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Previous release (v1)
2024-04-19 11:40:00, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_103754 1647 bp RNA linear PRI 31-JUL-2023
DEFINITION Homo sapiens long intergenic non-protein coding RNA 491
(LINC00491), transcript variant 2, long non-coding RNA.
ACCESSION NR_103754
VERSION NR_103754.1
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 1647)
AUTHORS Zhou S, Wu C, Tang Q, Zhou X, He B, Chang P and He X.
TITLE Silencing LINC00491 inhibits prostate cancer development through
the miR-384/TRIM44 axis
JOURNAL J Biochem Mol Toxicol 37 (7), e23370 (2023)
PUBMED 37070216
REMARK GeneRIF: Silencing LINC00491 inhibits prostate cancer development
through the miR-384/TRIM44 axis.
REFERENCE 2 (bases 1 to 1647)
AUTHORS Wang W, Yang T, Li D, Huang Y, Bai G and Li Q.
TITLE LINC00491 promotes cell growth and metastasis through
miR-324-5p/ROCK1 in liver cancer
JOURNAL J Transl Med 19 (1), 504 (2021)
PUBMED 34876144
REMARK GeneRIF: LINC00491 promotes cell growth and metastasis through
miR-324-5p/ROCK1 in liver cancer.
Publication Status: Online-Only
REFERENCE 3 (bases 1 to 1647)
AUTHORS Ye H, Mulmi Shrestha S, Zhu J, Ding Y and Shi R.
TITLE Long non-coding RNA LINC00491 promotes proliferation and inhibits
apoptosis in esophageal squamous cell carcinoma
JOURNAL Int J Mol Med 47 (4) (2021)
PUBMED 33537830
REMARK GeneRIF: Long noncoding RNA LINC00491 promotes proliferation and
inhibits apoptosis in esophageal squamous cell carcinoma.
REFERENCE 4 (bases 1 to 1647)
AUTHORS Li J, Liu D, Hua R, Zhang J, Liu W, Huo Y, Cheng Y, Hong J and Sun
Y.
TITLE Long non-coding RNAs expressed in pancreatic ductal adenocarcinoma
and lncRNA BC008363 an independent prognostic factor in PDAC
JOURNAL Pancreatology 14 (5), 385-390 (2014)
PUBMED 25200694
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
DA458823.1, CN270888.1 and AC099487.2.
Transcript Variant: This variant (2) lacks an internal exon and
contains two alternate internal exons, resulting in a shorter
transcript, compared to variant 1.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
##Evidence-Data-START##
Transcript exon combination :: SRR14038193.2604230.1 [ECO:0000332]
RNAseq introns :: partial sample support SAMEA2148874,
SAMEA2149398 [ECO:0000350]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-201 DA458823.1 1-201
202-819 CN270888.1 45-662
820-1647 AC099487.2 57724-58551 c
FEATURES Location/Qualifiers
source 1..1647
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="5"
/map="5q21.1"
gene 1..1647
/gene="LINC00491"
/note="long intergenic non-protein coding RNA 491"
/db_xref="GeneID:285708"
/db_xref="HGNC:HGNC:43428"
ncRNA 1..1647
/ncRNA_class="lncRNA"
/gene="LINC00491"
/product="long intergenic non-protein coding RNA 491,
transcript variant 2"
/db_xref="GeneID:285708"
/db_xref="HGNC:HGNC:43428"
exon 1..238
/gene="LINC00491"
/inference="alignment:Splign:2.1.0"
variation 2
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1747280534"
variation 3
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1747280469"
variation 4
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:182627692"
variation 5
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:951211421"
variation 6
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1034873694"
variation 7
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1456999565"
variation 9
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1747280167"
variation 10
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1747280106"
variation 11
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:2149566169"
variation 12
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1243974676"
variation 13
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1054038517"
variation 14..16
/gene="LINC00491"
/replace="aac"
/replace="aacaac"
/db_xref="dbSNP:1392497570"
variation 15
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:971597132"
variation 16
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1003448079"
variation 18
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1378808438"
variation 19
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:905149644"
variation 20
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1377370362"
variation 26
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:2149566161"
variation 27
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1580618725"
variation 30
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242158267"
variation 31
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044697734"
variation 32
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:570082604"
variation 33
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:2149566151"
variation 36..38
/gene="LINC00491"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1459390768"
variation 36
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:551539768"
variation 37
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:533476772"
variation 38
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1052157304"
variation 39
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:559954542"
variation 40
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1422708992"
variation 44
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1170256731"
variation 45
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:572045419"
variation 47
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1412691634"
variation 51
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1051737267"
variation 53
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:933765270"
variation 55
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:560033813"
variation 56..66
/gene="LINC00491"
/replace=""
/replace="gccctgcttcg"
/db_xref="dbSNP:1747277068"
variation 56
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:529539760"
variation 57
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1483673449"
variation 58
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1040544005"
variation 59
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1747277647"
variation 62
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1277211162"
variation 63
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1218194390"
variation 64
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:372919434"
variation 65
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:910790480"
variation 66
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:562228935"
variation 67
/gene="LINC00491"
/replace=""
/replace="a"
/db_xref="dbSNP:1258935094"
variation 67
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:6885654"
variation 68
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:919260566"
variation 70..86
/gene="LINC00491"
/replace="cgcgca"
/replace="cgcgcatggtgcgcgca"
/db_xref="dbSNP:1424141767"
variation 70
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:972106456"
variation 71
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:971495394"
variation 72
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:917347423"
variation 73
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1338475580"
variation 74
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1747275816"
variation 75
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1399523214"
variation 76
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:577572299"
variation 77..88
/gene="LINC00491"
