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Previous release (v1)
2026-10-05 17:50:30, GGRNA.v2 : RefSeq release 233 (Jan, 2026)
LOCUS NR_131250 780 bp RNA linear PRI 19-APR-2022 DEFINITION Homo sapiens Rhox homeobox family member 1 pseudogene 1 (RHOXF1P1), non-coding RNA. ACCESSION NR_131250 VERSION NR_131250.1 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 780) AUTHORS Penkala I, Wang J, Syrett CM, Goetzl L, Lopez CB and Anguera MC. TITLE lncRHOXF1, a Long Noncoding RNA from the X Chromosome That Suppresses Viral Response Genes during Development of the Early Human Placenta JOURNAL Mol. Cell. Biol. 36 (12), 1764-1775 (2016) PUBMED 27066803 REMARK GeneRIF: Results show that lncRHOXF1 RNA is the first example of a lncRNA that regulates the host response to viral infections in human placental progenitor cells, suggesting that it functions as a repressor of the viral response during early human development. Publication Status: Online-Only COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AC240732.2. 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 :: BX331476.2, ERR3218373.241138.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA2145544, SAMEA2146411 [ECO:0000348] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-229 AC240732.2 121596-121824 230-563 AC240732.2 122033-122366 564-705 AC240732.2 123693-123834 706-780 AC240732.2 126356-126430 FEATURES Location/Qualifiers source 1..780 /organism="Homo sapiens" /mol_type="transcribed RNA" /db_xref="taxon:9606" /chromosome="X" /map="Xq24" gene 1..780 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /note="Rhox homeobox family member 1 pseudogene 1" /pseudo /db_xref="GeneID:101928941" /db_xref="HGNC:HGNC:51580" /db_xref="MIM:300973" misc_RNA 1..780 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /product="Rhox homeobox family member 1 pseudogene 1" /pseudo /db_xref="GeneID:101928941" /db_xref="HGNC:HGNC:51580" /db_xref="MIM:300973" exon 1..229 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /inference="alignment:Splign:2.1.0" /pseudo variation 1 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:1360648797" variation 2 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2521767954" variation 3 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1439965488" variation 5 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057029730" variation 6 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2521767934" variation 10 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="t" /db_xref="dbSNP:2521767926" variation 24 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:963838645" variation 25 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057029706" variation 27..29 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="ctc" /db_xref="dbSNP:1377006615" variation 34 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521767899" variation 35..38 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="ccc" /replace="cccc" /db_xref="dbSNP:2057029657" variation 35 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1018621810" variation 36 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2521767884" variation 38 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1005445807" variation 39 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="" /replace="t" /db_xref="dbSNP:1300611322" variation 40 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1343941027" variation 42 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:2521767856" variation 43 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1219416958" variation 44 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:1281227020" variation 46 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2057029586" variation 49 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:1555990806" variation 50 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2521767833" variation 52..54 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="ccc" /replace="cccc" /db_xref="dbSNP:2521767820" variation 52 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521767831" variation 53 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521767827" variation 54 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2057029560" variation 56 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="t" /db_xref="dbSNP:2057029547" variation 60 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:782356410" variation 63 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:782219502" variation 66 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057029519" variation 67 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057029505" variation 68 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1198604021" variation 70 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2521767792" variation 73 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1555990803" variation 74 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="t" /db_xref="dbSNP:1239249737" variation 75 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:782649874" variation 76 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1377132964" variation 81 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521767773" variation 87 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057029458" variation 88 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1478500740" variation 91 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1174488435" variation 92 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521767760" variation 93 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057029430" variation 94 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1427048889" variation 96 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:994123348" variation 97 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:2057029389" variation 100 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:2057029377" variation 107 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521767742" variation 108 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:895946692" variation 113 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2057029358" variation 115 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:1169896821" variation 117 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1057107926" variation 118 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1401015163" variation 121 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057029316" variation 125 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="t" /db_xref="dbSNP:782506662" variation 127 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1323358177" variation 130 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:2521767707" variation 132 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057029274" variation 134 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057029265" variation 135 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:2057029251" variation 143 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:2521767687" variation 144 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057029238" variation 147 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057029229" variation 148 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1329980742" variation 150 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1436776439" variation 162 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="t" /db_xref="dbSNP:2521767669" variation 164 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2521767667" variation 165 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:2057029213" variation 166 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:906015737" variation 171 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1555990786" variation 177 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="" /replace="c" /db_xref="dbSNP:2521767647" variation 179 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521767643" variation 180 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:1218342826" variation 181 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1259090689" variation 183 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:2521767637" variation 191 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2057029140" variation 199 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057029121" variation 200 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="t" /db_xref="dbSNP:2147872824" variation 203 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:16995714" variation 