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Previous release (v1)
2025-10-28 02:14:41, GGRNA.v2 : RefSeq release 232 (Sep, 2025)
LOCUS NR_144387 1068 bp RNA linear PRI 17-SEP-2024
DEFINITION Homo sapiens fibronectin leucine rich transmembrane protein 2
(FLRT2), transcript variant 7, non-coding RNA.
ACCESSION NR_144387
VERSION NR_144387.2
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 1068)
AUTHORS Hwang,H.J., Kang,D., Kim,J.R., Choi,J.H., Ryu,J.K., Herman,A.B.,
Ko,Y.G., Park,H.J., Gorospe,M. and Lee,J.S.
TITLE FLRT2 prevents endothelial cell senescence and vascular aging by
regulating the ITGB4/mTORC2/p53 signaling pathway
JOURNAL JCI Insight 9 (7), e172678 (2024)
PUBMED 38587072
REMARK GeneRIF: FLRT2 prevents endothelial cell senescence and vascular
aging by regulating the ITGB4/mTORC2/p53 signaling pathway.
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 1068)
AUTHORS Jiang,P., Ning,J., Yu,W., Rao,T., Ruan,Y. and Cheng,F.
TITLE FLRT2 suppresses bladder cancer progression through inducing
ferroptosis
JOURNAL J Cell Mol Med 28 (5), e17855 (2024)
PUBMED 37480224
REMARK GeneRIF: FLRT2 suppresses bladder cancer progression through
inducing ferroptosis.
REFERENCE 3 (bases 1 to 1068)
AUTHORS Bae,H., Kim,B., Lee,H., Lee,S., Kang,H.S. and Kim,S.J.
TITLE Epigenetically regulated Fibronectin leucine rich transmembrane
protein 2 (FLRT2) shows tumor suppressor activity in breast cancer
cells
JOURNAL Sci Rep 7 (1), 272 (2017)
PUBMED 28325946
REMARK GeneRIF: Taken together, these results provide insights into the
role of FLRT2 as a novel tumor suppressor in the breast, which is
inactivated by hypermethylation during tumor development.
Publication Status: Online-Only
REFERENCE 4 (bases 1 to 1068)
AUTHORS Jackson,V.A., Mehmood,S., Chavent,M., Roversi,P., Carrasquero,M.,
Del Toro,D., Seyit-Bremer,G., Ranaivoson,F.M., Comoletti,D.,
Sansom,M.S., Robinson,C.V., Klein,R. and Seiradake,E.
TITLE Super-complexes of adhesion GPCRs and neural guidance receptors
JOURNAL Nat Commun 7, 11184 (2016)
PUBMED 27091502
REMARK Publication Status: Online-Only
REFERENCE 5 (bases 1 to 1068)
AUTHORS Wu,Y., Davison,J., Qu,X., Morrissey,C., Storer,B., Brown,L.,
Vessella,R., Nelson,P. and Fang,M.
TITLE Methylation profiling identified novel differentially methylated
markers including OPCML and FLRT2 in prostate cancer
JOURNAL Epigenetics 11 (4), 247-258 (2016)
PUBMED 26890304
REMARK GeneRIF: OPCML and FLRT2 were further validated in an independent
cohort consisting of 20 low-Gleason and 33 high-Gleason tissues. We
then compared patients with biochemical recurrence (n=70) vs. those
without (n=86) in a third cohort, and they showed no difference in
methylation at these DMR loci
REFERENCE 6 (bases 1 to 1068)
AUTHORS Kuo,J.C., Han,X., Hsiao,C.T., Yates,J.R. 3rd and Waterman,C.M.
TITLE Analysis of the myosin-II-responsive focal adhesion proteome
reveals a role for beta-Pix in negative regulation of focal
adhesion maturation
JOURNAL Nat Cell Biol 13 (4), 383-393 (2011)
PUBMED 21423176
REFERENCE 7 (bases 1 to 1068)
AUTHORS Wheeler,H.E., Metter,E.J., Tanaka,T., Absher,D., Higgins,J.,
Zahn,J.M., Wilhelmy,J., Davis,R.W., Singleton,A., Myers,R.M.,
Ferrucci,L. and Kim,S.K.
