ver.2
Home
|
Help
|
Advanced search
Previous release (v1)
2024-04-25 09:39:18, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001185117 3499 bp mRNA linear PRI 22-SEP-2023 DEFINITION Homo sapiens claudin 19 (CLDN19), transcript variant 3, mRNA. ACCESSION NM_001185117 VERSION NM_001185117.2 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 3499) 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 3499) 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 3499) 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 3499) 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 3499) 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 3499) 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 3499) 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 3499) 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 3499) 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 3499) 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, AK298992.1 and AC098484.2. On Aug 13, 2020 this sequence version replaced NM_001185117.1. 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 (3) lacks an exon in the CDS, which results in frame-shift, and contains an additional segment in the 3' region compared to variant 1. The resulting isoform (c) is shorter and has a distinct C-terminus compared to isoform a. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. 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 :: AK298992.1 [ECO:0000332] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-6 AK096063.1 19-24 7-728 AK298992.1 4-725 729-3499 AC098484.2 81071-83841 c FEATURES Location/Qualifiers source 1..3499 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="1" /map="1p34.2" gene 1..3499 /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..830 /gene="CLDN19" /gene_synonym="HOMG5" /note="isoform c is encoded by transcript variant 3" /codon_start=1 /product="claudin-19 isoform c" /protein_id="NP_001172046.1" /db_xref="CCDS:CCDS53306.1" /db_xref="GeneID:149461" /db_xref="HGNC:HGNC:2040" /db_xref="MIM:610036" /translation="
MANSGLQLLGYFLALGGWVGIIASTALPQWKQSSYAGDAIITAVGLYEGLWMSCASQSTGQVQCKLYDSLLALDGHIQSARALMVVAVLLGFVAMVLSVVGMKCTRVGDSNPIAKGRVAIAGGALFILAGMNLAQPCSWAGPQLAWPCWAAPSSAAHARSQRDPTAAHSPIGLDPLLLPESTSELRLPWPAPHPVAPLPSIQPASQHPGQGHWGIGWA"
misc_feature 183..>590
/gene="CLDN19"
/gene_synonym="HOMG5"
/note="PMP-22/EMP/MP20/Claudin family; Region:
PMP22_Claudin; cl21598"
/db_xref="CDD:451326"
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..3499
/gene="CLDN19"
/gene_synonym="HOMG5"
/inference="alignment:Splign:2.1.0"
variation 562
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651360381"
variation 564
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651360279"
variation 570
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651360194"
variation 574
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:962614350"
variation 578
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651359971"
variation 579..586
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="ccctgttc"
/db_xref="dbSNP:1651359589"
variation 580
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:762618011"
variation 581
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651359777"
variation 583
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1216799895"
variation 586
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:776225389"
variation 587
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163560341"
variation 589
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316432824"
variation 590
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1473655950"
variation 591
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:866174535"
variation 593
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570442822"
variation 594
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124036870"
variation 597
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768639835"
variation 598
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651358674"
variation 606
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:747223067"
variation 608
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570442807"
variation 611
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263949970"
variation 612
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124036796"
variation 613
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:138355552"
variation 614
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:772247940"
variation 616
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1289785127"
variation 617
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:867926864"
variation 618
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651357824"
variation 622
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:140842024"
variation 623
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:145591298"
variation 624
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1217588010"
variation 625
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:749872474"
variation 627
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201399564"
variation 628
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651357109"
variation 629
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035217156"
variation 630
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1003712779"
variation 631
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124036565"
variation 634
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1403033958"
variation 635
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1330521485"
variation 636
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1164602961"
variation 637
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324117597"
variation 638
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367075794"
variation 639
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124036479"
variation 641
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332219103"
variation 643
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:369184924"
variation 644
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1394029284"
variation 648
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:531931336"
variation 649
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:9660973"
variation 650
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1300085775"
variation 652
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1424431332"
variation 653
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1196017795"
variation 655..661
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="agaga"
/replace="agagaga"
/db_xref="dbSNP:1341096574"
variation 658
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651353668"
variation 659
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1477074057"
variation 660
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124036280"
variation 663
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1246687752"
variation 667
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:758094656"
variation 670
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1453711939"
variation 673
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651352981"
variation 674
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256503881"
variation 675
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:749847290"
variation 676
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651352001"
variation 679
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:764811412"
variation 680
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1259589527"
variation 681
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:549476247"
variation 684
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:114350566"
variation 686
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:763959764"
variation 687
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:116804195"
variation 689
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1333791679"
variation 690
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:775446633"
variation 693
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651350767"
variation 694
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651350663"
variation 695..697
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:772887123"
variation 697
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651350389"
variation 704
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1401372077"
variation 705
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:772360364"
variation 707
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1412877618"
variation 708
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424493671"
variation 710
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011136678"
variation 711
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:894082758"
variation 714
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:145157550"
variation 715
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:774289795"
variation 718
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376266757"
variation 719
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:373130417"
variation 723
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1188616660"
variation 728
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1207548434"
variation 729..731
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cgc"
/replace="tgt"
/db_xref="dbSNP:1557550020"
variation 729
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:4660658"
variation 730
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:866489456"
variation 731
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278656048"
variation 733
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:890540431"
variation 734
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1351503503"
variation 735
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:867345315"
variation 741
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:866665590"
variation 743
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:748466759"
variation 744
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1038523634"
variation 745..750
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cccccc"
/replace="ccccccc"
/replace="cccccccc"
/db_xref="dbSNP:1396440246"
variation 745
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378795834"
variation 746
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1300141317"
variation 747
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1301048287"
variation 748..755
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccca"
/replace="cccaccca"
/db_xref="dbSNP:1238469200"
variation 748
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446024618"
variation 749
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1358664309"
variation 750
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:948161573"
variation 751
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570442470"
variation 752
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416239266"
variation 754
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1379067335"
variation 756
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:781553369"
variation 761
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651346724"
variation 763
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1440746078"
variation 765
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570442455"
variation 767
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:757926348"
variation 768
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1179779575"
variation 770
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482692439"
variation 772
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1309461123"
variation 773
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:750160816"
variation 775
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:916659139"
variation 776..785
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccagcc"
/replace="ccagccagcc"
/db_xref="dbSNP:1651345724"
variation 776
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:778274875"
variation 777
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651345917"
variation 778
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1207362128"
variation 785
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1254784973"
variation 787
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756840769"
variation 788
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1285270660"
variation 789
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:199656937"
variation 790
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1355608797"
