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Previous release (v1)
2025-10-29 01:22:30, GGRNA.v2 : RefSeq release 232 (Sep, 2025)
LOCUS NR_125790 553 bp RNA linear PRI 19-APR-2022
DEFINITION Homo sapiens CCND2 antisense RNA 1 (CCND2-AS1), transcript variant
3, long non-coding RNA.
ACCESSION NR_125790
VERSION NR_125790.1
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 553)
AUTHORS Xia E, Bhandari A, Shen Y, Zhou X, Sindan N, Xiang J, Guan Y, Yang
F and Wang O.
TITLE LncRNA CCND2-AS1 promotes proliferation, migration, and invasion in
papillary thyroid carcinoma
JOURNAL Biochem. Biophys. Res. Commun. 496 (2), 628-632 (2018)
PUBMED 29366479
REMARK GeneRIF: CCND2-AS1 expression was significantly over-expressed in
papillary thyroid carcinoma cell lines compared to normal thyroid
epithelial cells.
REFERENCE 2 (bases 1 to 553)
AUTHORS Zhang H, Wei DL, Wan L, Yan SF and Sun YH.
TITLE Highly expressed lncRNA CCND2-AS1 promotes glioma cell
proliferation through Wnt/beta-catenin signaling
JOURNAL Biochem. Biophys. Res. Commun. 482 (4), 1219-1225 (2017)
PUBMED 27923660
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AC006122.24.
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 :: BG413373.1, SRR5189667.319444.1
[ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA2142586, SAMEA2144120
[ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-126 AC006122.24 60049-60174
127-553 AC006122.24 87040-87466
FEATURES Location/Qualifiers
source 1..553
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="12"
/map="12p13.32"
gene 1..553
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/note="CCND2 antisense RNA 1"
/db_xref="GeneID:103752584"
/db_xref="HGNC:HGNC:49398"
ncRNA 1..553
/ncRNA_class="lncRNA"
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/product="CCND2 antisense RNA 1, transcript variant 3"
/db_xref="GeneID:103752584"
/db_xref="HGNC:HGNC:49398"
exon 1..126
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/inference="alignment:Splign:2.1.0"
variation 3
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1863871409"
variation 4
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2120523396"
variation 7
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751723166"
variation 10
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1863871296"
variation 11
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2120523372"
variation 13
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1055859383"
variation 16
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1487280180"
variation 17
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1345554353"
variation 18
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2120523318"
variation 19
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1591643892"
variation 20
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2120523300"
variation 22
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1233414806"
variation 24
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:766500677"
variation 25
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:763529306"
variation 26
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:867376054"
variation 27
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2120523230"
variation 28
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773652105"
variation 29
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:765770986"
variation 31
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2120523194"
variation 32
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:762132499"
variation 33
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2497486973"
variation 34
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2120523172"
variation 35
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:776929300"
variation 36
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2497486956"
variation 40
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:759699380"
variation 41
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2120523142"
variation 46..47
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2497486929"
variation 46
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1863870570"
variation 48
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2120523118"
variation 49
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1311963474"
variation 50
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2120523085"
variation 51
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2120523066"
variation 55
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2120523057"
variation 60
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1863870425"
variation 61
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:771743347"
variation 62
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2120523011"
variation 64
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2497486890"
variation 66
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2120523000"
variation 67
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2497486881"
variation 68
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2120522991"
variation 69
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2120522978"
variation 71
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2120522964"
variation 75
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2497486858"
variation 76
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:745455734"
variation 78
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2120522945"
variation 79
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2497486847"
variation 82
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200880354"
variation 84
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1863870231"
variation 86
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2497486823"
variation 94
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770403051"
variation 95
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1019910889"
variation 96
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2497486809"
variation 97
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748823991"
variation 98
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2497486795"
variation 99
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1189680723"
variation 100
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1591643857"
variation 101
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2497486780"
variation 102
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2120522831"
variation 103
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424514247"
variation 104
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2120522797"
variation 105
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2120522783"
variation 106
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:777614015"
variation 107
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2120522758"
variation 108
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2120522746"
variation 110
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2120522735"
variation 111
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441700094"
variation 114
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1863869849"
variation 118
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2120522696"
variation 119
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2120522686"
variation 121
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:756058431"
variation 123
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2120522661"
variation 124
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:878898553"
variation 126
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2497486693"
exon 127..553
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/inference="alignment:Splign:2.1.0"
variation 127
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2497445352"
variation 129
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1591636152"
variation 145
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1489896941"
variation 151
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1863491952"
variation 152
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:755432343"
variation 155
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201682435"
variation 166
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:190637705"
variation 168
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1863491799"
variation 173
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1863491775"
variation 174
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1863491745"
variation 180
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:745420148"
variation 181
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1863491668"
variation 188
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1309847955"
variation 192..193
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1375177872"
variation 193
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:780729624"
variation 194
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:148172200"
variation 200..201
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace=""
/replace="tg"
/db_xref="dbSNP:1168183694"
variation 200
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2120451275"
variation 208
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2120451262"
variation 209
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1032061937"
variation 211
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1863491381"
variation 218
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430319435"
variation 219
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2120451228"
variation 224
