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Previous release (v1)
2024-04-28 14:23:21, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_110884 545 bp RNA linear PRI 27-APR-2021
DEFINITION Homo sapiens ZNF652 antisense RNA 1 (ZNF652-AS1), transcript
variant 3, long non-coding RNA.
ACCESSION NR_110884 XR_424845 XR_429993 XR_433413
VERSION NR_110884.1
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 545)
AUTHORS Coviello AD, Haring R, Wellons M, Vaidya D, Lehtimaki T, Keildson
S, Lunetta KL, He C, Fornage M, Lagou V, Mangino M, Onland-Moret
NC, Chen B, Eriksson J, Garcia M, Liu YM, Koster A, Lohman K,
Lyytikainen LP, Petersen AK, Prescott J, Stolk L, Vandenput L, Wood
AR, Zhuang WV, Ruokonen A, Hartikainen AL, Pouta A, Bandinelli S,
Biffar R, Brabant G, Cox DG, Chen Y, Cummings S, Ferrucci L, Gunter
MJ, Hankinson SE, Martikainen H, Hofman A, Homuth G, Illig T,
Jansson JO, Johnson AD, Karasik D, Karlsson M, Kettunen J, Kiel DP,
Kraft P, Liu J, Ljunggren O, Lorentzon M, Maggio M, Markus MR,
Mellstrom D, Miljkovic I, Mirel D, Nelson S, Morin Papunen L,
Peeters PH, Prokopenko I, Raffel L, Reincke M, Reiner AP, Rexrode
K, Rivadeneira F, Schwartz SM, Siscovick D, Soranzo N, Stockl D,
Tworoger S, Uitterlinden AG, van Gils CH, Vasan RS, Wichmann HE,
Zhai G, Bhasin S, Bidlingmaier M, Chanock SJ, De Vivo I, Harris TB,
Hunter DJ, Kahonen M, Liu S, Ouyang P, Spector TD, van der Schouw
YT, Viikari J, Wallaschofski H, McCarthy MI, Frayling TM, Murray A,
Franks S, Jarvelin MR, de Jong FH, Raitakari O, Teumer A, Ohlsson
C, Murabito JM and Perry JR.
TITLE A genome-wide association meta-analysis of circulating sex
hormone-binding globulin reveals multiple Loci implicated in sex
steroid hormone regulation
JOURNAL PLoS Genet 8 (7), e1002805 (2012)
PUBMED 22829776
REFERENCE 2 (bases 1 to 545)
AUTHORS Haiman CA, Chen GK, Blot WJ, Strom SS, Berndt SI, Kittles RA,
Rybicki BA, Isaacs WB, Ingles SA, Stanford JL, Diver WR, Witte JS,
Hsing AW, Nemesure B, Rebbeck TR, Cooney KA, Xu J, Kibel AS, Hu JJ,
John EM, Gueye SM, Watya S, Signorello LB, Hayes RB, Wang Z, Yeboah
E, Tettey Y, Cai Q, Kolb S, Ostrander EA, Zeigler-Johnson C,
Yamamura Y, Neslund-Dudas C, Haslag-Minoff J, Wu W, Thomas V, Allen
GO, Murphy A, Chang BL, Zheng SL, Leske MC, Wu SY, Ray AM, Hennis
AJ, Thun MJ, Carpten J, Casey G, Carter EN, Duarte ER, Xia LY,
Sheng X, Wan P, Pooler LC, Cheng I, Monroe KR, Schumacher F, Le
Marchand L, Kolonel LN, Chanock SJ, Van Den Berg D, Stram DO and
Henderson BE.
