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Previous release (v1)
2024-04-26 10:14:54, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_148960 2841 bp mRNA linear PRI 16-SEP-2023 DEFINITION Homo sapiens claudin 19 (CLDN19), transcript variant 1, mRNA. ACCESSION NM_148960 VERSION NM_148960.3 KEYWORDS RefSeq; MANE Select. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. REFERENCE 1 (bases 1 to 2841) 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 2841) 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 2841) 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 2841) 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 2841) 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 2841) 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 2841) 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 2841) 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 2841) 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 2841) AUTHORS Kniesel U and Wolburg H. TITLE Tight junctions of the blood-brain barrier JOURNAL Cell Mol Neurobiol 20 (1), 57-76 (2000) PUBMED 10690502 REMARK Review article COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK096063.1, BC030524.1 and AC098484.2. This sequence is a reference standard in the RefSeqGene project. On May 17, 2019 this sequence version replaced NM_148960.2. 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 (1) represents the shortest transcript, but encodes the longest isoform (a). Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: AK096063.1, SRR9304715.579845.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1970526, SAMEA2142853 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000296387.6/ ENSP00000296387.1 RefSeq Select criteria :: based on conservation, expression, longest protein ##RefSeq-Attributes-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-309 AK096063.1 19-327 310-799 BC030524.1 214-703 800-1078 AK096063.1 818-1096 1079-1079 AC098484.2 82833-82833 c 1080-2841 AK096063.1 1098-2859 FEATURES Location/Qualifiers source 1..2841 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="1" /map="1p34.2" gene 1..2841 /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..848 /gene="CLDN19" /gene_synonym="HOMG5" /note="isoform a is encoded by transcript variant 1" /codon_start=1 /product="claudin-19 isoform a" /protein_id="NP_683763.2" /db_xref="CCDS:CCDS471.1" /db_xref="GeneID:149461" /db_xref="HGNC:HGNC:2040" /db_xref="MIM:610036" /translation="
MANSGLQLLGYFLALGGWVGIIASTALPQWKQSSYAGDAIITAVGLYEGLWMSCASQSTGQVQCKLYDSLLALDGHIQSARALMVVAVLLGFVAMVLSVVGMKCTRVGDSNPIAKGRVAIAGGALFILAGLCTLTAVSWYATLVTQEFFNPSTPVNARYEFGPALFVGWASAGLAVLGGSFLCCTCPEPERPNSSPQPYRPGPSAAAREPVVKLPASAKGPLGV"
misc_feature 183..719
/gene="CLDN19"
/gene_synonym="HOMG5"
/note="PMP-22/EMP/MP20/Claudin family; Region:
PMP22_Claudin; cl21598"
/db_xref="CDD:451326"
misc_feature 195..257
/gene="CLDN19"
/gene_synonym="HOMG5"
/note="propagated from UniProtKB/Swiss-Prot (Q8N6F1.2);
transmembrane region"
misc_feature 417..479
/gene="CLDN19"
/gene_synonym="HOMG5"
/note="propagated from UniProtKB/Swiss-Prot (Q8N6F1.2);
transmembrane region"
misc_feature 525..587
/gene="CLDN19"
/gene_synonym="HOMG5"
/note="propagated from UniProtKB/Swiss-Prot (Q8N6F1.2);
transmembrane region"
misc_feature 654..716
/gene="CLDN19"
/gene_synonym="HOMG5"
/note="propagated from UniProtKB/Swiss-Prot (Q8N6F1.2);
transmembrane region"
misc_feature 744..845
/gene="CLDN19"
/gene_synonym="HOMG5"
/note="propagated from UniProtKB/Swiss-Prot (Q8N6F1.2);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
variation 181
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2124050883"
variation 187
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007717189"
variation 188
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:763498750"
variation 191
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651500994"
variation 195
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1030881254"
variation 197
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651500767"
variation 200
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:748664372"
variation 203
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124050794"
variation 204
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:755733650"
variation 206
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651500390"
variation 207
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:368192028"
variation 209
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1334937552"
variation 211
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:767519642"
variation 212
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:12065961"
variation 213
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1381084957"
variation 214
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:751251811"
variation 216
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469998876"
variation 218
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:139675253"
variation 220
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651499300"
variation 221
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570446700"
variation 222
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:555427014"
variation 224
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1452486962"
variation 226
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1363837773"
variation 227
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1180463718"
variation 232
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:118203979"
variation 236
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242311210"
variation 237
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:773544283"
variation 238
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:140913043"
variation 243
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:761923272"
variation 244
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1057515456"
variation 247
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124050531"
variation 249
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:866406931"
variation 252
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:776725990"
variation 253
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:769104160"
variation 256
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:553635114"
variation 257
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124050460"
variation 258
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1357851582"
variation 260
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1375501298"
variation 262
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1314960755"
variation 265
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:780216494"
variation 266
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1342611487"
variation 269
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315830730"
variation 274
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:867223625"
variation 275
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381262078"
variation 278
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:760544476"
variation 279
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1033106967"
variation 280
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422671061"
variation 282
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442564894"
variation 284
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:748869909"
variation 285
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:777520292"
variation 287
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:755860892"
variation 288
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1240115369"
variation 289
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1191344664"
variation 291
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651495650"
variation 295
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:752202900"
variation 301
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:387907421"
variation 302
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780859720"
variation 303
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:751576939"
variation 305
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1407788763"
variation 312..314
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="t"
/replace="tat"
/db_xref="dbSNP:1229360131"
variation 313
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1291749652"
variation 319
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358943115"
variation 321
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:762859529"
variation 323
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:750581981"
variation 326
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:387907418"
variation 329
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:762045827"
variation 331
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402626520"
variation 332
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:776635994"
variation 335
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303732063"
variation 336
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:768727872"
variation 341
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:907045006"
variation 342
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:118203980"
variation 343
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:761073623"
variation 344
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651493539"
variation 345
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1475211264"
variation 349
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339250013"
variation 350
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124049938"
variation 351..353
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="ggg"
/db_xref="dbSNP:1159781653"
variation 351
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1347509413"
variation 355
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1439229751"
variation 362
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:776112203"
variation 365
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:772291750"
variation 374
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:746201648"
variation 375
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:779164813"
variation 376
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1434953393"
variation 378
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1222974414"
variation 379
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:373645751"
variation 380
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:539643806"
variation 386
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780841156"
variation 387
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:571067526"
variation 395
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1279756315"
variation 396
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:780082160"
exon 397..561
/gene="CLDN19"
/gene_synonym="HOMG5"
/inference="alignment:Splign:2.1.0"
variation 397
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1355679787"
variation 402..409
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="atccaatc"
/replace="atccaatccaatc"
/db_xref="dbSNP:1557551861"
variation 402
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:140190002"
variation 407
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451717579"
variation 408
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1227282179"
variation 412
