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Previous release (v1)
2024-04-28 09:48:35, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_125788 565 bp RNA linear PRI 11-SEP-2020
DEFINITION Homo sapiens long intergenic non-protein coding RNA 1065
(LINC01065), long non-coding RNA.
ACCESSION NR_125788
VERSION NR_125788.1
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 565)
AUTHORS Kimura K, Wakamatsu A, Suzuki Y, Ota T, Nishikawa T, Yamashita R,
Yamamoto J, Sekine M, Tsuritani K, Wakaguri H, Ishii S, Sugiyama T,
Saito K, Isono Y, Irie R, Kushida N, Yoneyama T, Otsuka R, Kanda K,
Yokoi T, Kondo H, Wagatsuma M, Murakawa K, Ishida S, Ishibashi T,
Takahashi-Fujii A, Tanase T, Nagai K, Kikuchi H, Nakai K, Isogai T
and Sugano S.
TITLE Diversification of transcriptional modulation: large-scale
identification and characterization of putative alternative
promoters of human genes
JOURNAL Genome Res. 16 (1), 55-65 (2006)
PUBMED 16344560
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
DB043011.1 and AL136359.13.
##Evidence-Data-START##
RNAseq introns :: single sample supports all introns SAMEA1968968,
SAMEA2148874 [ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-117 DB043011.1 1-117
118-141 AL136359.13 117488-117511
142-565 DB043011.1 145-568
FEATURES Location/Qualifiers
source 1..565
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="13"
/map="13q14.3"
gene 1..565
/gene="LINC01065"
/note="long intergenic non-protein coding RNA 1065"
/db_xref="GeneID:102723875"
/db_xref="HGNC:HGNC:49103"
ncRNA 1..565
/ncRNA_class="lncRNA"
/gene="LINC01065"
/product="long intergenic non-protein coding RNA 1065"
/db_xref="GeneID:102723875"
/db_xref="HGNC:HGNC:49103"
exon 1..197
/gene="LINC01065"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="LINC01065"
/replace="a"
/replace="t"
/db_xref="dbSNP:1955220661"
variation 3
/gene="LINC01065"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:932982216"
variation 5
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250763004"
variation 6
/gene="LINC01065"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593513421"
variation 7
/gene="LINC01065"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955220563"
variation 11
/gene="LINC01065"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593513419"
variation 12
/gene="LINC01065"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593513417"
variation 14
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955220499"
variation 21
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370912907"
variation 22
/gene="LINC01065"
/replace="c"
/replace="g"
/db_xref="dbSNP:901640525"
variation 23
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1489736516"
variation 28
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393603582"
variation 29
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1459774941"
variation 31
/gene="LINC01065"
/replace=""
/replace="g"
/db_xref="dbSNP:1955220283"
variation 31
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955220270"
variation 32
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1327693793"
variation 35
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955220251"
variation 37
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955220236"
variation 38
/gene="LINC01065"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:963889525"
variation 47..49
/gene="LINC01065"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1955220209"
variation 57
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955220197"
variation 58
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1381867346"
variation 64
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1267493008"
variation 66
/gene="LINC01065"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593513401"
variation 68
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1017166551"
variation 71..76
/gene="LINC01065"
/replace="cac"
/replace="caccac"
/db_xref="dbSNP:2138298259"
variation 74
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:573200917"
variation 75..80
/gene="LINC01065"
/replace="acaaca"
/replace="acaacaaca"
/db_xref="dbSNP:1228213326"
variation 76
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:2138298255"
variation 81
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955220117"
variation 82
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955220106"
variation 84
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:940899540"
variation 90
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:909385025"
variation 93
/gene="LINC01065"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:887022780"
variation 94
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:553333037"
variation 95
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:984937385"
variation 96..97
/gene="LINC01065"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1025297953"
variation 96
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1333370326"
variation 98
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:539707024"
variation 99
/gene="LINC01065"
/replace="a"
/replace="t"
/db_xref="dbSNP:1317338168"
variation 100
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:948311593"
variation 101
/gene="LINC01065"
/replace="c"
/replace="g"
/db_xref="dbSNP:747492823"
variation 105
/gene="LINC01065"
/replace="a"
/replace="t"
/db_xref="dbSNP:1274206057"
variation 106
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1485745971"
variation 111
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955219911"
variation 118
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955219896"
variation 120
/gene="LINC01065"
/replace="g"
/replace="t"
/db_xref="dbSNP:1003126625"
variation 122..123
/gene="LINC01065"
/replace=""
/replace="acatcatttaatgtca"
/db_xref="dbSNP:764119289"
variation 122..123
/gene="LINC01065"
/replace="g"
/replace="gg"
/db_xref="dbSNP:559549667"
variation 124
/gene="LINC01065"
/replace="a"
/replace="t"
/db_xref="dbSNP:1429817448"
variation 125..126
/gene="LINC01065"
/replace=""
/replace="at"
/db_xref="dbSNP:758466311"
variation 126
/gene="LINC01065"
/replace="a"
/replace="t"
/db_xref="dbSNP:577484633"
variation 128..129
/gene="LINC01065"
/replace=""
/replace="atttaatgtcagacatttaatgtgg"
/db_xref="dbSNP:556806091"
variation 128
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955219785"