variation 792
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456719872"
variation 794
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381079432"
variation 795
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1310238805"
variation 797
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651344732"
variation 798
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651344659"
variation 800
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1226823680"
variation 804
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378806839"
variation 806
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284992714"
variation 811
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:866413020"
variation 813
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:778620439"
variation 814
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416757983"
variation 816
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1314103036"
variation 819
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1358672309"
variation 820
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1298153440"
variation 821
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:565025655"
variation 823
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1362861718"
variation 826
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:764084498"
variation 830
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:760700236"
variation 832
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:977990338"
variation 834
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1466485858"
variation 835
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:967912511"
variation 839
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1330499189"
variation 840
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:544937247"
variation 841
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651342944"
variation 844
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022106419"
variation 845
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772513053"
variation 847
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1366405529"
variation 859
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651342598"
variation 860
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:567128668"
variation 864
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:774741981"
variation 865
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651342298"
variation 868
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:759663769"
variation 869
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1018692736"
variation 871
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651342000"
variation 874
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651341512"
variation 890
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124034842"
variation 892
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1314531151"
variation 893
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="a"
/db_xref="dbSNP:1651341350"
variation 893
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1009023125"
variation 896
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651341219"
variation 901
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651341136"
variation 902
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651341089"
variation 906
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651341023"
variation 909
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651340952"
variation 911
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:950371999"
variation 915
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651340773"
variation 919
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456719913"
variation 920
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1390669324"
variation 923
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1320998903"
variation 924
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1239070859"
variation 925
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1025957490"
variation 926
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:994439822"
variation 928
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651340259"
variation 929
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427342313"
variation 931
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:555913979"
variation 940
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651340035"
variation 941
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1433791171"
variation 942
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1169882297"
variation 945
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570442247"
variation 950
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:898731607"
variation 951..953
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cac"
/replace="cacac"
/db_xref="dbSNP:1331759851"
variation 953
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1038973831"
variation 954
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:550620549"
variation 957
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651339377"
variation 963
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:536058712"
variation 964
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370684135"
variation 965
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557549800"
variation 966
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570442219"
variation 967
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570442214"
variation 970
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:573614349"
variation 971
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651338833"
variation 974
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651338767"
variation 975
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570442209"
variation 982
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1367710944"
variation 985
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1167233205"
variation 986
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1278153633"
variation 988
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056556314"
variation 989
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424598155"
variation 991
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651336218"
variation 992
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:958266587"
variation 996
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651336052"
variation 1001
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651335943"
variation 1005
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274145956"
variation 1006
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1321411740"
variation 1009
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:140498057"
variation 1012
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651333329"
variation 1021
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:181776711"
variation 1022
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1490544441"
variation 1023
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1042348540"
variation 1024
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1192984336"
variation 1026
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1260998336"
variation 1027
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651332744"
variation 1029
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651332665"
variation 1030
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651332594"
variation 1031
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:571260727"
variation 1034
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:558473657"
variation 1035
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651332354"
variation 1037
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651332273"
variation 1041
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651332197"
variation 1046
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651332117"
variation 1047
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:12141833"
variation 1050
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403329333"
variation 1053
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:915151352"
variation 1057
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:993965686"
variation 1059
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:975020708"
variation 1060
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:964577864"
variation 1061
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:780389459"
variation 1062
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1487739799"
variation 1065
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651331169"
variation 1067
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1267596829"
variation 1068
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651331002"
variation 1069
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223403161"
variation 1070
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2124033931"
variation 1072
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651330831"
variation 1073..1083
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tagag"
/replace="tagagatagag"
/db_xref="dbSNP:1226928582"
variation 1073
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651330755"
variation 1075
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651330667"
variation 1079
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770205728"
variation 1080
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651330477"
variation 1081
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1378911877"
variation 1085
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1292323792"
variation 1089
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1360406686"
variation 1095
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1216029747"
variation 1096
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651330010"
variation 1097
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:745928043"
variation 1098
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651329838"
variation 1100
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651329757"
variation 1109
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651329673"
variation 1110
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570442088"
variation 1111
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651329531"
variation 1116
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570442086"
variation 1118
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:781433880"
variation 1120
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570442076"
variation 1121
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:941232493"
variation 1122
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651329153"
variation 1124
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651329078"
variation 1125
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651329000"
variation 1126
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651328911"
variation 1130..1132
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2124033603"
variation 1133
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651328824"
variation 1134
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:571548302"
variation 1138
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570442065"
variation 1139
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:950424439"
variation 1141
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:569593546"
variation 1143
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1054990359"
variation 1145
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:937667307"
variation 1147
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298289259"
variation 1148
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026009370"
variation 1153
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:927592582"
variation 1156
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2124033479"
variation 1158
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1414120405"
variation 1162
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651327829"
variation 1163..1166
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ca"
/replace="caca"
/db_xref="dbSNP:1651327691"
variation 1165
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1418710998"
variation 1168
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:994493897"
variation 1172
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:981821556"
variation 1173..1176
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="ccac"
/db_xref="dbSNP:913683166"
variation 1174
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:115864005"