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:768309387"
variation 413
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:896880334"
variation 414
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450421453"
variation 415
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:901442993"
variation 416
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1299357363"
variation 421
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651447341"
variation 422
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651447252"
variation 423
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1439120120"
variation 430
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651447047"
variation 432
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1158407262"
variation 434
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:746656339"
variation 435
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:538666680"
variation 438
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:771549550"
variation 440
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1444446063"
variation 442
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:118203981"
variation 443
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651446362"
variation 444
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1553139268"
variation 449
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:778861111"
variation 450
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:34374110"
variation 451
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557551799"
variation 454
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651445702"
variation 456
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749031151"
variation 466
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:777556169"
variation 467
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:756289810"
variation 468
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:752926836"
variation 474
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:387907419"
variation 475
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651444990"
variation 480..481
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1651444883"
variation 482
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:748824249"
variation 485
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1289562292"
variation 486
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1466588520"
variation 487
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200640147"
variation 488
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201994736"
variation 489
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:752086015"
variation 490
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:766957259"
variation 492
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651443997"
variation 498
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651443863"
variation 503
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2124045042"
variation 506
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1349368590"
variation 507
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651443699"
variation 508
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:867064302"
variation 509
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:763579075"
variation 510
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:755364712"
variation 511
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:948617979"
variation 514
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:989252379"
variation 522
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:765527366"
variation 523
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:377319583"
variation 527
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124044916"
variation 530
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651442786"
variation 533
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:763138436"
variation 534
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:750311451"
variation 535
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570444933"
variation 536
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:771578996"
variation 537..541
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1288612884"
variation 537
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:759006357"
variation 538
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651441969"
variation 539
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:773871683"
variation 543
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1478541411"
variation 544
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1266106532"
variation 549
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:770796801"
variation 553
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1488735388"
variation 559
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:143479131"
variation 561
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557551678"
exon 562..646
/gene="CLDN19"
/gene_synonym="HOMG5"
/inference="alignment:Splign:2.1.0"
variation 562
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:769597140"
variation 568
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378831110"
variation 572
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1474323316"
variation 574..579
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tg"
/replace="tgactg"
/db_xref="dbSNP:762736103"
variation 584
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:747861227"
variation 586
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781067170"
variation 587
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370124717"
variation 591
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557551562"
variation 593
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:200835353"
variation 595
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375722346"
variation 598..600
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2124044159"
variation 598
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:780278993"
variation 600
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:906095096"
variation 602
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746364980"
variation 606
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:779246616"
variation 607
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1237543232"
variation 608
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651434298"
variation 609
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651434213"
variation 611
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651434118"
variation 612
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651434032"
variation 613
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386978279"
variation 617
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:11810617"
variation 618
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:757804403"
variation 619
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651433568"
variation 625
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1310630314"
variation 627
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242843559"
variation 628
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1442512269"
variation 633
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1381010022"
variation 634
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1333146300"
variation 635
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396212645"
variation 645
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651432829"
exon 647..799
/gene="CLDN19"
/gene_synonym="HOMG5"
/inference="alignment:Splign:2.1.0"
variation 647
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651360381"
variation 649
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651360279"
variation 655
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651360194"
variation 659
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:962614350"
variation 663
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651359971"
variation 664..671
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="ccctgttc"
/db_xref="dbSNP:1651359589"
variation 665
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:762618011"
variation 666
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651359777"
variation 668
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1216799895"
variation 671
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:776225389"
variation 672
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163560341"
variation 674
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316432824"
variation 675
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1473655950"
variation 676
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:866174535"
variation 678
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570442822"
variation 679
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124036870"
variation 682
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768639835"
variation 683
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651358674"
variation 691
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:747223067"
variation 693
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570442807"
variation 696
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263949970"
variation 697
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124036796"
variation 698
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:138355552"
variation 699
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:772247940"
variation 701
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1289785127"
variation 702
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:867926864"
variation 703
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651357824"
variation 707
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:140842024"
variation 708
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:145591298"
variation 709
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1217588010"
variation 710
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:749872474"
variation 712
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201399564"
variation 713
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651357109"
variation 714
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035217156"
variation 715
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1003712779"
variation 716
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124036565"
variation 719
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1403033958"
variation 720
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1330521485"
variation 721
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1164602961"
variation 722
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324117597"
variation 723
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367075794"
variation 724
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124036479"
variation 726
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332219103"
variation 728
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:369184924"
variation 729
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1394029284"
variation 733
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:531931336"
variation 734
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:9660973"
variation 735
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1300085775"
variation 737
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1424431332"
variation 738