/replace="g"
/replace="ggtgcgcgcacg"
/db_xref="dbSNP:1747274245"
variation 77
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:556085244"
variation 78
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1278279243"
variation 79
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1747275463"
variation 80..85
/gene="LINC00491"
/replace="gcgc"
/replace="gcgcgc"
/db_xref="dbSNP:1476150517"
variation 80
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313166415"
variation 81
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1309607623"
variation 82
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1434090075"
variation 83
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:563304229"
variation 84
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:958801271"
variation 86
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:745509092"
variation 87
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409050547"
variation 88
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:982846183"
variation 89..105
/gene="LINC00491"
/replace="cactgacctgcgcccac"
/replace="cactgacctgcgcccacactgacctgcgcccac"
/db_xref="dbSNP:1747272778"
variation 89
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:951470356"
variation 91
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1034842399"
variation 93
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298954485"
variation 94
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1003790480"
variation 95
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1747273549"
variation 96
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189814426"
variation 98
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1019900406"
variation 99..105
/gene="LINC00491"
/replace="c"
/replace="cgcccac"
/db_xref="dbSNP:1747272682"
variation 99
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:998299772"
variation 100
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:544741974"
variation 103
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:969299395"
variation 104
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:900902174"
variation 106
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1223979886"
variation 107
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1217994738"
variation 108
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1747272417"
variation 113
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1023987897"
variation 114
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1747272218"
variation 115
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:577338489"
variation 116
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1245806927"
variation 117
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1267578510"
variation 118
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1747271844"
variation 119
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:893457255"
variation 121
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1747271614"
variation 122..123
/gene="LINC00491"
/replace=""
/replace="a"
/db_xref="dbSNP:1329750932"
variation 123
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1438937872"
variation 125
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1370198621"
variation 126
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1747271257"
variation 127
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:919540468"
variation 129
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1036348327"
variation 133
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1217432988"
variation 134
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780865696"
variation 135
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1366578973"
variation 136
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756763528"
variation 138..143
/gene="LINC00491"
/replace=""
/replace="acctca"
/db_xref="dbSNP:1747270304"
variation 140
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:890241550"
variation 142
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281808992"
variation 147
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051231903"
variation 148
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:934158930"
variation 152
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1288690469"
variation 155
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451894097"
variation 157
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:958526866"
variation 160
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1747269669"
variation 161..165
/gene="LINC00491"
/replace="ca"
/replace="cacca"
/db_xref="dbSNP:1747269340"
variation 162
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:552675720"
variation 163
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:376273848"
variation 165
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:534492051"
variation 168
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:941616937"
variation 169..170
/gene="LINC00491"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1747268937"
variation 171
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:751582047"
variation 172
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:909870456"
variation 173
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1457352024"
variation 174
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:3114587"
variation 175
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:997849044"
variation 176..177
/gene="LINC00491"
/replace=""
/replace="tc"
/db_xref="dbSNP:1747268179"
variation 177
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:965429469"
variation 178
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:930006460"
variation 179
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1747267843"
variation 181
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1747267748"
variation 182
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:928047277"
variation 183
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1747267541"
variation 185
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1331430568"
variation 186
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1747267379"
variation 187..189
/gene="LINC00491"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1747267112"
variation 187
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339289379"
variation 188
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1445172644"
variation 189
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1426235298"
variation 192
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1747266907"
variation 194
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1017999722"
variation 195
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1747266857"
variation 196
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1747266799"
variation 197
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1255794557"
variation 198
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:981939377"
variation 199
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1199099270"
variation 200..202
/gene="LINC00491"
/replace="cgg"
/replace="gga"
/db_xref="dbSNP:796805507"
variation 200
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:969645827"
variation 201
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:3105473"
variation 202
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:898069452"
variation 205
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423239283"