variation 1179
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124033343"
variation 1182
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651327264"
variation 1184
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651327171"
variation 1188
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:189463551"
variation 1189
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295063346"
variation 1200
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:146829937"
variation 1201
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017856464"
variation 1202
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:895328399"
variation 1203
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205745945"
variation 1206
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1166828875"
variation 1216
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441990"
variation 1217
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1057009534"
variation 1218
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651326301"
variation 1220
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651326224"
variation 1222
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1431750471"
variation 1226
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212055901"
variation 1233
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651325985"
variation 1238
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441977"
variation 1244
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:547115625"
variation 1249
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651325743"
variation 1251
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651325660"
variation 1253
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:955001262"
variation 1254
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:752275663"
variation 1259
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570441964"
variation 1260
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651325274"
variation 1261
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1470222436"
variation 1264..1268
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ggggg"
/replace="gggggg"
/db_xref="dbSNP:1171463827"
variation 1264
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1557549605"
variation 1269
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1425128711"
variation 1271
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651324772"
variation 1273
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651324655"
variation 1276
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1269922455"
variation 1278
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441948"
variation 1279
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651324363"
variation 1288..1315
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gg"
/replace="ggtcggaccatggcgcccctgcccccgg"
/db_xref="dbSNP:1220887984"
variation 1291
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:533160815"
variation 1292
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:993520421"
variation 1298
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407311555"
variation 1300
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:902591128"
variation 1301
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:564169958"
variation 1302..1409
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gcccctgcccccg"
/replace="gcccctgcccccgggaatgggccccaggcagggctgctgtgagggcca
aggtctggccacgctggccagtacccatgtccgggcctgaatgcacagcccctgcccc
cg"
/db_xref="dbSNP:1651318199"
variation 1302
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1042403857"
variation 1303
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1005324205"
variation 1305
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:766985702"
variation 1309
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:867072861"
variation 1310
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1160256565"
variation 1313
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:544224952"
variation 1314..1316
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1263612424"
variation 1314
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:531471001"
variation 1319
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2124032758"
variation 1326
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651322461"
variation 1330
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651322377"
variation 1331
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557549561"
variation 1332
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651322226"
variation 1333
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1038958519"
variation 1334
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:937904168"
variation 1335
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:751482708"
variation 1339
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651321885"
variation 1343
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124032667"
variation 1346
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651321814"
variation 1351
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1310295582"
variation 1353
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651321238"
variation 1360
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:911748345"
variation 1361
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:562452279"
variation 1362
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:143708479"
variation 1363
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:573827426"
variation 1364
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:553575963"
variation 1365
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651320439"
variation 1368
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651320363"
variation 1374
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387097409"
variation 1375
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:919004200"
variation 1376
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:868235687"
variation 1380..1383
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="ccgg"
/db_xref="dbSNP:989256170"
variation 1381
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376759002"
variation 1382
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:913634313"
variation 1384
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1398992220"
variation 1386
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651319662"
variation 1389
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:963044897"
variation 1393
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:577543955"
variation 1394
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:910699717"
variation 1395
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651319288"
variation 1398..1401
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1030616687"
variation 1398
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:372581520"
variation 1399
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:955095486"
variation 1404..1408
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cccc"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:376221466"
variation 1404
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:184994488"
variation 1405
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:972471763"
variation 1407
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651318655"
variation 1408..1409
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="t"
/db_xref="dbSNP:1557549490"
variation 1408
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:74885359"
variation 1409
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:569528348"
variation 1412
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:763045798"
variation 1413
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:773299018"
variation 1414
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1220634133"
variation 1417
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:770230972"
variation 1421
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1290915035"
variation 1422
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:528764011"
variation 1422
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235329729"
variation 1424
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748661119"
variation 1425
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:781537112"
variation 1426
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1477762274"
variation 1428
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1364784331"
variation 1433
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:769126862"
variation 1435
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441741"
variation 1436..1445
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ctctctctct"
/replace="ctctctctctctctctct"
/db_xref="dbSNP:1651316147"
variation 1438
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:374216538"
variation 1441
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778667951"
variation 1448
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651316071"
variation 1449
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1166673287"
variation 1452
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651315898"
variation 1459
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:756892751"
variation 1462
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651315741"
variation 1464
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422290318"
variation 1466
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651315592"
variation 1470
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1193831713"
variation 1472
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:753338977"
variation 1476
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777425105"
variation 1477
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147528059"
variation 1479
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651315070"
variation 1482
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:752738519"
variation 1483
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:535667246"
variation 1488
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1215803586"
variation 1489
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:200491942"
variation 1490
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1257662822"
variation 1491
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1219376620"
variation 1492
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1279949075"
variation 1493
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1309299294"
variation 1494
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:371686331"
variation 1501
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:766571498"
variation 1502
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:387907420"
variation 1503
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:764858690"
variation 1505
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:773211263"
variation 1507
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328261253"
variation 1508
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:769931882"
variation 1513
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:762297703"
variation 1515
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:777172207"
variation 1516
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:768871931"
variation 1517
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:747361042"
variation 1520
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:775740656"
variation 1523
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:770548857"
variation 1524
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:367910861"
variation 1525
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:777408812"
variation 1526
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:546757402"
variation 1531
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:755733771"
variation 1532
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:748064968"
variation 1534
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1177658979"
variation 1536
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:781140631"
variation 1538
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651312522"
variation 1539
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429507975"
variation 1540
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:373755403"
variation 1544
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:750026527"
variation 1547
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651312175"
variation 1551
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200471599"
variation 1552
