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Previous release (v1)
2024-11-01 10:32:07, GGRNA.v2 : RefSeq release 226 (Sep, 2024)
LOCUS XM_047438139 614 bp mRNA linear PRI 25-AUG-2024 DEFINITION PREDICTED: Homo sapiens claudin domain containing 2 (CLDND2), transcript variant X3, mRNA. ACCESSION XM_047438139 VERSION XM_047438139.1 DBLINK BioProject: PRJNA168 KEYWORDS RefSeq. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. COMMENT MODEL REFSEQ: This record is predicted by automated computational analysis. This record is derived from a genomic sequence (NC_000019.10) annotated using gene prediction method: Gnomon, supported by EST evidence. Also see: Documentation of NCBI's Annotation Process ##Genome-Annotation-Data-START## Annotation Provider :: NCBI RefSeq Annotation Status :: Updated annotation Annotation Name :: GCF_000001405.40-RS_2024_08 Annotation Pipeline :: NCBI eukaryotic genome annotation pipeline Annotation Software Version :: 10.3 Annotation Method :: Best-placed RefSeq; Gnomon; RefSeqFE; cmsearch; tRNAscan-SE Features Annotated :: Gene; mRNA; CDS; ncRNA Annotation Date :: 08/23/2024 ##Genome-Annotation-Data-END## FEATURES Location/Qualifiers source 1..614 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="19" gene 1..614 /gene="CLDND2" /note="claudin domain containing 2; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 56 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns" /db_xref="GeneID:125875" /db_xref="HGNC:HGNC:28511" misc_feature 1 /gene="CLDND2" /experiment="COORDINATES: cap analysis [ECO:0007248]" /note="transcription start site" variation 1 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:914526138" variation 2 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1986559581" variation 4 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1394702753" variation 10 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1391173834" variation 12..15 /gene="CLDND2" /replace="ct" /replace="ctct" /db_xref="dbSNP:887267045" variation 12 /gene="CLDND2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1419305633" variation 15..19 /gene="CLDND2" /replace="tgt" /replace="tgtgt" /db_xref="dbSNP:1188234260" variation 17 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1352543403" variation 20 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1292709796" variation 23 /gene="CLDND2" /replace="a" /replace="g" /db_xref="dbSNP:989802041" variation 28 /gene="CLDND2" /replace="a" /replace="c" /db_xref="dbSNP:1223595861" variation 31 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:995281097" variation 36 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1986558519" variation 42 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1480223490" variation 48 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1986558195" variation 50 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:953045985" variation 52 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1986557983" variation 54 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:749488865" variation 56 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1986557750" variation 57 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:376369107" variation 59 /gene="CLDND2" /replace="g" /replace="t" /db_xref="dbSNP:1367870523" variation 61 /gene="CLDND2" /replace="a" /replace="aa" /db_xref="dbSNP:1986540370" variation 63 /gene="CLDND2" /replace="c" /replace="t" /db_xref="dbSNP:1986540253" variation 65 /gene="CLDND2" /replace="c" /replace="g" /db_xref="dbSNP:1392241759" CDS 67..570 /gene="CLDND2" /codon_start=1 /product="claudin domain-containing protein 2 isoform X2" /protein_id="XP_047294095.1" /db_xref="GeneID:125875" /db_xref="HGNC:HGNC:28511" /translation="
MGVKRSLQSGGILLSLVANVLMVLSTATNYWTRQQEGHSGLWQECNHGICSSIPCQTTLAVTVACMVLAVGVGVVGMVMGLRIRCDEGESLRGQTTSAFLFLGGLLLLTALIGYTVKNAWKNNVFFSWSYFSGWLALPFSILAGFCFLLADMIMQSTDAISGFPVCL"
misc_feature 94..498
/gene="CLDND2"
/note="PMP-22/EMP/MP20/Claudin family; Region:
PMP22_Claudin; cl21598"
/db_xref="CDD:473919"
variation 69..73
/gene="CLDND2"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1437433976"
variation 69
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:758921395"
variation 70
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1986539816"
variation 71
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200312007"
variation 72
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:538045785"
variation 73
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1351339775"
variation 76
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2123633567"
variation 77
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:777335261"
variation 78
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1230101024"
variation 79
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371550969"
variation 80
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:143028916"
variation 82
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:754799498"
variation 83
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:751289647"
variation 85
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369800546"
variation 86
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762873455"
variation 88..89
/gene="CLDND2"
/replace=""
/replace="ca"
/db_xref="dbSNP:753083530"
variation 89
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397526552"
variation 93
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1181982791"
variation 93
/gene="CLDND2"
/replace="t"
/replace="tt"
/db_xref="dbSNP:765717056"
variation 94
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568474544"
variation 95
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:765336897"
variation 96
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1366435982"
variation 97
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1229737224"
variation 98
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:141927207"
variation 99
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354887417"
variation 102
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986535878"
variation 104
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1986535732"
variation 106
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986535614"
variation 108
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1756564974"
variation 111
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986535481"
variation 114
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1475521451"
variation 115
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1986535216"
variation 117
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1986535084"
variation 118
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:150482801"
variation 119
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:907270970"
variation 122
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1291041024"
variation 123
/gene="CLDND2"
/replace=""
/replace="c"
/db_xref="dbSNP:1986534455"
variation 124