TITLE Genome-wide association study of prostate cancer in men of African
ancestry identifies a susceptibility locus at 17q21
JOURNAL Nat Genet 43 (6), 570-573 (2011)
PUBMED 21602798
REFERENCE 3 (bases 1 to 545)
AUTHORS Newton-Cheh C, Johnson T, Gateva V, Tobin MD, Bochud M, Coin L,
Najjar SS, Zhao JH, Heath SC, Eyheramendy S, Papadakis K, Voight
BF, Scott LJ, Zhang F, Farrall M, Tanaka T, Wallace C, Chambers JC,
Khaw KT, Nilsson P, van der Harst P, Polidoro S, Grobbee DE,
Onland-Moret NC, Bots ML, Wain LV, Elliott KS, Teumer A, Luan J,
Lucas G, Kuusisto J, Burton PR, Hadley D, McArdle WL, Brown M,
Dominiczak A, Newhouse SJ, Samani NJ, Webster J, Zeggini E,
Beckmann JS, Bergmann S, Lim N, Song K, Vollenweider P, Waeber G,
Waterworth DM, Yuan X, Groop L, Orho-Melander M, Allione A, Di
Gregorio A, Guarrera S, Panico S, Ricceri F, Romanazzi V, Sacerdote
C, Vineis P, Barroso I, Sandhu MS, Luben RN, Crawford GJ,
Jousilahti P, Perola M, Boehnke M, Bonnycastle LL, Collins FS,
Jackson AU, Mohlke KL, Stringham HM, Valle TT, Willer CJ, Bergman
RN, Morken MA, Doring A, Gieger C, Illig T, Meitinger T, Org E,
Pfeufer A, Wichmann HE, Kathiresan S, Marrugat J, O'Donnell CJ,
Schwartz SM, Siscovick DS, Subirana I, Freimer NB, Hartikainen AL,
McCarthy MI, O'Reilly PF, Peltonen L, Pouta A, de Jong PE, Snieder
H, van Gilst WH, Clarke R, Goel A, Hamsten A, Peden JF, Seedorf U,
Syvanen AC, Tognoni G, Lakatta EG, Sanna S, Scheet P, Schlessinger
D, Scuteri A, Dorr M, Ernst F, Felix SB, Homuth G, Lorbeer R,
Reffelmann T, Rettig R, Volker U, Galan P, Gut IG, Hercberg S,
Lathrop GM, Zelenika D, Deloukas P, Soranzo N, Williams FM, Zhai G,
Salomaa V, Laakso M, Elosua R, Forouhi NG, Volzke H, Uiterwaal CS,
van der Schouw YT, Numans ME, Matullo G, Navis G, Berglund G,
Bingham SA, Kooner JS, Connell JM, Bandinelli S, Ferrucci L,
Watkins H, Spector TD, Tuomilehto J, Altshuler D, Strachan DP, Laan
M, Meneton P, Wareham NJ, Uda M, Jarvelin MR, Mooser V, Melander O,
Loos RJ, Elliott P, Abecasis GR, Caulfield M and Munroe PB.
CONSRTM Wellcome Trust Case Control Consortium
TITLE Genome-wide association study identifies eight loci associated with
blood pressure
JOURNAL Nat Genet 41 (6), 666-676 (2009)
PUBMED 19430483
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
DA017831.1.
On or before Mar 1, 2014 this sequence version replaced
XR_429993.1, XR_424845.1, XR_433413.1.
Transcript Variant: This variant (3) uses an alternate 5' terminal
exon, resulting in a shorter transcript, compared to variant 1.
##Evidence-Data-START##
Transcript exon combination :: DA017831.1, SRR1803611.228159.1
[ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1968968, SAMEA2150385
[ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-545 DA017831.1 1-545
FEATURES Location/Qualifiers
source 1..545
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="17"
/map="17q21.33"
gene 1..545
/gene="ZNF652-AS1"
/note="ZNF652 antisense RNA 1"
/db_xref="GeneID:102724596"
/db_xref="HGNC:HGNC:55582"
ncRNA 1..545
/ncRNA_class="lncRNA"
/gene="ZNF652-AS1"
/product="ZNF652 antisense RNA 1, transcript variant 3"
/db_xref="GeneID:102724596"
/db_xref="HGNC:HGNC:55582"
exon 1..57
/gene="ZNF652-AS1"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:573378233"
variation 2
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070388414"
variation 8
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1480682763"
variation 10
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070388474"
variation 12
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1054890119"
variation 15
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:542260692"
variation 16
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070388568"
variation 17
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:916350332"
variation 25..29
/gene="ZNF652-AS1"
/replace="ag"
/replace="agaag"
/db_xref="dbSNP:1234176494"
variation 27
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070388687"
variation 30
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070388726"
variation 31
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201230370"
variation 32
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070388819"
variation 35
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070388858"
variation 36
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:761541421"
variation 41
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1263354121"
variation 43..44
/gene="ZNF652-AS1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2070388928"
variation 46
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2070388963"
variation 48
/gene="ZNF652-AS1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2070388989"
variation 49
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:991157492"
exon 58..128
/gene="ZNF652-AS1"
/inference="alignment:Splign:2.1.0"
variation 58
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2143187474"
variation 61
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279696726"
variation 63
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070431965"
variation 65
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1676505241"
variation 72
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070431985"
variation 73
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070432011"
variation 79
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1597809534"
variation 81
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070432054"
variation 82
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211909554"
variation 84
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070432093"
variation 89
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070432119"
variation 94
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070432137"
variation 95
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:62076449"
variation 96
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:751691029"
variation 97
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035667021"
variation 101
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1374703565"
variation 104
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070432281"
variation 117
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070432302"
variation 118..119
/gene="ZNF652-AS1"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2070432343"
variation 118
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070432326"
variation 121
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:956101436"
variation 122
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281725470"
variation 123
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1010280011"
variation 127