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1313365002"
variation 1553
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039423338"
variation 1560
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651311814"
variation 1561
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651311737"
variation 1562
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:910316814"
variation 1563..1569
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:1351281461"
variation 1564
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230470801"
variation 1569
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651311406"
variation 1573
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:943323880"
variation 1575
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651311245"
variation 1577
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1290591903"
variation 1585..1592
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="catccagc"
/db_xref="dbSNP:369052611"
variation 1585
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1312372093"
variation 1588
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:890355984"
variation 1589
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:796219031"
variation 1591
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651310688"
variation 1592..1595
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1310273077"
variation 1592
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051634158"
polyA_site 1597
/gene="CLDN19"
/gene_synonym="HOMG5"
/note="major polyA site"
variation 1597
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:77236131"
variation 1600
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651309054"
variation 1601
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:919054603"
variation 1606
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651308898"
variation 1609
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651308816"
variation 1611
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:765909170"
variation 1612
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:550521995"
variation 1615
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:958751979"
variation 1617
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441516"
variation 1619
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486463471"
variation 1625
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376052803"
variation 1626
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:915602099"
variation 1628
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651306549"
variation 1633
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:991547265"
variation 1636
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1412202056"
variation 1637
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1184440731"
variation 1640
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002446383"
variation 1641
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1437925300"
variation 1645
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2124031042"
variation 1650
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651305332"
variation 1653
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651305260"
variation 1655
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:959681582"
variation 1659
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651305109"
variation 1660
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:530817596"
variation 1662
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1035678117"
variation 1664
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:140105842"
variation 1666
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:966857083"
variation 1667
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1408035464"
variation 1668
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651304418"
variation 1669
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:372780855"
variation 1671
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330294458"
variation 1675
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651304187"
variation 1676
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374175709"
variation 1677
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651304043"
variation 1681
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1225012393"
variation 1683
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:371735000"
variation 1684
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="a"
/db_xref="dbSNP:1651303556"
variation 1685
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441448"
variation 1689
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651303395"
variation 1692
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651303321"
variation 1693
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651303242"
variation 1702
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651303183"
variation 1703
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:762336108"
variation 1705
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651303028"
variation 1708
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651302955"
variation 1709
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1017633734"
variation 1710
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651302791"
variation 1711
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1233170783"
variation 1713
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007966109"
variation 1719
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1266027309"
variation 1721
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210312530"
variation 1725
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204652754"
variation 1727
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651302185"
variation 1729
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:890420008"
variation 1736
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="t"
/db_xref="dbSNP:1237852963"
variation 1737
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:912075"
variation 1738
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651301614"
variation 1740
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1179091682"
variation 1741
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124030579"
variation 1742
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441403"
variation 1745
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:936351398"
variation 1752
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651301325"
variation 1753
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651301258"
variation 1756
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651301175"
variation 1760
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651301086"
variation 1763
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:796637327"
variation 1764
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1173907268"
variation 1766
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1431290070"
variation 1767
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557549135"
variation 1768..1770
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1470171925"
variation 1770..1772
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="t"
/replace="tct"
/db_xref="dbSNP:1651300214"
variation 1771
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169660133"
variation 1777
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651300144"
variation 1778..1783
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccccc"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:532996510"
variation 1778
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1397759529"
variation 1781
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651299939"
variation 1782
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557549123"
variation 1785
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:374721300"
variation 1791
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:897677267"
variation 1793..1808
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tggccttggccttggc"
/replace="tggccttggccttggccttggc"
/db_xref="dbSNP:1382161816"
variation 1795
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651299417"
variation 1801
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:769241790"
variation 1802
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1037519071"
variation 1803
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1313526522"
variation 1809
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1651298963"
variation 1816
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1224550639"
variation 1817
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1257815975"
variation 1819
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306041428"
variation 1821..1822
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1387012858"
variation 1822
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651298546"
variation 1825
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:560322698"
variation 1828
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:923428502"
variation 1830..1831
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="tt"
/db_xref="dbSNP:1651298185"
variation 1830
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441330"
variation 1833
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651298103"
variation 1835
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1488210994"
variation 1837
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651297939"
variation 1838
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651297853"
variation 1845
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189528235"
variation 1846
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:972643328"
variation 1847
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651297622"
variation 1855
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:940921614"
variation 1861
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651297444"
variation 1862
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:915635301"
variation 1863
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651297274"
variation 1870
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192750059"
variation 1872
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651297101"
variation 1873
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:909480057"
variation 1880
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651296925"
variation 1881
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1411376424"
variation 1882
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1170743499"
variation 1883
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651296740"
variation 1887
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348885607"
variation 1888
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651296606"
variation 1892
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:540075482"
variation 1893
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1458132860"
variation 1897
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1304397001"
variation 1899
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651296322"
variation 1901
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1348005048"
variation 1905
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406074500"
variation 1908
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:991208270"
variation 1909
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1360351404"
variation 1910
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651295905"
variation 1913
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1216643137"
variation 1917
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:938348889"
variation 1921
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651295666"
variation 1926
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651295584"
variation 1927..1928
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1557549040"
variation 1927
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:958740672"
variation 1928
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:577777997"
variation 1929
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557549032"
variation 1936
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1220436490"
variation 1941
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651295069"
variation 1942
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651294954"
variation 1944..1945
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="ct"
/db_xref="dbSNP:1651294861"
variation 1951
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651294764"
variation 1958