204 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2521767615" variation 207 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521767613" variation 210 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521767608" variation 213 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:1212327597" variation 214 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1266821235" variation 215 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:947691393" variation 218 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1452215545" variation 220 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521767601" variation 221..227 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="aaga" /replace="aagaaga" /db_xref="dbSNP:2521767586" variation 223 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1201290917" variation 225 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:2057029013" variation 226 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2521767591" variation 228 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1240519901" variation 229 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2057028992" exon 230..563 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /inference="alignment:Splign:2.1.0" /pseudo variation 232 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="gg" /db_xref="dbSNP:1358034417" variation 234 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521767288" variation 235 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521767284" variation 237..238 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="" /replace="ttc" /db_xref="dbSNP:2521767273" variation 237 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2521767279" variation 239 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057028459" variation 241 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1418760496" variation 243 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:994133156" variation 247 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1569302385" variation 251 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2057028423" variation 257 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2057028412" variation 258 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1298373316" variation 265 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:868988585" variation 269 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1394595950" variation 270..273 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="agac" /replace="agacagac" /db_xref="dbSNP:1312444814" variation 271 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057028386" variation 273 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2521767223" variation 276 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="t" /db_xref="dbSNP:2521767217" variation 279 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2521767212" variation 286 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:2521767206" variation 288 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:17327277" variation 289 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1035753498" variation 290 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521767186" variation 293 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1247587619" variation 298 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:2057028288" variation 299 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1307237960" variation 300 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1353017371" variation 303 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1217659142" variation 308 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1001595402" variation 312 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:2057028215" variation 313 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:905927803" variation 314 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057028197" variation 316 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521767148" variation 318 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057028182" variation 320 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2521767142" variation 330 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1198576466" variation 335 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:1255206284" variation 336 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1424366030" variation 339 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521767127" variation 340 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2057028122" variation 341 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521767113" variation 342 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521767108" variation 343 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1569302369" variation 344 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2057028101" variation 346 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2057028089" variation 347 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521767096" variation 349 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521767091" variation 350 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1189502599" variation 351 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521767081" variation 354..357 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="ccc" /replace="cccc" /db_xref="dbSNP:2521767078" variation 354 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1043263080" variation 355 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057028052" variation 359 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057028044" variation 362 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521767074" variation 363 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521767069" variation 366 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2057028032" variation 367 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1012155533" variation 373 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:781866558" variation 378 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1053330051" variation 379 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1464230654" variation 381 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521767052" variation 382 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:1302674806" variation 383 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057027994" variation 386 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1403331193" variation 387 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057027973" variation 390 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057027961" variation 393 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2057027955" variation 398 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="aa" /db_xref="dbSNP:34238633" variation 399 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:1398331201" variation 401 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:934998463" variation 402 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521767027" variation 405..415 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="gcagcagcagc" /replace="gcagcagcagcagc" /db_xref="dbSNP:1240891277" variation 405 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521767023" variation 407 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1376256393" variation 410 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:2521767018" variation 413 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="" /replace="a" /db_xref="dbSNP:2521767012" variation 413 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="t" /db_xref="dbSNP:2057027910" variation 416 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:900815231" variation 426 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:782757244" variation 427 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057027871" variation 428 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057027858" variation 434 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="t" /db_xref="dbSNP:2057027850" variation 435 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2521766990" variation 436 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="" /replace="t" /db_xref="dbSNP:1311537906" variation 440 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2521766981" variation 441 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:942456620" variation 442 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1310732196" variation 445 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057027832" variation 