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Previous release (v1)
2024-04-24 19:16:26, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_110547 752 bp RNA linear PRI 11-SEP-2020
DEFINITION Homo sapiens long intergenic non-protein coding RNA 1500
(LINC01500), long non-coding RNA.
ACCESSION NR_110547 XR_424508 XR_429368 XR_432985
VERSION NR_110547.1
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 752)
AUTHORS Comuzzie AG, Cole SA, Laston SL, Voruganti VS, Haack K, Gibbs RA
and Butte NF.
TITLE Novel genetic loci identified for the pathophysiology of childhood
obesity in the Hispanic population
JOURNAL PLoS ONE 7 (12), e51954 (2012)
PUBMED 23251661
REFERENCE 2 (bases 1 to 752)
AUTHORS Otowa T, Yoshida E, Sugaya N, Yasuda S, Nishimura Y, Inoue K,
Tochigi M, Umekage T, Miyagawa T, Nishida N, Tokunaga K, Tanii H,
Sasaki T, Kaiya H and Okazaki Y.
TITLE Genome-wide association study of panic disorder in the Japanese
population
JOURNAL J. Hum. Genet. 54 (2), 122-126 (2009)
PUBMED 19165232
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
CR739775.1 and AW102585.1.
On or before Feb 12, 2014 this sequence version replaced
XR_424508.1, XR_429368.1, XR_432985.1.
##Evidence-Data-START##
Transcript exon combination :: SRR5189667.85555.1,
SRR5189667.266345.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1968968, SAMEA2148874
[ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-686 CR739775.1 1-686
687-752 AW102585.1 3-68 c
FEATURES Location/Qualifiers
source 1..752
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="14"
/map="14q23.1"
gene 1..752
/gene="LINC01500"
/note="long intergenic non-protein coding RNA 1500"
/db_xref="GeneID:102723742"
/db_xref="HGNC:HGNC:51166"
ncRNA 1..752
/ncRNA_class="lncRNA"
/gene="LINC01500"
/product="long intergenic non-protein coding RNA 1500"
/db_xref="GeneID:102723742"
/db_xref="HGNC:HGNC:51166"
exon 1..268
/gene="LINC01500"
/inference="alignment:Splign:2.1.0"
variation 3
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1045124831"
variation 4
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1274585849"
variation 8
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:1215306488"
variation 12
/gene="LINC01500"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:926709131"
variation 13
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1881939748"
variation 14
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:563235044"
variation 16
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1356448232"
variation 17
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1293030007"
variation 25
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1413395198"
variation 26
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1364685552"
variation 28
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1213561566"
variation 29
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1054195826"
variation 30
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:892504759"
variation 34
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1343544803"
variation 41
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:1167310955"
variation 43..48
/gene="LINC01500"
/replace="atggca"
/replace="atggcatggca"
/db_xref="dbSNP:1462146076"
variation 43
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:2139486653"
variation 44
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1021125813"
variation 46
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1881940693"
variation 47..55
/gene="LINC01500"
/replace="ca"
/replace="caactatca"
/db_xref="dbSNP:1881940768"
variation 49
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1881940821"
variation 52
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566554247"
variation 53
/gene="LINC01500"
/replace=""
/replace="t"
/db_xref="dbSNP:532743555"
variation 54
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:1881940975"
variation 55
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1881941025"
variation 58
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1209423471"
variation 59
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:967289757"
variation 60
/gene="LINC01500"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1003707631"
variation 61
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:770329774"
variation 65
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:1881941232"
variation 67
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1881941304"
variation 69
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1881941375"
variation 71
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1881941445"
variation 74
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:186017406"
variation 75
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1484584116"
variation 83
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:991617292"
variation 84
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1881941786"
variation 88
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:915597925"
variation 94
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1881941868"
variation 95
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1881941922"
variation 96
/gene="LINC01500"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1178460786"
variation 103..104
/gene="LINC01500"
/replace=""
/replace="at"
/db_xref="dbSNP:1254358477"
variation 103
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:952318131"
variation 105
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:890941058"
variation 106
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1333701765"
variation 112
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1594633451"
variation 113
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1418198288"
variation 115
/gene="LINC01500"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1008485016"
variation 125
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:984045423"
variation 127
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176295179"
variation 128..129
/gene="LINC01500"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2139486693"
variation 130
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1881942755"
variation 134..135
/gene="LINC01500"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1881942822"
variation 142
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1881942895"
variation 143
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:367909190"
variation 145
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1881943037"
variation 146
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:908449876"
variation 147
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1881943157"
variation 150
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1881943225"
variation 151
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1881943296"
variation 153
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:773649936"
variation 154