TITLE Sequential use of transcriptional profiling, expression
quantitative trait mapping, and gene association implicates MMP20
in human kidney aging
JOURNAL PLoS Genet 5 (10), e1000685 (2009)
PUBMED 19834535
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 8 (bases 1 to 1068)
AUTHORS Haines,B.P., Wheldon,L.M., Summerbell,D., Heath,J.K. and Rigby,P.W.
TITLE Regulated expression of FLRT genes implies a functional role in the
regulation of FGF signalling during mouse development
JOURNAL Dev Biol 297 (1), 14-25 (2006)
PUBMED 16872596
REFERENCE 9 (bases 1 to 1068)
AUTHORS Zhang,Z. and Henzel,W.J.
TITLE Signal peptide prediction based on analysis of experimentally
verified cleavage sites
JOURNAL Protein Sci 13 (10), 2819-2824 (2004)
PUBMED 15340161
REFERENCE 10 (bases 1 to 1068)
AUTHORS Lacy,S.E., Bonnemann,C.G., Buzney,E.A. and Kunkel,L.M.
TITLE Identification of FLRT1, FLRT2, and FLRT3: a novel family of
transmembrane leucine-rich repeat proteins
JOURNAL Genomics 62 (3), 417-426 (1999)
PUBMED 10644439
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AL049775.2 and BX119446.1.
On Aug 14, 2020 this sequence version replaced NR_144387.1.
Summary: This gene encodes a member of the fibronectin leucine rich
transmembrane (FLRT) family of cell adhesion molecules, which
regulate early embryonic vascular and neural development. The
encoded type I transmembrane protein has an extracellular region
consisting of an N-terminal leucine-rich repeat domain and a type 3
fibronectin domain, followed by a transmembrane domain and a short
C-terminal cytoplasmic tail domain. It functions as both a
homophilic cell adhesion molecule and a heterophilic chemorepellent
through its interaction with members of the uncoordinated-5
receptor family. Proteolytic removal of the extracellular region
controls the migration of neurons in the developing cortex.
Alternative splicing results in multiple transcript variants.
[provided by RefSeq, Sep 2016].
Transcript Variant: This variant (7) uses an alternate exon
structure compared to variant 1 and lacks the coding region found
in variant 1. This variant is represented as non-coding because it
lacks the entire coding region found in 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.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: CF128778.1 [ECO:0000332]
RNAseq introns :: partial sample support SAMEA1965299,
SAMEA1966682 [ECO:0000350]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-391 AL049775.2 95847-96237
392-447 AL049775.2 96870-96925
448-558 AL049775.2 118436-118546
559-586 AL049775.2 126893-126920
587-1068 BX119446.1 1-482
FEATURES Location/Qualifiers
source 1..1068
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="14"
/map="14q31.3"
gene 1..1068
/gene="FLRT2"
/note="fibronectin leucine rich transmembrane protein 2"
/db_xref="GeneID:23768"
/db_xref="HGNC:HGNC:3761"
/db_xref="MIM:604807"
misc_RNA 1..1068
/gene="FLRT2"
/product="fibronectin leucine rich transmembrane protein
2, transcript variant 7"
/db_xref="GeneID:23768"
/db_xref="HGNC:HGNC:3761"
/db_xref="MIM:604807"
exon 1..391
/gene="FLRT2"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1888180495"
variation 3
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:775726523"
variation 4
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:887157230"
variation 6
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888180732"
variation 8
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1281900910"
variation 9
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:974461203"
variation 12
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1319728529"
variation 19
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1432821843"
variation 22
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2503404629"
variation 25
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1346690866"
variation 26
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888181503"
variation 30
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1888181634"
variation 31..32
/gene="FLRT2"
/replace=""
/replace="tt"
/db_xref="dbSNP:1488906559"
variation 34
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1159598297"
variation 36
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1401484231"
variation 39
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1413420693"
variation 42
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1888182438"
variation 43
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:919965514"
variation 44
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888182793"
variation 46
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888182917"
variation 48
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888183034"
variation 49
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1446455214"
variation 51
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1057339717"
variation 52
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888183329"
variation 53
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2139786646"
variation 60
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:150485276"
variation 62
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1265282513"
variation 63
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1888183806"
variation 67
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:982837263"
variation 70
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:912688720"
variation 73
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888184286"
variation 74
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1450670428"
variation 77
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:944219944"
variation 78
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1566709351"
variation 79
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888184657"
variation 80
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888184786"
variation 81
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:895761087"
variation 83..89
/gene="FLRT2"
/replace="atca"
/replace="atcatca"
/db_xref="dbSNP:2503404797"
variation 87
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2503404804"
variation 88
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247721490"
variation 95
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1888185171"
variation 96
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:573586763"
variation 97
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1182429349"
variation 102
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1039926925"
variation 105
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1888185970"
variation 106
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1888186175"
variation 107
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1411232560"
variation 108
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566709372"
variation 109
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1888186828"
variation 110
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888186999"
variation 112
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1364035282"
variation 115
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1455427007"
variation 116
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1435583532"
variation 117
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2139786802"
variation 120
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2139786810"
variation 121
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:796457612"
variation 125..129
/gene="FLRT2"
/replace="ct"
/replace="ctcct"
/db_xref="dbSNP:1394988750"
variation 126
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1022622846"
variation 127
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2139786825"
variation 128
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301466591"
variation 131