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441257"
variation 1963
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:927363928"
variation 1964
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651294479"
variation 1966
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1490516616"
variation 1968
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1215809504"
variation 1974
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651294239"
variation 1976
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1240247833"
variation 1978
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651294088"
variation 1981
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651294006"
variation 1983
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1476285590"
variation 1995
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557549013"
variation 1997
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762244030"
variation 2007
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651293632"
variation 2014
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:971891724"
variation 2015
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:982342001"
variation 2018
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1421685531"
variation 2020
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2124029487"
variation 2021
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651293273"
variation 2022
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:966911128"
variation 2025
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="a"
/db_xref="dbSNP:1651293052"
variation 2027
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651292928"
variation 2028
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570441205"
variation 2029
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:776804215"
variation 2036
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="c"
/db_xref="dbSNP:138777333"
variation 2036
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570441195"
variation 2036
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2124029388"
variation 2038
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651292465"
variation 2042
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1057515528"
variation 2044
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1433378024"
variation 2044
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124029327"
variation 2045
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000530698"
variation 2052
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441171"
variation 2053
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:549719300"
variation 2055
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1378789687"
variation 2057
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:529459531"
variation 2067
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1317340602"
variation 2068
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1050521162"
variation 2070
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:958183930"
variation 2071
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651291501"
variation 2073
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124029210"
variation 2074
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557548969"
variation 2075
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651291298"
variation 2076
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:901605896"
variation 2079
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651291140"
variation 2081
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1036501699"
variation 2082
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:746091783"
variation 2083
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1465219512"
variation 2086
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651290809"
variation 2087
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651290725"
variation 2092
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651290639"
variation 2093
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651290539"
variation 2094
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="c"
/db_xref="dbSNP:2124029075"
variation 2094
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236668999"
variation 2097
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651290394"
variation 2102
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288859510"
variation 2103
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1018104979"
variation 2104
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651290159"
variation 2108
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1570441109"
variation 2111
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651290016"
variation 2113
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651289946"
variation 2116
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1208353733"
variation 2117
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1358653297"
variation 2119
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1007604392"
variation 2123
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1266123585"
variation 2124
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1227696453"
variation 2127
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:940889035"
variation 2128..2132
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:551118125"
variation 2128
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441086"
variation 2130
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:761260010"
variation 2132
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1406509120"
variation 2135
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:909468672"
variation 2142
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:954884639"
variation 2143
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570441069"
variation 2144
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651288831"
variation 2145
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030310070"
variation 2147
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:563880269"
variation 2148
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:781380872"
variation 2150
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651288511"
variation 2152
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:993435665"
variation 2157
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651288359"
variation 2158
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450854555"
variation 2166
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:927279008"
variation 2170
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570441044"
variation 2171
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1383775010"
variation 2173
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:981869447"
variation 2174
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:897729862"
variation 2175
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651287512"
variation 2176
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651287434"
variation 2178
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651287367"
variation 2179
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651287302"
variation 2180
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441028"
variation 2189
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651287140"
variation 2192
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:544178185"
variation 2197
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376179882"
variation 2200
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:770893678"
variation 2209..2215
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gaggtcc"
/replace="gaggtccgaggtcc"
/db_xref="dbSNP:1224286686"
variation 2216
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651286686"
variation 2217
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:894268522"
variation 2219
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651286537"
variation 2220..2224
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tcttt"
/replace="tctttcttt"
/db_xref="dbSNP:1651286378"
variation 2221
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1055959077"
variation 2241
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:142957479"
variation 2243
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557548866"
variation 2246
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651286100"
variation 2248
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651285812"
variation 2249
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163371071"
variation 2251
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:956565410"
variation 2254
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205305296"
variation 2258
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124028436"
variation 2260
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651285410"
variation 2261
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651285325"
variation 2263
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651285222"
variation 2267
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1032252022"
variation 2273..2276
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1651284899"
variation 2275
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1457037795"
variation 2278
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1179119133"
variation 2287
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570440973"
variation 2289
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651284640"
variation 2290
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651284567"
variation 2298
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428584044"
variation 2299
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000749435"
variation 2300
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651284324"
variation 2306
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777568849"
variation 2307
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1041346817"
variation 2317
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1028632951"
variation 2318
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1245915070"
variation 2319
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1429147609"
variation 2320
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651283714"
variation 2324
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651283626"
variation 2325..2326
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1651283478"
variation 2325
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651283551"
variation 2326
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:368436876"
variation 2334
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651283324"
variation 2337..2338
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="cccctt"
/db_xref="dbSNP:1651283244"
variation 2340..2343
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="gtac"
/db_xref="dbSNP:1651282989"
variation 2340
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651283164"
variation 2342
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196406854"
variation 2347..2352
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:1049224758"
variation 2348
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:181070200"
variation 2349
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:914148776"
variation 2350
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268267008"
variation 2351
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:377585440"
variation 2352
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:887914551"
variation 2356
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1225184734"
variation 2359
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651282146"
variation 2361
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651282052"
variation 2366
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263511720"
variation 2369
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651281877"
variation 2370
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124027921"
variation 2371
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651281784"
variation 2373
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:796839004"
variation 2375
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651281593"
variation 2376
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1274622493"
variation 2378
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651281450"
variation 2379
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370331996"
variation 2382
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1273470824"
variation 2384
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651281232"
