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Previous release (v1)
2024-04-26 01:49:51, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_131903 583 bp RNA linear PRI 11-SEP-2020
DEFINITION Homo sapiens long intergenic non-protein coding RNA 566
(LINC00566), long non-coding RNA.
ACCESSION NR_131903
VERSION NR_131903.1
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 583)
AUTHORS Strausberg RL, Feingold EA, Grouse LH, Derge JG, Klausner RD,
Collins FS, Wagner L, Shenmen CM, Schuler GD, Altschul SF, Zeeberg
B, Buetow KH, Schaefer CF, Bhat NK, Hopkins RF, Jordan H, Moore T,
Max SI, Wang J, Hsieh F, Diatchenko L, Marusina K, Farmer AA, Rubin
GM, Hong L, Stapleton M, Soares MB, Bonaldo MF, Casavant TL,
Scheetz TE, Brownstein MJ, Usdin TB, Toshiyuki S, Carninci P,
Prange C, Raha SS, Loquellano NA, Peters GJ, Abramson RD, Mullahy
SJ, Bosak SA, McEwan PJ, McKernan KJ, Malek JA, Gunaratne PH,
Richards S, Worley KC, Hale S, Garcia AM, Gay LJ, Hulyk SW,
Villalon DK, Muzny DM, Sodergren EJ, Lu X, Gibbs RA, Fahey J,
Helton E, Ketteman M, Madan A, Rodrigues S, Sanchez A, Whiting M,
Madan A, Young AC, Shevchenko Y, Bouffard GG, Blakesley RW,
Touchman JW, Green ED, Dickson MC, Rodriguez AC, Grimwood J,
Schmutz J, Myers RM, Butterfield YS, Krzywinski MI, Skalska U,
Smailus DE, Schnerch A, Schein JE, Jones SJ and Marra MA.
CONSRTM Mammalian Gene Collection Program Team
TITLE Generation and initial analysis of more than 15,000 full-length
human and mouse cDNA sequences
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 99 (26), 16899-16903 (2002)
PUBMED 12477932
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
BC038727.1 and AL359763.9.
##Evidence-Data-START##
Transcript exon combination :: BC038727.1, BI460035.1 [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
1-524 BC038727.1 1-524
525-525 AL359763.9 5406-5406
526-583 BC038727.1 526-583
FEATURES Location/Qualifiers
source 1..583
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="13"
/map="13q12.12"
gene 1..583
/gene="LINC00566"
/note="long intergenic non-protein coding RNA 566"
/db_xref="GeneID:100861547"
/db_xref="HGNC:HGNC:43710"
ncRNA 1..583
/ncRNA_class="lncRNA"
/gene="LINC00566"
/product="long intergenic non-protein coding RNA 566"
/db_xref="GeneID:100861547"
/db_xref="HGNC:HGNC:43710"
exon 1..87
/gene="LINC00566"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1400633024"
variation 3
/gene="LINC00566"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1406429785"
variation 11
/gene="LINC00566"
/replace="a"
/replace="c"
/db_xref="dbSNP:549231710"
variation 13
/gene="LINC00566"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878508781"
variation 17
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878508861"
variation 24
/gene="LINC00566"
/replace="a"
/replace="c"
/db_xref="dbSNP:1878508916"
variation 27
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1280470639"
variation 29
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1878508996"
variation 32
/gene="LINC00566"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:58867384"
variation 33
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1192580053"
variation 34
/gene="LINC00566"
/replace="a"
/replace="t"
/db_xref="dbSNP:1466894946"
variation 37
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1565961239"
variation 41
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:771174367"
variation 42
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:1234493333"
variation 43
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:537959727"
variation 44
/gene="LINC00566"
/replace=""
/replace="t"
/db_xref="dbSNP:1222123282"
variation 46
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:375401660"
variation 50
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282084346"
variation 56
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1206925887"
variation 59..66
/gene="LINC00566"
/replace="aagaa"
/replace="aagaagaa"
/db_xref="dbSNP:1878509677"
variation 59
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1878509643"
variation 60
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1009851251"
variation 61
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1022553508"
variation 64
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1176467943"
variation 68
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1878509836"
variation 70
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236130887"
variation 76
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878510352"
variation 78..80
/gene="LINC00566"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1275741802"
variation 81
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878510467"
variation 82..85
/gene="LINC00566"
/replace="aa"
/replace="aaaa"
/db_xref="dbSNP:1878510524"
variation 83
/gene="LINC00566"
/replace="a"
/replace="c"
/db_xref="dbSNP:1878510588"
variation 87
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1438109104"
exon 88..570
/gene="LINC00566"
/inference="alignment:Splign:2.1.0"
variation 89
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1447640061"
variation 90
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878617378"
variation 91
/gene="LINC00566"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1442178348"
variation 96
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1878617490"
variation 102
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205752232"
variation 103
/gene="LINC00566"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1482979890"
variation 106
/gene="LINC00566"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1254427722"
variation 107
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1878617685"
variation 111
/gene="LINC00566"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:977180845"
variation 116
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1159917664"
variation 118
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:1878617821"
variation 120
/gene="LINC00566"
/replace="a"
/replace="c"
/db_xref="dbSNP:1878617851"
variation 123
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1361159325"
variation 124
/gene="LINC00566"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1044927889"
variation 128
/gene="LINC00566"
/replace="a"
/replace="t"
/db_xref="dbSNP:1226807706"
variation 129
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:775735461"
variation 130
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878618069"
variation 135
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593543746"
variation 136
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:905010844"
variation 144
/gene="LINC00566"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1001660335"
variation 146
/gene="LINC00566"
/replace="a"
/replace="t"
/db_xref="dbSNP:1057141261"
variation 148
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:555111453"
variation 149
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400006572"
variation 152
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:895871537"
variation 155
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360630257"
variation 158
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878618492"
variation 159
/gene="LINC00566"
/replace="a"
/replace="c"
/db_xref="dbSNP:1878618529"
variation 163
/gene="LINC00566"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1467314173"