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1888188768"
variation 133
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1426814507"
variation 134
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:543945882"
variation 135
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1168084849"
variation 139
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448182839"
variation 140
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1422342907"
variation 141
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1187465545"
variation 143
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:947688646"
variation 144
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1888190262"
variation 146
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2139786895"
variation 147
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1457055010"
variation 148
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1888190669"
variation 150
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1594972542"
variation 151
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1888190884"
variation 152
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1042744587"
variation 154
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:902887542"
variation 155
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:998571175"
variation 157
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1035442666"
variation 158
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888192005"
variation 160
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2139786950"
variation 161
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1309184983"
variation 162..205
/gene="FLRT2"
/replace="gtg"
/replace="gtgcccagcagcggcgaggcggcatctccgctcccgccgccgtg"
/db_xref="dbSNP:2503405016"
variation 164
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888192451"
variation 167
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2503405029"
variation 169
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888192667"
variation 170
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296128445"
variation 172
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2139786979"
variation 174
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888193066"
variation 175
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:895627417"
variation 176
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1594972583"
variation 177
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888193623"
variation 179
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1365164677"
variation 182
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:999781230"
variation 184
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:113033644"
variation 185
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:56105610"
variation 186
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1460588007"
variation 190
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022820245"
variation 191
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1171664289"
variation 192
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1414419072"
variation 193
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1594972642"
variation 196
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1427586538"
variation 203
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1350455864"
variation 204
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:988342472"
variation 206
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:963622059"
variation 210
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295447985"
variation 211
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1322707560"
variation 214
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:531114003"
variation 221
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:546450205"
variation 222
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026908377"
variation 223
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1888196334"
variation 224
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1263966815"
variation 228
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:564768939"
variation 232
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:528825348"
variation 237
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1594972721"
variation 239
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1888196816"
variation 240
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888196924"
variation 242
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1888197020"
variation 243
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223954310"
variation 248
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888197239"
variation 251
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888197363"
variation 252
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1206022443"
variation 253
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:376621464"
variation 258
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888197747"
variation 262
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888197869"
variation 264
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:912657780"
variation 267
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888198134"
variation 268
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:931310231"
variation 269
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1414178422"
variation 271
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:751097239"
variation 273
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1423033197"
variation 275
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:965517807"
variation 276
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:984083142"
variation 278
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:547279808"
variation 281
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1470471181"
variation 283
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1594972790"
variation 285
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888199421"
variation 289..292
/gene="FLRT2"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1888199565"
variation 293
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1355976787"
variation 301
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:975969774"
variation 305
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:754553949"
variation 308
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:895634398"
variation 311
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250579776"
variation 313
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888200395"
variation 318
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:948671605"
variation 319
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:118107793"
variation 324
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888200903"
variation 325
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2139787291"
variation 326
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888201042"
variation 333
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1244962100"
variation 335
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1888201155"
variation 336
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:904407174"
variation 338
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328156236"
variation 342..344
/gene="FLRT2"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1888201675"
variation 342
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:561884493"
variation 343
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2503405377"
variation 348
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:529307953"
variation 349..350
/gene="FLRT2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1318993624"
variation 354
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380339426"
