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Previous release (v1)
2024-04-19 11:29:27, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_110883 558 bp RNA linear PRI 19-APR-2022
DEFINITION Homo sapiens ZNF652 antisense RNA 1 (ZNF652-AS1), transcript
variant 2, long non-coding RNA.
ACCESSION NR_110883
VERSION NR_110883.1
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 558)
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 558)
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 558)
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
AC091180.20.
Transcript Variant: This variant (2) contains multiple differences
at both the 5' and 3' ends, resulting in a shorter transcript,
compared to variant 1.
Sequence Note: The RefSeq transcript was derived from the reference
genome assembly. The genomic coordinates were determined from
alignments.
##Evidence-Data-START##
Transcript exon combination :: SRR3476690.116507.1,
SRR1803617.421143.1 [ECO:0000332]
RNAseq introns :: mixed sample support SAMEA1965299,
SAMEA1966682 [ECO:0006172]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-30 AC091180.20 68456-68485
31-101 AC091180.20 71365-71435
102-243 AC091180.20 80099-80240
244-443 AC091180.20 82396-82595
444-558 AC091180.20 87066-87180
FEATURES Location/Qualifiers
source 1..558
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="17"
/map="17q21.33"
gene 1..558
/gene="ZNF652-AS1"
/note="ZNF652 antisense RNA 1"
/db_xref="GeneID:102724596"
/db_xref="HGNC:HGNC:55582"
ncRNA 1..558
/ncRNA_class="lncRNA"
/gene="ZNF652-AS1"
/product="ZNF652 antisense RNA 1, transcript variant 2"
/db_xref="GeneID:102724596"
/db_xref="HGNC:HGNC:55582"
exon 1..30
/gene="ZNF652-AS1"
/inference="alignment:Splign:2.1.0"
variation 2
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:962267370"
variation 5
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1289539433"
variation 6
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:973655301"
variation 7
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1026618302"
variation 11
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070391377"
variation 14
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:944569705"
variation 16
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1324956019"
variation 20
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070391495"
variation 21
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1598323829"
variation 26
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1036281686"
variation 28
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070391619"
variation 30
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1407086324"
exon 31..101
/gene="ZNF652-AS1"
/inference="alignment:Splign:2.1.0"
variation 31
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2143187474"
variation 34
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279696726"
variation 36
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070431965"
variation 38
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1676505241"
variation 45
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070431985"
variation 46
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070432011"
variation 52
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1597809534"
variation 54
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070432054"
variation 55
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211909554"
variation 57
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070432093"
variation 62
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070432119"
variation 67
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070432137"
variation 68
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:62076449"
variation 69
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:751691029"
variation 70
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035667021"
variation 74
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1374703565"
variation 77
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070432281"
variation 90
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070432302"
variation 91..92
/gene="ZNF652-AS1"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2070432343"
variation 91
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070432326"
variation 94
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:956101436"
variation 95
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281725470"
variation 96
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1010280011"
variation 100
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070432434"
exon 102..243
/gene="ZNF652-AS1"
/inference="alignment:Splign:2.1.0"
variation 103
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070481208"
variation 104
/gene="ZNF652-AS1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2070481225"
variation 106
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1479587457"
variation 109
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1597812522"
variation 114
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070481264"
variation 123
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:991575094"
variation 124
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:898121561"
variation 125
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:916981428"
variation 127
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:185097938"
variation 135
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416752310"
variation 137
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070481366"
variation 139
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1041521982"
variation 141
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:567027571"
variation 146
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:774940675"
variation 149
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:115087312"
variation 150
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1567708383"
variation 156
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070481455"
variation 157
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400484225"
variation 158
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:899762382"
variation 159
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070481506"
variation 162..173
/gene="ZNF652-AS1"
/replace="cc"
/replace="cctggacctccc"
/db_xref="dbSNP:2070481516"
variation 164
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1371191468"
variation 167
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:977445387"
variation 169
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1431701685"
variation 171
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070481580"
variation 173
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070481589"
variation 180
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1424723577"
variation 185
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1192199043"
variation 186
/gene="ZNF652-AS1"
/replace=""
/replace="t"
/db_xref="dbSNP:2070481625"
variation 187..191
/gene="ZNF652-AS1"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:2070481676"
variation 187
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070481667"
variation 191
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1567708389"
variation 193
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070481700"
variation 194
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070481713"
variation 202
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2070481729"
variation 203
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070481743"
variation 216
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:923844324"
variation 219
/gene="ZNF652-AS1"
/replace="t"
/replace="tt"
/db_xref="dbSNP:2070481784"
variation 220
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1597812556"
variation 221
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250257658"
variation 224
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070481830"
variation 226
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070481851"
variation 227
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1182023763"
variation 228
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:956655822"
variation 230
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:989677507"
variation 235
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070481912"
variation 237
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:996837243"
variation 238
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070481942"
variation 239
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1207404411"
variation 240
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1398905979"
exon 244..443
/gene="ZNF652-AS1"
/inference="alignment:Splign:2.1.0"
variation 244
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1220342051"