variation 143
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955219765"
variation 148
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955219746"
variation 149
/gene="LINC01065"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:533953870"
variation 151
/gene="LINC01065"
/replace="a"
/replace="t"
/db_xref="dbSNP:1955219711"
variation 155
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955219697"
variation 156
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955219684"
variation 161
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:374531570"
variation 162
/gene="LINC01065"
/replace="c"
/replace="g"
/db_xref="dbSNP:1955219658"
variation 164
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1166923626"
variation 166
/gene="LINC01065"
/replace="a"
/replace="c"
/db_xref="dbSNP:1955219641"
variation 169
/gene="LINC01065"
/replace="c"
/replace="g"
/db_xref="dbSNP:1955219627"
variation 173
/gene="LINC01065"
/replace="c"
/replace="g"
/db_xref="dbSNP:1395029472"
variation 177
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955219609"
variation 184
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955219591"
variation 185..188
/gene="LINC01065"
/replace=""
/replace="gact"
/db_xref="dbSNP:2138298188"
variation 185..188
/gene="LINC01065"
/replace="gact"
/replace="gactgact"
/db_xref="dbSNP:61425436"
variation 186
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:2138298189"
variation 188
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:752514479"
variation 194
/gene="LINC01065"
/replace="a"
/replace="c"
/db_xref="dbSNP:1955219524"
exon 198..345
/gene="LINC01065"
/inference="alignment:Splign:2.1.0"
variation 205
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1459356091"
variation 210
/gene="LINC01065"
/replace="a"
/replace="t"
/db_xref="dbSNP:572643926"
variation 214
/gene="LINC01065"
/replace="a"
/replace="t"
/db_xref="dbSNP:1314027910"
variation 215
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:754665123"
variation 218
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:971655698"
variation 219
/gene="LINC01065"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1054941565"
variation 221
/gene="LINC01065"
/replace="c"
/replace="g"
/db_xref="dbSNP:937914648"
variation 222
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955208670"
variation 225
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:927833188"
variation 226
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955208648"
variation 233..234
/gene="LINC01065"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1955208618"
variation 233
/gene="LINC01065"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1955208630"
variation 234
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378804944"
variation 237
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211922869"
variation 245
/gene="LINC01065"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1046100007"
variation 246
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566081584"
variation 247
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:945017765"
variation 249
/gene="LINC01065"
/replace="a"
/replace="t"
/db_xref="dbSNP:1955208516"
variation 251
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955208502"
variation 253
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955208497"
variation 255
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169855815"
variation 256
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:190322220"
variation 258..264
/gene="LINC01065"
/replace="atca"
/replace="atcatca"
/db_xref="dbSNP:1371202707"
variation 259
/gene="LINC01065"
/replace="a"
/replace="t"
/db_xref="dbSNP:1955208465"
variation 264
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:913679722"
variation 265
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:959044897"
variation 269
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390321748"
variation 274
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1033070625"
variation 282
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955208384"
variation 284
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:111869894"
variation 285
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1423228636"
variation 288
/gene="LINC01065"
/replace="g"
/replace="t"
/db_xref="dbSNP:1385231646"
variation 290
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1399986620"
variation 293
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:532475988"
variation 298
/gene="LINC01065"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593512605"
variation 299
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955208201"
variation 301
/gene="LINC01065"
/replace="a"
/replace="t"
/db_xref="dbSNP:921433920"
variation 305
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955208190"
variation 306
/gene="LINC01065"
/replace="a"
/replace="c"
/db_xref="dbSNP:1219663961"
variation 316
/gene="LINC01065"
/replace="g"
/replace="t"
/db_xref="dbSNP:975517285"
variation 317
/gene="LINC01065"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1955208165"
variation 318
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265176296"
variation 319
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:965632576"
variation 320..321
/gene="LINC01065"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1955208126"
variation 320
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1355221882"
variation 322
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:2138296912"
variation 326
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955208110"
variation 339
/gene="LINC01065"
/replace="a"
/replace="c"
/db_xref="dbSNP:1955208094"
variation 345
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1207631499"
exon 346..453
/gene="LINC01065"
/inference="alignment:Splign:2.1.0"
variation 347
/gene="LINC01065"
/replace="a"
/replace="t"
/db_xref="dbSNP:1274057502"
variation 363
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1229730237"
variation 365
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:759905930"
variation 368
/gene="LINC01065"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955203108"
variation 371
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344953003"
variation 376
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955203066"