variation 355
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888202267"
variation 357
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888202459"
variation 359
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1395581317"
variation 360
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1888202911"
variation 362
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1339206104"
variation 363
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1888203281"
variation 364
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888203400"
variation 366
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1031727861"
variation 367
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1888203672"
variation 370
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1388317923"
variation 372
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888203907"
variation 374
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888204037"
variation 377
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1287530347"
variation 378
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:947620442"
variation 380
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1009046187"
variation 381
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163458319"
variation 382
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:776772455"
variation 384..385
/gene="FLRT2"
/replace=""
/replace="gtaa"
/db_xref="dbSNP:1888204724"
variation 385
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:924235174"
variation 387
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1310816648"
variation 388
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:934333959"
variation 389
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1888205272"
exon 392..447
/gene="FLRT2"
/inference="alignment:Splign:2.1.0"
variation 394
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1422054024"
variation 395
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:747169641"
variation 396
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1888245706"
variation 403
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187518381"
variation 404
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1275458765"
variation 409
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:377079360"
variation 410
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:537191156"
variation 414
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1888246307"
variation 415
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201139581"
variation 416..417
/gene="FLRT2"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1888246714"
variation 416
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:768830897"
variation 417..435
/gene="FLRT2"
/replace="tggagagcatacgaggcgg"
/replace="tggagagcatacgaggcggtggagagcatacgaggcgg"
/db_xref="dbSNP:1490353833"
variation 419..431
/gene="FLRT2"
/replace="gagagcatacgag"
/replace="gagagcatacgagagcatacgag"
/db_xref="dbSNP:1231833331"
variation 421
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1286335902"
variation 422
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1202305620"
variation 423
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1309238848"
variation 425
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:935961617"
variation 426
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1888247616"
variation 427..443
/gene="FLRT2"
/replace="acgaggcggaatccgga"
/replace="acgaggcggaatccggacgaggcggaatccgga"
/db_xref="dbSNP:1207930316"
variation 428
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1265811968"
variation 428
/gene="FLRT2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1774614257"
variation 429
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:187518764"
variation 431
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1199161318"
variation 433..436
/gene="FLRT2"
/replace=""
/replace="cgga"
/db_xref="dbSNP:1297719417"
variation 433
/gene="FLRT2"
/replace=""
/replace="c"
/db_xref="dbSNP:1245569653"
variation 433
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:913113979"
variation 434
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:978912257"
variation 435..437
/gene="FLRT2"
/replace=""
/replace="gaa"
/db_xref="dbSNP:1566710161"
variation 435
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1888249059"
variation 437
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469551709"
variation 438
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888249487"
variation 439
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:146131114"
variation 440
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:776567449"
variation 441..442
/gene="FLRT2"
/replace=""
/replace="gg"
/db_xref="dbSNP:1491582080"
variation 441
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1414911350"
variation 442
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:555154149"
variation 442
/gene="FLRT2"
/replace="g"
/replace="ggcgag"
/db_xref="dbSNP:1491181388"
variation 443
/gene="FLRT2"
/replace=""
/replace="a"
/db_xref="dbSNP:1888251247"
variation 443
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:916862217"
variation 444
/gene="FLRT2"
/replace=""
/replace="t"
/db_xref="dbSNP:1888251649"
variation 444
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:140120710"
variation 445
/gene="FLRT2"
/replace=""
/replace="c"
/db_xref="dbSNP:1888252041"
variation 445
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1005683094"
variation 446
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:562639400"
variation 447
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1888252458"
exon 448..558
/gene="FLRT2"
/inference="alignment:Splign:2.1.0"
variation 448
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1889713951"
variation 450
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1435514259"
variation 453
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1178240518"
variation 458
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:893617994"
variation 460
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376485759"
variation 461
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344208551"
variation 469
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1889715392"
variation 470
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:577906954"
variation 471
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2503460825"
variation 476
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566723603"
variation 480
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1889716104"
variation 481
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:181165903"
variation 491
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1889716673"
variation 493
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1225052167"
variation 494
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1167425730"
variation 495
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386093369"
variation 499
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1042326764"
variation 500
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1284109137"
variation 504
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1441722854"
variation 505
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:756811734"
variation 506
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330974060"
variation 508
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1595009071"
variation 510
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1392540007"
variation 512
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1889718998"
variation 519
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1889719262"
variation 520
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2139828163"
variation 523
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1595009095"
variation 524..527
