2024-04-20 16:49:21, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_146456 1080 bp RNA linear PRI 19-APR-2022 DEFINITION Homo sapiens long intergenic non-protein coding RNA 2446 (LINC02446), transcript variant 2, long non-coding RNA. ACCESSION NR_146456 VERSION NR_146456.1 KEYWORDS RefSeq. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AC068775.52. Transcript Variant: This variant (2) differs in the 3' end compared to variant 1. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments. ##Evidence-Data-START## Transcript exon combination :: SRR1163655.58686.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA2155628, SAMEA2159764 [ECO:0000348] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-138 AC068775.52 137564-137701 139-215 AC068775.52 156423-156499 216-1080 AC068775.52 159009-159873 FEATURES Location/Qualifiers source 1..1080 /organism="Homo sapiens" /mol_type="transcribed RNA" /db_xref="taxon:9606" /chromosome="12" /map="12p13.2" gene 1..1080 /gene="LINC02446" /note="long intergenic non-protein coding RNA 2446" /db_xref="GeneID:101060038" /db_xref="HGNC:HGNC:53378" ncRNA 1..1080 /ncRNA_class="lncRNA" /gene="LINC02446" /product="long intergenic non-protein coding RNA 2446, transcript variant 2" /db_xref="GeneID:101060038" /db_xref="HGNC:HGNC:53378" exon 1..138 /gene="LINC02446" /inference="alignment:Splign:2.1.0" variation 1 /gene="LINC02446" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1487738683" variation 2 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1022717895" variation 3..10 /gene="LINC02446" /replace="ttggccca" /replace="ttggcccattggccca" /db_xref="dbSNP:1865128583" variation 11 /gene="LINC02446" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:546163935" variation 13 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865128624" variation 14 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1205898389" variation 15 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865128646" variation 17 /gene="LINC02446" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:138159046" variation 18 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:184682972" variation 20..23 /gene="LINC02446" /replace="tg" /replace="tgtg" /db_xref="dbSNP:2120375559" variation 20 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1033842594" variation 22 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1865128735" variation 28 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865128754" variation 29 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:141617836" variation 30 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1304935309" variation 33 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:1865128860" variation 39 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1591646765" variation 42 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1346790019" variation 43 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1026588924" variation 47 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:950971154" variation 54..62 /gene="LINC02446" /replace="tttttttt" /replace="ttttttttt" /replace="tttttttttt" /db_xref="dbSNP:202150189" variation 54 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:992548639" variation 57 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:1591646775" variation 60 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:917020320" variation 62 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865129057" variation 63 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1414698544" variation 64 /gene="LINC02446" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1289068642" variation 67 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:1352355764" variation 69..77 /gene="LINC02446" /replace="tttgt" /replace="tttgtttgt" /db_xref="dbSNP:1399467768" variation 69 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865129109" variation 71 /gene="LINC02446" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1865129146" variation 75 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:929599010" variation 81 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865129200" variation 86 /gene="LINC02446" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2120375705" variation 87 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:866275744" variation 88 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:1865129232" variation 91..92 /gene="LINC02446" /replace="tt" /replace="ttt" /db_xref="dbSNP:1168399964" variation 91 /gene="LINC02446" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:943533447" variation 93 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:1565537729" variation 94 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:982430956" variation 98 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865129352" variation 101..104 /gene="LINC02446" /replace="aaaa" /replace="aaaaa" /db_xref="dbSNP:1175674901" variation 110 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865129386" variation 113 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:190181194" variation 114 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:377653105" variation 120 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:933347231" variation 122..124 /gene="LINC02446" /replace="cc" /replace="ccc" /db_xref="dbSNP:1312966467" variation 122 /gene="LINC02446" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1212036044" variation 124 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1206098966" variation 126 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865129507" variation 128 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1325119899" variation 130 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:1865129535" variation 132 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:1865129560" variation 134..135 /gene="LINC02446" /replace="a" /replace="aa" /db_xref="dbSNP:1865129577" variation 135 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865129592" exon 139..215 /gene="LINC02446" /inference="alignment:Splign:2.1.0" variation 142..150 /gene="LINC02446" /replace="agaa" /replace="agaagagaa" /db_xref="dbSNP:1437032672" variation 143 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1376889243" variation 145 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1865290007" variation 151 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:1173920220" variation 152 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1865290078" variation 155 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865290099" variation 160 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1169402058" variation 162 /gene="LINC02446" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1591651990" variation 166 /gene="LINC02446" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:779600028" variation 167 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1178835451" variation 174 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865290276" variation 177 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:527643618" variation 180 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865290325" variation 184 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1057297938" variation 185 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:1470482122" variation 190 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:2120421292" variation 192 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865290473" variation 204 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865290510" variation 205 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:1865290533" variation 206 /gene="LINC02446" /replace="" /replace="a" /db_xref="dbSNP:1232294391" variation 208 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:1409315590" variation 215 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865290601" exon 216..1080 /gene="LINC02446" /inference="alignment:Splign:2.1.0" variation 217 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:2120427163" variation 223 