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Previous release (v1)
2024-04-28 04:50:28, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_147010 813 bp RNA linear PRI 06-SEP-2020
DEFINITION Homo sapiens long intergenic non-protein coding RNA 1795
(LINC01795), long non-coding RNA.
ACCESSION NR_147010
VERSION NR_147010.1
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
BI825310.1 and AC007250.2.
##Evidence-Data-START##
RNAseq introns :: single sample supports all introns SAMEA2151119,
SAMEA2161674 [ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-754 BI825310.1 1-754
755-813 AC007250.2 37817-37875 c
FEATURES Location/Qualifiers
source 1..813
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="2"
/map="2p16.1"
gene 1..813
/gene="LINC01795"
/note="long intergenic non-protein coding RNA 1795"
/db_xref="GeneID:105374744"
/db_xref="HGNC:HGNC:52585"
ncRNA 1..813
/ncRNA_class="lncRNA"
/gene="LINC01795"
/product="long intergenic non-protein coding RNA 1795"
/db_xref="GeneID:105374744"
/db_xref="HGNC:HGNC:52585"
exon 1..306
/gene="LINC01795"
/inference="alignment:Splign:2.1.0"
variation 2
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:938305390"
variation 3
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1573878554"
variation 4..5
/gene="LINC01795"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1695097592"
variation 5
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695097614"
variation 8
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1483390556"
variation 11
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:2084534524"
variation 15
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:757050044"
variation 17
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695097679"
variation 18
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1238652621"
variation 21
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:537328498"
variation 22
/gene="LINC01795"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1314682083"
variation 24
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:1383773198"
variation 25
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:982835215"
variation 27
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1311783565"
variation 33
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:555521562"
variation 34
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1284237008"
variation 39
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:187461386"
variation 40
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:535129603"
variation 47
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1260835094"
variation 48
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486582266"
variation 55
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:754982367"
variation 58
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1164544184"
variation 59
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423972079"
variation 61
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1695098112"
variation 63..85
/gene="LINC01795"
/replace=""
/replace="tcactgggttccacggttctctt"
/db_xref="dbSNP:527931408"
variation 63
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695098128"
variation 68
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186349901"
variation 70
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1444857896"
variation 76
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:904066231"
variation 77
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:996875107"
variation 78
/gene="LINC01795"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1487479091"
variation 81
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695098754"
variation 84
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695098770"
variation 86
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1028387066"
variation 88
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695098817"
variation 92..94
/gene="LINC01795"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1264581171"
variation 92
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:920483915"
variation 96
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:891227701"
variation 97
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:376658497"
variation 98
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695098957"
variation 105
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695098976"
variation 108
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:1226532260"
variation 110
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:1016016482"
variation 113
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:553456656"
variation 117
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1050215261"
variation 118
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1695099720"
variation 119
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1384368097"
variation 120
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695099775"
variation 121
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:372995979"
variation 125
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1573878618"
variation 127
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1293230871"
variation 128
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:974436642"
variation 129
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:1026810891"
variation 130
/gene="LINC01795"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:969906490"
variation 133
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1448540880"
variation 134
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454728128"
variation 137
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390206223"
variation 138
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695100325"
variation 143
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:138424423"
variation 145
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1189957895"
variation 147
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695100377"
variation 155
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008643976"
variation 156
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373003406"
variation 157
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695100456"
variation 158
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695100472"
variation 160
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695100492"
variation 161
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1558849523"
variation 162
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:1695100532"
variation 166
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695100549"
variation 169
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1052131192"
variation 170
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:892112499"
variation 171..200
/gene="LINC01795"
/replace="cca"
/replace="ccaggtcagagaacacgaggcttgccacca"
/db_xref="dbSNP:1272264084"
variation 171
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:979951508"
variation 184
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1573878646"
variation 186
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:545584703"
variation 187
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:11888657"
variation 195
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695100847"
variation 197
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1573878650"
variation 202
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201300641"
variation 204
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1298344498"
variation 210
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1229704228"
variation 211
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695101381"
variation 214..221
/gene="LINC01795"
/replace="ccgcc"
/replace="ccgccgcc"
/db_xref="dbSNP:1695101401"
variation 215
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:193047415"
variation 216
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:543297785"
variation 217..218
/gene="LINC01795"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1695101485"
variation 218
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:748375345"
variation 219
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:183929237"
variation 220
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1480210430"
variation 221
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428643137"
variation 222
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1035141332"
variation 224
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1177546663"
variation 230
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:960819542"
variation 235
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695101754"
variation 236
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695101778"
variation 242
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210941283"
variation 243
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:945643848"
variation 246
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695101854"
variation 251
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1044401075"
variation 253
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:1695101927"