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070432434"
exon 129..545
/gene="ZNF652-AS1"
/inference="alignment:Splign:2.1.0"
variation 133
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:905466009"
variation 136
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070440446"
variation 146
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:978219459"
variation 150
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1284462241"
variation 153
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070440518"
variation 157
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205488458"
variation 158
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1343792582"
variation 159
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1336215255"
variation 164
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232176024"
variation 171
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070440602"
variation 173
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2143190692"
variation 176
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070440615"
variation 179
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070440633"
variation 182
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070440652"
variation 186
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331626200"
variation 187
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070440692"
variation 188
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070440709"
variation 191
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1303394561"
variation 193
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1001594035"
variation 194
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348754881"
variation 198
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:957797532"
variation 200
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070440796"
variation 202
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070440811"
variation 203
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1033988919"
variation 215
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:974404808"
variation 221
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070440867"
variation 222
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:921633552"
variation 223
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:933519301"
variation 224
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:987758280"
variation 226
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070440939"
variation 229
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070440956"
variation 233
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378566373"
variation 239
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:959758613"
variation 244
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:879703397"
variation 245
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250454146"
variation 246..247
/gene="ZNF652-AS1"
/replace=""
/replace="a"
/db_xref="dbSNP:35862262"
variation 246
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070441104"
variation 249
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1182219509"
variation 250
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070441148"
variation 252
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1597810001"
variation 254
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2143190894"
variation 255..257
/gene="ZNF652-AS1"
/replace="tgt"
/replace="tgtgt"
/db_xref="dbSNP:2070441184"
variation 260
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2143190905"
variation 270
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1257183509"
variation 271
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2143190922"
variation 276
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:908006715"
variation 281..283
/gene="ZNF652-AS1"
/replace=""
/replace="cca"
/db_xref="dbSNP:1197510371"
variation 283..284
/gene="ZNF652-AS1"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2070441268"
variation 286
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1276373279"
variation 288
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199516656"
variation 290
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1345534493"
variation 294
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1440813987"
variation 296
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2070441360"
variation 297
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1209479896"
variation 298
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070441402"
variation 307
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1013958666"
variation 311..319
/gene="ZNF652-AS1"
/replace="agagggctg"
/replace="agagggctgagagggctg"
/db_xref="dbSNP:2070441456"
variation 311
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441443"
variation 315
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258556996"
variation 316
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:940855518"
variation 319..320
/gene="ZNF652-AS1"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:2070441509"
variation 320
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441529"
variation 321
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1287847648"
variation 326
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2143191021"
variation 330
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1410447647"
variation 337
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441572"
variation 341
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441589"
variation 345
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441603"
variation 348
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1020039862"
variation 351
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1332515730"
variation 354
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441645"
variation 356
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1191696486"
variation 362
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441688"
variation 370
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395634477"
variation 374
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070441709"
variation 375
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:967607281"
variation 377
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1478324545"
variation 379
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2143191129"
variation 380
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:755422394"
variation 384
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441803"
variation 386
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1304907500"
variation 387
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1456141120"
variation 388