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1594633467"
variation 158
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1881943535"
variation 163
/gene="LINC01500"
/replace=""
/replace="c"
/db_xref="dbSNP:112747759"
variation 163
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:995300634"
variation 165
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1881943782"
variation 168
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:549927256"
variation 171
/gene="LINC01500"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1881943937"
variation 172
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1040864462"
variation 173
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:922705602"
variation 176
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1779377387"
variation 180
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1594633484"
variation 182
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:1444238759"
variation 185
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:571628455"
variation 186
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1881944407"
variation 189
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1881944477"
variation 190
/gene="LINC01500"
/replace=""
/replace="a"
/db_xref="dbSNP:1881944604"
variation 190
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:932767046"
variation 191
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281398118"
variation 192
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1881944763"
variation 193
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1881944830"
variation 206
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1371240800"
variation 208
/gene="LINC01500"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1049778374"
variation 209
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1304417925"
variation 212
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:893813774"
variation 215
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:567771316"
variation 220
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1881945292"
variation 227
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1232555498"
variation 228
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1042652862"
variation 230
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:538898720"
variation 231
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:918180230"
variation 232
/gene="LINC01500"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:547482509"
variation 233
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1881945842"
variation 240
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1689604816"
variation 242
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:970888606"
variation 244
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1881945967"
variation 245
/gene="LINC01500"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:190057116"
variation 246..249
/gene="LINC01500"
/replace="ccc"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1396885317"
variation 246
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1881946130"
variation 247
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193700964"
variation 249
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:182711644"
variation 250
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1881946268"
variation 251
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566554339"
variation 252
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1881946364"
variation 259..261
/gene="LINC01500"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:1881946409"
variation 264
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:1663292165"
variation 267
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:766298851"
variation 268
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:1881946520"
exon 269..457
/gene="LINC01500"
/inference="alignment:Splign:2.1.0"
variation 269
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1883102000"
variation 270
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446101749"
variation 273
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1883102063"
variation 274
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:536245144"
variation 275
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:985812805"
variation 276
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:2348816"
variation 279
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:553372787"
variation 280
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1883102295"
variation 281
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1883102334"
variation 283
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:997086239"
variation 286..287
/gene="LINC01500"
/replace="aa"
/replace="aaaa"
/db_xref="dbSNP:879294994"
variation 286
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:2139526663"
variation 292
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1157130420"
variation 297..311
/gene="LINC01500"
/replace=""
/replace="gttgatggataagtg"
/db_xref="dbSNP:1446647108"
variation 297..300
/gene="LINC01500"
/replace=""
/replace="gttg"
/db_xref="dbSNP:1883102501"
variation 299
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1385678535"
variation 300
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:2139526673"
variation 302..313
/gene="LINC01500"
/replace="t"
/replace="tggataagtgtt"
/db_xref="dbSNP:1883102604"
variation 302
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1182748181"
variation 303
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442772267"
variation 305
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1050462002"
variation 309
/gene="LINC01500"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1883102681"
variation 312
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1205214068"
variation 314
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1485238691"
variation 316
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430871834"
variation 318
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1883102823"
variation 328
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1258602161"
variation 329
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:888611590"
variation 331
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:947141922"
variation 334
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1175331401"
variation 335
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1354849851"
variation 340
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:779177650"
variation 341
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1381241144"
variation 346
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1883103158"
variation 348
/gene="LINC01500"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1463359192"
variation 351
/gene="LINC01500"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:571671709"
variation 355
