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Previous release (v1)
2020-11-27 01:07:16, GGRNA.v2 : RefSeq release 202 (Sep, 2020)
LOCUS NM_016932 2206 bp mRNA linear PRI 25-JUL-2020
DEFINITION Homo sapiens SIX homeobox 2 (SIX2), mRNA.
ACCESSION NM_016932
VERSION NM_016932.5
KEYWORDS RefSeq; MANE Select.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 2206)
AUTHORS Luck K, Kim DK, Lambourne L, Spirohn K, Begg BE, Bian W, Brignall
R, Cafarelli T, Campos-Laborie FJ, Charloteaux B, Choi D, Cote AG,
Daley M, Deimling S, Desbuleux A, Dricot A, Gebbia M, Hardy MF,
Kishore N, Knapp JJ, Kovacs IA, Lemmens I, Mee MW, Mellor JC,
Pollis C, Pons C, Richardson AD, Schlabach S, Teeking B, Yadav A,
Babor M, Balcha D, Basha O, Bowman-Colin C, Chin SF, Choi SG,
Colabella C, Coppin G, D'Amata C, De Ridder D, De Rouck S,
Duran-Frigola M, Ennajdaoui H, Goebels F, Goehring L, Gopal A,
Haddad G, Hatchi E, Helmy M, Jacob Y, Kassa Y, Landini S, Li R, van
Lieshout N, MacWilliams A, Markey D, Paulson JN, Rangarajan S,
Rasla J, Rayhan A, Rolland T, San-Miguel A, Shen Y, Sheykhkarimli
D, Sheynkman GM, Simonovsky E, Tasan M, Tejeda A, Tropepe V,
Twizere JC, Wang Y, Weatheritt RJ, Weile J, Xia Y, Yang X,
Yeger-Lotem E, Zhong Q, Aloy P, Bader GD, De Las Rivas J, Gaudet S,
Hao T, Rak J, Tavernier J, Hill DE, Vidal M, Roth FP and Calderwood
MA.
TITLE A reference map of the human binary protein interactome
JOURNAL Nature 580 (7803), 402-408 (2020)
PUBMED 32296183
REFERENCE 2 (bases 1 to 2206)
AUTHORS Wan ZH, Ma YH, Jiang TY, Lin YK, Shi YY, Tan YX, Dong LW and Wang
HY.
TITLE Six2 is negatively correlated with prognosis and facilitates
epithelial-mesenchymal transition via TGF-beta/Smad signal pathway
in hepatocellular carcinoma
JOURNAL HBPD INT 18 (6), 525-531 (2019)
PUBMED 31564506
REMARK GeneRIF: Elevated Six2 expression in hepatocellular carcinoma
patients was associated with negative prognosis. Upregulated Six2
promoted tumor growth and facilitated HCC metastasis via
TGF-beta/Smad signal pathway.
REFERENCE 3 (bases 1 to 2206)
AUTHORS Cheng N, Li H, Han Y and Sun S.
TITLE Transcription factor Six2 induces a stem cell-like phenotype in
renal cell carcinoma cells
JOURNAL FEBS Open Bio 9 (10), 1808-1816 (2019)
PUBMED 31420918
REMARK GeneRIF: The six2 knockdown attenuated the stemness of Renal cell
carcinoma (RCC) cells, which was evident by decreased spheroid
formation ability and stemness marker (sox2 and nanog) expression.
REFERENCE 4 (bases 1 to 2206)
AUTHORS Wu Y, Song T, Liu M, He Q, Chen L, Liu Y, Ni D, Liu J, Hu Y, Gu Y,
Li Q, Zhou Q and Xie Y.
TITLE PPARG Negatively Modulates Six2 in Tumor Formation of Clear Cell
Renal Cell Carcinoma
JOURNAL DNA Cell Biol. 38 (7), 700-707 (2019)
PUBMED 31090452
REMARK GeneRIF: Six2 expression negatively correlated with the overall
survival of clear cell renal cell carcinoma patients.