variation 165
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:543286579"
variation 168
/gene="LINC00566"
/replace="a"
/replace="c"
/db_xref="dbSNP:1878618693"
variation 173
/gene="LINC00566"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1025577332"
variation 184
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:574957631"
variation 185
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878618838"
variation 187
/gene="LINC00566"
/replace="a"
/replace="c"
/db_xref="dbSNP:953014542"
variation 198
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193827610"
variation 204
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1878618954"
variation 205
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423252874"
variation 206
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1878619035"
variation 211
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1254251268"
variation 221
/gene="LINC00566"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:537681788"
variation 222
/gene="LINC00566"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1018476780"
variation 224
/gene="LINC00566"
/replace="a"
/replace="c"
/db_xref="dbSNP:976876464"
variation 228
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:922356455"
variation 231..235
/gene="LINC00566"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1244704238"
variation 231
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1320585660"
variation 237
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1310020111"
variation 240
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1311551889"
variation 242
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878619486"
variation 243
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:372601984"
variation 245
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:956416388"
variation 249
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:2138825143"
variation 251
/gene="LINC00566"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1407709532"
variation 254
/gene="LINC00566"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1372185218"
variation 255
/gene="LINC00566"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1355097258"
variation 256
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:745774701"
variation 257
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:914874617"
variation 258
/gene="LINC00566"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:772083634"
variation 259
/gene="LINC00566"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1045379048"
variation 261
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1878620144"
variation 265
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:1878620198"
variation 267
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:926516737"
variation 276
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:775140882"
variation 277
/gene="LINC00566"
/replace="a"
/replace="c"
/db_xref="dbSNP:867709771"
variation 278
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:2138825168"
variation 282
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:2138825169"
variation 284
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281547966"
variation 289
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1878620423"
variation 290
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1878620460"
variation 292
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:746876358"
variation 293
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242210145"
variation 294
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:1878620662"
variation 295
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:2138825175"
variation 296
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:2138825181"
variation 298
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1487815704"
variation 299
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1459696513"
variation 300
/gene="LINC00566"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1180010601"
variation 301
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:2138825187"
variation 303
/gene="LINC00566"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1334937711"
variation 304
/gene="LINC00566"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1056196513"
variation 307
/gene="LINC00566"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768134176"
variation 311
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:557673390"
variation 312
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:2138825198"
variation 314
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1878621196"
variation 317
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:75910494"
variation 318..319
/gene="LINC00566"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2138825204"
variation 318
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878621321"
variation 320..324
/gene="LINC00566"
/replace="ag"
/replace="aggag"
/db_xref="dbSNP:1878621354"
variation 320..321
/gene="LINC00566"
/replace=""
/replace="ag"
/db_xref="dbSNP:2138825206"
variation 322
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1329348208"
variation 324
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1878621436"
variation 325..326
/gene="LINC00566"
/replace=""
/replace="gt"
/db_xref="dbSNP:2138825212"
variation 327
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878621473"
variation 331
/gene="LINC00566"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593543817"
variation 338
/gene="LINC00566"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427017372"
variation 340
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1047085155"
variation 341
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:888435988"
variation 342
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1414769654"
variation 345
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:1461978477"
variation 349
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1335829117"
variation 352
/gene="LINC00566"
/replace="a"
/replace="t"
/db_xref="dbSNP:1878622443"
variation 353
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1005838664"
variation 354
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1018942923"
variation 356
/gene="LINC00566"
/replace="a"
/replace="c"
/db_xref="dbSNP:1878622571"
variation 362
/gene="LINC00566"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199922884"
variation 364
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878622721"
variation 365..366
/gene="LINC00566"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1431825092"
variation 367
/gene="LINC00566"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:114205275"
variation 370
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:564881131"
variation 372
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878622983"
variation 373..379
/gene="LINC00566"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:1878623037"
variation 381
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1214872406"
variation 388
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1468538759"
variation 390
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1333506585"
variation 392
/gene="LINC00566"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:796616601"
variation 394
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:956468294"