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1883103273"
variation 358
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1003470314"
variation 363
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1883103430"
variation 364
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:903334995"
variation 365
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1883103490"
variation 366
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:2139526711"
variation 372
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1883103524"
variation 374
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:2139526715"
variation 375
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368962100"
variation 379
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1883103615"
variation 381
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1035001659"
variation 382
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1409506020"
variation 384
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1883103804"
variation 387
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1283996220"
variation 390
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1883103910"
variation 392
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1369871717"
variation 393
/gene="LINC01500"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:934840465"
variation 395
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:1883104061"
variation 399
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1883104111"
variation 400
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287156851"
variation 401
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1883104209"
variation 404
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1426863781"
variation 405
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1217958314"
variation 407
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1883104356"
variation 411
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1366409747"
variation 412
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1883104411"
variation 416
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1883104442"
variation 418
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1883104474"
variation 419
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1883104518"
variation 421
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1883104548"
variation 422
/gene="LINC01500"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:184166997"
variation 427
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1883104654"
variation 432
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:896072975"
variation 433
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1442473462"
variation 435
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1883104755"
variation 439
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1883104796"
variation 440
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:959387758"
variation 442
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1853799323"
variation 443
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1883104880"
variation 444
/gene="LINC01500"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:370934630"
variation 447
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:1013624114"
variation 449
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:968542600"
exon 458..537
/gene="LINC01500"
/inference="alignment:Splign:2.1.0"
variation 458
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326700718"
variation 460
/gene="LINC01500"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1317243907"
variation 461
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1383274323"
variation 462
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1883352661"
variation 463
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:536250521"
variation 464
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1426001352"
variation 468
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1385142952"
variation 479
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1181877171"
variation 481
/gene="LINC01500"
/replace=""
/replace="c"
/db_xref="dbSNP:1451373155"
variation 481
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1883352885"
variation 482
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242733333"
variation 484
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:142588285"
variation 485
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:921338362"
variation 487
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1876240074"
variation 489
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:936756841"
variation 490
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:576145339"
variation 491
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002427471"
variation 494
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1883353201"
variation 496
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:546708020"
variation 498
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:543481314"
variation 499
/gene="LINC01500"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1883353309"
variation 500
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:150272888"
variation 503
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:989592546"
variation 505
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1339512929"
variation 506
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1883353462"
variation 508
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:1883353494"
variation 510
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:138683738"
variation 516..518
/gene="LINC01500"
/replace="agg"
/replace="aggagg"
/db_xref="dbSNP:1332454829"
variation 517
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:2139536436"
variation 518
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1883353652"
variation 519
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1286092216"
variation 520
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1448918875"
variation 528..533
/gene="LINC01500"
/replace="aaaaaa"
/replace="aaaaaaa"
/db_xref="dbSNP:1883353812"
variation 530
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:987557170"
variation 532..536
/gene="LINC01500"
/replace="aa"
/replace="aataa"
/db_xref="dbSNP:1883353921"
variation 533
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1191335154"
variation 537
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:911890591"
exon 538..566
/gene="LINC01500"
/inference="alignment:Splign:2.1.0"
variation 538
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1335401693"
variation 542
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1883980615"
variation 545
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:749960820"
variation 546
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:556390849"
variation 549
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1883980741"
variation 551