/gene="FLRT2"
/replace="tatt"
/replace="tatttatt"
/db_xref="dbSNP:1889719815"
variation 525
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:983415413"
variation 530
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1174735333"
variation 531
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1889720547"
variation 541
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:117266817"
variation 542
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:572320814"
variation 548
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035711378"
variation 554
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1889721935"
exon 559..658
/gene="FLRT2"
/inference="alignment:Splign:2.1.0"
variation 560
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2139844815"
variation 562
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1890296807"
variation 570
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:952479748"
variation 571
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890297167"
variation 574
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:755589217"
variation 578
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:908367733"
variation 579
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1890297628"
variation 582
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1299066340"
variation 583
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316786846"
variation 584
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2139844862"
variation 590..591
/gene="FLRT2"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1890298073"
variation 595
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2139844870"
variation 610
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890298240"
variation 611
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:187873507"
variation 614
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1167075369"
variation 617
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890298680"
variation 620
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890298848"
variation 621
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890299000"
variation 624
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424468957"
variation 627
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:879456951"
variation 628
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:767246801"
variation 629
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1294014707"
variation 630
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1890299838"
variation 633
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1890299976"
variation 634
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1185226191"
variation 640
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:193018774"
variation 641
/gene="FLRT2"
/replace=""
/replace="a"
/db_xref="dbSNP:1264294890"
variation 646
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2139844944"
variation 648
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1199125474"
variation 653
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890300749"
variation 654
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1040948130"
variation 657
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1890301206"
exon 659..1068
/gene="FLRT2"
/inference="alignment:Splign:2.1.0"
variation 660
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2139847685"
variation 662
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:987218903"
variation 664
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1169888477"
variation 668
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890418284"
variation 670
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1018252140"
variation 672
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1890418651"
variation 676
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1321091764"
variation 680
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1387939130"
variation 681
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2503485214"
variation 683
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:770070687"
variation 687
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:964119982"
variation 688
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1595027794"
variation 690
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2139847742"
variation 696
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1890419506"
variation 699
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1890419670"
variation 709
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1890419835"
variation 713..727
/gene="FLRT2"
/replace="agg"
/replace="agggcagtattcagg"
/db_xref="dbSNP:1890420134"
variation 713
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1595027801"
variation 717
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777990680"
variation 721
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2503485325"
variation 722
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:974115504"
variation 728
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1425564082"
variation 733
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:749298971"
variation 734
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1377276003"
variation 735
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196847725"
variation 744
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:770744618"
variation 745
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1054252875"
variation 750
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890421759"
variation 753
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:535414728"
variation 754
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1198524321"
variation 756
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377261277"
variation 757
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1415338241"
variation 758
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:137873561"
variation 767
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890423365"
variation 770
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890423594"
variation 775
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890423839"
variation 776
/gene="FLRT2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1890424078"
variation 784
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2503485456"
variation 787
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:539784298"
variation 795
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010101157"
variation 797
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272660114"
variation 801
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1595027935"
variation 802
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890425415"
variation 803
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1020140923"
variation 804
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:928552403"
variation 805
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1270452644"
variation 812
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:938585564"
variation 813
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1890426680"
variation 819
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890426925"
variation 822
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890427178"
variation 823
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:907106316"
variation 826
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:894130240"
variation 831
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1890427801"
variation 833..849
/gene="FLRT2"
/replace="aat"
/replace="aatgacctgggggaaat"
/db_xref="dbSNP:1352150121"
variation 835
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1890428099"
variation 838
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1329367242"
variation 839