variation 2386
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268854758"
variation 2395
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1045719913"
variation 2397
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="g"
/db_xref="dbSNP:1651280966"
variation 2400
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:910688779"
variation 2402
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1332005923"
variation 2407
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:375306800"
variation 2410
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:913313445"
variation 2412
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:988929125"
variation 2413..2421
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ag"
/replace="aggccagag"
/db_xref="dbSNP:2124027665"
variation 2414
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:758420361"
variation 2416
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124027693"
variation 2418
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302621983"
variation 2421
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:148594631"
variation 2424
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651280180"
variation 2427
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1368236439"
variation 2428
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:954754714"
variation 2430
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651279898"
variation 2431
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:369724376"
variation 2434
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124027562"
variation 2435
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1406709368"
variation 2442
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:925067368"
variation 2445
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1030363830"
variation 2446
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124027513"
variation 2447
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1224900327"
variation 2449
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651279231"
variation 2455
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410475059"
variation 2461..2464
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1651278770"
variation 2463
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424315949"
variation 2464
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651278627"
variation 2467
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:570565492"
variation 2468
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651278296"
variation 2469
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:550710062"
variation 2470
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:961993377"
variation 2480
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1016190439"
variation 2481
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006102105"
variation 2482
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:894312717"
variation 2491
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1055609220"
variation 2492
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1003059924"
variation 2495
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440821"
variation 2500
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1490681272"
variation 2501
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1377976423"
variation 2503
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651276774"
variation 2504
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:906949228"
variation 2505
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651276379"
variation 2510
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440801"
variation 2511
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:966138586"
variation 2514
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482159495"
variation 2517
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1191445002"
variation 2524
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:114944537"
variation 2525
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:568148786"
variation 2526
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:945714612"
variation 2528
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442385976"
variation 2537
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124027137"
variation 2545
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651272818"
variation 2550
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124027109"
variation 2551
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651272715"
variation 2553
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1277175863"
variation 2556
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1426580574"
variation 2560
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440761"
variation 2561
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303707822"
variation 2562
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651272059"
variation 2563
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:914201766"
variation 2566
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651271743"
variation 2567
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651271624"
variation 2577
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1380357646"
variation 2578
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:887547668"
variation 2579
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1057515527"
variation 2580
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1243631825"
variation 2580
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651271035"
variation 2581..2582
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="acctccccttcc"
/db_xref="dbSNP:1651270946"
variation 2583
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651270816"
variation 2591
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:548984051"
variation 2592
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124026869"
variation 2593
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1361015949"
variation 2595
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651270491"
variation 2600
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651270406"
variation 2601
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:189819580"
variation 2603..2609
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ctggcct"
/replace="ctggcctggcct"
/db_xref="dbSNP:1651269933"
variation 2604
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1002138865"
variation 2606
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651270061"
variation 2607..2614
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cctcc"
/replace="cctcctcc"
/db_xref="dbSNP:1651269737"
variation 2609
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1203815179"
variation 2614
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:906096762"
variation 2620
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124026713"
variation 2622
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:564714068"
variation 2623
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1227401183"
variation 2628
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348176800"
variation 2631
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651268960"
variation 2634
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:950072291"
variation 2641
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1363228211"
variation 2643
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1451529541"
variation 2644
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2124026616"
variation 2646
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:529158343"
variation 2647
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1391371008"
variation 2650
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651268246"
variation 2651
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651268154"
variation 2660..2661
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="gcttctccttcg"
/db_xref="dbSNP:1385411183"
variation 2665
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:891756677"
variation 2666
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332181117"
variation 2668
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:184596944"
variation 2678
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:796988312"
variation 2680
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651267544"
variation 2681
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651267448"
variation 2684
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406550607"
variation 2685
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:144430420"
variation 2688
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471748356"
variation 2691
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262971116"
variation 2692
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124026409"
variation 2693
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651266929"
variation 2695
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:910732047"
variation 2698
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1351873770"
variation 2711
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:778687377"
variation 2712
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:986301112"
variation 2719
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651266461"
variation 2724
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1241571392"
variation 2726
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651266301"
variation 2728
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651266207"
variation 2731
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:754589000"
variation 2735
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:926038941"
variation 2738
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1184356468"
variation 2741
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1472535414"
variation 2742
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1249928199"
variation 2746
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651264513"
variation 2748
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:753515106"
variation 2759
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:933422896"
variation 2765
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212936203"
variation 2768
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651264106"
variation 2769
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651264023"
variation 2776
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651263951"
variation 2778
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651263878"
variation 2786
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651263788"
variation 2790
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:976373319"
variation 2792
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:766100803"
variation 2795
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:546730630"
variation 2796
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:965993611"
variation 2799
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1321561594"
variation 2802
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1470006770"
variation 2803
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651263108"
variation 2807
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651263025"
variation 2808..2809
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="ac"
/db_xref="dbSNP:1297176277"
variation 2808
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440619"
variation 2809
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651262799"
variation 2811
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651262709"
variation 2814
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440610"
variation 2815
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:923346842"
variation 2816
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1014521584"
variation 2817
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1351603683"
variation 2818
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:972101560"
variation 2819
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651262102"
variation 2820
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651262021"
variation 2821
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1326675459"
variation 2823
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651261851"
variation 2825
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1204553607"
variation 2828
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1289876170"
variation 2829
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:760068656"
variation 2830
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1479712621"