variation 210..211
/gene="LINC00491"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1747265940"
variation 210
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1254354264"
variation 211
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1747265875"
variation 212
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1747265820"
variation 213
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1747265740"
variation 214..215
/gene="LINC00491"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1170077959"
variation 215
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1466460730"
variation 216
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400525903"
variation 217
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:989792798"
variation 218
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1747265191"
variation 219
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1311535803"
variation 220
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1747264993"
variation 221..225
/gene="LINC00491"
/replace=""
/replace="atctt"
/db_xref="dbSNP:1275889685"
variation 222
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1747264904"
variation 224
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301712271"
variation 226
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:957983706"
variation 227
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:191360414"
variation 228
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1580618310"
variation 230
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1362545600"
variation 231
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:569912623"
variation 233..235
/gene="LINC00491"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1580618295"
variation 233
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1747264239"
variation 234
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172310843"
variation 235
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:950059414"
variation 236
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:890168078"
exon 239..309
/gene="LINC00491"
/inference="alignment:Splign:2.1.0"
variation 240
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1280126590"
variation 244
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1418649987"
variation 247
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:975331829"
variation 248
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1240913584"
variation 250
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1745985512"
variation 252
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1434283874"
variation 256
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1329072172"
variation 259
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745985325"
variation 266
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745985265"
variation 267
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745985222"
variation 269..274
/gene="LINC00491"
/replace=""
/replace="aacatc"
/db_xref="dbSNP:762353394"
variation 276
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:962335435"
variation 277
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1388581027"
variation 278
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1580586265"
variation 280
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1580586262"
variation 283
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304892428"
variation 288
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745984871"
variation 290
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745984824"
variation 291
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745984771"
variation 296
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1723883933"
variation 297..298
/gene="LINC00491"
/replace=""
/replace="ac"
/db_xref="dbSNP:1241097110"
variation 298
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386942832"
variation 300
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:986107096"
variation 301..302
/gene="LINC00491"
/replace=""
/replace="taa"
/db_xref="dbSNP:1357713474"
variation 308
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396263515"
exon 310..372
/gene="LINC00491"
/inference="alignment:Splign:2.1.0"
variation 311
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:918038721"
variation 313
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1745848895"
variation 314
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745848854"
variation 315
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:537503006"
variation 317
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745848768"
variation 328
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1226997775"
variation 329
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1745848673"
variation 331..333
/gene="LINC00491"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:35344064"
variation 332
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1283968990"
variation 333
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1745848526"
variation 335
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448144626"
variation 337
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745848445"
variation 338
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1580582329"
variation 345..347
/gene="LINC00491"
/replace="c"
/replace="cac"
/db_xref="dbSNP:1745848365"
variation 347
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:535125810"
variation 348
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:914434972"
variation 350
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1269211443"
variation 351
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1349276388"
variation 354
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1165198042"
variation 359
/gene="LINC00491"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1745848075"
variation 359
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:753652295"
variation 363
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1405539304"
variation 365
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:2149548291"
variation 368
/gene="LINC00491"
/replace=""
/replace="a"
/db_xref="dbSNP:1745847915"
variation 368
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:955685282"
variation 370
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745847820"
variation 371
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:568001405"
exon 373..1647
/gene="LINC00491"
/inference="alignment:Splign:2.1.0"
variation 377
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:938821816"
variation 380
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1310791920"
variation 381
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1745795476"
variation 384
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1029714140"
variation 393
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1561532874"
variation 394
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745795318"
variation 395
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:977277774"
variation 403
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745795234"
variation 407
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1290091051"
variation 410
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:963911643"
variation 413
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323319499"
variation 414
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745795073"