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1413627510"
variation 841..845
/gene="FLRT2"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1566729611"
variation 841
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:774306944"
variation 843
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1281864993"
variation 845
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:112458751"
variation 851
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1170985510"
variation 855
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:575303911"
variation 860
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:947152323"
variation 864..871
/gene="FLRT2"
/replace="aag"
/replace="aagcaaag"
/db_xref="dbSNP:1890429767"
variation 864
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:539937698"
variation 869
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890429935"
variation 871
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890430090"
variation 873
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2503485701"
variation 874
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2139848018"
variation 876
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1890430299"
variation 878
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1178075714"
variation 883
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890430810"
variation 884
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1002758519"
variation 885
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:187574706"
variation 887
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1441092249"
variation 890
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1183004537"
variation 892..895
/gene="FLRT2"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1000109268"
variation 892
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1216469403"
variation 897
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1276106897"
variation 899
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:959402849"
variation 900
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1212631264"
variation 910
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:991308854"
variation 911
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1284765311"
variation 920
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890433804"
variation 921
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:558412946"
variation 930
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1375444592"
variation 936..938
/gene="FLRT2"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1280005989"
variation 938
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1447040972"
variation 944
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890435131"
variation 948
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1890435365"
variation 949
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:189447924"
variation 952
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1475117434"
variation 957
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2139848120"
variation 961
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1335901808"
variation 965
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890436312"
variation 966
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890436579"
variation 969
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2503485897"
variation 971
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890436813"
variation 973
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1436870871"
variation 976
/gene="FLRT2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1008461176"
variation 977
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1158128526"
variation 980
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:866319884"
variation 981
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890438005"
variation 991
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890438246"
variation 992
/gene="FLRT2"
/replace=""
/replace="c"
/db_xref="dbSNP:1166171479"
variation 995
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:963189164"
variation 997
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1890438998"
variation 998
/gene="FLRT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1890439238"
variation 1000..1011
/gene="FLRT2"
/replace="tctacttatcta"
/replace="tctacttatctacttatcta"
/db_xref="dbSNP:561145817"
variation 1003
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1890439756"
variation 1005..1011
/gene="FLRT2"
/replace=""
/replace="ttatcta"
/db_xref="dbSNP:1890440089"
variation 1005
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1018720168"
variation 1007
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:964006488"
variation 1008
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1435214732"
variation 1010
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1890440238"
variation 1013
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:972918389"
variation 1014
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:562004715"
variation 1018..1021
/gene="FLRT2"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1485835171"
variation 1019
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1890440957"
variation 1022
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2139848222"
variation 1024
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1890441117"
variation 1025
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:934199559"
variation 1026
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1261929846"
variation 1027
/gene="FLRT2"
/replace=""
/replace="t"
/db_xref="dbSNP:1213837506"
variation 1029
/gene="FLRT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318146602"
variation 1031
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:573993910"
variation 1035
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1383776939"
variation 1039
/gene="FLRT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1027030889"
variation 1044..1051
/gene="FLRT2"
/replace="aataa"
/replace="aataataa"
/db_xref="dbSNP:1325433013"
variation 1046
/gene="FLRT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1890442730"
variation 1051
/gene="FLRT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2503486145"
variation 1059
/gene="FLRT2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1294963248"
variation 1062..1066
/gene="FLRT2"
/replace="tt"
/replace="ttttt"
/db_xref="dbSNP:2503486164"
variation 1066
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1890443117"
variation 1067..1068
/gene="FLRT2"
/replace=""
/replace="g"
/replace="t"
/db_xref="dbSNP:1356352378"
variation 1068
/gene="FLRT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:987055995"
ORIGIN
agttgtacgttcgaaacctgtcgccgtcacttgcgcgtttggcattatccattgtcaccgcggaggaacgagcgctcgagatatcatcagtgcccgcaaatctccgcgccaaggcgctgagctactcctttccgaggtgcgcctctggtcctccgtccctggtgcccagcagcggcgaggcggcatctccgctcccgccgccgtgtccaccgagccctgggatcagggtggcagttctcaacgatgggcaggagggacctcggcggcgacccctaaaacaataccatgccccgggatccccgctgctgccgcgccagcgtcttccctttccacctccctgaccctgtcggattcggatgagcccattgcaaggagaagacgcagccgtcagagcgcctgcggaggtggcgaaggcttggagagcatacgaggcggaatccggatcgaacaggtaagacacggagacctttgggttgatggcaagatttggagggctgattatggcgcctttgatgtgaggaggtattcctgcaatccttccgagacacctaagctgcttttcagaagctatctcctgagcagtgtgtaattctctcctggctgtttgatggtaatgggagctgtacatgtatctggagagaggagaaccagcctggggactcaagatatattaaagactatgctcatggacatcaattctttcctgtcctttagggcagtattcaggccacacggttcaataacgggaaagaatgtcgtcacatgattgcatcatgttcttcaaaatgaaatctattgaacagtataaacaacaaagaacatcatttgtcagaatgacctgggggaaatagtccagtgaaactaagcaaagggaactttataccgtgagggaaaatcaatggattgtaacagaaccctgcaagaagagacatagctttcaagttccagagacctagaggtgactgagaagcaggatgtaccagaaactgggcttcttgttctacttatctagcgcccttttcacagtgttgtatatgtaaataaataataaagcagtgtgatttttaa
//
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]