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Previous release (v1)
2024-04-25 10:45:43, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_110733 580 bp RNA linear PRI 19-APR-2022
DEFINITION Homo sapiens ZNF649 antisense RNA 1 (ZNF649-AS1), long non-coding
RNA.
ACCESSION NR_110733 XR_244010 XR_248587 XR_253903
VERSION NR_110733.1
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 580)
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
DB080180.1 and AI458876.1.
On or before Feb 25, 2014 this sequence version replaced
XR_244010.2, XR_248587.2, XR_253903.2.
##Evidence-Data-START##
Transcript exon combination :: DB080180.1, SRR5189667.287021.1
[ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1968968, SAMEA2148093
[ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-448 DB080180.1 1-448
449-579 AI458876.1 5-135 c
580-580 DB080180.1 580-580
FEATURES Location/Qualifiers
source 1..580
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="19"
/map="19q13.41"
gene 1..580
/gene="ZNF649-AS1"
/note="ZNF649 antisense RNA 1"
/db_xref="GeneID:101928571"
/db_xref="HGNC:HGNC:51285"
ncRNA 1..580
/ncRNA_class="lncRNA"
/gene="ZNF649-AS1"
/product="ZNF649 antisense RNA 1"
/db_xref="GeneID:101928571"
/db_xref="HGNC:HGNC:51285"
exon 1..102
/gene="ZNF649-AS1"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2084983215"
variation 2
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122746566"
variation 3
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:75075099"
variation 7
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1426998091"
variation 12
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1265945574"
variation 15
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:555352692"
variation 17
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:184558993"
variation 19
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2084983429"
variation 21
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:919502084"
variation 22
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:534736751"
variation 23
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1177236037"
variation 24
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2084983586"
variation 25
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:982656401"
variation 26
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568453444"
variation 27
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1018306035"
variation 28
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568453450"
variation 29
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2084983744"
variation 30..31
/gene="ZNF649-AS1"
/replace="t"
/replace="tt"
/db_xref="dbSNP:2122746704"
variation 30
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1186742181"
variation 31
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2084983808"
variation 32
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:778295510"
variation 33
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:529437402"
variation 34
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:547984827"
variation 36
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2084983933"
variation 46..49
/gene="ZNF649-AS1"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1290747797"
variation 48
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2084983988"
variation 52
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2084984026"
variation 53
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2084984051"
variation 58
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2084984081"
variation 62
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:938071527"
variation 64
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1337386347"
variation 66
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1197599004"
variation 67
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2084984191"
variation 68
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2084984217"
variation 70
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1391985904"
variation 72
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:868821696"
variation 73
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1306446764"
variation 74
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1366643125"
variation 76
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:915269185"
variation 79
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1456868040"
variation 80
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2084984404"
variation 81..84
/gene="ZNF649-AS1"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1470559776"
variation 82
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:988675391"
variation 83
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2084984492"
variation 86..87
/gene="ZNF649-AS1"
/replace=""
/replace="c"
/db_xref="dbSNP:1179222265"
variation 86
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122746879"
variation 87
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386819403"
variation 88
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1457105378"
variation 89
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568453478"
variation 91
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1418044678"
variation 92
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1289652284"
variation 93
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1364409417"
variation 94
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2084984721"
variation 95
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2084984752"
variation 96..97
/gene="ZNF649-AS1"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2084984810"
variation 96
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2084984787"
variation 97
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1385120965"
variation 99
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2084984865"
variation 100
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:912980630"
variation 101
/gene="ZNF649-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1267928554"
variation 102
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2084984950"
exon 103..238
/gene="ZNF649-AS1"
/inference="alignment:Splign:2.1.0"
variation 108
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1013323595"
variation 114
/gene="ZNF649-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2122764858"
variation 117
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427335087"
variation 118..121
/gene="ZNF649-AS1"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1267126338"
variation 122
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568456120"
variation 124
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:868173169"
variation 131
/gene="ZNF649-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2085061224"
variation 132..140
/gene="ZNF649-AS1"
/replace="gaagaa"
/replace="gaagaagaa"
/db_xref="dbSNP:752783031"
variation 132
/gene="ZNF649-AS1"
/replace=""
/replace="g"
/db_xref="dbSNP:2085061242"
variation 134..136
/gene="ZNF649-AS1"
/replace="a"
/replace="aga"
/db_xref="dbSNP:2085061283"
variation 135
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2085061301"
variation 139
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242341734"
variation 140
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2122764905"
variation 144
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2085061341"
variation 147
/gene="ZNF649-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1201525180"
variation 150
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:570992247"
variation 153..156
/gene="ZNF649-AS1"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:2085061398"
variation 164..171
/gene="ZNF649-AS1"
/replace="aagaa"
/replace="aagaagaa"
/db_xref="dbSNP:1717301510"
variation 169
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:148926580"
variation 176
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1159148551"
variation 182
/gene="ZNF649-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2085061458"
variation 186
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:969076783"
variation 190
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2085061490"
variation 194
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:767697292"
variation 196..203
/gene="ZNF649-AS1"
/replace="aagaa"
/replace="aagaagaa"
/db_xref="dbSNP:2085061561"
variation 196
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1248497963"
variation 197
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1032559144"
variation 200
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:956859346"
variation 201..208
/gene="ZNF649-AS1"
/replace="gaa"
/replace="gaaatgaa"
/db_xref="dbSNP:766090643"
variation 201
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1394647033"
variation 208
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1399259416"
variation 209
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2085061672"
variation 211
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:931052386"
variation 213
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2085061713"
