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Previous release (v1)
2024-04-28 01:31:35, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_033826 776 bp RNA linear PRI 02-SEP-2020
DEFINITION Homo sapiens small nuclear ribonucleoprotein D2 pseudogene 2
(SNRPD2P2), non-coding RNA.
ACCESSION NR_033826 XR_078245 XR_078885 XR_079392
VERSION NR_033826.1
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 776)
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
BC014600.1.
On or before Jun 30, 2010 this sequence version replaced
XR_079392.1, XR_078245.1, XR_078885.1.
##Evidence-Data-START##
Transcript is intronless :: BC014600.1, BG722592.1 [ECO:0000345]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-776 BC014600.1 7-782
FEATURES Location/Qualifiers
source 1..776
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="1"
/map="1q42.2"
gene 1..776
/gene="SNRPD2P2"
/note="small nuclear ribonucleoprotein D2 pseudogene 2"
/pseudo
/db_xref="GeneID:645339"
/db_xref="HGNC:HGNC:38598"
misc_RNA 1..776
/gene="SNRPD2P2"
/product="small nuclear ribonucleoprotein D2 pseudogene 2"
/pseudo
/db_xref="GeneID:645339"
/db_xref="HGNC:HGNC:38598"
exon 1..764
/gene="SNRPD2P2"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 10
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1292254248"
variation 11
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1657564412"
variation 13
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369670385"
variation 21
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213347218"
variation 27
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:112510644"
variation 28
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1476503361"
variation 37
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:989234005"
variation 40
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:936509665"
variation 48
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657564130"
variation 53
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657564114"
variation 54
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1384610160"
variation 55
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:779461903"
variation 57
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1443345589"
variation 60
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1165970981"
variation 62
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657563870"
variation 63
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657563835"
variation 64
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:755463000"
variation 68
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657563791"
variation 78
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657563768"
variation 85
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:986435939"
variation 87
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124837648"
variation 88
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:954679455"
variation 89
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1029641506"
variation 91
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1657563620"
variation 92
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376007622"
variation 93
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657563566"
variation 95
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:973367083"
variation 98
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1204485941"
variation 100
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657563470"
variation 106
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1657563449"
variation 110
/gene="SNRPD2P2"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1257861397"
variation 110
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1348583739"
variation 112
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:976769341"
variation 117
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:558219849"
variation 119
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1015697467"
variation 120
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:375511113"
variation 121
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:540745459"
variation 123
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315692977"
variation 124
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1349841201"
variation 126
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2124837615"
variation 128
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:888608818"
variation 129
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:780001863"
variation 134
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002854294"
variation 135
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1657563003"
variation 139
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657562972"
variation 142
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327401737"
variation 144
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657562915"
variation 145
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:756175110"
variation 147
/gene="SNRPD2P2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1657562839"
variation 150
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1448957840"
variation 157
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:578000792"
variation 158
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:906796335"
variation 172
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:982657371"
variation 179
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1657562670"
variation 181
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657562643"
variation 188
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657562605"
variation 189
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1657562566"
variation 192
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1657562527"
variation 195
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657562489"
variation 197
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:555755489"
variation 198
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:150649132"
variation 201..206
/gene="SNRPD2P2"
/replace="gag"
/replace="gaggag"
/db_xref="dbSNP:1185467186"
variation 207
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657562327"
variation 208
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:892181599"
variation 210
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1001930420"
variation 220
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1572074302"
variation 222
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1657562207"
variation 226
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1470063089"
variation 227
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:141834027"
variation 228
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010521951"
variation 230
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657562049"
variation 231
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1053460443"
variation 232
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403401255"
variation 234
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:762879024"
variation 236
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1336803615"
variation 237
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657561829"
variation 239
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:556018068"
variation 244
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1434944966"
variation 249
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657561674"
variation 251
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657561637"
variation 252
/gene="SNRPD2P2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1657561586"
variation 252
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657561543"
variation 253
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1281081557"