variation 419
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745795029"
variation 420
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196497055"
variation 421
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1445931186"
variation 434
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1237547879"
variation 442
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:2149547723"
variation 443
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458149512"
variation 444
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1018087745"
variation 446
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745794796"
variation 451
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1180662545"
variation 453
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745794712"
variation 460
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1745794672"
variation 461..463
/gene="LINC00491"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1745794545"
variation 462
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1401010161"
variation 465
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1235811498"
variation 470
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1580580845"
variation 473
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:2149547712"
variation 475
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745794405"
variation 477
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1044260691"
variation 478
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745794304"
variation 479
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1745794263"
variation 480
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:2149547708"
variation 483
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:947258897"
variation 484
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416176826"
variation 485
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1005412501"
variation 486
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1745794070"
variation 487
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1408611532"
variation 490..491
/gene="LINC00491"
/replace=""
/replace="c"
/db_xref="dbSNP:1170379936"
variation 502
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745793914"
variation 503
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1745793876"
variation 505
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1401731886"
variation 508
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:561063618"
variation 511
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1449641847"
variation 516
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:888335554"
variation 517
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1745793620"
variation 531..532
/gene="LINC00491"
/replace=""
/replace="ct"
/db_xref="dbSNP:1338219392"
variation 532
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025536341"
variation 534
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:182534989"
variation 535
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:988769251"
variation 541
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745793354"
variation 545
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745793308"
variation 549
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1380862281"
variation 551
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1745793214"
variation 561
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:906224959"
variation 562
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1216635662"
variation 564
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1745793055"
variation 571
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1046144547"
variation 576..578
/gene="LINC00491"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1318251356"
variation 586
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:771704250"
variation 588
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:986916438"
variation 590
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1745792801"
variation 593
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:947819220"
variation 595
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745792704"
variation 597
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:953803955"
variation 601
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1163426909"
variation 603
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1476955246"
variation 609
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1193475425"
variation 614
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745792456"
variation 615
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473591708"
variation 618..623
/gene="LINC00491"
/replace="ga"
/replace="gagaga"
/db_xref="dbSNP:1745792207"
variation 618
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:894628195"
variation 621
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745792312"
variation 622
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1029087457"
variation 624..632
/gene="LINC00491"
/replace="aagaag"
/replace="aagaagaag"
/db_xref="dbSNP:1745792096"
variation 625
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1467469853"
variation 630
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:2149547673"
variation 632
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:747637941"
variation 640
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:370906737"
variation 641
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402084143"
variation 642
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:974899253"
variation 644
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778973212"
variation 646
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:192742199"
variation 648..650
/gene="LINC00491"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1360608293"
variation 648
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745791639"
variation 649
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745791590"
variation 651
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:926156268"
variation 653
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458603870"
variation 654
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1240499523"
variation 655
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1580580745"
variation 657
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:977679127"
variation 658
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745791259"
variation 662
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745791197"
variation 664
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745791175"
variation 670
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1016913818"
variation 671
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277116142"
variation 677
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745791024"
variation 680
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:946063512"
variation 681
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1005165853"
variation 684
/gene="LINC00491"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1745790848"
variation 691
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:2149547658"
variation 693
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745790803"
variation 694..695
/gene="LINC00491"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1220195521"
variation 697
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745790738"