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1196017795"
variation 740..746
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="agaga"
/replace="agagaga"
/db_xref="dbSNP:1341096574"
variation 743
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651353668"
variation 744
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1477074057"
variation 745
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124036280"
variation 748
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1246687752"
variation 752
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:758094656"
variation 755
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1453711939"
variation 758
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651352981"
variation 759
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256503881"
variation 760
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:749847290"
variation 761
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651352001"
variation 764
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:764811412"
variation 765
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1259589527"
variation 766
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:549476247"
variation 769
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:114350566"
variation 771
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:763959764"
variation 772
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:116804195"
variation 774
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1333791679"
variation 775
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:775446633"
variation 778
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651350767"
variation 779
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651350663"
variation 780..782
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:772887123"
variation 782
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651350389"
variation 789
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1401372077"
variation 790
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:772360364"
variation 792
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1412877618"
variation 793
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424493671"
variation 795
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011136678"
variation 796
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:894082758"
variation 799
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:145157550"
exon 800..2841
/gene="CLDN19"
/gene_synonym="HOMG5"
/inference="alignment:Splign:2.1.0"
variation 801
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:756892751"
variation 804
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651315741"
variation 806
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422290318"
variation 808
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651315592"
variation 812
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1193831713"
variation 814
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:753338977"
variation 818
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777425105"
variation 819
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147528059"
variation 821
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651315070"
variation 824
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:752738519"
variation 825
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:535667246"
variation 830
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1215803586"
variation 831
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:200491942"
variation 832
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1257662822"
variation 833
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1219376620"
variation 834
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1279949075"
variation 835
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1309299294"
variation 836
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:371686331"
variation 843
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:766571498"
variation 844
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:387907420"
variation 845
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:764858690"
variation 847
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:773211263"
variation 849
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328261253"
variation 850
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:769931882"
variation 855
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:762297703"
variation 857
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:777172207"
variation 858
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:768871931"
variation 859
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:747361042"
variation 862
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:775740656"
variation 865
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:770548857"
variation 866
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:367910861"
variation 867
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:777408812"
variation 868
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:546757402"
variation 873
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:755733771"
variation 874
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:748064968"
variation 876
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1177658979"
variation 878
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:781140631"
variation 880
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651312522"
variation 881
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429507975"
variation 882
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:373755403"
variation 886
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:750026527"
variation 889
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651312175"
variation 893
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200471599"
variation 894
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1313365002"
variation 895
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039423338"
variation 902
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651311814"
variation 903
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651311737"
variation 904
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:910316814"
variation 905..911
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:1351281461"
variation 906
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230470801"
variation 911
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651311406"
variation 915
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:943323880"
variation 917
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651311245"
variation 919
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1290591903"
variation 927..934
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="catccagc"
/db_xref="dbSNP:369052611"
variation 927
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1312372093"
variation 930
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:890355984"
variation 931
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:796219031"
variation 933
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651310688"
variation 934..937
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1310273077"
variation 934
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051634158"
polyA_site 939
/gene="CLDN19"
/gene_synonym="HOMG5"
/note="major polyA site"
variation 939
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:77236131"
variation 942
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651309054"
variation 943
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:919054603"
variation 948
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651308898"
variation 951
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651308816"
variation 953
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:765909170"
variation 954
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:550521995"
variation 957
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:958751979"
variation 959
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441516"
variation 961
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486463471"
variation 967
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376052803"
variation 968
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:915602099"
variation 970
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651306549"
variation 975
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:991547265"
variation 978
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1412202056"
variation 979
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1184440731"
variation 982
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002446383"
variation 983
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1437925300"
variation 987
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2124031042"
variation 992
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651305332"
variation 995
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651305260"
variation 997
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:959681582"
variation 1001
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651305109"
variation 1002
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:530817596"
variation 1004
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1035678117"
variation 1006
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:140105842"
variation 1008
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:966857083"
variation 1009
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1408035464"
variation 1010
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651304418"
variation 1011
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:372780855"
variation 1013
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330294458"
variation 1017
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651304187"
variation 1018
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374175709"
variation 1019
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651304043"
variation 1023
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1225012393"
variation 1025
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:371735000"
variation 1026
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="a"
/db_xref="dbSNP:1651303556"
variation 1027
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441448"
variation 1031
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651303395"
variation 1034
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651303321"
variation 1035
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651303242"
variation 1044
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651303183"
variation 1045
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:762336108"
variation 1047
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651303028"
variation 1050
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651302955"
variation 1051
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1017633734"
variation 1052
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651302791"
variation 1053
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1233170783"
variation 1055
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007966109"
variation 1061
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1266027309"
variation 1063
