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Previous release (v1)
2024-11-21 21:30:04, GGRNA.v2 : RefSeq release 226 (Sep, 2024)
LOCUS NM_001145465 907 bp mRNA linear PRI 01-JUN-2024 DEFINITION Homo sapiens NANOG neighbor homeobox (NANOGNB), mRNA. ACCESSION NM_001145465 XR_040558 XR_040559 XR_040560 VERSION NM_001145465.1 KEYWORDS RefSeq; MANE Select. 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 907) AUTHORS Lovering,R.C., Gaudet,P., Acencio,M.L., Ignatchenko,A., Jolma,A., Fornes,O., Kuiper,M., Kulakovskiy,I.V., Laegreid,A., Martin,M.J. and Logie,C. TITLE A GO catalogue of human DNA-binding transcription factors JOURNAL Biochim Biophys Acta Gene Regul Mech 1864 (11-12), 194765 (2021) PUBMED 34673265 REFERENCE 2 (bases 1 to 907) AUTHORS Dunwell,T.L. and Holland,P.W.H. TITLE A sister of NANOG regulates genes expressed in pre-implantation human development JOURNAL Open Biol 7 (4) (2017) PUBMED 28446706 REFERENCE 3 (bases 1 to 907) AUTHORS Zhong,Y.F. and Holland,P.W. TITLE The dynamics of vertebrate homeobox gene evolution: gain and loss of genes in mouse and human lineages JOURNAL BMC Evol Biol 11, 169 (2011) PUBMED 21679462 REMARK Erratum:[BMC Evol Biol. 2011;11:204] Publication Status: Online-Only COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AY151139.1. On or before Mar 1, 2009 this sequence version replaced XR_040559.1, XR_040560.1, XR_040558.1. ##Evidence-Data-START## Transcript exon combination :: AY151139.1, BI464932.1 [ECO:0000332] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000382119.1/ ENSP00000371553.1 RefSeq Select criteria :: based on single protein-coding transcript ##RefSeq-Attributes-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-907 AY151139.1 1-907 FEATURES Location/Qualifiers source 1..907 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="12" /map="12p13.31" gene 1..907 /gene="NANOGNB" /note="NANOG neighbor homeobox" /db_xref="GeneID:360030" /db_xref="HGNC:HGNC:24958" /db_xref="MIM:620692" exon 1..172 /gene="NANOGNB" /inference="alignment:Splign:2.1.0" variation 1 /gene="NANOGNB" /replace="a" /replace="t" /db_xref="dbSNP:1416111754" variation 2 /gene="NANOGNB" /replace="a" /replace="t" /db_xref="dbSNP:1440123987" variation 6 /gene="NANOGNB" /replace="c" /replace="t" /db_xref="dbSNP:1865234121" variation 11 /gene="NANOGNB" /replace="c" /replace="t" /db_xref="dbSNP:1382053352" variation 14..21 /gene="NANOGNB" /replace="ggtcggtc" /replace="ggtcggtcggtc" /db_xref="dbSNP:1176727122" variation 15 /gene="NANOGNB" /replace="a" /replace="g" /db_xref="dbSNP:994566100" variation 17 /gene="NANOGNB" /replace="c" /replace="g" /db_xref="dbSNP:1267447451" variation 18 /gene="NANOGNB" /replace="a" /replace="g" /db_xref="dbSNP:1865234219" variation 24 /gene="NANOGNB" /replace="a" /replace="c" /db_xref="dbSNP:1276978348" variation 26 /gene="NANOGNB" /replace="c" /replace="t" /db_xref="dbSNP:1340431886" variation 27 /gene="NANOGNB" /replace="c" /replace="t" /db_xref="dbSNP:1227975968" variation 28 /gene="NANOGNB" /replace="a" /replace="g" /db_xref="dbSNP:2120506789" variation 32..33 /gene="NANOGNB" /replace="c" /replace="cc" /db_xref="dbSNP:1865234333" variation 32 /gene="NANOGNB" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1027803122" variation 34 /gene="NANOGNB" /replace="c" /replace="t" /db_xref="dbSNP:1865234359" variation 35 /gene="NANOGNB" /replace="c" /replace="g" /db_xref="dbSNP:1865234378" variation 36 /gene="NANOGNB" /replace="c" /replace="g" /db_xref="dbSNP:1264545944" variation 37 /gene="NANOGNB" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1275685376" variation 40 /gene="NANOGNB" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:772529209" variation 42..43 /gene="NANOGNB" /replace="a" /replace="aa" /db_xref="dbSNP:1865234484" variation 42 /gene="NANOGNB" /replace="a" /replace="g" /db_xref="dbSNP:1217771380" variation 45 /gene="NANOGNB" /replace="a" /replace="g" /db_xref="dbSNP:1208211508" variation 51 /gene="NANOGNB" /replace="c" /replace="t" /db_xref="dbSNP:926006043" variation 52 /gene="NANOGNB" /replace="c" /replace="t" /db_xref="dbSNP:1865234541" variation 53 /gene="NANOGNB" /replace="c" /replace="g" /db_xref="dbSNP:1266685158" variation 56 /gene="NANOGNB" /replace="c" /replace="t" /db_xref="dbSNP:1452111469" misc_feature 59..61 /gene="NANOGNB" /note="upstream in-frame stop codon" variation 60 /gene="NANOGNB" /replace="a" /replace="g" /db_xref="dbSNP:2120506880" variation 62 /gene="NANOGNB" /replace="a" /replace="g" /db_xref="dbSNP:1592108974" variation 64 /gene="NANOGNB" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1200856657" variation 66 /gene="NANOGNB" /replace="a" /replace="c" /db_xref="dbSNP:1245982840" variation 69 /gene="NANOGNB" /replace="c" /replace="t" /db_xref="dbSNP:1332242226" CDS 71..637 /gene="NANOGNB" /note="homeobox protein C14; homeobox C14" /codon_start=1 /product="NANOG neighbor homeobox" /protein_id="NP_001138937.1" /db_xref="CCDS:CCDS44826.1" /db_xref="GeneID:360030" /db_xref="HGNC:HGNC:24958" /db_xref="MIM:620692" /translation="
MHRARWLTPVIPALWEAEAGRSRGQEIETILANKKQSAMPWDQDPEQSTGNYSEDEQNGKQKWREEGEAGRKREREKEEKNEKELQDEQENKRKRENEKQKQYPEKRLVSKSLMHTLWAKFKLNRCPTIQESLSLSFEFDMTHKQISQWFCKTRKKYNKEMSKRKHKKKHMRWRSLCCQGWSRTPALK"
misc_feature 152..388
/gene="NANOGNB"
/note="propagated from UniProtKB/Swiss-Prot (Q7Z5D8.1);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
variation 71
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1303482725"
variation 74
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1448697391"
variation 77
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775855759"
variation 78
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:866678269"
variation 79
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:1865234906"
variation 81
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1004499232"
variation 82
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1162145398"
variation 83
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:747317808"
variation 84
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:141049797"
variation 85
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:905546336"
variation 86
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193948826"
variation 89
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1865235150"
variation 91