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1453747054"
variation 125
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:137890141"
variation 128
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:747388530"
variation 129
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1490479401"
variation 130
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1473019042"
variation 131
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273287505"
variation 136
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:766705239"
variation 141
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:892985932"
variation 143
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1163841957"
variation 144..159
/gene="CLDND2"
/replace="gg"
/replace="ggccaccaactactgg"
/db_xref="dbSNP:1286962093"
variation 144
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368172559"
variation 145
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265286290"
variation 148
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1986532815"
variation 150..153
/gene="CLDND2"
/replace="caac"
/replace="caacaac"
/db_xref="dbSNP:1986532411"
variation 150
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1234260170"
variation 152
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:931887664"
variation 154
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1307144896"
variation 157
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986532297"
variation 159
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:746357149"
variation 160
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1310555112"
variation 161
/gene="CLDND2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:34633086"
variation 163
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370928932"
variation 164
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:199591571"
variation 168
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1331139384"
variation 173
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:780828288"
variation 175
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:944395544"
variation 176
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375294321"
variation 177
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:141435818"
variation 178
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:779793613"
variation 180
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1156786260"
variation 182
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:758314796"
variation 183
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568474407"
variation 184
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:566771736"
variation 186
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1183337530"
variation 187
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201357238"
variation 190
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1986529600"
variation 192
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1432886304"
variation 195
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1986529320"
variation 197
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:765042158"
variation 199
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:761954347"
variation 200
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1337348640"
variation 201
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:753908258"
variation 203
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1254335351"
variation 207
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:145587573"
variation 208
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352030933"
variation 211
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1239174330"
variation 215
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:776039544"
variation 216
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1231115650"
variation 218
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:772546495"
variation 221
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326767106"
variation 222
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1167750554"
variation 223
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1986527530"
variation 225
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1441380989"
variation 226
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1387872499"
variation 227
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396317297"
variation 228
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1347860377"
variation 229
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1431258664"
variation 230
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:149708978"
variation 236
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1435993047"
variation 238
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1310043039"
variation 239
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1208844685"
variation 240..245
/gene="CLDND2"
/replace="gc"
/replace="gctggc"
/db_xref="dbSNP:766420239"
variation 241
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:746481949"
variation 244
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1169234910"
variation 246
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:199854670"
variation 249
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:771562132"
variation 251
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:558697101"
variation 252..255
/gene="CLDND2"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:760657397"
variation 253
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:778565175"
variation 256
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568473823"
variation 257
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986494403"
variation 258
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:374413392"
variation 261
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:181014895"
variation 263
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:749220517"
variation 266
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1449292548"
variation 268
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:777808790"
variation 270
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1207141951"
variation 271
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1421949058"
variation 272
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:756295215"
variation 275
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1343062109"
variation 278
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:752758697"
variation 279
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:767795968"
variation 280
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274929937"
variation 286
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231206904"
variation 287..300
/gene="CLDND2"
/replace="tggtgggcatggtg"
/replace="tggtgggcatggtgggcatggtg"
/db_xref="dbSNP:773407298"
variation 287
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:140994018"
variation 288
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318528069"