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:978643313"
variation 389
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070441871"
variation 392
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:899250740"
variation 394
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1159278090"
variation 395
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070441920"
variation 399
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070441939"
variation 401
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473321378"
variation 406
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415014465"
variation 411
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070441995"
variation 414
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186450846"
variation 416
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:937459472"
variation 422..427
/gene="ZNF652-AS1"
/replace="gtc"
/replace="gtcgtc"
/db_xref="dbSNP:2070442045"
variation 424
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:9903556"
variation 425
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:530454855"
variation 441
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070442144"
variation 444
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1836749782"
variation 446
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:766612819"
variation 447..451
/gene="ZNF652-AS1"
/replace="tagtt"
/replace="tagttagtt"
/db_xref="dbSNP:2070442186"
variation 448
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1268753848"
variation 455
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1413456203"
variation 456
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070442245"
variation 457
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1597810054"
variation 461
/gene="ZNF652-AS1"
/replace=""
/replace="c"
/db_xref="dbSNP:2070442304"
variation 461
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070442286"
variation 462..465
/gene="ZNF652-AS1"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:2070442334"
variation 462
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070442318"
variation 467
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2143191377"
variation 474
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070442349"
variation 478
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070442366"
variation 480
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230144193"
variation 481
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1334228746"
variation 486
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070442412"
variation 487..488
/gene="ZNF652-AS1"
/replace=""
/replace="tg"
/db_xref="dbSNP:2070442432"
variation 488
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2070442442"
variation 494
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070442454"
variation 496
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1282475193"
variation 497
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244359600"
variation 500
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070442485"
variation 502
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:975390511"
variation 504..517
/gene="ZNF652-AS1"
/replace="tttt"
/replace="ttttttcttttttt"
/db_xref="dbSNP:2070442561"
variation 504
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070442541"
variation 510
/gene="ZNF652-AS1"
/replace=""
/replace="c"
/db_xref="dbSNP:2070442596"
variation 510
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070442584"
variation 511..517
/gene="ZNF652-AS1"
/replace="tttttt"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:1024907772"
variation 516
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:550550265"
variation 517
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:77101414"
variation 518
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070442678"
variation 519
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070442693"
variation 520..521
/gene="ZNF652-AS1"
/replace=""
/replace="ttttt"
/db_xref="dbSNP:76269324"
variation 520
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:539705846"
variation 521..523
/gene="ZNF652-AS1"
/replace="gtt"
/replace="gttgtt"
/replace="gttgtttttgtt"
/db_xref="dbSNP:2070442757"
variation 521
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1459258844"
variation 523..524
/gene="ZNF652-AS1"
/replace=""
/replace="g"
/db_xref="dbSNP:2070442782"
variation 524
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:79645723"
variation 525..527
/gene="ZNF652-AS1"
/replace="ttg"
/replace="ttgctgttg"
/db_xref="dbSNP:2143191600"
variation 525
/gene="ZNF652-AS1"
/replace="t"
/replace="tgt"
/replace="tgttgt"
/db_xref="dbSNP:2070442820"
variation 526..530
/gene="ZNF652-AS1"
/replace="tgttg"
/replace="tgttgctgttg"
/db_xref="dbSNP:1467045457"
variation 527
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070442930"
variation 528..532
/gene="ZNF652-AS1"
/replace="ttgtt"
/replace="ttgttttgtt"
/db_xref="dbSNP:2143191657"
variation 528
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:879034747"
variation 532..536
/gene="ZNF652-AS1"
/replace="tgttg"
/replace="tgttgctgttg"
/db_xref="dbSNP:1287850207"
variation 534..538
/gene="ZNF652-AS1"
/replace="ttgtt"
/replace="ttgttattgtt"
/db_xref="dbSNP:1340933321"
variation 537..541
/gene="ZNF652-AS1"
/replace="ttgtt"
/replace="ttgtttttgtt"
/db_xref="dbSNP:2070442970"
variation 539..545
/gene="ZNF652-AS1"
/replace=""
/replace="gttgttg"
/db_xref="dbSNP:2070443004"
variation 539
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070442991"
variation 540..544
/gene="ZNF652-AS1"
/replace="ttgtt"
/replace="ttgttattgtt"
/db_xref="dbSNP:2070443016"
variation 542..545
/gene="ZNF652-AS1"
/replace=""
/replace="gttg"
/db_xref="dbSNP:1357336412"
variation 542
/gene="ZNF652-AS1"
/replace=""
/replace="g"
/db_xref="dbSNP:1229298248"
variation 543
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2070443055"
variation 545
/gene="ZNF652-AS1"
/replace=""
/replace="g"
/db_xref="dbSNP:374051404"
variation 545
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:144621505"
ORIGIN
gtgatcaaagctggaccttttcagagaaggtctcgaatcctgaagacagacttcgaggggatgatgcagcaagaagacccacaccagatgagggcgccttgatattggatttcccagcctccagaactaagcctgggacttgcctctgtgatctggtgctttggagggccttgggcctcagggctagcaaggtccctttctggagattccagttcctctgcccgccctcctttacctctttctcctcacacatctgtctgagggatggggatgagggctgccaaccaatgttaccacttgacagaccacaagagggctggttccagtgcctcccttgttcagctgctgacactgcagcttggcagtcattgaaggcaatatttagctcctacatctgacctgattggaagatcaggcttctgtcgtcctggtttcctggccttggatagttcttcactaacttttattcattaaggcagtgggcagaaagcagcagaaccctgttttttctttttttggggtttttgttgttgttgttgttgttg
//
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]