variation 255
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1351070463"
variation 256
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1229279999"
variation 257
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1657561216"
variation 258
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657561174"
variation 259
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1053097959"
variation 262
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1558101374"
variation 264
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2124837523"
variation 265
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:752538109"
variation 268
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1191378475"
variation 269
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:765325508"
variation 272
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1451028991"
variation 273
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1050287820"
variation 274
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657560802"
variation 279
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1205714984"
variation 282
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1657560717"
variation 286
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:933210516"
variation 292
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657560654"
variation 294
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:536090305"
variation 295
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:567468672"
variation 300
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:923188263"
variation 301
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657560526"
variation 303
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657560483"
variation 309
/gene="SNRPD2P2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1445256569"
variation 310
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:976716975"
variation 312
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258309560"
variation 313
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:759562821"
variation 317
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1479491596"
variation 318
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1199122040"
variation 319..320
/gene="SNRPD2P2"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1657560260"
variation 320
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:908585090"
variation 321
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:371547683"
variation 322
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:920668324"
variation 323
/gene="SNRPD2P2"
/replace=""
/replace="a"
/db_xref="dbSNP:1395066982"
variation 330
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124837487"
variation 334
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1408159821"
variation 336
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:973439081"
variation 337
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657559981"
variation 338
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:952853393"
variation 339
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:547246113"
variation 342
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1230889101"
variation 348
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1558101345"
variation 356
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657559828"
variation 361
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1657559800"
variation 362
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:908486767"
variation 363..372
/gene="SNRPD2P2"
/replace="acaacaa"
/replace="acaacaacaa"
/db_xref="dbSNP:1225511937"
variation 367
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657559750"
variation 368
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1657559676"
variation 370
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1034233648"
variation 371
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1343943393"
variation 375
/gene="SNRPD2P2"
/replace=""
/replace="t"
/db_xref="dbSNP:2124837463"
variation 376
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2124837459"
variation 385
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:960634955"
variation 386
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002393394"
variation 390
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:970913715"
variation 396
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:112527476"
variation 402
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1483660101"
variation 403
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199231051"
variation 405
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009808624"
variation 407
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:969145175"
variation 411
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021998415"
variation 412
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:571320057"
variation 414
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1199067806"
variation 416
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657559186"
variation 419
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1010552983"
variation 420
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1414806259"
variation 423
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657559016"
variation 425
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:892138654"
variation 430
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657558937"
variation 431
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:892114444"
variation 436
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030642858"
variation 438
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1423927453"
variation 443
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009565726"
variation 444
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:138261140"
variation 447
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1171322592"
variation 450
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302291020"
variation 454
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1657558550"
variation 455..460
/gene="SNRPD2P2"
/replace="gggggg"
/replace="ggggggg"
/db_xref="dbSNP:1167145257"
variation 455
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1411327901"
variation 456
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:531326988"
variation 457
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1657558356"
variation 459
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:888891020"
variation 461
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657558220"
variation 463
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657558179"
variation 464
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1222320842"
variation 465
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:751308377"
variation 473
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657558082"
variation 476
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1657558048"
variation 477..485
/gene="SNRPD2P2"
/replace="aagaag"
/replace="aagaagaag"
/db_xref="dbSNP:1657557942"
variation 478
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1474381045"
variation 480
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1490930766"
variation 481
/gene="SNRPD2P2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1558101309"
variation 485
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1657557911"
variation 487
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:933178070"
variation 488
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1657557866"
variation 492
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1210780506"
variation 498
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1260668554"
variation 500
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1657557774"