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210312530"
variation 1067
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204652754"
variation 1069
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651302185"
variation 1071
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:890420008"
variation 1078
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="t"
/db_xref="dbSNP:1237852963"
variation 1079
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:912075"
variation 1080
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651301614"
variation 1082
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1179091682"
variation 1083
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124030579"
variation 1084
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441403"
variation 1087
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:936351398"
variation 1094
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651301325"
variation 1095
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651301258"
variation 1098
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651301175"
variation 1102
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651301086"
variation 1105
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:796637327"
variation 1106
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1173907268"
variation 1108
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1431290070"
variation 1109
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557549135"
variation 1110..1112
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1470171925"
variation 1112..1114
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="t"
/replace="tct"
/db_xref="dbSNP:1651300214"
variation 1113
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169660133"
variation 1119
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651300144"
variation 1120..1125
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccccc"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:532996510"
variation 1120
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1397759529"
variation 1123
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651299939"
variation 1124
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557549123"
variation 1127
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:374721300"
variation 1133
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:897677267"
variation 1135..1150
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tggccttggccttggc"
/replace="tggccttggccttggccttggc"
/db_xref="dbSNP:1382161816"
variation 1137
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651299417"
variation 1143
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:769241790"
variation 1144
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1037519071"
variation 1145
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1313526522"
variation 1151
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1651298963"
variation 1158
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1224550639"
variation 1159
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1257815975"
variation 1161
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306041428"
variation 1163..1164
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1387012858"
variation 1164
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651298546"
variation 1167
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:560322698"
variation 1170
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:923428502"
variation 1172..1173
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="tt"
/db_xref="dbSNP:1651298185"
variation 1172
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570441330"
variation 1175
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651298103"
variation 1177
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1488210994"
variation 1179
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651297939"
variation 1180
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651297853"
variation 1187
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189528235"
variation 1188
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:972643328"
variation 1189
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651297622"
variation 1197
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:940921614"
variation 1203
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651297444"
variation 1204
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:915635301"
variation 1205
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651297274"
variation 1212
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192750059"
variation 1214
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651297101"
variation 1215
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:909480057"
variation 1222
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651296925"
variation 1223
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1411376424"
variation 1224
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1170743499"
variation 1225
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651296740"
variation 1229
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348885607"
variation 1230
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651296606"
variation 1234
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:540075482"
variation 1235
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1458132860"
variation 1239
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1304397001"
variation 1241
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651296322"
variation 1243
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1348005048"
variation 1247
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406074500"
variation 1250
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:991208270"
variation 1251
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1360351404"
variation 1252
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651295905"
variation 1255
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1216643137"
variation 1259
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:938348889"
variation 1263
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651295666"
variation 1268
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651295584"
variation 1269..1270
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1557549040"
variation 1269
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:958740672"
variation 1270
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:577777997"
variation 1271
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557549032"
variation 1278
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1220436490"
variation 1283
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651295069"
variation 1284
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651294954"
variation 1286..1287
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="ct"
/db_xref="dbSNP:1651294861"
variation 1293
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651294764"
variation 1300
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441257"
variation 1305
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:927363928"
variation 1306
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651294479"
variation 1308
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1490516616"
variation 1310
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1215809504"
variation 1316
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651294239"
variation 1318
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1240247833"
variation 1320
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651294088"
variation 1323
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651294006"
variation 1325
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1476285590"
variation 1337
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557549013"
variation 1339
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762244030"
variation 1349
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651293632"
variation 1356
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:971891724"
variation 1357
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:982342001"
variation 1360
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1421685531"
variation 1362
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2124029487"
variation 1363
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651293273"
variation 1364
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:966911128"
variation 1367
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="a"
/db_xref="dbSNP:1651293052"
variation 1369
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651292928"
variation 1370
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570441205"
variation 1371
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:776804215"
variation 1378
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="c"
/db_xref="dbSNP:138777333"
variation 1378
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570441195"
variation 1378
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2124029388"
variation 1380
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651292465"
variation 1384
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1057515528"
variation 1386
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1433378024"
variation 1386
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124029327"
variation 1387
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000530698"
variation 1394
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441171"
variation 1395
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:549719300"
variation 1397
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1378789687"
variation 1399
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:529459531"
variation 1409
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1317340602"
variation 1410
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1050521162"
variation 1412
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:958183930"
variation 1413
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651291501"
variation 1415
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124029210"
variation 1416
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557548969"
variation 1417
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651291298"
variation 1418
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:901605896"
variation 1421
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651291140"
variation 1423
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1036501699"
variation 1424
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:746091783"
variation 1425
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1465219512"
variation 1428
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651290809"
variation 1429
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651290725"
variation 1434
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651290639"
variation 1435
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651290539"
variation 1436
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="c"
/db_xref="dbSNP:2124029075"
variation 1436
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236668999"
variation 1439
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651290394"
variation 1444
