2024-04-28 12:39:03, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_133932 602 bp RNA linear PRI 11-SEP-2020 DEFINITION Homo sapiens TMEM139 antisense RNA 1 (TMEM139-AS1), long non-coding RNA. ACCESSION NR_133932 XR_928069 XR_956257 VERSION NR_133932.1 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 602) AUTHORS Kimura K, Wakamatsu A, Suzuki Y, Ota T, Nishikawa T, Yamashita R, Yamamoto J, Sekine M, Tsuritani K, Wakaguri H, Ishii S, Sugiyama T, Saito K, Isono Y, Irie R, Kushida N, Yoneyama T, Otsuka R, Kanda K, Yokoi T, Kondo H, Wagatsuma M, Murakawa K, Ishida S, Ishibashi T, Takahashi-Fujii A, Tanase T, Nagai K, Kikuchi H, Nakai K, Isogai T and Sugano S. TITLE Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes JOURNAL Genome Res. 16 (1), 55-65 (2006) PUBMED 16344560 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from DB173620.1 and DA339204.1. On or before Dec 11, 2015 this sequence version replaced XR_928069.1, XR_956257.1. ##Evidence-Data-START## Transcript exon combination :: DA339204.1, DB173620.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1968968, SAMEA2145743 [ECO:0000348] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-26 DB173620.1 3-28 27-602 DA339204.1 1-576 FEATURES Location/Qualifiers source 1..602 /organism="Homo sapiens" /mol_type="transcribed RNA" /db_xref="taxon:9606" /chromosome="7" /map="7q34" gene 1..602 /gene="TMEM139-AS1" /note="TMEM139 antisense RNA 1" /db_xref="GeneID:105375545" /db_xref="HGNC:HGNC:40988" ncRNA 1..602 /ncRNA_class="lncRNA" /gene="TMEM139-AS1" /product="TMEM139 antisense RNA 1" /db_xref="GeneID:105375545" /db_xref="HGNC:HGNC:40988" exon 1..358 /gene="TMEM139-AS1" /inference="alignment:Splign:2.1.0" variation 5 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:1801304206" variation 7 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1455486208" variation 9 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:1801303833" variation 13..16 /gene="TMEM139-AS1" /replace="ccc" /replace="cccc" /db_xref="dbSNP:2116736489" variation 13 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:2116736512" variation 16 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1801303642" variation 18 /gene="TMEM139-AS1" /replace="c" /replace="g" /db_xref="dbSNP:910450675" variation 23 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:575917301" variation 24 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:986101673" variation 29 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:189768168" variation 31 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1801302843" variation 34 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1030296076" variation 38 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:993475172" variation 41 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801301954" variation 48 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1299572014" variation 50 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801301407" variation 52..57 /gene="TMEM139-AS1" /replace="ctct" /replace="ctctct" /db_xref="dbSNP:1801300100" variation 52 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1801301132" variation 53 /gene="TMEM139-AS1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1586441178" variation 54 /gene="TMEM139-AS1" /replace="c" /replace="g" /db_xref="dbSNP:1319112282" variation 56 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:2116736197" variation 58 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1240695760" variation 59 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1801299580" variation 61 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:1801299433" variation 62 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1260971797" variation 64 /gene="TMEM139-AS1" /replace="c" /replace="g" /db_xref="dbSNP:962080797" variation 73 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:1206329886" variation 74 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801298927" variation 81 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:185502601" variation 82 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:772100190" variation 85 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:749280980" variation 86 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:780315841" variation 87 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:2116735957" variation 88 /gene="TMEM139-AS1" /replace="a" /replace="t" /db_xref="dbSNP:1801298022" variation 91 /gene="TMEM139-AS1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:113745741" variation 93 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:754497885" variation 99 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:756340162" variation 100 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1368749609" variation 105 /gene="TMEM139-AS1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:955634668" variation 107 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1431078847" variation 108 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1264917759" variation 111 /gene="TMEM139-AS1" /replace="a" /replace="aa" /db_xref="dbSNP:1182737658" variation 111 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:201211574" variation 112 /gene="TMEM139-AS1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:554399738" variation 113 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1259534084" variation 115 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:757558709" variation 116 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1174310964" variation 117..119 /gene="TMEM139-AS1" /replace="cc" /replace="ccc" /db_xref="dbSNP:1433133384" variation 117 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1801295083" variation 118 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:752003889" variation 119 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:764459504" variation 120 /gene="TMEM139-AS1" /replace="a" /replace="t" /db_xref="dbSNP:758973964" variation 121..123 /gene="TMEM139-AS1" /replace="cc" /replace="ccc" /db_xref="dbSNP:1801293781" variation 121 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:752134733" variation 122 /gene="TMEM139-AS1" /replace="c" /replace="g" /db_xref="dbSNP:764737512" variation 124 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:1801293634" variation 127 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1224545048" variation 132 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:759102304" variation 133 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:146790657" variation 134 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:201395654" variation 135 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:372836265" variation 136 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:773085821" variation 138 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1182526563" variation 142 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1801292192" variation 143 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:573205507" variation 148 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:1563055266" variation 150 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1586440626" variation 151 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:771866608" variation 153 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:748124760" variation 155 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1177469185" variation 159 /gene="TMEM139-AS1" /replace="c" /replace="g" /db_xref="dbSNP:775655032" variation 160 