REFERENCE 5 (bases 1 to 2206)
AUTHORS Rodas LM, Garcia-Herrera A, Ramirez Bajo M, Fernandez-Larrea C,
Cibeira MT, Blasco M, Rosinol L, Sole M, Blade J, Campistol JM and
Quintana LF.
TITLE Six-2 glomerular expression for the prediction of renal outcome in
systemic amyloidosis
JOURNAL Amyloid 26 (sup1), 97-98 (2019)
PUBMED 31343337
REMARK GeneRIF: Glomerular Six-2 deposits in renal biopsy should be
validated in prospective series as a predictor of renal outcome in
renal amyloidosis
REFERENCE 6 (bases 1 to 2206)
AUTHORS Weber S, Taylor JC, Winyard P, Baker KF, Sullivan-Brown J, Schild
R, Knuppel T, Zurowska AM, Caldas-Alfonso A, Litwin M, Emre S,
Ghiggeri GM, Bakkaloglu A, Mehls O, Antignac C, Network E, Schaefer
F and Burdine RD.
TITLE SIX2 and BMP4 mutations associate with anomalous kidney development
JOURNAL J. Am. Soc. Nephrol. 19 (5), 891-903 (2008)
PUBMED 18305125
REMARK GeneRIF: Defects in these proteins could affect kidney development
at multiple stages, leading to the congenital anomalies observed in
patients with renal hypodysplasia
REFERENCE 7 (bases 1 to 2206)
AUTHORS Buller C, Xu X, Marquis V, Schwanke R and Xu PX.
TITLE Molecular effects of Eya1 domain mutations causing organ defects in
BOR syndrome
JOURNAL Hum. Mol. Genet. 10 (24), 2775-2781 (2001)
PUBMED 11734542
REFERENCE 8 (bases 1 to 2206)
AUTHORS Boucher CA, Winchester CL, Hamilton GM, Winter AD, Johnson KJ and
Bailey ME.
TITLE Structure, mapping and expression of the human gene encoding the
homeodomain protein, SIX2
JOURNAL Gene 247 (1-2), 145-151 (2000)
PUBMED 10773454
REFERENCE 9 (bases 1 to 2206)
AUTHORS Celli J, van Beusekom E, Hennekam RC, Gallardo ME, Smeets DF, de
Cordoba SR, Innis JW, Frydman M, Konig R, Kingston H, Tolmie J,
Govaerts LC, van Bokhoven H and Brunner HG.
TITLE Familial syndromic esophageal atresia maps to 2p23-p24
JOURNAL Am. J. Hum. Genet. 66 (2), 436-444 (2000)
PUBMED 10677303
REFERENCE 10 (bases 1 to 2206)
AUTHORS Kawakami K, Ohto H, Takizawa T and Saito T.
TITLE Identification and expression of six family genes in mouse retina
JOURNAL FEBS Lett. 393 (2-3), 259-263 (1996)
PUBMED 8814301
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AC012354.11, AF332197.1,
BC024033.2, AI697804.1 and AI299144.1.
This sequence is a reference standard in the RefSeqGene project.
On Nov 23, 2018 this sequence version replaced NM_016932.4.
Summary: This gene is a member of the vertebrate gene family which
encode proteins homologous to the Drosophila 'sine oculis' homeobox
protein. The encoded protein is a transcription factor which, like
other members of this gene family, may be involved in limb or eye
development. [provided by RefSeq, Dec 2008].