variation 698
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1273045919"
variation 699
/gene="LINC00491"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1344186995"
variation 705
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745790593"
variation 706
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1201162416"
variation 709
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:922636006"
variation 712
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1280819055"
variation 714
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1487308661"
variation 715
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745790342"
variation 718
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1216175546"
variation 719
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1264126509"
variation 722
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1745790204"
variation 727
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745788313"
variation 729
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:545278073"
variation 730
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745788202"
variation 734
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1561532764"
variation 738
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451347826"
variation 745
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745788083"
variation 746
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377616847"
variation 748
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:574366566"
variation 752
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:552912109"
variation 755
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1230213057"
variation 758
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1035699599"
variation 761
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1297233703"
variation 765
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745787603"
variation 766
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1745787533"
variation 769
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:72781850"
variation 776
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1580580668"
variation 779
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:911321038"
variation 781
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:905961410"
variation 788
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1321320592"
variation 798
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:983897286"
variation 799
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:753740225"
variation 804
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745786848"
variation 823
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1241041758"
variation 824..831
/gene="LINC00491"
/replace="aag"
/replace="aagtaaag"
/db_xref="dbSNP:1745786617"
variation 824
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1233880946"
variation 831
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276480217"
variation 833
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1351644624"
variation 834
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745786395"
variation 836
/gene="LINC00491"
/replace=""
/replace="g"
/db_xref="dbSNP:1287073494"
variation 836
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:114522914"
variation 840
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:535054006"
variation 841
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1281152176"
variation 842
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1370692425"
variation 846
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:994530856"
variation 847
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:567632258"
variation 850
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1053437642"
variation 853
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745785598"
variation 858
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:2149547616"
variation 859
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:934598149"
variation 860
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378962261"
variation 863
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745785480"
variation 865
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025088456"
variation 866..885
/gene="LINC00491"
/replace=""
/replace="tgagttcattagtcagaaaa"
/db_xref="dbSNP:1358307067"
variation 866
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:555804389"
variation 868..903
/gene="LINC00491"
/replace=""
/replace="agttcattagtcagaaaaagggaaaataccaccacc"
/db_xref="dbSNP:1026486700"
variation 871
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745785195"
variation 872
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745785003"
variation 880
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1161026103"
variation 882
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1011925803"
variation 888..903
/gene="LINC00491"
/replace=""
/replace="ggaaaataccaccacc"
/db_xref="dbSNP:1439714456"
variation 890..893
/gene="LINC00491"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1157681358"
variation 895..903
/gene="LINC00491"
/replace="accaccacc"
/replace="accaccaccacc"
/db_xref="dbSNP:1745784282"
variation 896
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:537165543"
variation 898
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1580580571"
variation 904
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1580580553"
variation 908
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1745784144"
variation 917
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:920993507"
variation 923
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:973820772"
variation 924
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:2149547600"
variation 926
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446212721"
variation 927
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1310074927"
variation 928
/gene="LINC00491"
/replace=""
/replace="c"
/db_xref="dbSNP:1745783847"
variation 930
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:963504148"
variation 932
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745783738"
variation 935
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745783694"
variation 937
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:2149547597"
variation 938
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:79439168"
variation 944
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745783583"
variation 947
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189945856"
variation 951
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745783464"
variation 962
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:984072856"
variation 964
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:757429098"
variation 967
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1457700051"
variation 968
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1478012575"
variation 977
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745783147"
variation 979
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1177536371"
variation 983
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1247637257"
variation 984
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:951007140"
variation 985
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1745782954"
variation 993
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1420289212"
variation 996..1013
/gene="LINC00491"