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288859510"
variation 1445
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1018104979"
variation 1446
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651290159"
variation 1450
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1570441109"
variation 1453
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651290016"
variation 1455
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651289946"
variation 1458
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1208353733"
variation 1459
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1358653297"
variation 1461
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1007604392"
variation 1465
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1266123585"
variation 1466
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1227696453"
variation 1469
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:940889035"
variation 1470..1474
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:551118125"
variation 1470
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441086"
variation 1472
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:761260010"
variation 1474
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1406509120"
variation 1477
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:909468672"
variation 1484
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:954884639"
variation 1485
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570441069"
variation 1486
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651288831"
variation 1487
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030310070"
variation 1489
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:563880269"
variation 1490
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:781380872"
variation 1492
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651288511"
variation 1494
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:993435665"
variation 1499
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651288359"
variation 1500
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450854555"
variation 1508
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:927279008"
variation 1512
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570441044"
variation 1513
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1383775010"
variation 1515
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:981869447"
variation 1516
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:897729862"
variation 1517
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651287512"
variation 1518
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651287434"
variation 1520
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651287367"
variation 1521
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651287302"
variation 1522
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570441028"
variation 1531
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651287140"
variation 1534
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:544178185"
variation 1539
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376179882"
variation 1542
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:770893678"
variation 1551..1557
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gaggtcc"
/replace="gaggtccgaggtcc"
/db_xref="dbSNP:1224286686"
variation 1558
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651286686"
variation 1559
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:894268522"
variation 1561
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651286537"
variation 1562..1566
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tcttt"
/replace="tctttcttt"
/db_xref="dbSNP:1651286378"
variation 1563
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1055959077"
variation 1583
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:142957479"
variation 1585
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557548866"
variation 1588
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651286100"
variation 1590
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651285812"
variation 1591
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163371071"
variation 1593
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:956565410"
variation 1596
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205305296"
variation 1600
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124028436"
variation 1602
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651285410"
variation 1603
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651285325"
variation 1605
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651285222"
variation 1609
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1032252022"
variation 1615..1618
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1651284899"
variation 1617
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1457037795"
variation 1620
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1179119133"
variation 1629
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570440973"
variation 1631
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651284640"
variation 1632
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651284567"
variation 1640
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428584044"
variation 1641
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000749435"
variation 1642
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651284324"
variation 1648
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777568849"
variation 1649
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1041346817"
variation 1659
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1028632951"
variation 1660
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1245915070"
variation 1661
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1429147609"
variation 1662
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651283714"
variation 1666
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651283626"
variation 1667..1668
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1651283478"
variation 1667
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651283551"
variation 1668
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:368436876"
variation 1676
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651283324"
variation 1679..1680
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="cccctt"
/db_xref="dbSNP:1651283244"
variation 1682..1685
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="gtac"
/db_xref="dbSNP:1651282989"
variation 1682
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651283164"
variation 1684
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196406854"
variation 1689..1694
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:1049224758"
variation 1690
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:181070200"
variation 1691
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:914148776"
variation 1692
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268267008"
variation 1693
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:377585440"
variation 1694
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:887914551"
variation 1698
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1225184734"
variation 1701
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651282146"
variation 1703
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651282052"
variation 1708
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263511720"
variation 1711
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651281877"
variation 1712
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124027921"
variation 1713
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651281784"
variation 1715
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:796839004"
variation 1717
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651281593"
variation 1718
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1274622493"
variation 1720
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651281450"
variation 1721
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370331996"
variation 1724
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1273470824"
variation 1726
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651281232"
variation 1728
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268854758"
variation 1737
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1045719913"
variation 1739
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="g"
/db_xref="dbSNP:1651280966"
variation 1742
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:910688779"
variation 1744
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1332005923"
variation 1749
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:375306800"
variation 1752
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:913313445"
variation 1754
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:988929125"
variation 1755..1763
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ag"
/replace="aggccagag"
/db_xref="dbSNP:2124027665"
variation 1756
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:758420361"
variation 1758
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124027693"
variation 1760
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302621983"
variation 1763
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:148594631"
variation 1766
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651280180"
variation 1769
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1368236439"
variation 1770
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:954754714"
variation 1772
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651279898"
variation 1773
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:369724376"
variation 1776
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124027562"
variation 1777
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1406709368"
variation 1784
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:925067368"
variation 1787
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1030363830"
variation 1788
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124027513"
variation 1789
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1224900327"
variation 1791
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651279231"
variation 1797
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410475059"
variation 1803..1806
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1651278770"
variation 1805
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424315949"
variation 1806
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651278627"
variation 1809
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:570565492"
variation 1810
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651278296"
variation 1811
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:550710062"
variation 1812
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:961993377"
variation 1822
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1016190439"
variation 1823
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006102105"
variation 1824
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:894312717"
variation 1833
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1055609220"
variation 1834
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1003059924"
variation 1837