447 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:141922356" variation 448 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1848421995" variation 452 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1255240794" variation 454 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:984013140" variation 456 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057027764" variation 457 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2521766951" variation 458 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2057027759" variation 460 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1202137029" variation 461 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:2057027740" variation 463 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2057027729" variation 467 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521766935" variation 469 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:1236231350" variation 472 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2147872694" variation 473 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1457255219" variation 477 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1178789326" variation 482 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521766918" variation 483 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1239440332" variation 484..493 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="" /replace="cccagcacgt" /db_xref="dbSNP:2057027661" variation 484 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1431144294" variation 491 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1174859278" variation 492 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057027670" variation 494 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2521766892" variation 495 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1378607276" variation 496 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1467843190" variation 500 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:1169178733" variation 501 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1555990727" variation 504 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:931102545" variation 514 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2521766872" variation 518 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1569302343" variation 519 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521766855" variation 520 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521766850" variation 524 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521766843" variation 531 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521766838" variation 536..540 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="ct" /replace="cttct" /db_xref="dbSNP:59381700" variation 536 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:1400284764" variation 537..538 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="t" /replace="tt" /db_xref="dbSNP:1555990725" variation 538..541 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="tc" /replace="tctc" /replace="tctctc" /db_xref="dbSNP:200142442" variation 538 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:918522255" variation 541 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:972598453" variation 542 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:782702001" variation 543 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521766818" variation 544 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="t" /db_xref="dbSNP:2521766814" variation 548 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2521766809" variation 549 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2057027488" variation 553 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2521766800" variation 559 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1302192273" variation 563 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:782047299" exon 564..705 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /inference="alignment:Splign:2.1.0" /pseudo variation 570 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1177440001" variation 584 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057023030" variation 586 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1555990597" variation 598 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521765438" variation 600 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1252302243" variation 604 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057022996" variation 624 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2057022982" variation 633 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1431095597" variation 638 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1555990595" variation 639 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:960999229" variation 640 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2057022924" variation 646 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:1198651836" variation 658 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:1430398859" variation 663 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="t" /db_xref="dbSNP:782723791" variation 668 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057022889" variation 672 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:1471257414" variation 677 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2057022866" variation 698 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057022856" variation 699 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057022848" variation 701 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2057022834" exon 706..780 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /inference="alignment:Splign:2.1.0" /pseudo variation 706 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2521763496" variation 712 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2057015867" variation 717 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:140110431" variation 718..719 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="gg" /db_xref="dbSNP:1414817119" variation 718 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057015835" variation 730 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1468359600" variation 733 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:1336124844" variation 737 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:1403240261" variation 748 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="t" /db_xref="dbSNP:963239356" variation 749 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2521763474" variation 752 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2521763471" variation 754 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:1397952770" variation 758 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057015755" variation 759 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:2057015745" variation 761 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="c" /db_xref="dbSNP:2057015735" variation 762 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="g" /replace="t" /db_xref="dbSNP:2057015718" variation 765 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:1014889728" variation 766 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="t" /db_xref="dbSNP:782029674" variation 773 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="t" /db_xref="dbSNP:970828210" variation 774 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="a" /replace="g" /db_xref="dbSNP:2057015660" variation 778 /gene="RHOXF1P1" /gene_synonym="lncRHOXF1; TCONS_00017086" /replace="c" /replace="g" /db_xref="dbSNP:2057015649" ORIGIN
ccggaggcgtcctgagcagcagcccactccctgtcccctgcaggcgtccgacccgaagtccacgcgccggaactcggaccaggagccagaggaccccagcgcagaatccgcggagacgcacggcttcgtcgaccacgctcccaggtggcgttccagcccagatccggccacgaagacaccggcgacctcggcctgggtttcctgttcgatgagctccagaaagaagacgatgcgaaggatatagagacttcagtgactgaagctggaggagacgatgagaagaaaatacggaccaaacccgagcagggagcaggagcaggaaaagaaagtcacgtgtacgcgggagctgcggaccccatgatccacgagaaccagaagggcggtggtggccaccaggagccctggcagcagcagcctgaggagttggcccaggactcctccgctgaggatccgcaaccccaagatcaggagcgtctattcagccccagcacgttcggcgggttgcacctgaaggagctagacagcattttctgaccttctcaatatccggacatgttcgcttgaaagcaactggcaatatgcatggatgtgagtgaagctgaagtggaagccagtaagcctgatgaaagcaattggtcagagtagccactctgaaacctgcctcagaccttggatactttgtcctacacattctccaattggcctggtaacttcaccggatgaagaaatctaggttgttggtgtttttctttgaacacctcttcttgctcttcgataggt
//
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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