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1326058017"
variation 92
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1865235190"
variation 93
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1363620658"
variation 94
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:974900907"
variation 105
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298795291"
variation 107
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344595825"
variation 108
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:796713985"
variation 109
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1216010563"
variation 110
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258329211"
variation 111
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1865235376"
variation 113
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1264965838"
variation 114
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1357079068"
variation 115
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1211690983"
variation 116
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865235456"
variation 117
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1266206139"
variation 118
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:886214263"
variation 120
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:149820722"
variation 121
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:145794794"
variation 122
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1249603000"
variation 123
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1421693425"
variation 125
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:12818448"
variation 126
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1368562230"
variation 127
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1459041537"
variation 130
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1156283220"
variation 131
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:913303343"
variation 132
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:1865235789"
variation 134
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1457167753"
variation 136
/gene="NANOGNB"
/replace="a"
/replace="attta"
/db_xref="dbSNP:1321645422"
variation 136
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402789211"
variation 137..138
/gene="NANOGNB"
/replace=""
/replace="ct"
/db_xref="dbSNP:1865235903"
variation 137
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367741383"
variation 138
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1394528557"
variation 143
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1464066389"
variation 144
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1384149279"
variation 146
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865235971"
variation 148
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1312335942"
variation 149
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1341261705"
variation 150
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:1427988437"
variation 151
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1247167975"
variation 152
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1266300920"
variation 153
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1478589413"
variation 154
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:143053607"
variation 155
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1193354082"
variation 157
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1443384832"
variation 158
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865236132"
variation 159
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1209208359"
variation 160
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:1199258327"
variation 161
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:981405973"
variation 164
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:763011633"
variation 169
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1865236233"
variation 170
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1258791968"
variation 171
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1199645570"
exon 173..505
/gene="NANOGNB"
/inference="alignment:Splign:2.1.0"
variation 175
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1183670554"
variation 177
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1865276788"
variation 178
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410886229"
variation 179
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1034341755"
variation 180
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1865276979"
variation 181
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1431929620"
variation 183
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:778968033"
variation 185
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865277056"
variation 187
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1260603097"
variation 189
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:755627184"
variation 191
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1433479206"
variation 194
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:1865277157"
variation 200
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:2120516503"
variation 201
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865277175"
variation 202
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:781482439"
variation 204
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1436850930"
variation 206
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:1463684279"
variation 208
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865277261"
variation 210
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1306356071"
variation 211
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1395119920"
variation 213
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1865277666"
variation 218
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1435887727"
variation 219
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865277717"
variation 220
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370164049"
variation 221
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1565471587"
variation 226
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:1427686963"
variation 229
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:995692914"
variation 230
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410560373"