variation 501
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2124837395"
variation 503
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657557750"
variation 506
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444913125"
variation 507
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1194787872"
variation 508
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657557660"
variation 509
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:770378687"
variation 513
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:563200954"
variation 515
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:181366523"
variation 521
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1386895733"
variation 524
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657557492"
variation 531
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1037774498"
variation 532
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1657557435"
variation 533
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657557370"
variation 538
/gene="SNRPD2P2"
/replace="a"
/replace="t"
/db_xref="dbSNP:940610438"
variation 550
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1288056899"
variation 551
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:112422735"
variation 552
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1380678409"
variation 554
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:984150519"
variation 559
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1255532239"
variation 563
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:952881995"
variation 564
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:560743039"
variation 565
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657557079"
variation 566
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657557045"
variation 570
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1313608021"
variation 571
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:981313268"
variation 575
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657556968"
variation 581
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:540433204"
variation 583
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1438648559"
variation 584
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:939275072"
variation 585
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272738741"
variation 594
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213239550"
variation 595
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124837334"
variation 600
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358926793"
variation 602
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657556756"
variation 607
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025137022"
variation 608
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1657556697"
variation 620
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657556670"
variation 621
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:569971578"
variation 622..625
/gene="SNRPD2P2"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:35344460"
variation 622
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657556597"
variation 624
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1294374922"
variation 626
/gene="SNRPD2P2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1657556435"
variation 627
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1657556395"
variation 628
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1233249062"
variation 637
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:980613103"
variation 642..643
/gene="SNRPD2P2"
/replace=""
/replace="a"
/db_xref="dbSNP:1657556246"
variation 642
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1657556289"
variation 643..652
/gene="SNRPD2P2"
/replace="ttttttttt"
/replace="tttttttttt"
/replace="ttttttttttt"
/replace="tttttttttttt"
/db_xref="dbSNP:915021115"
variation 643
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:76031188"
variation 648
/gene="SNRPD2P2"
/replace="a"
/replace="t"
/db_xref="dbSNP:969176096"
variation 649
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354219265"
variation 653
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1389611391"
variation 655
/gene="SNRPD2P2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1310601268"
variation 656
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1443879492"
variation 658
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1572074112"
variation 659
/gene="SNRPD2P2"
/replace="g"
/replace="t"
/db_xref="dbSNP:772789661"
variation 661..665
/gene="SNRPD2P2"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1382052719"
variation 661
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:771684016"
variation 665
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1334775121"
variation 666
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354817811"
variation 669..677
/gene="SNRPD2P2"
/replace="aaca"
/replace="aacataaca"
/db_xref="dbSNP:1657555641"
variation 671
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2124837289"
variation 672
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1009761890"
variation 675
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:578079639"
variation 678
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1327921308"
variation 691
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1229887839"
variation 693
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268417041"
variation 694
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657555539"
variation 695
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1657555513"
variation 700
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407942957"
variation 702
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201302215"
variation 706
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657555435"
variation 708
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1657555406"
variation 710
/gene="SNRPD2P2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1657555384"
variation 713
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:956965524"
variation 719
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1032401235"
variation 728
/gene="SNRPD2P2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1572074099"
variation 732
/gene="SNRPD2P2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1000540154"
variation 741
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2124837263"
variation 742
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1657555257"
variation 746..751
/gene="SNRPD2P2"
/replace="aaaaa"
/replace="aaaaaa"
/replace="aaaaaaa"
/db_xref="dbSNP:1176499332"
variation 746
/gene="SNRPD2P2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1657555233"
variation 755
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:956442961"
variation 763
/gene="SNRPD2P2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1657555124"
ORIGIN
gaatttacaccatggaaactggcaaacgctgcaaacactgcctcccaccatcacagacagccagttattaagcatttatcagcacattatgttgccagggactgtgctcagagttattggggggagaggcagtagcagtgttatgtagtcaagcttataactgataaactgtagtcatttggaaaaacagaagcaacgcagaggagatgggagtgaaccaagaacatagtaaccaccctgaacctcctcaacaaaccccagagggacatgtccccagaggagatgcagaagcacggggaggagggtccactctgtgctccgcagtcagtcaagaacaacactgaagtgctcaccaactactgacaacaacaagctgctgggctgcgaaggccttgagtagacactgcaacatggtgctggagaatgtgaaggagatgtgtactgaggtccccaaggggggcaacggtggcaagggcaagaagaagtccaagccagccaacaaagaccacttcatctccaagctcttcctgtgcagggactcagtcatcaccaacaagtgggggccacctccccattgacagaactcactccctcatcctatgaagacctaccctttgttatggggataataaagccctgtgcttttttttttctagtagtaaaaacaaaacataacaacaacaataaaactttagtcatttggtcatattagggaagtcatttattattctgtttcttcagaaataaaaaacagataacaaaaaaaaaaaaaaaaa
//
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]