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:376312753"
variation 231
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:979597608"
variation 235
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:963666788"
variation 236..238
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="ccc"
/db_xref="dbSNP:1369775559"
variation 240
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:756913420"
variation 240
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2497445292"
variation 244
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1863491110"
variation 247
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1863491078"
variation 248
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1863491050"
variation 249
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:537996828"
variation 250
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1345531082"
variation 251
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1381600856"
variation 252
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1863490922"
variation 263
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1863490894"
variation 266
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1863490865"
variation 268
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1024416310"
variation 269
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:568904740"
variation 271
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:891575312"
variation 272
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1863490715"
variation 273
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1801488854"
variation 276
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:891074718"
variation 281
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1863490654"
variation 282
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2120451053"
variation 291
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1025587610"
variation 292
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:935826005"
variation 296
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:774926547"
variation 309
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1863490516"
variation 311
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1292621910"
variation 322
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1863490459"
variation 329
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1863490435"
variation 334
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:186263937"
variation 335
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473943837"
variation 338..340
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2497445203"
variation 341
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1253342354"
variation 345..351
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="tttttt"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:932576665"
variation 347
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:993988307"
variation 351
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203940541"
variation 352..354
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:976522818"
variation 352
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:921942706"
variation 359
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace=""
/replace="c"
/db_xref="dbSNP:1442408171"
variation 359
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2497445158"
variation 364..366
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="cac"
/db_xref="dbSNP:776088082"
variation 364
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:12318331"
variation 365
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037753934"
variation 366
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:942149934"
variation 367
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1863490011"
variation 368
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1274496462"
variation 369
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:560645809"
variation 370
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2497444985"
variation 375
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:183381060"
variation 376
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1863489872"
variation 384
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1287104330"
variation 386
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1863489811"
variation 391
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace=""
/replace="c"
/db_xref="dbSNP:1387044601"
variation 396
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1863489759"
variation 397
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1382647860"
variation 401
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1863489709"
variation 404
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1335858783"
variation 406
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1863489637"
variation 407
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1380247158"
variation 408
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:143750586"
variation 409
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1227954292"
variation 410
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353708742"
variation 412
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1315962282"
variation 415
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:564728997"
variation 419
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1290267864"
variation 420
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1027839491"
variation 421
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1863489297"
variation 423
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1349828797"
variation 426..429
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1486480550"
variation 427
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1863489228"
variation 428
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1863489190"
variation 430
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1863489132"
variation 433
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1863489112"
variation 439
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1203521960"
variation 441
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:918145635"
variation 447
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1591636091"
variation 448
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1591636088"
variation 451
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1863488982"
variation 455
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1241705576"
variation 457
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1296335457"
variation 463
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:988811244"
variation 464
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:970747168"
variation 466
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:935478063"
variation 467
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:569246364"
variation 470
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1863488729"
variation 478
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1863488690"
variation 479
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1364968945"
variation 481
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1863488610"
variation 483
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374291176"
variation 495
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:979201133"
variation 496
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2358723"
variation 497
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403691167"
variation 499
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1863488446"
variation 506
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1565423571"
variation 507
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1454360538"
variation 508
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1863488331"
variation 514..515
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace=""
/replace="a"
/db_xref="dbSNP:34898844"
variation 514
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1863488302"
variation 520
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:575450020"
variation 523
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1863488210"
variation 525
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:891506445"
variation 529
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1350188089"
variation 532..539
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="taaa"
/replace="taaataaa"
/db_xref="dbSNP:547336966"
variation 536
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2120450415"
variation 540
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1565423567"
variation 541
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1863488030"
variation 543
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1389819681"
variation 545
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:191552531"
variation 548
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1863487917"
variation 551
/gene="CCND2-AS1"
/gene_synonym="CCND2-AS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1863487883"
ORIGIN
aatgcacagcttctccgcggtcagcgggctggtctctttgagtttggaggccaggaacatgcagacagcacccaggagttgcagatgggacttcggagtcgggaccccagccaagaaacggtccagaagaatctaccataaaaccaacagactcctcctgatctctacctgtgctgtctgcctctctagttccggacactgagagctggtgccctgtggccacctcaagctggaaccctgcaagatcaccaagaagactgcatgcctcgctctagccttcctaagggaaagtagactcctgtttttgagagaaattacctgatttcaagagaaacataaaggactttttttcccttaacattccactcgtaaaaatgaagtttggaagaacttctgcaaactctgagtgttttggtcaattgaccttttactgtactaagcaaatctgaagccacaaatacattggggaggaaggtatacccttcacaaaagatccgtcacttagccagatactctgttgccatgcttctttaaataaagcacatttctggta
//
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]