variation 241..260
/gene="NANOGNB"
/replace="aaatgga"
/replace="aaatggaaagcagaaatgga"
/db_xref="dbSNP:1299967768"
variation 243..244
/gene="NANOGNB"
/replace=""
/replace="gatacag"
/db_xref="dbSNP:1189936959"
variation 243
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:114136506"
variation 244
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1865277855"
variation 245..246
/gene="NANOGNB"
/replace=""
/replace="aagat"
/db_xref="dbSNP:1256131840"
variation 246
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1218520248"
variation 247..249
/gene="NANOGNB"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1865277939"
variation 247
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1357847720"
variation 249
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1592110296"
variation 256
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:887365634"
variation 257
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1008856218"
variation 258
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865278044"
variation 259
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:1225869520"
variation 261
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1249277936"
variation 262..269
/gene="NANOGNB"
/replace="agaag"
/replace="agaagaag"
/db_xref="dbSNP:1019315174"
variation 265
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1865278157"
variation 266
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1865278184"
variation 268..272
/gene="NANOGNB"
/replace="ag"
/replace="aggag"
/db_xref="dbSNP:1865278213"
variation 269
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:1322694842"
variation 270
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865278248"
variation 275
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:758922229"
variation 280
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:920696549"
variation 281..287
/gene="NANOGNB"
/replace="aga"
/replace="agaaaga"
/db_xref="dbSNP:1565471600"
variation 285..291
/gene="NANOGNB"
/replace="agaga"
/replace="agagaga"
/db_xref="dbSNP:1865278309"
variation 288
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865278331"
variation 290
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:929362242"
variation 293
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:185000545"
variation 294
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244414463"
variation 296
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1487793811"
variation 297
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:769053712"
variation 300..307
/gene="NANOGNB"
/replace="aagaa"
/replace="aagaagaa"
/db_xref="dbSNP:1268522129"
variation 305
/gene="NANOGNB"
/replace=""
/replace="g"
/db_xref="dbSNP:1308642724"
variation 305
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865278548"
variation 306..312
/gene="NANOGNB"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:1455893486"
variation 306
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865278600"
variation 308
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865278662"
variation 309
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1167068511"
variation 312
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:774570733"
variation 313
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:75086416"
variation 314
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:143895543"
variation 319
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1865278908"
variation 321
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1348135869"
variation 324
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:776296089"
variation 325
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:968413945"
variation 331
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1865279071"
variation 334
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373051639"
variation 335
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:899708417"
variation 340
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1565471636"
variation 348
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1432713702"
variation 349
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:932491421"
variation 350..353
/gene="NANOGNB"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1865279267"
variation 354
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:763066551"
variation 356
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1365487163"
variation 363
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1417091123"
variation 365
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1181833946"
variation 367
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1215892636"
variation 374
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:373676869"
variation 375
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:924409705"
variation 380
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1320541317"
variation 381
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1221633120"
variation 382
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:774424251"
variation 383
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1470218122"
variation 389
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1233487378"
variation 390
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:759460411"
variation 391
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:993148562"
variation 393
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:767321679"
variation 394
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:917955933"
variation 395
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1053589945"
variation 400
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1865280019"
variation 405
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:948031139"
variation 406
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450333281"
variation 410
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865280130"
variation 411
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:1865280163"
variation 413
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2120517041"
variation 414
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:752332013"
variation 417
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:749994978"
variation 422
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:763596163"
variation 424