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440821"
variation 1842
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1490681272"
variation 1843
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1377976423"
variation 1845
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651276774"
variation 1846
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:906949228"
variation 1847
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651276379"
variation 1852
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440801"
variation 1853
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:966138586"
variation 1856
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482159495"
variation 1859
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1191445002"
variation 1866
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:114944537"
variation 1867
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:568148786"
variation 1868
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:945714612"
variation 1870
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442385976"
variation 1879
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124027137"
variation 1887
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651272818"
variation 1892
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124027109"
variation 1893
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651272715"
variation 1895
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1277175863"
variation 1898
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1426580574"
variation 1902
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440761"
variation 1903
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303707822"
variation 1904
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651272059"
variation 1905
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:914201766"
variation 1908
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651271743"
variation 1909
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651271624"
variation 1919
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1380357646"
variation 1920
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:887547668"
variation 1921
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1057515527"
variation 1922
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1243631825"
variation 1922
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651271035"
variation 1923..1924
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="acctccccttcc"
/db_xref="dbSNP:1651270946"
variation 1925
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651270816"
variation 1933
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:548984051"
variation 1934
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124026869"
variation 1935
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1361015949"
variation 1937
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651270491"
variation 1942
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651270406"
variation 1943
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:189819580"
variation 1945..1951
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ctggcct"
/replace="ctggcctggcct"
/db_xref="dbSNP:1651269933"
variation 1946
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1002138865"
variation 1948
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651270061"
variation 1949..1956
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cctcc"
/replace="cctcctcc"
/db_xref="dbSNP:1651269737"
variation 1951
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1203815179"
variation 1956
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:906096762"
variation 1962
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124026713"
variation 1964
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:564714068"
variation 1965
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1227401183"
variation 1970
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348176800"
variation 1973
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651268960"
variation 1976
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:950072291"
variation 1983
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1363228211"
variation 1985
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1451529541"
variation 1986
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2124026616"
variation 1988
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:529158343"
variation 1989
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1391371008"
variation 1992
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651268246"
variation 1993
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651268154"
variation 2002..2003
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="gcttctccttcg"
/db_xref="dbSNP:1385411183"
variation 2007
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:891756677"
variation 2008
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332181117"
variation 2010
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:184596944"
variation 2020
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:796988312"
variation 2022
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651267544"
variation 2023
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651267448"
variation 2026
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406550607"
variation 2027
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:144430420"
variation 2030
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471748356"
variation 2033
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262971116"
variation 2034
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124026409"
variation 2035
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651266929"
variation 2037
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:910732047"
variation 2040
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1351873770"
variation 2053
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:778687377"
variation 2054
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:986301112"
variation 2061
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651266461"
variation 2066
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1241571392"
variation 2068
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651266301"
variation 2070
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651266207"
variation 2073
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:754589000"
variation 2077
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:926038941"
variation 2080
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1184356468"
variation 2083
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1472535414"
variation 2084
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1249928199"
variation 2088
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651264513"
variation 2090
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:753515106"
variation 2101
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:933422896"
variation 2107
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212936203"
variation 2110
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651264106"
variation 2111
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651264023"
variation 2118
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651263951"
variation 2120
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651263878"
variation 2128
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651263788"
variation 2132
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:976373319"
variation 2134
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:766100803"
variation 2137
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:546730630"
variation 2138
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:965993611"
variation 2141
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1321561594"
variation 2144
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1470006770"
variation 2145
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651263108"
variation 2149
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651263025"
variation 2150..2151
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="ac"
/db_xref="dbSNP:1297176277"
variation 2150
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440619"
variation 2151
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651262799"
variation 2153
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651262709"
variation 2156
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440610"
variation 2157
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:923346842"
variation 2158
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1014521584"
variation 2159
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1351603683"
variation 2160
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:972101560"
variation 2161
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651262102"
variation 2162
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651262021"
variation 2163
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1326675459"
variation 2165
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651261851"
variation 2167
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1204553607"
variation 2170
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1289876170"
variation 2171
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:760068656"
variation 2172
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1479712621"
variation 2173
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:962046453"
variation 2174
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124025830"
variation 2175
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:76855155"
variation 2177
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651261007"
variation 2179..2197
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gcaca"
/replace="gcacatccaccggggcaca"
/db_xref="dbSNP:1169331973"
variation 2179
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570440564"
variation 2180
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1480061117"
variation 2181
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1281856305"
variation 2183
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1197119795"
variation 2184
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651260597"
variation 2185
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651260497"
variation 2186
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:985131155"
variation 2187
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440550"
variation 2189
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:958630245"
variation 2190
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651260155"
variation 2191
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651260083"
variation 2193
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651260006"
variation 2199
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651259846"
variation 2201
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:745884385"
variation 2205
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200527665"
variation 2207..2210
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tgtc"
/replace="tgtctgtc"
/db_xref="dbSNP:1001707873"
variation 2209
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440539"
variation 2210
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651259427"