/replace="gcagaatgtttcctttac"
/replace="gcagaatgtttcctttacgcagaatgtttcctttac"
/db_xref="dbSNP:1745782766"
variation 1006
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1162281237"
variation 1007
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:2149547585"
variation 1012
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:141837376"
variation 1023..1027
/gene="LINC00491"
/replace="ctc"
/replace="ctctc"
/db_xref="dbSNP:1745782712"
variation 1031
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1580580486"
variation 1032
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1458268051"
variation 1039
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745782587"
variation 1042..1046
/gene="LINC00491"
/replace=""
/replace="acata"
/db_xref="dbSNP:1398112179"
variation 1046
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:533436827"
variation 1047
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1465044683"
variation 1049
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745782409"
variation 1050
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:7723461"
variation 1052
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:904727875"
variation 1054
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1041991126"
variation 1058
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1312326878"
variation 1059
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:188560442"
variation 1062
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256553749"
variation 1067
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745781807"
variation 1070
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1317602683"
variation 1073..1074
/gene="LINC00491"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1276625480"
variation 1073
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745781720"
variation 1076
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745781629"
variation 1078
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1199833757"
variation 1085
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745781534"
variation 1089
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1260492509"
variation 1090
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:7723320"
variation 1094
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745780467"
variation 1095
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1179589806"
variation 1096
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1041415255"
variation 1097
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:868573996"
variation 1099
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1255117963"
variation 1100
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1424028749"
variation 1107
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1189540974"
variation 1111
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:942736718"
variation 1112
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745779908"
variation 1113
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1421227529"
variation 1114
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:911268399"
variation 1115
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1745779774"
variation 1117
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745779729"
variation 1118
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745779686"
variation 1119
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745779638"
variation 1127
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:370267671"
variation 1128
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:139987955"
variation 1133
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1356173407"
variation 1136
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1685610137"
variation 1137
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745779442"
variation 1138
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1338164463"
variation 1140
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1302321051"
variation 1141
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745779296"
variation 1144
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:3105485"
variation 1145
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745779045"
variation 1146
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416857237"
variation 1147
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:892920752"
variation 1150
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276470908"
variation 1151
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1340317454"
variation 1153
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745778648"
variation 1155
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:952544002"
variation 1159
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1219585904"
variation 1163
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1487063798"
variation 1170
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:918443329"
variation 1172
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745778276"
variation 1173
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745778229"
variation 1175
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1052965513"
variation 1178
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:569394714"
variation 1181
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1173407550"
variation 1183
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1414392176"
variation 1187
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1426562316"
variation 1189..1195
/gene="LINC00491"
/replace="aaaaa"
/replace="aaaaaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:891061516"
variation 1189
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:183558415"
variation 1191
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1477010925"
variation 1204
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1487863559"
variation 1205
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1194086754"
variation 1206
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:971020335"
variation 1207
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745777526"
variation 1215
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:765800602"
variation 1216
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745777408"
variation 1221
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745777333"
variation 1222
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:537936462"
variation 1226
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:2149547513"
variation 1232
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745777243"
variation 1238
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745777205"
variation 1239
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:563472919"
variation 1243
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1012284962"
variation 1244
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:545267367"
variation 1245
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1194605319"
variation 1248
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745776941"
variation 1250
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745776902"
variation 1251
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1486994166"
variation 1255
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1175190424"
variation 1260
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1254308230"
variation 1261