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:1226022188" variation 162 /gene="TMEM139-AS1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:769982248" variation 163 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1022629796" variation 166 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:1172443698" variation 169 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:746012011" variation 174 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:781534226" variation 178 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:757520950" variation 179 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:747294170" variation 180 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:2116735061" variation 181 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:562740614" variation 186 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:1212944507" variation 187 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:758770757" variation 188 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:568548190" variation 191 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801288404" variation 193 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:754449756" variation 195 /gene="TMEM139-AS1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:765903986" variation 197 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801287682" variation 198 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:760409081" variation 201 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1250075701" variation 202 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801287094" variation 206 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:772819941" variation 207 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:767360375" variation 208 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:761760839" variation 209 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:143413842" variation 213 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1391107352" variation 215 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:774426300" variation 223 /gene="TMEM139-AS1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1169445191" variation 225 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:1462392981" variation 229..237 /gene="TMEM139-AS1" /replace="aagaag" /replace="aagaagaag" /db_xref="dbSNP:756241602" variation 231 /gene="TMEM139-AS1" /replace="c" /replace="g" /db_xref="dbSNP:768755912" variation 233 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801285168" variation 235 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:138052864" variation 236 /gene="TMEM139-AS1" /replace="a" /replace="t" /db_xref="dbSNP:776803380" variation 239 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1801284486" variation 241 /gene="TMEM139-AS1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1385387897" variation 242 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1348768392" variation 244 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801283837" variation 245 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:770989765" variation 247 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:556354422" variation 250..258 /gene="TMEM139-AS1" /replace="agaaa" /replace="agaaagaaa" /db_xref="dbSNP:750635612" variation 256 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:538352460" variation 261 /gene="TMEM139-AS1" /replace="a" /replace="t" /db_xref="dbSNP:570716990" variation 262 /gene="TMEM139-AS1" /replace="c" /replace="g" /db_xref="dbSNP:1309253564" variation 263 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:946802603" variation 265 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:772477803" variation 266 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:748548549" variation 267 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:954620689" variation 268 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801280465" variation 269 /gene="TMEM139-AS1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:779366702" variation 270 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1416365836" variation 271 /gene="TMEM139-AS1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1315827627" variation 273 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1238529182" variation 276 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:552547079" variation 278 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:144836832" variation 279 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:371442140" variation 280 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:368800303" variation 283 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:142807595" variation 284 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:1426476391" variation 289..291 /gene="TMEM139-AS1" /replace="cc" /replace="ccc" /db_xref="dbSNP:767655806" variation 289 /gene="TMEM139-AS1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:559802428" variation 290 /gene="TMEM139-AS1" /replace="c" /replace="g" /db_xref="dbSNP:751450443" variation 291 /gene="TMEM139-AS1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:764082489" variation 292..315 /gene="TMEM139-AS1" /replace="ag" /replace="agcaaagccagccccagtaggaag" /db_xref="dbSNP:762035470" variation 292 /gene="TMEM139-AS1" /replace="a" /replace="t" /db_xref="dbSNP:762988837" variation 298 /gene="TMEM139-AS1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:529082006" variation 299 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1360082241" variation 300 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1436991801" variation 303 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:375464913" variation 305 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1801274993" variation 306 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1563054877" variation 309 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:760730072" variation 310..317 /gene="TMEM139-AS1" /replace="aggaagga" /replace="aggaaggaagga" /db_xref="dbSNP:1446647920" variation 315 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1179273664" variation 316 /gene="TMEM139-AS1" /replace="c" /replace="g" /db_xref="dbSNP:1801274238" variation 318 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1220819427" variation 320 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:202131612" variation 321 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:772325965" variation 323 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801273516" variation 325 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1801273356" variation 329 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:2116733681" variation 332 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1563054833" variation 334 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801272972" variation 335 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1204666543" variation 339 /gene="TMEM139-AS1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:748466860" variation 340 /gene="TMEM139-AS1" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1296816028" variation 345 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1281470821" variation 347 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1240109086" variation 352 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:2116733539" variation 354..357 /gene="TMEM139-AS1" /replace="ccc" /replace="cccc" /db_xref="dbSNP:1801271676" variation 358 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:1586439652" exon 