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1165562657"
variation 426
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1396670870"
variation 432
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1455520176"
variation 433..437
/gene="NANOGNB"
/replace="taagt"
/replace="taagtaagt"
/db_xref="dbSNP:1865280377"
variation 435
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1216201382"
variation 436
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1396995137"
variation 437
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1865280471"
variation 441
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045049151"
variation 442
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1389050325"
variation 444
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1459694844"
variation 445
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1259832671"
variation 447..463
/gene="NANOGNB"
/replace="g"
/replace="gccccactatacaagag"
/db_xref="dbSNP:1432487883"
variation 447
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1159073365"
variation 448
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1865280849"
variation 449
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282118809"
variation 451
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1377951213"
variation 453
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:893631836"
variation 454
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1180497149"
variation 455
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1228464836"
variation 457
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1294583298"
variation 458
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1337603031"
variation 459
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1207316556"
variation 465
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1009345618"
variation 467
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1865281140"
variation 469
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:753353332"
variation 470
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1447982666"
variation 473
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1218342743"
variation 475
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1463286081"
variation 476
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:2120517245"
variation 478
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1021121764"
variation 479
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1865281379"
variation 480
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:906235511"
variation 485
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:756756506"
variation 488
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1453256049"
variation 489
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1301512948"
variation 490
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:747102390"
variation 491
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1420028097"
variation 493
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1565471700"
variation 494..498
/gene="NANOGNB"
/replace="aca"
/replace="acaca"
/db_xref="dbSNP:1423648840"
variation 495
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1471587269"
variation 497
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1393420217"
variation 498
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1421305006"
variation 500
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1033935847"
variation 505
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:959864912"
exon 506..585
/gene="NANOGNB"
/inference="alignment:Splign:2.1.0"
variation 506
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748408334"
variation 509
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1471113052"
variation 511
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1291754698"
variation 514
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1170611480"
variation 515
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1865282997"
variation 517
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865283023"
variation 518
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1424127864"
variation 522
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:1435307624"
variation 524
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1376715336"
variation 527
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:968445530"
variation 528
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:77290736"
variation 529
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:749443725"
variation 532
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:771119714"
variation 534
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865283235"
variation 538
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:960133035"
variation 540
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1336880724"
variation 541
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:199917356"
variation 542
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:548793247"
variation 543
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1273473394"
variation 545..551
/gene="NANOGNB"
/replace="aaa"
/replace="aaagaaa"
/db_xref="dbSNP:1865283405"
variation 545
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344691464"
variation 547
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235452606"
variation 548
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:1486969213"
variation 551
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1282785980"
variation 552
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:992784929"
variation 553
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1340297913"
variation 556..560
/gene="NANOGNB"
/replace=""
/replace="caaga"
/db_xref="dbSNP:915833253"
variation 557
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1251265431"
variation 559
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:1439498615"
variation 560
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196616546"
variation 561
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:932585824"
variation 567
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1308232216"
variation 573
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1275362113"
variation 574
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865283628"
variation 576