variation 214
/gene="ZNF649-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:557115401"
variation 218
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2085061756"
variation 222
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2085061769"
variation 227
/gene="ZNF649-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1299183865"
variation 233..235
/gene="ZNF649-AS1"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2085061805"
variation 234..236
/gene="ZNF649-AS1"
/replace="aag"
/replace="aagaag"
/db_xref="dbSNP:2085061821"
variation 238
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1461063721"
exon 239..580
/gene="ZNF649-AS1"
/inference="alignment:Splign:2.1.0"
variation 239
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:543216153"
variation 246
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2085086699"
variation 247
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2085086719"
variation 248
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:754109950"
variation 249
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2085086755"
variation 254
/gene="ZNF649-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2085086767"
variation 255
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:762186189"
variation 256
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1055084853"
variation 258
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199959359"
variation 264
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:114365071"
variation 265
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:758435751"
variation 271
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:766295631"
variation 276
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2085086935"
variation 277
/gene="ZNF649-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2085086954"
variation 286
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:540901521"
variation 288..290
/gene="ZNF649-AS1"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:991238332"
variation 288
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1254895491"
variation 294..296
/gene="ZNF649-AS1"
/replace=""
/replace="att"
/db_xref="dbSNP:2085087017"
variation 298
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1206403134"
variation 299
/gene="ZNF649-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2122771397"
variation 301
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:886163248"
variation 304
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1194677208"
variation 310
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2085087084"
variation 311
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:769694266"
variation 315..318
/gene="ZNF649-AS1"
/replace="tc"
/replace="tctc"
/db_xref="dbSNP:1194064009"
variation 317
/gene="ZNF649-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2085087137"
variation 322
/gene="ZNF649-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1358380465"
variation 328
/gene="ZNF649-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:559578602"
variation 329
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568457111"
variation 330
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1018988495"
variation 333
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2085087200"
variation 335
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:773346258"
variation 340..346
/gene="ZNF649-AS1"
/replace="atga"
/replace="atgatga"
/db_xref="dbSNP:2122771466"
variation 340
/gene="ZNF649-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1291705223"
variation 341
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444602765"
variation 342
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2085087251"
variation 344
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1438893950"
variation 352
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2085087286"
variation 353
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2085087300"
variation 357
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328597512"
variation 363..364
/gene="ZNF649-AS1"
/replace="c"
/replace="cc"
/db_xref="dbSNP:574837286"
variation 365
/gene="ZNF649-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:527721875"
variation 373
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1165037507"
variation 374
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2085087393"
variation 378
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1475109742"
variation 379
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1549931"
variation 380
/gene="ZNF649-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1414983439"
variation 387
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1178626272"
variation 388
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1420234846"
variation 392
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232161381"
variation 399
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2085087556"
variation 403
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1474559418"
variation 404
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:975396031"
variation 414
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1033245345"
variation 416
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2085087627"
variation 423
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1420384662"
variation 433
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1599889541"
variation 438
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1411566456"
variation 447
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287791196"
variation 448
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:772046016"
variation 450
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:934970133"
variation 453
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1311033787"
variation 454
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:957520080"
variation 460
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2085087754"
variation 461
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122771607"
variation 462
/gene="ZNF649-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2085087774"
variation 463
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:988910061"
variation 466
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:775230053"
variation 472
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1314504286"
variation 479
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2085087851"
variation 487
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:890633163"
variation 496
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2085087885"
variation 498
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2085087903"
variation 504
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2085087917"
variation 505
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373867120"
variation 506
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:564467676"
variation 507
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2085087949"
variation 510..512
/gene="ZNF649-AS1"
/replace=""
/replace="ata"
/db_xref="dbSNP:761789466"
variation 523
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1270257838"
variation 525..527
/gene="ZNF649-AS1"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1340924962"
variation 534
/gene="ZNF649-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1440792227"
variation 538
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1007645035"
variation 548
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2085088055"
variation 553
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2085088074"
variation 557..559
/gene="ZNF649-AS1"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1160650743"
variation 558
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1400940434"
variation 559
/gene="ZNF649-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1406720551"
variation 560
/gene="ZNF649-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2085088154"
variation 563
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2085088172"
variation 564..567
/gene="ZNF649-AS1"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1156619334"
variation 566..572
/gene="ZNF649-AS1"
/replace="aaca"
/replace="aacaaca"
/db_xref="dbSNP:1455450390"
variation 568
/gene="ZNF649-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2085088232"
variation 573
/gene="ZNF649-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2085088247"
ORIGIN
gatgcaatatgtctgcgcccaggggacgcttgctgggagcagccattttcaaccctactgccgtagagcaggcggagtccctcttttcgcgccttaagacagaaacacaaaatgatcctctgacaagtgatgaagaagaatgggaagatgtgaaaatccaagcaagaagaacttaggggaagcaactcaacatctaagaagaaatgaatagggatcagttccaagaagagataaaggggaaatacccaagaactgggatgcttcgtctttggtttcttctggatcctccctaaattttggctaagaaatctgagtctccatttaagagtgttcccagaaatgatgacatccacatccaggaacctcctccttccttcatttgaactctcttgcttctggggagccaggacctatggagtaaaaatcaagttcatttggtgacacattccctccgggcccagatgctgtctctgctgctgtaaactctcctgcagtcaaggccaagcaatatatctaagcatccctttgtcaggtgtccccaagtctttacatcccagggcaataaaacaacactctgaat
//
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]