variation 290
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1364344485"
variation 292
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1986491266"
variation 294
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:751993787"
variation 297
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:766628417"
variation 300
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2123629995"
variation 302
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:763254992"
variation 304
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:750065635"
variation 307
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:765661741"
variation 309
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163274581"
variation 310
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1461215602"
variation 312
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419236582"
variation 316
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:995987172"
variation 317
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1167661295"
variation 321
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:3745403"
variation 322
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:61736500"
variation 325
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2123629821"
variation 329
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1177841337"
variation 330
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:771821890"
variation 331
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:139548240"
variation 333
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1211608610"
variation 334
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986487715"
variation 335
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:756866627"
variation 336
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1467817776"
variation 337
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273741707"
variation 338
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:35337369"
variation 339
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1206256235"
variation 340
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:376652333"
variation 341
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:749054663"
variation 342
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:373643518"
variation 344
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756057433"
variation 347
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2123629581"
variation 348
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1323420932"
variation 349
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:748298147"
variation 350
/gene="CLDND2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1395591812"
variation 351
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:536390977"
variation 353
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1452333172"
variation 354
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:550109619"
variation 356
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143947857"
variation 357
/gene="CLDND2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1420901645"
variation 358
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:765786340"
variation 359
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:74538792"
variation 360
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469070489"
variation 363
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2123629356"
variation 365
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1253453283"
variation 366
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:775103545"
variation 367
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1986483492"
variation 372..373
/gene="CLDND2"
/replace=""
/replace="tt"
/db_xref="dbSNP:1568473600"
variation 373
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568473594"
variation 374
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1054818020"
variation 375
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986482685"
variation 376
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:766917605"
variation 378
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:886252090"
variation 379..390
/gene="CLDND2"
/replace="ctgctgctg"
/replace="ctgctgctgctg"
/replace="ctgctgctgctgctg"
/db_xref="dbSNP:774085638"
variation 381
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1357375096"
variation 386
/gene="CLDND2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:762502780"
variation 387
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397458806"
variation 388
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:750129630"
variation 389
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:764916263"
variation 390
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1986454475"
variation 393
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761525613"
variation 394
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1164044064"
variation 396
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:776470517"
variation 397
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1369751601"
variation 401
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:764001121"
variation 403..404
/gene="CLDND2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1986452504"
variation 403
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:760627572"
variation 404
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:775592435"
variation 407
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1986452211"
variation 410
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:867796482"
variation 412
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:772164503"
variation 419
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1038380123"
variation 420
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1467373673"
variation 421
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:745910460"
variation 423
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1599851554"
variation 424
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1234509795"
variation 430..435
/gene="CLDND2"
/replace="aac"
/replace="aacaac"
/db_xref="dbSNP:1599851539"
variation 432
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1337569389"
variation 433
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1986450972"
variation 435..438
/gene="CLDND2"
/replace="c"
/replace="cgtc"
/db_xref="dbSNP:1051331535"
variation 435
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986450693"
variation 436
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:61737052"
variation 437..445
/gene="CLDND2"
/replace="tcttct"
/replace="tcttcttct"
/db_xref="dbSNP:768471991"
variation 437
/gene="CLDND2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1986450238"
variation 438
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1238386392"
variation 441
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986449786"
variation 443
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1331082939"