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865283643"
variation 577
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:376922335"
variation 578
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:2120517830"
variation 579
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:774477338"
variation 582
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1865283703"
variation 583
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1865283717"
variation 584
/gene="NANOGNB"
/replace=""
/replace="a"
/db_xref="dbSNP:1865283762"
variation 584
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1865283740"
variation 585
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1454576237"
exon 586..907
/gene="NANOGNB"
/inference="alignment:Splign:2.1.0"
variation 586
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:2120525377"
variation 587
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1000835827"
variation 593..597
/gene="NANOGNB"
/replace="tct"
/replace="tctct"
/db_xref="dbSNP:1374665107"
variation 593
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:1195276652"
variation 594
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1862611278"
variation 595
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:991494441"
variation 596
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1862611343"
variation 604
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1862611374"
variation 605
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1350012375"
variation 606
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1033363486"
variation 609
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:955955665"
variation 610
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1293584049"
variation 612
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:2120525436"
variation 613
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1448531706"
variation 614
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:1592111454"
variation 616
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226222532"
variation 617
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:184126538"
variation 618
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:538087276"
variation 619
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1862611725"
variation 620
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1592111465"
variation 623
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:1862611774"
variation 624
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1408625352"
variation 626
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1862611823"
variation 627
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1024117210"
variation 628
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:1862611879"
variation 629
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1160291210"
variation 630
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1468109251"
variation 631
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:1205896812"
variation 636
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471546293"
variation 638
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1162123566"
variation 639
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1394470453"
variation 642
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:971203479"
variation 644
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:979855998"
variation 645
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1016232767"
variation 646..649
/gene="NANOGNB"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1482300668"
variation 647..676
/gene="NANOGNB"
/replace=""
/replace="tttggcctccagaaatgctgtgattacaag"
/db_xref="dbSNP:1862612141"
variation 647
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190485827"
variation 648
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1862612174"
variation 649
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:1286939423"
variation 662
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1328354978"
variation 664
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1862612279"
variation 666
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386862725"
variation 672
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:927012773"
variation 673
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:972164299"
variation 675
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:962710452"
variation 676
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1296626547"
variation 678
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:919448010"
variation 685
/gene="NANOGNB"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1862612540"
variation 685
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1406939623"
variation 687
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:973736040"
variation 688
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1293229165"
variation 690
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:918233613"
variation 699
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:58053555"
variation 707
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1862612711"
variation 708
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1345585207"
variation 709
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1862612768"
variation 710
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:930266006"
variation 713
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1862612829"
variation 720
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1443711272"
variation 722
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051779750"
variation 724
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:2120525723"
regulatory 726..731
/regulatory_class="polyA_signal_sequence"
/gene="NANOGNB"
/note="hexamer: AATAAA"
variation 734
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:1410520905"
variation 735
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1862612925"
variation 736
/gene="NANOGNB"
/replace=""
/replace="g"
/db_xref="dbSNP:1236586022"
variation 738
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:910816810"
variation 739
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1426763645"
variation 745
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:943585259"
variation 746
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:912768251"
variation 752