359..479 /gene="TMEM139-AS1" /inference="alignment:Splign:2.1.0" variation 359 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801262265" variation 365 /gene="TMEM139-AS1" /replace="c" /replace="g" /db_xref="dbSNP:1194817741" variation 366 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:1246450255" variation 367 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:543114986" variation 369 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1801260918" variation 370 /gene="TMEM139-AS1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1186998899" variation 372..379 /gene="TMEM139-AS1" /replace="aaat" /replace="aaataaat" /db_xref="dbSNP:1801260090" variation 373 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1586439119" variation 374 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:888875160" variation 375 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:1485858729" variation 383 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:1801259940" variation 385 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:183233212" variation 390 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801259579" variation 391 /gene="TMEM139-AS1" /replace="" /replace="t" /db_xref="dbSNP:933174639" variation 392 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1801259264" variation 396 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:2116732390" variation 399 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801259108" variation 404 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1013898853" variation 405 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801258442" variation 408 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:971992073" variation 413..414 /gene="TMEM139-AS1" /replace="" /replace="a" /db_xref="dbSNP:1443617453" variation 413 /gene="TMEM139-AS1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1210255503" variation 416..418 /gene="TMEM139-AS1" /replace="t" /replace="tat" /db_xref="dbSNP:1801257439" variation 417 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:543888880" variation 421 /gene="TMEM139-AS1" /replace="c" /replace="g" /db_xref="dbSNP:1801257297" variation 423 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:2116732252" variation 428 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1031555206" variation 429 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801257012" variation 431 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:1586438988" variation 433..446 /gene="TMEM139-AS1" /replace="ggaa" /replace="ggaatagccaggaa" /db_xref="dbSNP:1801256565" variation 444 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1586438980" variation 449 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:999183251" variation 452 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1434089925" variation 455 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801256126" variation 456 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1801255948" variation 459 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1233150816" variation 465 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:1586438949" variation 467 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1586438941" variation 468 /gene="TMEM139-AS1" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1801255315" variation 473 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1342364428" exon 480..602 /gene="TMEM139-AS1" /inference="alignment:Splign:2.1.0" variation 483 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:897135530" variation 486 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:1800625241" variation 495 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1800625203" variation 496 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1800625175" variation 497 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1038790835" variation 500 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:1408780924" variation 508 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1800625076" variation 509 /gene="TMEM139-AS1" /replace="a" /replace="t" /db_xref="dbSNP:1800625041" variation 511 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1182383764" variation 512 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:941400547" variation 513 /gene="TMEM139-AS1" /replace="c" /replace="g" /db_xref="dbSNP:1800624933" variation 518 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1586416868" variation 520 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:906091349" variation 521 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1474179991" variation 526 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:994902394" variation 527 /gene="TMEM139-AS1" /replace="c" /replace="g" /db_xref="dbSNP:1400727483" variation 530 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:1044691042" variation 541 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1335065975" variation 544 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1800624686" variation 547 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:899336855" variation 550 /gene="TMEM139-AS1" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:950211293" variation 551 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1044529354" variation 554 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1800624381" variation 555 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:576383992" variation 557 /gene="TMEM139-AS1" /replace="" /replace="g" /db_xref="dbSNP:749489765" variation 562..566 /gene="TMEM139-AS1" /replace="tct" /replace="tctct" /db_xref="dbSNP:1800623797" variation 562 /gene="TMEM139-AS1" /replace="a" /replace="t" /db_xref="dbSNP:752507881" variation 563 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:139541615" variation 564 /gene="TMEM139-AS1" /replace="g" /replace="t" /db_xref="dbSNP:1800623832" variation 569 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:934427263" variation 571 /gene="TMEM139-AS1" /replace="c" /replace="g" /db_xref="dbSNP:1192039476" variation 573 /gene="TMEM139-AS1" /replace="c" /replace="g" /db_xref="dbSNP:925610075" variation 581 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1423965085" variation 582 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1194905428" variation 584 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:1270367800" variation 586 /gene="TMEM139-AS1" /replace="a" /replace="c" /db_xref="dbSNP:150507582" variation 591 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1210284148" variation 592 /gene="TMEM139-AS1" /replace="t" /replace="tt" /db_xref="dbSNP:1800623247" variation 598 /gene="TMEM139-AS1" /replace="a" /replace="g" /db_xref="dbSNP:2116674982" variation 599 /gene="TMEM139-AS1" /replace="c" /replace="t" /db_xref="dbSNP:1800623200" ORIGIN
gttggcctctgacccctcctcccgctgatgccaatgacaggaaaccagagactctctgcctcagagactacagggagagagggaggatgggcccaaggtgtattcctcttacgatgcccacccttaactcaccgtgcattgcctgagggccctgggctctcagtctgcattgattggagctgggaccgaagcccccattccagaaaccggaccaggagataggcaaacaagaagaagccacccaatgtgagaaagaaataagcaacgggggtgatgtccgtctttatgcccagcaaagccagccccagtaggaaggaggcgcagcacaggaggagaagcggcttctccagtctccccagttcttcaatctcaaataaatcatctgtagagtcccctccagttccgaaattctctctatgtcttggagtgtgtggaatagccaggaaaccagcccaggagctttgactcccagccattctgcaccttaagcaaaaaggaagttagccacacatggtggctcatgactgtagtctcagctacatgggaggcaaggcgagaggatctcttgagcccaggagttcgaggccagcctaggcaatgta
//
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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