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1865314532" variation 230 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1211580205" variation 231 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:2120427180" variation 245 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865314602" variation 249 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865314617" variation 251 /gene="LINC02446" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1242676367" variation 260 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:944128328" variation 265 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:1259500496" variation 268 /gene="LINC02446" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:561528426" variation 269 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1036586606" variation 271 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:899339382" variation 274 /gene="LINC02446" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1042360852" variation 275 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1289662736" variation 277 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1230787942" variation 278 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:530644541" variation 282 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:1865315415" variation 287 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1865315427" variation 288 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:923959945" variation 289..291 /gene="LINC02446" /replace="" /replace="aaa" /db_xref="dbSNP:953523589" variation 290..297 /gene="LINC02446" /replace="aagaa" /replace="aagaagaa" /db_xref="dbSNP:1865315483" variation 291..293 /gene="LINC02446" /replace="a" /replace="aga" /db_xref="dbSNP:1865315497" variation 298 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1865315559" variation 302 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865315571" variation 303 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865315593" variation 309 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:778327196" variation 312 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1428999586" variation 317 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865315622" variation 318 /gene="LINC02446" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1378929942" variation 320 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1304509348" variation 324 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1865315688" variation 326 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:2120427302" variation 327 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865315710" variation 328 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1009384428" variation 334..335 /gene="LINC02446" /replace="t" /replace="tt" /db_xref="dbSNP:1364647046" variation 337 /gene="LINC02446" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1865315757" variation 340 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865315785" variation 343 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865315804" variation 351 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865315826" variation 357 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865315846" variation 359 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865315862" variation 362 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1018926361" variation 367 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1865315893" variation 368 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1431158061" variation 370 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1591652707" variation 375 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:576082438" variation 380..385 /gene="LINC02446" /replace="a" /replace="agagaa" /db_xref="dbSNP:1865315968" variation 381 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:1865315985" variation 384..387 /gene="LINC02446" /replace="aaa" /replace="aaaa" /db_xref="dbSNP:1865316007" variation 388 /gene="LINC02446" /replace="" /replace="g" /db_xref="dbSNP:1174874959" variation 391 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:1053949314" variation 392 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:895437446" variation 396 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865316097" variation 405 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1865316113" variation 406 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:988704511" variation 407 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865316149" variation 411 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1490245340" variation 415 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:2120427460" variation 417 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865316185" variation 421 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1267083924" variation 424 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:749682935" variation 425 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865316223" variation 426..427 /gene="LINC02446" /replace="" /replace="g" /db_xref="dbSNP:1865316237" variation 427 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1047007139" variation 428 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:1865316274" variation 435 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:2120427491" variation 443 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865316297" variation 444 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:2120427497" variation 445 /gene="LINC02446" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:906919186" variation 451 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1333607167" variation 453 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1272872862" variation 454 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865316369" variation 456 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1003049977" variation 460..465 /gene="LINC02446" /replace="gaa" /replace="gaagaa" /db_xref="dbSNP:1444716164" variation 463 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:550617391" variation 464 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1352776611" variation 466 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:76872865" variation 468 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:961014717" variation 469 /gene="LINC02446" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2125096" variation 470 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865316614" variation 476 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1281005783" variation 478..482 /gene="LINC02446" /replace="tt" /replace="ttctt" /db_xref="dbSNP:202068470" variation 480 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1026900156" variation 485..491 /gene="LINC02446" /replace="aaaaaa" /replace="aaaaaaa" /db_xref="dbSNP:940303796" variation 485 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1408124788" variation 490..492 /gene="LINC02446" /replace="" /replace="aag" /db_xref="dbSNP:1865316769" variation 490 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1404345342" variation 497 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865316782" variation 502 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:1865316806" variation 509 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865316824" variation 511 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1865316840" variation 512 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865316859" variation 513 /gene="LINC02446" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1439038786" variation 516..524 /gene="LINC02446" /replace="tatatat" /replace="tatatatat" /db_xref="dbSNP:1036618697" variation 517 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865316898" variation 519 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:2120427672" variation 520..529 /gene="LINC02446" /replace="tatat" /replace="tatattatat" /db_xref="dbSNP:1865316935" variation 520 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865316913" variation 