
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1404978019"
variation 3011
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124025433"
variation 3014
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009910087"
variation 3019
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:149256970"
variation 3020
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557548354"
variation 3021
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651257129"
variation 3031
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1054107067"
variation 3033
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651256977"
variation 3035
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:904588472"
variation 3040..3043
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="t"
/replace="ttct"
/db_xref="dbSNP:529449539"
variation 3041
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:796175275"
variation 3043..3052
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="tcctctgggt"
/db_xref="dbSNP:796901250"
variation 3045
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651256649"
variation 3046..3052
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="tctgggt"
/db_xref="dbSNP:562296433"
variation 3047
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:889365281"
variation 3049
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1490465444"
variation 3050
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1049876055"
variation 3053
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651256206"
variation 3064
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247904427"
variation 3068
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1170642886"
variation 3073
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651256000"
variation 3074
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1051069098"
variation 3082
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:931824276"
variation 3083
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651255779"
variation 3085
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124025179"
variation 3088
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651255704"
variation 3089
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651255626"
variation 3095
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301862960"
variation 3097
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651255479"
variation 3098
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:933476755"
variation 3100
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288652453"
variation 3103
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651255231"
variation 3108
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1360239083"
variation 3109
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:770989443"
variation 3111
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:923397849"
variation 3115
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124025040"
variation 3116
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651254904"
variation 3117
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651254819"
variation 3119
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1298557597"
variation 3120
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:71654253"
variation 3123
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1040226305"
variation 3124
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:944594774"
variation 3125
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1293905748"
variation 3126..3129
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tcca"
/replace="tccatcca"
/db_xref="dbSNP:1651252045"
variation 3126
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651252143"
variation 3134
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1452102004"
variation 3137
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651251901"
variation 3140
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:556016559"
variation 3142
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651251709"
variation 3150
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1320683263"
variation 3151
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651251523"
variation 3154
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1287161397"
variation 3160
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:972155294"
variation 3175
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651251285"
variation 3177
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1486687028"
variation 3182
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:371301647"
variation 3185
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:113021721"
variation 3187
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:763565629"
variation 3188
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1296855045"
variation 3189..3190
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="cc"
/db_xref="dbSNP:1432786550"
variation 3190
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651250450"
variation 3195
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:951754166"
variation 3196
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1289160691"
variation 3197
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:984795189"
variation 3198
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1158931903"
variation 3201
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1343831685"
variation 3204
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1433265834"
variation 3205
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651249964"
variation 3212
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1057515454"
variation 3219
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1436042894"
variation 3223
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1348305840"
variation 3224
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651249597"
variation 3227
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1382267259"
variation 3228
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651249434"
variation 3231
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:958906433"
variation 3232
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651249261"
variation 3233
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:56345167"
variation 3234
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:969836365"
variation 3235
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651248882"
variation 3237
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223154374"
variation 3239
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651248719"
variation 3240
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:573446568"
variation 3241
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1209098870"
variation 3246
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651248461"
variation 3249
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:981285231"
variation 3250
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651248287"
variation 3252
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:553394106"
variation 3254..3257
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1651248113"
variation 3258
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1184964715"
variation 3260
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:866481412"
variation 3262
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1570440321"
variation 3263
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651247803"