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1592111504"
polyA_site 754
/gene="NANOGNB"
/note="major polyA site"
variation 755
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1053425092"
variation 760
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1214218681"
variation 762
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1412373903"
variation 764
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:757831943"
variation 766
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:768067755"
variation 768
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:2092716517"
variation 769
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1225427333"
variation 770
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:942809617"
variation 771
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039811035"
variation 773
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1862613237"
variation 779
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1156669920"
variation 780
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:903917570"
variation 783
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:2120525833"
variation 785
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:1001289355"
variation 792
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432699078"
variation 800
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1387780679"
variation 801
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:187979580"
variation 803
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1470661683"
variation 805
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1356943760"
variation 808
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1862613402"
variation 810
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1862613425"
variation 811
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1862613662"
variation 814
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174835273"
variation 820
/gene="NANOGNB"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1862613754"
variation 820
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1862613717"
variation 821..825
/gene="NANOGNB"
/replace="tgt"
/replace="tgtgt"
/db_xref="dbSNP:906254332"
variation 822
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:2120525901"
variation 829
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1592111525"
variation 830..834
/gene="NANOGNB"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1862613867"
variation 831
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1422030138"
variation 833
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1565472523"
variation 837
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1185116691"
variation 839
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:2120525933"
variation 843
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:1862613955"
variation 845
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1862614035"
variation 847
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:756382011"
variation 848
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:1176845936"
variation 853
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:180838803"
variation 854
/gene="NANOGNB"
/replace="c"
/replace="g"
/db_xref="dbSNP:1862614118"
variation 855
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1862614137"
variation 860
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244282458"
variation 861
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:1862614183"
variation 863
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1862614209"
variation 864
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1862614247"
variation 865
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:148911844"
variation 866
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:1459987733"
variation 868
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:1759689596"
variation 869
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1862614373"
variation 870
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:895065338"
variation 874
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:147013986"
variation 875
/gene="NANOGNB"
/replace="c"
/replace="t"
/db_xref="dbSNP:778391180"
variation 885
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1310258194"
variation 887
/gene="NANOGNB"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1364264925"
variation 888
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1862614613"
variation 889..896
/gene="NANOGNB"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/replace="aaaaaaaaa"
/db_xref="dbSNP:533703331"
variation 890
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:963395868"
variation 893
/gene="NANOGNB"
/replace="a"
/replace="c"
/db_xref="dbSNP:1462091746"
variation 895
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:971212024"
variation 897
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:2120526095"
variation 898
/gene="NANOGNB"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1862614760"
variation 899
/gene="NANOGNB"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:768139037"
variation 900
/gene="NANOGNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:371494215"
variation 901
/gene="NANOGNB"
/replace="a"
/replace="g"
/db_xref="dbSNP:1862614802"
variation 907
/gene="NANOGNB"
/replace="g"
/replace="t"
/db_xref="dbSNP:1862614827"
ORIGIN
atctaccttatctggtcggtcatctctgtaacctccctaccaaggactaattggtctttaaaactcctcaatgcaccgggcgcggtggctcacgcctgtaatcccagcactttgggaggccgaggcgggcagatcacgaggtcaggaaatcgagaccatcttggctaacaagaaacaatcagctatgccttgggatcaagatccagaacaatcaactggaaattacagtgaagatgaacaaaatggaaagcagaaatggagagaagaaggagaagcaggcagaaagagagaacgagaaaaagaagaaaaaaacgaaaaggagctgcaagatgaacaggaaaacaaaaggaaaagggaaaatgagaaacagaaacagtatcccgagaaaagattagtcagcaaatccctcatgcatactctctgggcaaagtttaagttaaacaggtgccccactatacaagagagtctatcactgtcatttgaatttgacatgacacataaacagataagtcaatggttttgtaaaacgaggaagaaatataataaagaaatgtccaagagaaagcataagaaaaaacatatgagatggagatctctgtgttgccaaggctggtctcgaactcctgccctcaagtgatcttcctattttggcctccagaaatgctgtgattacaagcatgagccatcgcactggctaagacattttacatgacaccattctcaccaataaatggagttctgaaaggataaacaagaaaacattaacagtcgttgattccgtggagtagaactaaatgaggggtatgcaaaggagtttttatgtgttttatttttaccctactgtagatttaaagtttttataatggatgttaattgattttatttaagaaaaaaaatcgagtcaagg
//
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]