variation 2831
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:962046453"
variation 2832
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124025830"
variation 2833
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:76855155"
variation 2835
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651261007"
variation 2837..2855
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gcaca"
/replace="gcacatccaccggggcaca"
/db_xref="dbSNP:1169331973"
variation 2837
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570440564"
variation 2838
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1480061117"
variation 2839
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1281856305"
variation 2841
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1197119795"
variation 2842
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651260597"
variation 2843
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651260497"
variation 2844
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:985131155"
variation 2845
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440550"
variation 2847
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:958630245"
variation 2848
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651260155"
variation 2849
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651260083"
variation 2851
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651260006"
variation 2857
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651259846"
variation 2859
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:745884385"
variation 2863
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200527665"
variation 2865..2868
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tgtc"
/replace="tgtctgtc"
/db_xref="dbSNP:1001707873"
variation 2867
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440539"
variation 2868
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651259427"
variation 2872
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651259312"
variation 2882
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651259241"
variation 2883
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:567823099"
variation 2884
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651259065"
variation 2885
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1024484460"
variation 2886
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651258894"
variation 2889
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651258809"
variation 2903
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281860320"
variation 2907
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:544361263"
variation 2909
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1014880889"
variation 2913..2916
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1651257735"
variation 2915
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651257827"
variation 2916
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:373188579"
variation 2920
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1404978019"
variation 2926
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124025433"
variation 2929
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009910087"
variation 2934
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:149256970"
variation 2935
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557548354"
variation 2936
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651257129"
variation 2946
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1054107067"
variation 2948
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651256977"
variation 2950
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:904588472"
variation 2955..2958
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="t"
/replace="ttct"
/db_xref="dbSNP:529449539"
variation 2956
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:796175275"
variation 2958..2967
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="tcctctgggt"
/db_xref="dbSNP:796901250"
variation 2960
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651256649"
variation 2961..2967
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="tctgggt"
/db_xref="dbSNP:562296433"
variation 2962
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:889365281"
variation 2964
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1490465444"
variation 2965
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1049876055"
variation 2968
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651256206"
variation 2979
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247904427"
variation 2983
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1170642886"
variation 2988
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651256000"
variation 2989
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1051069098"
variation 2997
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:931824276"
variation 2998
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651255779"
variation 3000
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124025179"
variation 3003
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651255704"
variation 3004
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651255626"
variation 3010
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301862960"
variation 3012
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651255479"
variation 3013
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:933476755"
variation 3015
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288652453"
variation 3018
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651255231"
variation 3023
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1360239083"
variation 3024
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:770989443"
variation 3026
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:923397849"
variation 3030
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124025040"
variation 3031
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651254904"
variation 3032
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651254819"
variation 3034
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1298557597"
variation 3035
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:71654253"
variation 3038
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1040226305"
variation 3039
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:944594774"
variation 3040
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1293905748"
variation 3041..3044
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tcca"
/replace="tccatcca"
/db_xref="dbSNP:1651252045"
variation 3041
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651252143"
variation 3049
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1452102004"
variation 3052
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651251901"
variation 3055
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:556016559"
variation 3057
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651251709"
variation 3065
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1320683263"
variation 3066
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651251523"
variation 3069
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1287161397"
variation 3075
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:972155294"
variation 3090
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651251285"
variation 3092
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1486687028"
variation 3097
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:371301647"
variation 3100
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:113021721"
variation 3102
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:763565629"
variation 3103
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1296855045"
variation 3104..3105
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="cc"
/db_xref="dbSNP:1432786550"
variation 3105
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651250450"
variation 3110
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:951754166"
variation 3111
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1289160691"
variation 3112
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:984795189"
variation 3113
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1158931903"
variation 3116
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1343831685"
variation 3119
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1433265834"
variation 3120
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651249964"
variation 3127
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1057515454"
variation 3134
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1436042894"
variation 3138
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1348305840"
variation 3139
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651249597"
variation 3142
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1382267259"
variation 3143
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651249434"
variation 3146
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:958906433"
variation 3147
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651249261"
variation 3148
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:56345167"
variation 3149
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:969836365"
variation 3150
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651248882"
variation 3152
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223154374"
variation 3154
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651248719"
variation 3155
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:573446568"
variation 3156
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1209098870"
variation 3161
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651248461"
variation 3164
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:981285231"
variation 3165
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651248287"
variation 3167
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:553394106"
variation 3169..3172
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1651248113"
variation 3173
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1184964715"
variation 3175
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:866481412"
variation 3177
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1570440321"
variation 3178
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651247803"
variation 3180..3183
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="ctgc"
/db_xref="dbSNP:1651247659"
variation 3180
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:539642986"
variation 3185
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451809122"
variation 3186
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1469144840"
variation 3187
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1177158947"
variation 3188
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651247303"
variation 3190..3198
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="agaa"
/replace="agaaaagaa"
/db_xref="dbSNP:1402844561"
variation 3196
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1406394767"
variation 3199
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651247012"
variation 3200
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651246942"
variation 3204
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765727450"
variation 3205
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651246621"
variation 3206..3208
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1458515379"
variation 3206
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2124024227"
variation 3208
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:546947188"
variation 3213
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262884502"
variation 3214
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651246309"
variation 3215
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:956260632"
variation 3218
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651246161"
variation 3224
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1020047992"
variation 3225
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1009962127"
variation 3228
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:147155302"
variation 3229
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1338872790"
variation 3231
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651245677"
variation 3232
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651245592"
variation 3236
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1244664749"
variation 3238
