2024-03-29 14:26:46, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
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="t" /db_xref="dbSNP:751723166" variation 10 /gene="CCND2-AS1" /gene_synonym="CCND2-AS2" /replace="c" /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="c" /replace="g" /db_xref="dbSNP:762132499" variation 34 /gene="CCND2-AS1" /gene_synonym="CCND2-AS2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2120523172" variation 35 /gene="CCND2-AS1" /gene_synonym="CCND2-AS2" /replace="c" /replace="t" /db_xref="dbSNP:776929300" variation 40 /gene="CCND2-AS1" /gene_synonym="CCND2-AS2" /replace="a" /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 /gene="CCND2-AS1" /gene_synonym="CCND2-AS2" /replace="a" /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="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="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 66 /gene="CCND2-AS1" /gene_synonym="CCND2-AS2" /replace="c" /replace="t" /db_xref="dbSNP:2120523000" 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 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 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 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 97 /gene="CCND2-AS1" /gene_synonym="CCND2-AS2" /replace="a" /replace="t" /db_xref="dbSNP:748823991" 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 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" /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" /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" /db_xref="dbSNP:2120522696" variation 119 /gene="CCND2-AS1" /gene_synonym="CCND2-AS2" /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" exon 127..553 /gene="CCND2-AS1" /gene_synonym="CCND2-AS2" /inference="alignment:Splign:2.1.0" 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 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" /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 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 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="t" /db_xref="dbSNP:1274496462" variation 369 /gene="CCND2-AS1" /gene_synonym="CCND2-AS2" /replace="a" /replace="g" /db_xref="dbSNP:560645809" 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.
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