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:762987732"
variation 1262
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296612883"
variation 1267
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745775815"
variation 1268
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1032087113"
variation 1275
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1000658022"
variation 1277
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745775669"
variation 1281
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:2149547506"
variation 1282
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:373533926"
variation 1283
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745775560"
variation 1286
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:551032940"
variation 1287
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1225298678"
variation 1291
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745775371"
variation 1297
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1315792725"
variation 1299
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1277375761"
variation 1308
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400207049"
variation 1310
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745775179"
variation 1312
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1363714043"
variation 1314
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745775037"
variation 1316
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:920961053"
variation 1317
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1302526228"
variation 1322
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348016856"
variation 1324..1327
/gene="LINC00491"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1283497928"
variation 1324
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1745774856"
variation 1325
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235813039"
variation 1331
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1038080705"
variation 1333
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1042309976"
variation 1336
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010419736"
variation 1337
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1243637891"
variation 1340
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1487348112"
variation 1341
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:192225692"
variation 1343
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:983652873"
variation 1346
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:765683622"
variation 1347
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:112722049"
variation 1350
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745774185"
variation 1353
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745774144"
variation 1354
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:911260158"
variation 1356
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1420547324"
variation 1357
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1048443365"
variation 1358
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:529590716"
variation 1359
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1348525268"
variation 1363
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1436159119"
variation 1364
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745773808"
variation 1368
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1745773775"
variation 1371
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745773725"
variation 1372
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745773661"
variation 1374..1379
/gene="LINC00491"
/replace="tt"
/replace="tttctt"
/db_xref="dbSNP:756980392"
variation 1376
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745773613"
variation 1377
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1294674171"
variation 1379
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:573945787"
variation 1383
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760047014"
variation 1384
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745773307"
variation 1385
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1352250954"
variation 1389
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1224005909"
variation 1390
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:972954818"
variation 1391
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:2149547462"
variation 1392
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285853194"
variation 1395
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:2149547460"
variation 1400
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1319732757"
variation 1404
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:555343945"
variation 1406
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745772958"
variation 1407
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1220513760"
variation 1408..1415
/gene="LINC00491"
/replace="taa"
/replace="taagttaa"
/db_xref="dbSNP:1745772776"
variation 1413
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1745772824"
variation 1421
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1430508085"
variation 1427
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1745772666"
variation 1429
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:56170429"
variation 1431
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:187388775"
variation 1434..1438
/gene="LINC00491"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1745772336"
variation 1435
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1237663539"
variation 1439
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745772287"
variation 1440
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:116239642"
variation 1441
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:959025549"
variation 1446
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745772105"
variation 1449
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1411860473"
variation 1450
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745772018"
variation 1451
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:760472655"
variation 1453
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745771918"
variation 1457
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1745771878"
variation 1459
/gene="LINC00491"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745771816"
variation 1461
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1745771735"
variation 1463
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1745771719"
variation 1464
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:2149547445"
variation 1467
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745771679"
variation 1468
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1050960697"
variation 1470
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:77026938"
variation 1470
/gene="LINC00491"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1745771570"
variation 1471
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1745771472"
variation 1472
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1745771428"
variation 1473
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745771392"
variation 1485
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:2149547442"
variation 1486
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745771350"
variation 1487
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1205451867"