variation 395
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1878623280"
variation 397
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:572070550"
variation 398
/gene="LINC00566"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:187694130"
variation 399..402
/gene="LINC00566"
/replace="tggc"
/replace="tggctggc"
/db_xref="dbSNP:914948025"
variation 400..401
/gene="LINC00566"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:968116207"
variation 400
/gene="LINC00566"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1878623554"
variation 402
/gene="LINC00566"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:140742378"
variation 403
/gene="LINC00566"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:192347882"
variation 407
/gene="LINC00566"
/replace=""
/replace="c"
/db_xref="dbSNP:939247054"
variation 409
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:991976022"
variation 410
/gene="LINC00566"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593543852"
variation 412
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385882570"
variation 414
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:1878624206"
variation 417
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1262872627"
variation 418
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1321027732"
variation 421
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:549604161"
variation 423
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:1878624451"
variation 429
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:563239302"
variation 433..434
/gene="LINC00566"
/replace="a"
/replace="aa"
/db_xref="dbSNP:151112067"
variation 434
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1379806269"
variation 441..445
/gene="LINC00566"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:2138825301"
variation 441
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1878624693"
variation 442
/gene="LINC00566"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:930093638"
variation 444
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1238283465"
variation 445
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1878624893"
variation 449
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593543873"
variation 452
/gene="LINC00566"
/replace="a"
/replace="t"
/db_xref="dbSNP:1190836335"
variation 457
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1449445843"
variation 458
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593543876"
variation 460
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:2138825314"
variation 461
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878625176"
variation 462
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1436659771"
variation 463
/gene="LINC00566"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1186075391"
variation 465
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1878625391"
variation 467
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:2138825326"
variation 468
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878625450"
variation 473
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878625507"
variation 477
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1878625561"
variation 480
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1878625579"
variation 483
/gene="LINC00566"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1448242089"
variation 484
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284443786"
variation 485
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:374486839"
variation 489
/gene="LINC00566"
/replace="a"
/replace="t"
/db_xref="dbSNP:1199529413"
variation 492
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:532133131"
variation 493
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:888496568"
variation 495
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:941364132"
variation 496
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1248447304"
variation 498
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:765722301"
variation 499
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:764748061"
variation 500
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:900105274"
variation 504
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1468455128"
variation 505
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:547324898"
variation 506
/gene="LINC00566"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1878626536"
variation 508
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:1878626605"
variation 511
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:2138825360"
variation 513
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:377355892"
variation 514
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1397319604"
variation 515
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:2138825363"
variation 516
/gene="LINC00566"
/replace="a"
/replace="c"
/db_xref="dbSNP:1377632912"
variation 517
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174704378"
variation 519
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:1878626855"
variation 521
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1429543745"
variation 524
/gene="LINC00566"
/replace="a"
/replace="c"
/db_xref="dbSNP:1409514066"
variation 525
/gene="LINC00566"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2862249"
variation 527..531
/gene="LINC00566"
/replace="g"
/replace="gcctg"
/db_xref="dbSNP:1170159222"
variation 527
/gene="LINC00566"
/replace="g"
/replace="t"
/db_xref="dbSNP:1878627278"
variation 528
/gene="LINC00566"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1878627392"
variation 532
/gene="LINC00566"
/replace="a"
/replace="t"
/db_xref="dbSNP:892631266"
variation 535
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878627552"
variation 537..543
/gene="LINC00566"
/replace="aaaaaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:1406063091"
variation 537
/gene="LINC00566"
/replace="a"
/replace="t"
/db_xref="dbSNP:1186384547"
variation 538
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1440385484"
variation 542
/gene="LINC00566"
/replace="a"
/replace="t"
/db_xref="dbSNP:1878627772"
variation 546..547
/gene="LINC00566"
/replace="aa"
/replace="aataaataa"
/db_xref="dbSNP:1283064262"
variation 548..561
/gene="LINC00566"
/replace="ataaa"
/replace="ataaaagctataaa"
/db_xref="dbSNP:1878627902"
variation 553
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:552112544"
variation 554
/gene="LINC00566"
/replace="c"
/replace="g"
/db_xref="dbSNP:1211276698"
variation 555
/gene="LINC00566"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878628078"
variation 570
/gene="LINC00566"
/replace="a"
/replace="g"
/db_xref="dbSNP:1878628140"
ORIGIN
ataattgctgccaaaatcatcacaagctgtacgtcatcaaggctccctttgcactcccaagaagaactgttcattttaaacaaaagtgatgagaattcctccagaggtgggaacagagaaaacttcatgcttggtaaagcacctgaggcacccattacaatctgggacaagatgaggacatcaacactcatgctgtattccacatgggaggccaagtcaacgcaagatgatttttaagagatataagagccaggcgcggtagctgacacctgtaatcccagcactttgggaagctgaggtgggaggctcacttgaggccaggagatcaagaccagcctaaccaacaaagcaagaccaagaccccttctctacaaaaaaataagaaaattagcctggcgtggcggtgcacacctgtggttccagctacactagaagctgaagggggaggttcacttgagccccgagtttgaggctgcagtgagccacattagcgccaccgcactacagcctgggtgacagagcaaaagcctgtctccaaaaaaataaaataaaagctataaatactgcaaaaaaaaaaaaaaaa
//
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]