variation 245
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1359017298"
variation 247
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:537037455"
variation 248
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:193241928"
variation 250
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:887735815"
variation 251
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:760708141"
variation 254
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1003507903"
variation 255
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1181318931"
variation 258
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:558232916"
variation 259
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1470546014"
variation 268
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070494775"
variation 269
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:185362744"
variation 270..294
/gene="ZNF652-AS1"
/replace="a"
/replace="atctactctttgggagttctccaga"
/db_xref="dbSNP:2070494822"
variation 271
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070494837"
variation 272
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070494848"
variation 274
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2143208986"
variation 279
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070494858"
variation 280
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1300750031"
variation 281
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:905578207"
variation 290
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:989563494"
variation 292
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1388851952"
variation 293
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:570485283"
variation 296
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1035331155"
variation 297..302
/gene="ZNF652-AS1"
/replace="aaaaaa"
/replace="aaaaaaa"
/db_xref="dbSNP:2070494976"
variation 297
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:891436552"
variation 301
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:548903225"
variation 306
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:568790729"
variation 307
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070495026"
variation 311
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1288246693"
variation 312
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1490196857"
variation 323
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070495064"
variation 324
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022285641"
variation 327
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:969035838"
variation 333
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070495104"
variation 334
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1479773152"
variation 341
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:775682957"
variation 342
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1251173368"
variation 353
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:763067178"
variation 359
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070495178"
variation 360
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1228528263"
variation 366
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:147601241"
variation 367
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2070495249"
variation 368
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1281874759"
variation 372
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070495282"
variation 376
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070495296"
variation 379
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1018403597"
variation 381
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:965402107"
variation 386
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1828615878"
variation 391
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070495332"
variation 394
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:912107186"
variation 395
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070495369"
variation 396
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070495379"
variation 410
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:764438547"
variation 411
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:376487379"
variation 412
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355229366"
variation 413
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:972321191"
variation 418
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070495427"
variation 423
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2070495441"
variation 432
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2143209165"
variation 433
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:751868172"
variation 435
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:918702041"
variation 436
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:77764116"
variation 438
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1175673529"
variation 439
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1480711923"
variation 440
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:984179825"
variation 441
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:571326556"
exon 444..558
/gene="ZNF652-AS1"
/inference="alignment:Splign:2.1.0"
variation 452
/gene="ZNF652-AS1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2070516760"
variation 452
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070516749"
variation 457
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:916434831"
variation 458
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1221609604"
variation 460
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1441894391"
variation 466
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070516803"
variation 468
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1756004349"
variation 470
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1597814773"
variation 473
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:949266811"
variation 475
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070516838"
variation 478
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070516853"
variation 480
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070516871"
variation 485
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2143215738"
variation 486
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273265679"
variation 491
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223331905"
variation 494
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1305351447"
variation 495
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:531126807"
variation 497
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1214984246"
variation 498
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:183904679"
variation 500
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367062333"
variation 501
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070517085"
variation 510
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2070517097"
variation 515
/gene="ZNF652-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070517113"
variation 519
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070517127"
variation 521
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301227289"
variation 522
/gene="ZNF652-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2070517157"
variation 523
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2070517171"
variation 539
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070517187"
variation 541
/gene="ZNF652-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:961987981"
variation 542
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2070517210"
variation 544
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:981870849"
variation 548
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:973113925"
variation 549
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1027780304"
variation 552
/gene="ZNF652-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:958452501"
variation 555
/gene="ZNF652-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147788625"
variation 556
/gene="ZNF652-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:917085932"
ORIGIN
ggtggagaaaggtctgcattacccactggggggatgatgcagcaagaagacccacaccagatgagggcgccttgatattggatttcccagcctccagaactacagagtcttgctctgtcactcgggctggagtacagtgacacaatcacggttcactgcagcctggacctcccaggctcaagtgatccccctgctgcagcctcctgagtagctgggactacaggcctgtgccaccatgtccaggtccggtccactgctaggagatccatatctactctttgggagttctccagaggaaaaaatcaacaggcgggagaaagatactctgctagcttcagattcattagtactaggaaatggagagataggaggtataatgtattagggaagcaagggattcagaaccaggtgcccactgactctgagaagcactgggtgcacagagggtagcagacaagcaagagggtggaatttgcagcatctcatcttggtgagacagttggaagacttttctgccaattatagtggttaaacactgactcaacatcaaacaacggc
//
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]