521 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1237170412" variation 524 /gene="LINC02446" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:953945077" variation 526 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1865316988" variation 528 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:139875901" variation 531 /gene="LINC02446" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1865317038" variation 533 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865317060" variation 534..535 /gene="LINC02446" /replace="" /replace="c" /db_xref="dbSNP:34674348" variation 535 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1379672317" variation 542 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:930885139" variation 543 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865317116" variation 548 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1232385775" variation 551 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1019878084" variation 553 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1172496308" variation 559 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865317181" variation 562 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865317195" variation 563 /gene="LINC02446" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:74897207" variation 566 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865317238" variation 572 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1591652749" variation 575 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:375496998" variation 585 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865317313" variation 589 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1329607514" variation 590 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865317341" variation 593 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865317361" variation 595..596 /gene="LINC02446" /replace="" /replace="g" /db_xref="dbSNP:35781159" variation 596 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:555332632" variation 597 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1865317425" variation 603 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1565542460" variation 604 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1321897309" variation 605 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865317470" variation 608 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:1591652754" variation 612 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1009002792" variation 615 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1441854806" variation 616..620 /gene="LINC02446" /replace="at" /replace="atgat" /db_xref="dbSNP:1865317537" variation 619 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865317565" variation 623 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:1865317580" variation 624 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1280902690" variation 626 /gene="LINC02446" /replace="" /replace="c" /db_xref="dbSNP:1865317639" variation 626 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1865317619" variation 629 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:531900520" variation 630 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1305376966" variation 638 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1329073404" variation 640 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:568644227" variation 642 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:775547317" variation 645 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1009560542" variation 646 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:1337333634" variation 650 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:564416972" variation 653 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:180987193" variation 656 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1196177730" variation 657 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865317955" variation 658 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1161481048" variation 659 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1401501335" variation 660 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:948314942" variation 663 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:371260584" variation 664 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865318110" variation 666 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:1468650534" variation 671 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865318171" variation 674 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865318194" variation 677 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:1865318213" variation 682 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:906714057" variation 683 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:958754755" variation 687 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1244251664" variation 688..693 /gene="LINC02446" /replace="aca" /replace="acaaca" /db_xref="dbSNP:1183524992" variation 689 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1865318372" variation 690 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:940894601" variation 697 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:992585410" variation 698 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1217034251" variation 702 /gene="LINC02446" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1036770465" variation 703 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:2125095" variation 710 /gene="LINC02446" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1865318627" variation 712 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865318655" variation 715 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1591652787" variation 718 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1198836290" variation 725 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865318721" variation 727 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:143762446" variation 728 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:572934854" variation 731 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1026659179" variation 732 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865318816" variation 735 /gene="LINC02446" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:920246051" variation 738 /gene="LINC02446" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:550498725" variation 741 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865318898" variation 745 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865318912" variation 750 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:889305180" variation 759 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:755594435" variation 760 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1849019274" variation 770 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1290382520" variation 773 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:2120428097" variation 774 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865319006" variation 780 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1431265306" variation 781 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865319034" variation 790 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1344782704" variation 791 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:1865319066" variation 796 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1295501553" variation 798 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:1865319131" variation 800..801 /gene="LINC02446" /replace="a" /replace="aa" /db_xref="dbSNP:1388382180" variation 800 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1865319151" variation 802 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1865319182" variation 804..806 /gene="LINC02446" /replace="aa" /replace="aaa" /db_xref="dbSNP:1865319200" variation 805 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1426558119" variation 806 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1865319238" variation 