variation 377
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1271000703"
variation 387
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955203031"
variation 396
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955203006"
variation 398
/gene="LINC01065"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1480694702"
variation 401
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:2138296241"
variation 403
/gene="LINC01065"
/replace="a"
/replace="c"
/db_xref="dbSNP:953305488"
variation 404
/gene="LINC01065"
/replace="a"
/replace="c"
/db_xref="dbSNP:2138296238"
variation 406..407
/gene="LINC01065"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1955202941"
variation 407
/gene="LINC01065"
/replace="c"
/replace="g"
/db_xref="dbSNP:1313289109"
variation 412..417
/gene="LINC01065"
/replace="ctg"
/replace="ctgctg"
/db_xref="dbSNP:1955202828"
variation 412
/gene="LINC01065"
/replace="c"
/replace="g"
/db_xref="dbSNP:114572265"
variation 414
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955202864"
variation 415
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955202849"
variation 417
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:187594981"
variation 419
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1168686714"
variation 422
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:961715464"
variation 426
/gene="LINC01065"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:181681964"
variation 428
/gene="LINC01065"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593512248"
variation 431
/gene="LINC01065"
/replace="a"
/replace="c"
/db_xref="dbSNP:536348409"
variation 437
/gene="LINC01065"
/replace="c"
/replace="g"
/db_xref="dbSNP:971922654"
variation 440
/gene="LINC01065"
/replace="g"
/replace="t"
/db_xref="dbSNP:2138296204"
variation 442
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955202675"
variation 443
/gene="LINC01065"
/replace=""
/replace="c"
/db_xref="dbSNP:1334444785"
variation 443
/gene="LINC01065"
/replace="a"
/replace="c"
/db_xref="dbSNP:2138296199"
variation 448
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1326903294"
variation 450..451
/gene="LINC01065"
/replace=""
/replace="g"
/db_xref="dbSNP:1955202590"
variation 450
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955202611"
variation 451
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955202569"
exon 454..489
/gene="LINC01065"
/inference="alignment:Splign:2.1.0"
variation 455
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955196588"
variation 462
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955196574"
variation 465..466
/gene="LINC01065"
/replace="ga"
/replace="gaga"
/db_xref="dbSNP:1358078824"
variation 467
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955196551"
variation 470
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1243738557"
variation 475
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:911058738"
variation 476
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1356890430"
variation 482..488
/gene="LINC01065"
/replace="aag"
/replace="aagtaag"
/db_xref="dbSNP:1955196483"
variation 483
/gene="LINC01065"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:767131616"
variation 486
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:2138295488"
variation 487
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204334671"
variation 489
/gene="LINC01065"
/replace="a"
/replace="c"
/db_xref="dbSNP:1259392696"
exon 490..565
/gene="LINC01065"
/inference="alignment:Splign:2.1.0"
variation 490
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1310638900"
variation 498
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:767875688"
variation 500
/gene="LINC01065"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:922515988"
variation 506
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955111295"
variation 513
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1281141776"
variation 518
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:2138286424"
variation 520
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1313633810"
variation 521
/gene="LINC01065"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1210386429"
variation 522
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955111229"
variation 523
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1035320660"
variation 525
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955111216"
variation 527
/gene="LINC01065"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1955111197"
variation 532
/gene="LINC01065"
/replace="a"
/replace="c"
/db_xref="dbSNP:1566344743"
variation 533
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002586487"
variation 536
/gene="LINC01065"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:575756728"
variation 537
/gene="LINC01065"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1307477660"
variation 543
/gene="LINC01065"
/replace="g"
/replace="t"
/db_xref="dbSNP:1955111141"
variation 545
/gene="LINC01065"
/replace="c"
/replace="g"
/db_xref="dbSNP:1955111128"
variation 548
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1955111102"
variation 552
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1490133749"
variation 553
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:1238744910"
variation 556
/gene="LINC01065"
/replace="c"
/replace="g"
/db_xref="dbSNP:976674199"
variation 558
/gene="LINC01065"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:762587576"
variation 559
/gene="LINC01065"
/replace="c"
/replace="t"
/db_xref="dbSNP:1955111029"
variation 563
/gene="LINC01065"
/replace="a"
/replace="g"
/db_xref="dbSNP:961043395"
ORIGIN
aaccagcagctcccttggtaggggcatgcagaagacctgatgacacaaaccctccaaagagtttcaccctcaccacaacaggtggcttcctgctcggcagcccatcctgcatcacttcagtggacttctctgacatctactagaccacattaaatgaatcacagccttgaaactgaactggaaggacttccttcaagatttttatctaattcctgttggacagtgtaaaatgccacttcttccagggttgcctgcatatcatcaaaagggaaatagtactcatcgaagatgtgcctttgctaggaactaggacaagggtggcctttataaattcatgaagagaaggagccagcatatgaacttgctgcctatctttagcaaggagatgcaaatgacatccacaaacctcttctgctgtatacctggatgaaagcaaggctagctgtgtgtcctatggcaccaaggactgaaagattgtaagaagtaagagtccatcatagaggccaagccaaatacaactatgttttcaagcataagatggatagatgtggtaaaccacaagaag
//
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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