variation 254
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695101951"
variation 259
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1481397198"
variation 268
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695101992"
variation 269
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1573878672"
variation 272
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:904013530"
variation 273
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:2104162197"
variation 276
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695102067"
variation 277
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1695102088"
variation 278
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1181201351"
variation 280
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695102135"
variation 282
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695102154"
variation 283
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1695102176"
variation 284
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1482811708"
variation 289
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1275610847"
variation 291
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1015626316"
variation 292
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1695102270"
variation 295
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1342929827"
variation 296
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1255526166"
variation 298
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695102329"
variation 302
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1695102353"
variation 303
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1695102378"
variation 306
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:528815223"
exon 307..662
/gene="LINC01795"
/inference="alignment:Splign:2.1.0"
variation 307
/gene="LINC01795"
/replace=""
/replace="c"
/db_xref="dbSNP:2104190325"
variation 314
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695335736"
variation 318
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695335771"
variation 321
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:746254956"
variation 322
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:758889424"
variation 327
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1558854058"
variation 330
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1451120768"
variation 331
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:568395980"
variation 335
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:535598115"
variation 336
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:979387451"
variation 337
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695336100"
variation 340
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:920777313"
variation 345
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1215835742"
variation 347
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1558854080"
variation 350..352
/gene="LINC01795"
/replace=""
/replace="gtc"
/db_xref="dbSNP:1695336374"
variation 350
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1354383031"
variation 353
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1311140085"
variation 355
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:925086330"
variation 358
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:2104190393"
variation 359
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243581508"
variation 360
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385324755"
variation 361
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695336543"
variation 363
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:1695336573"
variation 364
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1695336598"
variation 366
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1312290455"
variation 368
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396608113"
variation 370
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:72618698"
variation 371
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695337305"
variation 376
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:986646933"
variation 378
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1334606759"
variation 384
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695337407"
variation 385
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1419605802"
variation 386
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780559081"
variation 389
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695337552"
variation 390
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:912348871"
variation 396
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1343925297"
variation 401
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:572434756"
variation 402
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:892437527"
variation 405
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:943703100"
variation 406
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192347740"
variation 410
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1042967868"
variation 411
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:747556347"
variation 412
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:546464599"
variation 414
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:898067657"
variation 418
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1334234275"
variation 421
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:769259174"
variation 424
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:141444773"
variation 430..438
/gene="LINC01795"
/replace="ct"
/replace="ctcgactct"
/db_xref="dbSNP:1695338117"
variation 432
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1265047438"
variation 433
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:748113710"
variation 441
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1245833954"
variation 445
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:1357658070"
variation 450
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:887902177"
variation 454
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695338302"
variation 455
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1399551147"
variation 461
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1341668520"
variation 466
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1300603077"
variation 467
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:576818099"
variation 468
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:1695338410"
variation 469
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261693398"
variation 471
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695338466"
variation 473..476
/gene="LINC01795"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1385387747"
variation 481
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1034179866"
variation 483
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1164248450"
variation 488
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:2104190603"
variation 491
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1459092047"
variation 492
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:960806256"
variation 494
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1169321965"
variation 495
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:528102008"
variation 496
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:562363183"
variation 499
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1202389974"
variation 505
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:961663532"
variation 506
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:966720237"
variation 507
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695338796"
variation 508
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1267766958"
variation 509
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695338844"
variation 510
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695338865"
variation 512
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:770072484"
variation 514
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695338912"
variation 521
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695338933"
variation 527
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1027890419"
variation 536
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:2104190689"
variation 538
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:529655543"
variation 542
/gene="LINC01795"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695339000"
variation 544
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695339020"
variation 546
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695339035"
variation 548
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1318701730"
variation 550
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:375366831"
variation 556
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:911997623"
variation 557
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:954005356"
variation 558
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:763235760"
variation 561