variation 2214
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651259312"
variation 2224
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651259241"
variation 2225
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:567823099"
variation 2226
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651259065"
variation 2227
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1024484460"
variation 2228
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651258894"
variation 2231
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651258809"
variation 2245
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281860320"
variation 2249
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:544361263"
variation 2251
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1014880889"
variation 2255..2258
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1651257735"
variation 2257
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651257827"
variation 2258
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:373188579"
variation 2262
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1404978019"
variation 2268
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124025433"
variation 2271
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009910087"
variation 2276
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:149256970"
variation 2277
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557548354"
variation 2278
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651257129"
variation 2288
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1054107067"
variation 2290
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651256977"
variation 2292
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:904588472"
variation 2297..2300
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="t"
/replace="ttct"
/db_xref="dbSNP:529449539"
variation 2298
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:796175275"
variation 2300..2309
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="tcctctgggt"
/db_xref="dbSNP:796901250"
variation 2302
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651256649"
variation 2303..2309
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="tctgggt"
/db_xref="dbSNP:562296433"
variation 2304
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:889365281"
variation 2306
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1490465444"
variation 2307
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1049876055"
variation 2310
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651256206"
variation 2321
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247904427"
variation 2325
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1170642886"
variation 2330
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651256000"
variation 2331
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1051069098"
variation 2339
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:931824276"
variation 2340
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651255779"
variation 2342
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124025179"
variation 2345
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651255704"
variation 2346
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651255626"
variation 2352
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301862960"
variation 2354
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651255479"
variation 2355
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:933476755"
variation 2357
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288652453"
variation 2360
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651255231"
variation 2365
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1360239083"
variation 2366
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:770989443"
variation 2368
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:923397849"
variation 2372
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124025040"
variation 2373
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651254904"
variation 2374
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651254819"
variation 2376
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1298557597"
variation 2377
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:71654253"
variation 2380
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1040226305"
variation 2381
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:944594774"
variation 2382
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1293905748"
variation 2383..2386
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="tcca"
/replace="tccatcca"
/db_xref="dbSNP:1651252045"
variation 2383
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651252143"
variation 2391
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1452102004"
variation 2394
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651251901"
variation 2397
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:556016559"
variation 2399
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651251709"
variation 2407
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1320683263"
variation 2408
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651251523"
variation 2411
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1287161397"
variation 2417
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:972155294"
variation 2432
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651251285"
variation 2434
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1486687028"
variation 2439
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:371301647"
variation 2442
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:113021721"
variation 2444
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:763565629"
variation 2445
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1296855045"
variation 2446..2447
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="cc"
/db_xref="dbSNP:1432786550"
variation 2447
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651250450"
variation 2452
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:951754166"
variation 2453
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1289160691"
variation 2454
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:984795189"
variation 2455
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1158931903"
variation 2458
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1343831685"
variation 2461
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1433265834"
variation 2462
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651249964"
variation 2469
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1057515454"
variation 2476
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1436042894"
variation 2480
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1348305840"
variation 2481
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651249597"
variation 2484
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1382267259"
variation 2485
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651249434"
variation 2488
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:958906433"
variation 2489
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651249261"
variation 2490
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:56345167"
variation 2491
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:969836365"
variation 2492
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651248882"
variation 2494
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223154374"
variation 2496
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651248719"
variation 2497
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:573446568"
variation 2498
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1209098870"
variation 2503
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651248461"
variation 2506
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:981285231"
variation 2507
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651248287"
variation 2509
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:553394106"
variation 2511..2514
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1651248113"
variation 2515
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1184964715"
variation 2517
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:866481412"
variation 2519
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1570440321"
variation 2520
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651247803"
variation 2522..2525
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="ctgc"
/db_xref="dbSNP:1651247659"
variation 2522
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:539642986"
variation 2527
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451809122"
variation 2528
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1469144840"
variation 2529
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1177158947"
variation 2530
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651247303"
variation 2532..2540
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="agaa"
/replace="agaaaagaa"
/db_xref="dbSNP:1402844561"
variation 2538
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1406394767"
variation 2541
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651247012"
variation 2542
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651246942"
variation 2546
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765727450"
variation 2547
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651246621"
variation 2548..2550
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1458515379"
variation 2548
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2124024227"
variation 2550
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:546947188"
variation 2555
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262884502"
variation 2556
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651246309"
variation 2557
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:956260632"
variation 2560
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651246161"
variation 2566
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1020047992"
variation 2567
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1009962127"
variation 2570
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:147155302"
variation 2571
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1338872790"
variation 2573
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651245677"
variation 2574
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651245592"
variation 2578
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1244664749"
variation 2580
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:892869640"
variation 2581
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:112310775"
variation 2582
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651245042"
variation 2583
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651244971"
variation 2589
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651244902"
variation 2591
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441510641"
variation 2595
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1000192988"
variation 2608
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:138082769"
variation 2609
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1262264797"
variation 2612