variation 446
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1229799125"
variation 449
/gene="CLDND2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771131130"
variation 455
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1986448995"
variation 456..460
/gene="CLDND2"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1273298552"
variation 456
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2123626658"
variation 459
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324972016"
variation 462
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461934179"
variation 463
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1392768297"
variation 464
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1156328694"
variation 465
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469147368"
variation 469
/gene="CLDND2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1986447921"
variation 469
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1364025183"
variation 470
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:150545272"
variation 472
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1452170652"
variation 473
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986447338"
variation 474
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1986447186"
variation 478..480
/gene="CLDND2"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:749182476"
variation 478
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:778195808"
variation 483
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1986446586"
variation 488
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1986446362"
variation 489
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373919523"
variation 493
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1986445876"
variation 494
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:748645509"
variation 495
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143501994"
variation 496
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:114975292"
variation 497
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:755754582"
variation 501
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:752559823"
variation 503
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1165758878"
variation 505..507
/gene="CLDND2"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1368913884"
variation 508..513
/gene="CLDND2"
/replace="ctg"
/replace="ctgctg"
/replace="ctgctgctg"
/db_xref="dbSNP:777453479"
variation 510
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1177936955"
variation 511
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:199756062"
variation 516
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1986426279"
variation 518
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:751539630"
variation 520..524
/gene="CLDND2"
/replace="at"
/replace="atgat"
/db_xref="dbSNP:1375455615"
variation 520
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298769311"
variation 521
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:766161552"
variation 528
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:185510103"
variation 529
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1223138752"
variation 530
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1986425063"
variation 532
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1314556151"
variation 534
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1311910677"
variation 536..537
/gene="CLDND2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1568472642"
variation 537
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1059344"
variation 540
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:141450057"
variation 542
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268759728"
variation 543
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1986423843"
variation 544
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:199917528"
variation 547
/gene="CLDND2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1986423336"
variation 549
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301760024"
variation 550
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1440564055"
variation 555..558
/gene="CLDND2"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:765627231"
variation 557
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:777181361"
variation 558
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1204637370"
variation 559
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1986422183"
variation 560
/gene="CLDND2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1337242900"
variation 561
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295730829"
variation 567
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:769162667"
variation 573..590
/gene="CLDND2"
/replace="g"
/replace="gcagcctgcctggggcag"
/db_xref="dbSNP:1191550743"
variation 574..582
/gene="CLDND2"
/replace=""
/replace="cagcctgcc"
/db_xref="dbSNP:1568472573"
variation 582
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:756560566"
variation 583
/gene="CLDND2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568472568"
variation 584
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1159320301"
variation 585
/gene="CLDND2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:761078378"
variation 586
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370612637"
variation 588
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368435588"
variation 590
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1481910306"
variation 594
/gene="CLDND2"
/replace="a"
/replace="g"
/db_xref="dbSNP:772403705"
variation 597..598
/gene="CLDND2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1267991046"
variation 601
/gene="CLDND2"
/replace="a"
/replace="c"
/db_xref="dbSNP:904812810"
variation 602
/gene="CLDND2"
/replace="c"
/replace="g"
/db_xref="dbSNP:748889646"
variation 604
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:777148133"
variation 605..611
/gene="CLDND2"
/replace="tttttt"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:5828475"
variation 610
/gene="CLDND2"
/replace="c"
/replace="t"
/db_xref="dbSNP:769476219"
variation 614
/gene="CLDND2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:112263850"
ORIGIN
gtctctctgggctctgtgtctaaggagccctagggcactgggtgtgagtcacttagcctcagtggcatgggggtgaagcggagcctccagagtgggggcattctgctcagcctcgtggccaacgtcctcatggtgctctccacggccaccaactactggacccgccaacaagagggccacagtggcctgtggcaggaatgcaaccacggcatctgctccagcatcccctgccagaccacgctggcggtgactgtggcgtgcatggtgctggcggtgggtgtcggcgtggtgggcatggtgatgggactgcggattcggtgcgacgagggcgagtcgctgcggggccagaccacgagcgccttcctcttcctcggcggactgctgctgctgaccgccttgataggctacaccgtgaagaatgcgtggaagaacaacgtcttcttctcttggtcctatttttctgggtggctggccttacccttctcaattctcgcgggcttctgctttctgctggcagacatgatcatgcagagcaccgacgccatcagtggattccccgtgtgtctgtgactgcagcctgcctggggcagaataaaggaacggctttttttagc
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
[Full Text]