variation 1488
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331194350"
variation 1496
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745771252"
variation 1497
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745771210"
variation 1498
/gene="LINC00491"
/replace=""
/replace="c"
/db_xref="dbSNP:1561532489"
variation 1498
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1375542608"
variation 1501
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1442243976"
variation 1510
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:566161685"
variation 1511
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:60284576"
variation 1512
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:747684484"
variation 1514
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010782778"
variation 1517
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745770770"
variation 1519
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:372808956"
variation 1520
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745770662"
variation 1521
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:182199550"
variation 1522
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1745770556"
variation 1525
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1020282343"
variation 1527
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1745770467"
variation 1528
/gene="LINC00491"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1196701183"
variation 1532
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1038010507"
variation 1538
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:567208956"
variation 1540
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1745770204"
variation 1542
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1047277231"
variation 1546
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745770106"
variation 1547..1551
/gene="LINC00491"
/replace="aagaa"
/replace="aagaagaa"
/db_xref="dbSNP:1310060746"
variation 1548..1555
/gene="LINC00491"
/replace="aga"
/replace="agaacaga"
/db_xref="dbSNP:1220701531"
variation 1549
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1472588800"
variation 1553
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1188839246"
variation 1559
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1420489315"
variation 1564
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:929478809"
variation 1571
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:928830831"
variation 1573
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:889769244"
variation 1574
/gene="LINC00491"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1048350557"
variation 1576
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:931331266"
variation 1580
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:2149547408"
variation 1582
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330292135"
variation 1583..1589
/gene="LINC00491"
/replace="tttttt"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:1356870487"
variation 1583
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745769260"
variation 1589
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745769094"
variation 1591
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:897191537"
variation 1592
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:149498756"
variation 1598
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1580580030"
variation 1599
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:990166576"
variation 1603
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:1745768208"
variation 1605
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1745768116"
variation 1606
/gene="LINC00491"
/replace="c"
/replace="g"
/db_xref="dbSNP:1745768023"
variation 1608
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745767951"
variation 1613
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1216535965"
variation 1614..1616
/gene="LINC00491"
/replace="a"
/replace="ata"
/db_xref="dbSNP:1745767798"
variation 1617
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:957624056"
variation 1620
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:530616133"
variation 1621..1623
/gene="LINC00491"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1339980026"
variation 1624
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:1745765557"
variation 1633
/gene="LINC00491"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332454253"
variation 1637
/gene="LINC00491"
/replace="c"
/replace="t"
/db_xref="dbSNP:1031741670"
variation 1639..1640
/gene="LINC00491"
/replace=""
/replace="atgcaaaaagtgc"
/db_xref="dbSNP:1197783780"
variation 1640..1641
/gene="LINC00491"
/replace=""
/replace="aactttttgcat"
/db_xref="dbSNP:1745765180"
variation 1640
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:202060431"
variation 1641..1642
/gene="LINC00491"
/replace=""
/replace="ctttttgcatcaa"
/db_xref="dbSNP:1554082265"
variation 1641..1642
/gene="LINC00491"
/replace="ca"
/replace="cactttttgcatca"
/replace="cactttttgcgtca"
/replace="cactttttgtatca"
/replace="catca"
/db_xref="dbSNP:rs59087646"
variation 1641
/gene="LINC00491"
/replace="c"
/replace="ctctttttgcatc"
/db_xref="dbSNP:1463799317"
variation 1642..1643
/gene="LINC00491"
/replace=""
/replace="ctttttgcatcc"
/db_xref="dbSNP:1745764690"
variation 1643
/gene="LINC00491"
/replace="a"
/replace="c"
/db_xref="dbSNP:201159036"
variation 1644
/gene="LINC00491"
/replace="g"
/replace="t"
/db_xref="dbSNP:200023150"
variation 1646
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:2149547376"
variation 1647
/gene="LINC00491"
/replace="a"
/replace="t"
/db_xref="dbSNP:1745764547"
ORIGIN
gactcggaaagggaactccctgaccccttgcgcttcccgagtgaggcaatgcctcgccctgcttcgactcgcgcatggtgcgcgcacgcactgacctgcgcccactgtctggcactccctagtgagatgaacccggtacctcagatggaaatgcagaaatcaccagtcttctgcgtcgctcacgctgggagctgtagaccggagctgttcctattcggccatcttgtctcctcccgtgggcttttggctcaattctgaataaacagtgaacatccatgtgggagcaatgaggaggaactgtagcatctggaacagtccaaaaaggaagctgggagtcagcccatcacgaggttgcttgatcagaatcacatgaactggaaattccctgtctccccttaaccagcactggaagcagatgggaagagaatagctgtgactgactcacactctaacccagcaaccctcagcatacaagtgggagaccataaagtttttcaagaccccaaaagaggccaaaggtctgataattgctgggagaaggtccactatccaagaagagaagaggaaaaggaattaaagtctccaagcactggggatgcaagaagagagttgcacaggagagaaagaagaagttgtccacggggtgaccctgcaattggagggaaatgcatgtggatatgtgcagggagtctaggaagtgaagccttagtgatcatttacaagaatgagggttaggtaaaataagggatgcaaagccacctgtagtctattctaacctcactccatcactctatacaatctgtgttttatcatctgaaatgttaagtaaagacctgtttgggtcttcttcagaatcccatacatttgagttcattagtcagaaaaagggaaaataccaccaccccatcctggaatggcagtcatgtacacttttataatgagagattgggcagcaaagggggccccttgtggacctcacccagccagagaaggaggcagaatgtttcctttactatcttttcctctccccagaggaacactacatattgttccctccatgggcttaagagaaggtgccagggttacagatagatatatcgctagctgtagagcacagggtgaattgggatgtccatgtacaaagctagggacaggagaatcagtttaaagactttaaaaataattaggaaaaaaaggaaggcctgacccaaagcttaggagtgcaggtagagaagagatggtgccatgatataccatgtctctgggacttttctgtattcctcttcctctgtatactgtattgccctcattccctatttattcaaaatctgtgctacctccactgcgaagacttccacgagaaaattcagatatttcttcttttgtggacactttctaccttacaaataagttaattttaattcaaggaagagtttttccggaaccctgttggcctgctcacaggaatgtaagttccttaaatctagggcacagtgtctttgagaactgcaatcacctacatcaacatgacatagctattaggactaagaacagagaccacctgtgtcaacatgagttactatttttttccgtgaaacatttgtccaagaaagataagactgtaaccaataaatagtttgcaagtaa
//
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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