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:892869640"
variation 3239
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:112310775"
variation 3240
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651245042"
variation 3241
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651244971"
variation 3247
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651244902"
variation 3249
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441510641"
variation 3253
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1000192988"
variation 3266
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:138082769"
variation 3267
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1262264797"
variation 3270
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:771252039"
variation 3271
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1226086135"
variation 3272
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651244247"
variation 3278
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440246"
variation 3280
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1344150641"
variation 3281
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651243960"
variation 3283
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651243885"
variation 3284
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1278827265"
variation 3294
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124023861"
variation 3297
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:889408741"
variation 3298
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651243607"
variation 3300
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651243524"
variation 3302
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1201787038"
variation 3303
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651243347"
variation 3311
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651243289"
variation 3315
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651243203"
variation 3317
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1050705706"
variation 3320
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651243058"
variation 3321..3324
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1651242896"
variation 3321
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124023737"
variation 3323
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473848049"
variation 3326
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651242802"
variation 3328
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651242713"
variation 3329..3332
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gt"
/replace="gtgt"
/db_xref="dbSNP:1295555220"
variation 3329
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:367871467"
variation 3332
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1365183958"
variation 3335
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:987445393"
variation 3349
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651242210"
variation 3350
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:997317672"
variation 3351
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1403157963"
variation 3355
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651241969"
variation 3356
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1405766198"
variation 3359
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1248423203"
variation 3360
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1326930691"
variation 3361..3370
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gtggtgg"
/replace="gtggtggtgg"
/db_xref="dbSNP:1432196945"
variation 3364
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:537175766"
variation 3365
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748058230"
variation 3366
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370272303"
variation 3369
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1306198755"
variation 3370
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1282513897"
variation 3372
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374100414"
variation 3383
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651240603"
variation 3389..3430
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="actcgggagg"
/replace="actcgggaggctgaggcaggagaatcgcttgaactcgggagg"
/db_xref="dbSNP:1651238961"
variation 3390
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1175941351"
variation 3392
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:747048669"
variation 3393
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:568235631"
variation 3397
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:940783155"
variation 3404
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1212346123"
variation 3408
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651240040"
variation 3409
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274512736"
variation 3414
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1178386071"
variation 3415
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:909291003"
variation 3416
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268742724"
variation 3418
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651239567"
variation 3421
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1250436417"
variation 3422
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651239378"
variation 3424
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:192923064"
variation 3425
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1201425315"
variation 3428
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378495316"
variation 3429
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1475201215"
variation 3431
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1436636389"
variation 3433
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124023222"
variation 3435
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651238700"
variation 3436
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1430430620"
variation 3437
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1258863550"
variation 3438
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651238299"
variation 3440..3446
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cagtcag"
/replace="cagtcagtcag"
/db_xref="dbSNP:1310279220"
variation 3440
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651238217"
variation 3444
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1232414045"
variation 3446
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1040599473"
variation 3452
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1224790665"
variation 3454
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1192721334"
variation 3455
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1291746752"
variation 3459..3466
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cac"
/replace="cactgcac"
/db_xref="dbSNP:1651237360"
variation 3459
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651237593"
variation 3460
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:534717853"
variation 3464
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:944567393"
variation 3467
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651237304"
variation 3471
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1224371085"
variation 3472
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:188969705"
variation 3473
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446719057"
variation 3475
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1350052976"
variation 3476..3477
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="gc"
/db_xref="dbSNP:2124022944"
variation 3477
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570440079"
variation 3478..3479
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="tg"
/db_xref="dbSNP:2124022913"
variation 3478
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440076"
variation 3479
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651236726"
variation 3481
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440067"
variation 3486
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651236556"
variation 3487
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1191329965"
variation 3490
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440058"
variation 3491
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250108113"
variation 3492
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440050"
variation 3494
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1286567517"
variation 3496..3497
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="tc"
/db_xref="dbSNP:1397277485"
variation 3496
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274704995"
variation 3497
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1411792184"
variation 3498
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1570440034"
variation 3499
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="c"
/db_xref="dbSNP:1464983949"
variation 3499
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:955329719"
variation 3499
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1651235684"
ORIGIN
actgcctttgctccagccgctgccgccgcaccacctctccttctctgcctctgaccctccttctcgctgctccccctgcccagctgctcctcccacctggccatgaccaaagcccctgctggcaccctggcccagctctgagtcctgggaccctcggtcctctctcctgggccatggccaactcaggcctccagctcctgggctacttcttggccctgggtggctgggtgggcatcattgctagcacagccctgccacagtggaagcagtcttcctacgcaggcgacgccatcatcactgccgtgggcctctatgaagggctctggatgtcctgcgcctcccagagcactgggcaagtgcagtgcaagctctacgactcgctgctcgccctggacggtcacatccaatcagcgcgggccctgatggtggtggccgtgctcctgggcttcgtggccatggtcctcagcgtagttggcatgaagtgtacgcgggtgggagacagcaaccccattgccaagggccgtgttgccatcgccgggggagccctcttcatcctggcaggtatgaatttggcccagccctgttcgtgggctgggcctcagctggcctggccgtgctgggcggctccttcctctgctgcacatgcccggagccagagagacccaacagcagcccacagccctatcggcctggaccctctgctgctgcccgagagtacgtctgagctccgcctgccctggccagccccccacccagtggcccccttgcccagcatccagccagcctcgcagcaccctgggcagggccactggggcataggatgggcataggtgctctgagcagcttgtcctcaacacaagcacccaccctgcaatctgagacccagatcctcagagagacaccagaggcaggacccagcccccaggcatacacacagatgcaggtccaggcacggtcttgtctgcacagcctggtgggcaccagcatgcatccctggagacaggccctcaggcaccagcccggctgtttactcactgaagagctgcttgggtgtctgctacgtgctgggccctagagatagagcagtggccaagacgtaccttagtacccaggtccttggggtgagcagaaaccttcaccctccccagtcccatgggctcctcacagcaaccccacaagggcagtgccgggatgctgaacgttcacacaaggacagggagggtctgagtttaggtctcaggttcttccagtgcgcccagggctgggggccacctacacagatggtgaggtcggaccatggcgcccctgcccccgggaatgggccccaggcagggctgctgtgagggccaaggtctggccacgctggccagtacccatgtccgggcctgaatgcacagcccctgcccccgaccccacagctcactccactaaccagctctctctcttttgactttcagaccagttgttaaattgcccgcctccgccaagggccccctgggtgtgtaatgtccagtccccagccaggctctgtcccctgccatacctagactgtgtgtttcatatttttttggaaagagaagtgaacatccagccccaatcatggtatcattcggtctgtcctcagcgtggcttggacggggcctgtgtcagagtggtcagtgctgacccctggggctcttgggcagaaagatgaggagacagaggtccagggtgggttacatagcacatccagggctaagcaagaaataattcagaggtcctaccctctgtctagggacccccctcccaagcctggccttggccttggcacaaagtcctccttgataggagatcccactcactcctggaggctgcccctgaggcttggcccagctctaggagcagtccccagggtcagggagcccctggtgtggaaagaggccccaaggtagtaaaccctgcccctgttactgtgctccagagacctcctaagggaagggacagttcctggaaggccctccagctggatgctggggatcagcgataggtgaggggacacagtgtaggagctccccatgtagaaaagggaatgtggggagggcgttaggagcttgcaggcattaggactgtcctgagcaaggtctgcagcccccagctctgctcaccccgaatcctgccccttgtttccacacctaccattcctcctctcctgatccccagcatccagctgaggtccaaggtctttgtcctagaatcagagtggggaggggacagcctggggctgcccagagactgtgggtggagctgcctgctgcactcagcagtgcggtcagagaagggcttttggtcttgaagtccaggtaccatccccccttagcatacagggggaagggcctgagaggaatgtaaggaaaccagcccagatcagtcccaaggccagagtcctttgtcctacatctccctgaaccagagtgtgccctgcccctcatgctcagacctctcccaccccaaaccctctcccgggactcagtctccctggccactgcgtatcaggcttctggggaaagcatccatcacagaacctccccttccctgccacgcaccttccttggccagctccattctggcctcctccaccacctgccttgtgaccacatctcccaccacgtccccagatctcaagaacgcagctcagcttctccttcgagcttgactctgagagggaaagtgacggaaaccaagtcagatgagatgactgccatgtacactgcagtcaagggcagggaggggaggaatgacacaaatggcagggagctgctgggggactgacccctcggcgcctggcctggccggtgctgcacatccaccggggcacaacagggacttgtccagcctctggtcagaggatgtggccacctgaccctaaataggttccccagagtcctgcccctctaatgaatgagaactgcaggagtttctcctctgggtgcctgaagctatagtgcaatggttcccaaccctgcatgcacattcgaatcacctgggggcacaatgcctaggctccaaccccagacactcttatttcattggtctgggtggacctggcatcagaagtcatgtagctcctcaggggactgtagtgtgtggtcagcactgagggctcctctatgaggcctcaagcccaggtgactctgtgaggtctgcagagggagaaaagaacccacaagggaagaggtggaggtcaggcacggtggctcacgcttgtaatcccagcactttgggaggccgaggtgggtagatacctgaagtcaggagttcgagactagcctggccaatatggtaaaaccccgtgtctattaaaaatacaaaaattagctggctgtggtggtgggcacctgtaatcccagctactcgggaggctgaggcaggagaatcgcttgaactcgggaggtggaggttgcagtcagccaagatcgtgccactgcacaccatcctggatgacagagcaagactccatcac
//
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]