811 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1385960228" variation 813 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:541697880" variation 816 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1443327282" variation 817..820 /gene="LINC02446" /replace="tg" /replace="tgtg" /db_xref="dbSNP:1865319325" variation 818 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1296262423" variation 829 /gene="LINC02446" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1865319385" variation 830 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:569999434" variation 834 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:892582124" variation 837 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1009591746" variation 838 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865319491" variation 842 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865319507" variation 844 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865319516" variation 849 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865319534" variation 853 /gene="LINC02446" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1213215879" variation 855 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1022274930" variation 858 /gene="LINC02446" /replace="" /replace="a" /db_xref="dbSNP:1865319742" variation 860 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:1865319761" variation 862 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1865319774" variation 867 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:762839392" variation 870 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1216674555" variation 871 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:146849577" variation 872 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865319851" variation 874 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1357164017" variation 884 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1865319876" variation 885 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1297668545" variation 894 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1000130007" variation 895 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865319929" variation 897 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:544081340" variation 908..910 /gene="LINC02446" /replace="a" /replace="ata" /db_xref="dbSNP:1865319987" variation 917 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:2120428287" variation 920 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:958567677" variation 921 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865320038" variation 922 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1865320063" variation 925 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865320083" variation 926 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1406984183" variation 934 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865320123" variation 936 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1591652819" variation 937 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865320148" variation 938 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:148994290" variation 943 /gene="LINC02446" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:958119141" variation 946 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1591652824" variation 947 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865320224" variation 949..953 /gene="LINC02446" /replace="tgt" /replace="tgtgt" /db_xref="dbSNP:1024137221" variation 949 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:1171766770" variation 953 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:989408578" variation 957..963 /gene="LINC02446" /replace="tta" /replace="ttagtta" /db_xref="dbSNP:1428217745" variation 959 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865320297" variation 966 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865320311" variation 968 /gene="LINC02446" /replace="" /replace="t" /db_xref="dbSNP:1417829029" variation 975 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:766028807" variation 982 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1209649628" variation 989 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:10772319" variation 991 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865320463" variation 993 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:60400937" variation 1002 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1269216366" variation 1003 /gene="LINC02446" /replace="" /replace="c" /db_xref="dbSNP:1591652836" variation 1004 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:185450400" variation 1011 /gene="LINC02446" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:767171962" variation 1014 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:143816606" variation 1015 /gene="LINC02446" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1205155888" variation 1019 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865320648" variation 1022 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1306908795" variation 1027 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:920294466" variation 1029 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865320708" variation 1030 /gene="LINC02446" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:189811458" variation 1031 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865320769" variation 1042 /gene="LINC02446" /replace="c" /replace="g" /db_xref="dbSNP:1591652853" variation 1044 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1366906388" variation 1045 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865320847" variation 1046 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:752229331" variation 1049 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1865320905" variation 1051 /gene="LINC02446" /replace="" /replace="a" /db_xref="dbSNP:1282904865" variation 1052 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:550130818" variation 1053 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:931063612" variation 1057 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1299182388" variation 1059 /gene="LINC02446" /replace="g" /replace="t" /db_xref="dbSNP:1865321079" variation 1061 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865321103" variation 1066 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1461907521" variation 1071 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1865321156" variation 1073 /gene="LINC02446" /replace="a" /replace="g" /db_xref="dbSNP:1289257608" variation 1076 /gene="LINC02446" /replace="a" /replace="t" /db_xref="dbSNP:1865321204" variation 1077 /gene="LINC02446" /replace="a" /replace="c" /db_xref="dbSNP:1178994164" variation 1078 /gene="LINC02446" /replace="c" /replace="t" /db_xref="dbSNP:1865321259" ORIGIN
gcttggcccactctcactctgtggagtgtacatttgtttccataaatctgtgctttttttttcattgttttgtttgtgcatttcatccaattgtttgttcaaaatgccaagaatctggacaccctccaccagtaacaggcaagaagagaatagaggcaaagcaagccactccagaagtcctctagccagctttgtctttagtttgatggccagagaggaaatccaagccaaaagctccttttggagacaagaatattctgacagcacctcctacgatgtgacagagtcaaagaagaaaatatacaagagaactctgctatagaaaattacaaattcaaaccatgggaaaatggggaatagaaaaattatctctttagacagagaaaagattataaatactgaaaattgtcatttctataaatgtcattgctcttctgttttacattgtgtaaatatttggaagaaaatggcacaattttctttcaaaaaaagggaaacattcaaaatatttaaattatatatattatatatgtaacatgatcagcaagtctggaaacataacgaagttttatagtattgatttattcctatcactctgagatatggtgacattacatgatatgttcaacgtgttgttcctcattagcaatgtgttatgcataatggggaccaacatgggacattaatacaacatttctatcagtgcctgcacatgcttctgtgatacgttgcctccaatgatttttgtctctaattttcagaatataaacctgctccattagcattttctggaagaagcaatcaaatgggttaatctgtgaaagtaaatgttatctatatttcccaacattatggccatcctgtattaacgtatattatgtatattctgaactgctccataattggaatagtcattccttatcaataatttacttgatatcatggatatgtgtcttttagttaatgatccctttgccaactagcctagtttataggcagtgactatatcatactcattttgaattcccaatacttaccacagcttcctatacatggtagttgtttaataaataattcttg
//
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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