variation 3265..3268
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="ctgc"
/db_xref="dbSNP:1651247659"
variation 3265
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:539642986"
variation 3270
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451809122"
variation 3271
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1469144840"
variation 3272
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1177158947"
variation 3273
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651247303"
variation 3275..3283
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="agaa"
/replace="agaaaagaa"
/db_xref="dbSNP:1402844561"
variation 3281
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1406394767"
variation 3284
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651247012"
variation 3285
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651246942"
variation 3289
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765727450"
variation 3290
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651246621"
variation 3291..3293
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1458515379"
variation 3291
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2124024227"
variation 3293
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:546947188"
variation 3298
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262884502"
variation 3299
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651246309"
variation 3300
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:956260632"
variation 3303
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651246161"
variation 3309
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1020047992"
variation 3310
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1009962127"
variation 3313
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:147155302"
variation 3314
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1338872790"
variation 3316
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651245677"
variation 3317
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651245592"
variation 3321
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1244664749"
variation 3323
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:892869640"
variation 3324
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:112310775"
variation 3325
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651245042"
variation 3326
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651244971"
variation 3332
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651244902"
variation 3334
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441510641"
variation 3338
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1000192988"
variation 3351
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:138082769"
variation 3352
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1262264797"
variation 3355
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:771252039"
variation 3356
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1226086135"
variation 3357
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651244247"
variation 3363
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440246"
variation 3365
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1344150641"
variation 3366
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651243960"
variation 3368
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651243885"
variation 3369
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1278827265"
variation 3379
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124023861"
variation 3382
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:889408741"
variation 3383
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651243607"
variation 3385
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651243524"
variation 3387
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1201787038"
variation 3388
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651243347"
variation 3396
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651243289"
variation 3400
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651243203"
variation 3402
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1050705706"
variation 3405
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651243058"
variation 3406..3409
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1651242896"
variation 3406
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124023737"
variation 3408
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473848049"
variation 3411
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651242802"
variation 3413
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651242713"
variation 3414..3417
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gt"
/replace="gtgt"
/db_xref="dbSNP:1295555220"
variation 3414
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:367871467"
variation 3417
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1365183958"
variation 3420
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:987445393"
variation 3434
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651242210"
variation 3435
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:997317672"
variation 3436
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1403157963"
variation 3440
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651241969"
variation 3441
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1405766198"
variation 3444
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1248423203"
variation 3445
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1326930691"
variation 3446..3455
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gtggtgg"
/replace="gtggtggtgg"
/db_xref="dbSNP:1432196945"
variation 3449
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:537175766"
variation 3450
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748058230"
variation 3451
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370272303"
variation 3454
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1306198755"
variation 3455
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1282513897"
variation 3457
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374100414"
variation 3468
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651240603"
variation 3474..3515
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="actcgggagg"
/replace="actcgggaggctgaggcaggagaatcgcttgaactcgggagg"
/db_xref="dbSNP:1651238961"
variation 3475
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1175941351"
variation 3477
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:747048669"
variation 3478
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:568235631"
variation 3482
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:940783155"
variation 3489
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1212346123"
variation 3493
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651240040"
variation 3494
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274512736"
variation 3499
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1178386071"
variation 3500
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:909291003"
variation 3501
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268742724"
variation 3503
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651239567"
variation 3506
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1250436417"
variation 3507