/gene="LINC01795"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1573885901"
variation 573
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1573885905"
variation 574
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:944779132"
variation 575
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1695339735"
variation 576
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397601886"
variation 577
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:563898368"
variation 580
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1330267153"
variation 587
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695339873"
variation 588
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:560220306"
variation 590
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1416952145"
variation 592
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1425184723"
variation 593..594
/gene="LINC01795"
/replace=""
/replace="ct"
/db_xref="dbSNP:1695340053"
variation 593
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:943817998"
variation 595
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695340093"
variation 596..601
/gene="LINC01795"
/replace="tttttt"
/replace="ttttttt"
/db_xref="dbSNP:1695340131"
variation 599
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1573885921"
variation 602
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:1036753702"
variation 604
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1695340239"
variation 610..612
/gene="LINC01795"
/replace=""
/replace="ctc"
/db_xref="dbSNP:149669823"
variation 610
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695340271"
variation 612
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:1695340363"
variation 614
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695340397"
variation 615
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:2104190872"
variation 621
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:918227516"
variation 623
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1573885929"
variation 630
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378203071"
variation 631
/gene="LINC01795"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695340514"
variation 634
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695340555"
variation 636
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695340592"
variation 637
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695340618"
variation 638
/gene="LINC01795"
/replace=""
/replace="g"
/db_xref="dbSNP:1695340691"
variation 638
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:527383092"
variation 639
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1049741861"
variation 640
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1456288747"
variation 644
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:1198288332"
variation 645
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695340844"
variation 646..648
/gene="LINC01795"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:35386409"
variation 649..650
/gene="LINC01795"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1455142591"
variation 649
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695340903"
variation 650
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1695340980"
variation 651..653
/gene="LINC01795"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:778797411"
variation 651
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1573885944"
variation 654
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:888067114"
variation 655
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695341551"
variation 656
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695341592"
variation 658
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1217609743"
variation 659
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1695341668"
exon 663..813
/gene="LINC01795"
/inference="alignment:Splign:2.1.0"
variation 663
/gene="LINC01795"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1303488246"
variation 664
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1222156153"
variation 664
/gene="LINC01795"
/replace="t"
/replace="ttttt"
/replace="tttttttt"
/db_xref="dbSNP:1695373262"
variation 665
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1695373296"
variation 668
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695373320"
variation 669..675
/gene="LINC01795"
/replace="aaaaaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:1390995660"
variation 670
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695373389"
variation 674
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1038704724"
variation 676
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1309208239"
variation 679..681
/gene="LINC01795"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1558854940"
variation 682
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1412275409"
variation 688
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695373528"
variation 689
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1695373554"
variation 694
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:2104194543"
variation 695
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:537162655"
variation 698
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025835725"
variation 699
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1695373635"
variation 700
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:2104194555"
variation 701
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:114254748"
variation 707
/gene="LINC01795"
/replace=""
/replace="c"
/db_xref="dbSNP:1352707311"
variation 709
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695373720"
variation 713
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360551684"
variation 715
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1156232351"
variation 718
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1695373813"
variation 724
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:984300473"
variation 727
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:2104194589"
variation 729
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1412560551"
variation 731
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:910005263"
variation 734
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1695373900"
variation 739
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1474209370"
variation 743
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:998370643"
variation 745
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1695373951"
variation 746
/gene="LINC01795"
/replace="c"
/replace="g"
/db_xref="dbSNP:1256537543"
variation 748
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:964161505"
variation 752
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:2104194611"
variation 755
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695374012"
variation 756
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051287930"
variation 757
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:887238960"
variation 760
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695374152"
variation 762
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1257992124"
variation 764
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695374198"
variation 767
/gene="LINC01795"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213686663"
variation 775
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:573657853"
variation 776
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:2104194639"
variation 778
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1695374280"
variation 779
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017431670"
variation 781
/gene="LINC01795"
/replace="a"
/replace="c"
/db_xref="dbSNP:1695374322"
variation 782
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1695374349"
variation 789
/gene="LINC01795"
/replace="a"
/replace="g"
/db_xref="dbSNP:962848397"
variation 793
/gene="LINC01795"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695374392"
variation 797
/gene="LINC01795"
/replace="g"
/replace="t"
/db_xref="dbSNP:1695374407"
variation 802
/gene="LINC01795"
/replace="a"
/replace="t"
/db_xref="dbSNP:1012907168"
variation 811
/gene="LINC01795"
/replace="c"
/replace="t"
/db_xref="dbSNP:762482463"
ORIGIN
ggcttgccactgttcccacacggctaagtgtccgggttcgtcctaatcaagctgaacactagtcactgggttccacggttctcttccatgacccacggcttctaatagagctataacactcactgcatggcccaagattccattccttggaatccgtgaggccaagaaccccaggtcagagaacacgaggcttgccaccatcttggaagcagcccgccgccattttggaagtggcccaccaccatcttgggagctctgggagcaaggaccacctggtaacaataggccaaatactgtgctgataagcttgaaagcctgccctgaatcctcatctattgatggagatggtgtcatcttgccttgattgtatccagaagcttcatccccaagataaaggatggacatctctccgatgaccagcttcttttgctcgactctagagaaggttgctttctgcattctggcaactgccctctgtctacatgattagactcgttggttgcagtgctttctggagtaatgaagggatccagtgcacagggtttaacttactgggcacaatctctaagccaactctgcctgaatgggtcccctgttttttctcttctgctcttgttgaaccatatctctgttccttgtgctcctgggaatttcttgctctggtcatgaaaaaaatggaaactctctcaaggaataacaatcagagctgtctggttgacaagggacattatggttgcaagaagaccctgaagcaaggattctacatcaaagattcaggggcaatctgagtttgcatttaagatccttctgcct
//
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]