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1883980785"
variation 555
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:962884623"
variation 558
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1433926641"
variation 560
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:1594673006"
variation 565
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:186729133"
variation 566
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1883981064"
exon 567..686
/gene="LINC01500"
/inference="alignment:Splign:2.1.0"
variation 568
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1019389033"
variation 569
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1482790156"
variation 570
/gene="LINC01500"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1272514602"
variation 574
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1020258882"
variation 575
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:971424609"
variation 576
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:981498342"
variation 581
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1034776795"
variation 584
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1885002563"
variation 586
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:959274431"
variation 587
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:2139594633"
variation 588
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:991137028"
variation 589
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1885002662"
variation 590
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:920551631"
variation 593
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:930287030"
variation 595
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:570626342"
variation 596
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:952405061"
variation 606
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:907554741"
variation 608
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1702151161"
variation 609
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566596395"
variation 616
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1885002904"
variation 617..627
/gene="LINC01500"
/replace="caa"
/replace="caatcacacaa"
/db_xref="dbSNP:1368415607"
variation 619
/gene="LINC01500"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:944406185"
variation 621
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1885003030"
variation 622
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295599372"
variation 624
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1885003107"
variation 625
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:1594693692"
variation 626
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:148946889"
variation 637
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1040151389"
variation 639
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:1479685318"
variation 643
/gene="LINC01500"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:531072509"
variation 644
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:755648722"
variation 648
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1055096823"
variation 657
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1468732066"
variation 658
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:938056500"
variation 659
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1661924450"
variation 664
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277886154"
variation 671
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:2139594675"
variation 673
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1885003736"
variation 676
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1885003786"
variation 679
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1215396386"
variation 680
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1055209808"
variation 682
/gene="LINC01500"
/replace="g"
/replace="t"
/db_xref="dbSNP:1885003958"
exon 687..752
/gene="LINC01500"
/inference="alignment:Splign:2.1.0"
variation 690
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1885116862"
variation 692
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:947080832"
variation 695..696
/gene="LINC01500"
/replace=""
/replace="aa"
/db_xref="dbSNP:1885117080"
variation 695
/gene="LINC01500"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:566206386"
variation 695
/gene="LINC01500"
/replace="g"
/replace="gaactg"
/db_xref="dbSNP:1343516550"
variation 696..697
/gene="LINC01500"
/replace=""
/replace="tga"
/db_xref="dbSNP:1885117159"
variation 696
/gene="LINC01500"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:969660833"
variation 700
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1043126068"
variation 701
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:924360244"
variation 710
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1594696290"
variation 713
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1194556726"
variation 715
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:1885117315"
variation 716
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1165847744"
variation 717
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1885117381"
variation 718
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1885117417"
variation 719
/gene="LINC01500"
/replace="c"
/replace="g"
/db_xref="dbSNP:191232297"
variation 722
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1885117489"
variation 724
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1885117518"
variation 726
/gene="LINC01500"
/replace="c"
/replace="t"
/db_xref="dbSNP:1057265377"
variation 727..733
/gene="LINC01500"
/replace="a"
/replace="acaataa"
/db_xref="dbSNP:1174718470"
variation 730
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:896019444"
variation 736
/gene="LINC01500"
/replace="a"
/replace="t"
/db_xref="dbSNP:369724905"
variation 740
/gene="LINC01500"
/replace="a"
/replace="g"
/db_xref="dbSNP:1885117709"
variation 744
/gene="LINC01500"
/replace=""
/replace="a"
/db_xref="dbSNP:1480408559"
variation 751
/gene="LINC01500"
/replace="a"
/replace="c"
/db_xref="dbSNP:1885117780"
ORIGIN
aaggctgcaaacgaagccagaaagatggtggccagcacacctatggcaactatcaccacggtctccatgcttccggggagctcctgactcagtcccgttcacatcgtcctcatgggctaaggctgctggaagtggcaaactgggggaagaggatggcaggagctaggttcctccacgacacctccagagacctgagggcctcaagctgcagctccggggcacatcccgctgcgctcccacgacggccccgcggatggcaaagtcagcggcatcgcctatgcaggcaatcaaaggatgttgatggataagtgtttcaggcagaataatggccctcaaagatgttgacaccagaatcttcagaacctttgcatatgttacctaacatgacaaaagggactttgctgatgtgattaaggttaagaactttgagaagggaagattatcctggattatacaggtcgacgtttatttctttctgaactttcctggaggatcatcggccatactccagcagaagggtggatttgaaaaaataacgtttccacggcaacagtggcagcaattcaaaggaagacgttggagaattcacatgctattttagctggctctgtgattgcaatcacacaaatcattacattccagcgagatcccatcaacagaaggtttttccatttcagtctgtcaagtttttcaggcatgaatactgtaagcaagaagagaaaagttacaataaattgacatttatagttgaa
//
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]