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651239378"
variation 3509
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:192923064"
variation 3510
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1201425315"
variation 3513
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378495316"
variation 3514
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1475201215"
variation 3516
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1436636389"
variation 3518
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124023222"
variation 3520
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651238700"
variation 3521
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1430430620"
variation 3522
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1258863550"
variation 3523
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651238299"
variation 3525..3531
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cagtcag"
/replace="cagtcagtcag"
/db_xref="dbSNP:1310279220"
variation 3525
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651238217"
variation 3529
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1232414045"
variation 3531
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1040599473"
variation 3537
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1224790665"
variation 3539
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1192721334"
variation 3540
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1291746752"
variation 3544..3551
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cac"
/replace="cactgcac"
/db_xref="dbSNP:1651237360"
variation 3544
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651237593"
variation 3545
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:534717853"
variation 3549
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:944567393"
variation 3552
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651237304"
variation 3556
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1224371085"
variation 3557
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:188969705"
variation 3558
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446719057"
variation 3560
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1350052976"
variation 3561..3562
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="gc"
/db_xref="dbSNP:2124022944"
variation 3562
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570440079"
variation 3563..3564
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="tg"
/db_xref="dbSNP:2124022913"
variation 3563
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440076"
variation 3564
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651236726"
variation 3566
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440067"
variation 3571
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651236556"
variation 3572
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1191329965"
variation 3575
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440058"
variation 3576
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250108113"
variation 3577
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440050"
variation 3579
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1286567517"
variation 3581..3582
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="tc"
/db_xref="dbSNP:1397277485"
variation 3581
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274704995"
variation 3582
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1411792184"
variation 3583
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1570440034"
variation 3584
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="c"
/db_xref="dbSNP:1464983949"
variation 3584
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:955329719"
variation 3584
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1651235684"
ORIGIN
actgcctttgctccagccgctgccgccgcaccacctctccttctctgcctctgaccctccttctcgctgctccccctgcccagctgctcctcccacctggccatgaccaaagcccctgctggcaccctggcccagctctgagtcctgggaccctcggtcctctctcctgggccatggccaactcaggcctccagctcctgggctacttcttggccctgggtggctgggtgggcatcattgctagcacagccctgccacagtggaagcagtcttcctacgcaggcgacgccatcatcactgccgtgggcctctatgaagggctctggatgtcctgcgcctcccagagcactgggcaagtgcagtgcaagctctacgactcgctgctcgccctggacggtcacatccaatcagcgcgggccctgatggtggtggccgtgctcctgggcttcgtggccatggtcctcagcgtagttggcatgaagtgtacgcgggtgggagacagcaaccccattgccaagggccgtgttgccatcgccgggggagccctcttcatcctggcaggcctctgcactttgactgctgtctcgtggtatgccaccctggtgacccaggagttcttcaacccaagcacacctgtcaatgccaggtatgaatttggcccagccctgttcgtgggctgggcctcagctggcctggccgtgctgggcggctccttcctctgctgcacatgcccggagccagagagacccaacagcagcccacagccctatcggcctggaccctctgctgctgcccgagagtacgtctgagctccgcctgccctggccagccccccacccagtggcccccttgcccagcatccagccagcctcgcagcaccctgggcagggccactggggcataggatgggcataggtgctctgagcagcttgtcctcaacacaagcacccaccctgcaatctgagacccagatcctcagagagacaccagaggcaggacccagcccccaggcatacacacagatgcaggtccaggcacggtcttgtctgcacagcctggtgggcaccagcatgcatccctggagacaggccctcaggcaccagcccggctgtttactcactgaagagctgcttgggtgtctgctacgtgctgggccctagagatagagcagtggccaagacgtaccttagtacccaggtccttggggtgagcagaaaccttcaccctccccagtcccatgggctcctcacagcaaccccacaagggcagtgccgggatgctgaacgttcacacaaggacagggagggtctgagtttaggtctcaggttcttccagtgcgcccagggctgggggccacctacacagatggtgaggtcggaccatggcgcccctgcccccgggaatgggccccaggcagggctgctgtgagggccaaggtctggccacgctggccagtacccatgtccgggcctgaatgcacagcccctgcccccgaccccacagctcactccactaaccagctctctctcttttgactttcagaccagttgttaaattgcccgcctccgccaagggccccctgggtgtgtaatgtccagtccccagccaggctctgtcccctgccatacctagactgtgtgtttcatatttttttggaaagagaagtgaacatccagccccaatcatggtatcattcggtctgtcctcagcgtggcttggacggggcctgtgtcagagtggtcagtgctgacccctggggctcttgggcagaaagatgaggagacagaggtccagggtgggttacatagcacatccagggctaagcaagaaataattcagaggtcctaccctctgtctagggacccccctcccaagcctggccttggccttggcacaaagtcctccttgataggagatcccactcactcctggaggctgcccctgaggcttggcccagctctaggagcagtccccagggtcagggagcccctggtgtggaaagaggccccaaggtagtaaaccctgcccctgttactgtgctccagagacctcctaagggaagggacagttcctggaaggccctccagctggatgctggggatcagcgataggtgaggggacacagtgtaggagctccccatgtagaaaagggaatgtggggagggcgttaggagcttgcaggcattaggactgtcctgagcaaggtctgcagcccccagctctgctcaccccgaatcctgccccttgtttccacacctaccattcctcctctcctgatccccagcatccagctgaggtccaaggtctttgtcctagaatcagagtggggaggggacagcctggggctgcccagagactgtgggtggagctgcctgctgcactcagcagtgcggtcagagaagggcttttggtcttgaagtccaggtaccatccccccttagcatacagggggaagggcctgagaggaatgtaaggaaaccagcccagatcagtcccaaggccagagtcctttgtcctacatctccctgaaccagagtgtgccctgcccctcatgctcagacctctcccaccccaaaccctctcccgggactcagtctccctggccactgcgtatcaggcttctggggaaagcatccatcacagaacctccccttccctgccacgcaccttccttggccagctccattctggcctcctccaccacctgccttgtgaccacatctcccaccacgtccccagatctcaagaacgcagctcagcttctccttcgagcttgactctgagagggaaagtgacggaaaccaagtcagatgagatgactgccatgtacactgcagtcaagggcagggaggggaggaatgacacaaatggcagggagctgctgggggactgacccctcggcgcctggcctggccggtgctgcacatccaccggggcacaacagggacttgtccagcctctggtcagaggatgtggccacctgaccctaaataggttccccagagtcctgcccctctaatgaatgagaactgcaggagtttctcctctgggtgcctgaagctatagtgcaatggttcccaaccctgcatgcacattcgaatcacctgggggcacaatgcctaggctccaaccccagacactcttatttcattggtctgggtggacctggcatcagaagtcatgtagctcctcaggggactgtagtgtgtggtcagcactgagggctcctctatgaggcctcaagcccaggtgactctgtgaggtctgcagagggagaaaagaacccacaagggaagaggtggaggtcaggcacggtggctcacgcttgtaatcccagcactttgggaggccgaggtgggtagatacctgaagtcaggagttcgagactagcctggccaatatggtaaaaccccgtgtctattaaaaatacaaaaattagctggctgtggtggtgggcacctgtaatcccagctactcgggaggctgaggcaggagaatcgcttgaactcgggaggtggaggttgcagtcagccaagatcgtgccactgcacaccatcctggatgacagagcaagactccatcac
//
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]