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:771252039"
variation 2613
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1226086135"
variation 2614
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651244247"
variation 2620
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440246"
variation 2622
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1344150641"
variation 2623
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651243960"
variation 2625
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651243885"
variation 2626
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1278827265"
variation 2636
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124023861"
variation 2639
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:889408741"
variation 2640
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651243607"
variation 2642
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651243524"
variation 2644
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1201787038"
variation 2645
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651243347"
variation 2653
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651243289"
variation 2657
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651243203"
variation 2659
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1050705706"
variation 2662
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1651243058"
variation 2663..2666
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1651242896"
variation 2663
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124023737"
variation 2665
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473848049"
variation 2668
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651242802"
variation 2670
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651242713"
variation 2671..2674
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gt"
/replace="gtgt"
/db_xref="dbSNP:1295555220"
variation 2671
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:367871467"
variation 2674
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1365183958"
variation 2677
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:987445393"
variation 2691
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1651242210"
variation 2692
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:997317672"
variation 2693
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1403157963"
variation 2697
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651241969"
variation 2698
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1405766198"
variation 2701
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1248423203"
variation 2702
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1326930691"
variation 2703..2712
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="gtggtgg"
/replace="gtggtggtgg"
/db_xref="dbSNP:1432196945"
variation 2706
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:537175766"
variation 2707
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748058230"
variation 2708
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370272303"
variation 2711
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1306198755"
variation 2712
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1282513897"
variation 2714
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374100414"
variation 2725
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651240603"
variation 2731..2772
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="actcgggagg"
/replace="actcgggaggctgaggcaggagaatcgcttgaactcgggagg"
/db_xref="dbSNP:1651238961"
variation 2732
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1175941351"
variation 2734
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:747048669"
variation 2735
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:568235631"
variation 2739
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:940783155"
variation 2746
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1212346123"
variation 2750
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651240040"
variation 2751
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274512736"
variation 2756
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1178386071"
variation 2757
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:909291003"
variation 2758
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268742724"
variation 2760
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651239567"
variation 2763
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1250436417"
variation 2764
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651239378"
variation 2766
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:192923064"
variation 2767
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1201425315"
variation 2770
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378495316"
variation 2771
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1475201215"
variation 2773
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1436636389"
variation 2775
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124023222"
variation 2777
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651238700"
variation 2778
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1430430620"
variation 2779
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1258863550"
variation 2780
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651238299"
variation 2782..2788
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cagtcag"
/replace="cagtcagtcag"
/db_xref="dbSNP:1310279220"
variation 2782
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651238217"
variation 2786
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1232414045"
variation 2788
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1040599473"
variation 2794
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1224790665"
variation 2796
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1192721334"
variation 2797
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1291746752"
variation 2801..2808
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="cac"
/replace="cactgcac"
/db_xref="dbSNP:1651237360"
variation 2801
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1651237593"
variation 2802
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:534717853"
variation 2806
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:944567393"
variation 2809
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1651237304"
variation 2813
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1224371085"
variation 2814
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:188969705"
variation 2815
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446719057"
variation 2817
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1350052976"
variation 2818..2819
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="gc"
/db_xref="dbSNP:2124022944"
variation 2819
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570440079"
variation 2820..2821
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="tg"
/db_xref="dbSNP:2124022913"
variation 2820
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440076"
variation 2821
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651236726"
variation 2823
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440067"
variation 2828
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1651236556"
variation 2829
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1191329965"
variation 2832
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1570440058"
variation 2833
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250108113"
variation 2834
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570440050"
variation 2836
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1286567517"
variation 2838..2839
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="tc"
/db_xref="dbSNP:1397277485"
variation 2838
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274704995"
variation 2839
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1411792184"
variation 2840
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1570440034"
variation 2841
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace=""
/replace="c"
/db_xref="dbSNP:1464983949"
variation 2841
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="a"
/replace="c"
/db_xref="dbSNP:955329719"
variation 2841
/gene="CLDN19"
/gene_synonym="HOMG5"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1651235684"
ORIGIN
actgcctttgctccagccgctgccgccgcaccacctctccttctctgcctctgaccctccttctcgctgctccccctgcccagctgctcctcccacctggccatgaccaaagcccctgctggcaccctggcccagctctgagtcctgggaccctcggtcctctctcctgggccatggccaactcaggcctccagctcctgggctacttcttggccctgggtggctgggtgggcatcattgctagcacagccctgccacagtggaagcagtcttcctacgcaggcgacgccatcatcactgccgtgggcctctatgaagggctctggatgtcctgcgcctcccagagcactgggcaagtgcagtgcaagctctacgactcgctgctcgccctggacggtcacatccaatcagcgcgggccctgatggtggtggccgtgctcctgggcttcgtggccatggtcctcagcgtagttggcatgaagtgtacgcgggtgggagacagcaaccccattgccaagggccgtgttgccatcgccgggggagccctcttcatcctggcaggcctctgcactttgactgctgtctcgtggtatgccaccctggtgacccaggagttcttcaacccaagcacacctgtcaatgccaggtatgaatttggcccagccctgttcgtgggctgggcctcagctggcctggccgtgctgggcggctccttcctctgctgcacatgcccggagccagagagacccaacagcagcccacagccctatcggcctggaccctctgctgctgcccgagaaccagttgttaaattgcccgcctccgccaagggccccctgggtgtgtaatgtccagtccccagccaggctctgtcccctgccatacctagactgtgtgtttcatatttttttggaaagagaagtgaacatccagccccaatcatggtatcattcggtctgtcctcagcgtggcttggacggggcctgtgtcagagtggtcagtgctgacccctggggctcttgggcagaaagatgaggagacagaggtccagggtgggttacatagcacatccagggctaagcaagaaataattcagaggtcctaccctctgtctagggacccccctcccaagcctggccttggccttggcacaaagtcctccttgataggagatcccactcactcctggaggctgcccctgaggcttggcccagctctaggagcagtccccagggtcagggagcccctggtgtggaaagaggccccaaggtagtaaaccctgcccctgttactgtgctccagagacctcctaagggaagggacagttcctggaaggccctccagctggatgctggggatcagcgataggtgaggggacacagtgtaggagctccccatgtagaaaagggaatgtggggagggcgttaggagcttgcaggcattaggactgtcctgagcaaggtctgcagcccccagctctgctcaccccgaatcctgccccttgtttccacacctaccattcctcctctcctgatccccagcatccagctgaggtccaaggtctttgtcctagaatcagagtggggaggggacagcctggggctgcccagagactgtgggtggagctgcctgctgcactcagcagtgcggtcagagaagggcttttggtcttgaagtccaggtaccatccccccttagcatacagggggaagggcctgagaggaatgtaaggaaaccagcccagatcagtcccaaggccagagtcctttgtcctacatctccctgaaccagagtgtgccctgcccctcatgctcagacctctcccaccccaaaccctctcccgggactcagtctccctggccactgcgtatcaggcttctggggaaagcatccatcacagaacctccccttccctgccacgcaccttccttggccagctccattctggcctcctccaccacctgccttgtgaccacatctcccaccacgtccccagatctcaagaacgcagctcagcttctccttcgagcttgactctgagagggaaagtgacggaaaccaagtcagatgagatgactgccatgtacactgcagtcaagggcagggaggggaggaatgacacaaatggcagggagctgctgggggactgacccctcggcgcctggcctggccggtgctgcacatccaccggggcacaacagggacttgtccagcctctggtcagaggatgtggccacctgaccctaaataggttccccagagtcctgcccctctaatgaatgagaactgcaggagtttctcctctgggtgcctgaagctatagtgcaatggttcccaaccctgcatgcacattcgaatcacctgggggcacaatgcctaggctccaaccccagacactcttatttcattggtctgggtggacctggcatcagaagtcatgtagctcctcaggggactgtagtgtgtggtcagcactgagggctcctctatgaggcctcaagcccaggtgactctgtgaggtctgcagagggagaaaagaacccacaagggaagaggtggaggtcaggcacggtggctcacgcttgtaatcccagcactttgggaggccgaggtgggtagatacctgaagtcaggagttcgagactagcctggccaatatggtaaaaccccgtgtctattaaaaatacaaaaattagctggctgtggtggtgggcacctgtaatcccagctactcgggaggctgaggcaggagaatcgcttgaactcgggaggtggaggttgcagtcagccaagatcgtgccactgcacaccatcctggatgacagagcaagactccatcac
//
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.
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