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 :: AF332197.1, BC024033.2 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1968540, SAMEA1968832
[ECO:0000348]
##Evidence-Data-END##
##RefSeq-Attributes-START##
MANE Ensembl match :: ENST00000303077.7/ ENSP00000304502.6
RefSeq Select criteria :: based on conservation, expression
##RefSeq-Attributes-END##
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-49 AC012354.11 166978-167026 c
50-995 AF332197.1 1-946
996-1840 BC024033.2 927-1771
1841-2185 AI697804.1 1-345 c
2186-2203 AI299144.1 25-42 c
2204-2206 AC012354.11 162756-162758 c
FEATURES Location/Qualifiers
source 1..2206
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="2"
/map="2p21"
gene 1..2206
/gene="SIX2"
/note="SIX homeobox 2"
/db_xref="GeneID:10736"
/db_xref="HGNC:HGNC:10888"
/db_xref="MIM:604994"
exon 1..902
/gene="SIX2"
/inference="alignment:Splign:2.1.0"
variation 1..5
/gene="SIX2"
/replace="aa"
/replace="aagaa"
/db_xref="dbSNP:1375869578"
variation 3
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1455107641"
variation 4
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1572650601"
variation 7
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045695560"
variation 9
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:930329175"
variation 11
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433695325"
variation 12
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1447429736"
variation 15
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:920220778"
variation 16
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:971697866"
variation 19
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1312949131"
variation 24
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:940485146"
variation 25
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:911613497"
variation 27
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1572650575"
variation 30
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:987351627"
variation 36
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:953308091"
variation 37
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1243947958"
variation 46
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1028930693"
variation 47
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:978637307"
variation 48
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:968047691"
variation 50
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1171945585"
variation 51
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1356973627"
variation 52
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:554687033"
variation 54
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1009566550"
variation 56
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1217829402"
variation 59
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454926060"
variation 60
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1318887551"
variation 63
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1365133933"
variation 66
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:952310972"
variation 69..77
/gene="SIX2"
/replace="gcgcggagc"
/replace="gcgcggagcgcgcggagc"
/db_xref="dbSNP:1043263252"
variation 70
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1024345714"
variation 75
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1487016006"
variation 78
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:866575066"
variation 79
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1233233594"
variation 83
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1329121680"
variation 86
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1264060486"
variation 87
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1462771515"
variation 89
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1206603957"
variation 90
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1003727325"
variation 94
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486055146"
variation 98
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1188260606"
variation 99..100
/gene="SIX2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:905334308"
variation 99
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1284691975"
variation 101
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1216206080"
variation 106..127
/gene="SIX2"
/replace="gggcttgggc"
/replace="gggcttgggcgagggcttgggc"
/db_xref="dbSNP:545280202"
variation 110
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1430996862"
variation 113
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1455275182"
variation 125
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318996159"
variation 129
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:930932115"
variation 137
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1291201835"
variation 140
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1366105661"
variation 143
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278370826"
variation 145
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:899422565"
variation 149
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1325954104"
variation 151
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1399879599"
variation 160
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1267718660"
variation 163
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1036010634"
variation 173..174
/gene="SIX2"
/replace=""
/replace="g"
/db_xref="dbSNP:1350158299"
variation 173
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1462815960"
variation 175
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1317359533"
variation 177
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1217674744"
variation 181
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1199546125"
variation 186
/gene="SIX2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471304683"
variation 190
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1158022244"
variation 200
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302029250"
variation 204
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:940348081"
variation 207
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:911661330"
variation 209
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1408160169"
variation 210
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:535223850"
variation 212
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1178709571"
variation 215
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:987603924"
variation 220
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:931838952"
variation 223
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1347521795"
variation 224
/gene="SIX2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:921728930"
variation 227..242
/gene="SIX2"
/replace="cc"
/replace="ccagggggccagcccc"
/db_xref="dbSNP:1225272566"
variation 229
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1430509283"
variation 230
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1254573956"
variation 234
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1200210494"
variation 239
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1374246345"
variation 241
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:569522660"
variation 243
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483882188"
variation 246
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:549628521"
variation 248
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:563220941"
variation 250
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1196224151"
variation 251
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:968660827"
variation 253
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1481819235"
variation 255
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1180815734"
variation 258
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1278270360"
variation 259..260
/gene="SIX2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:913132667"
variation 263
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:533097092"
variation 267
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1338311284"
variation 270
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424400501"
variation 273
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1164841634"
variation 274
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:988166599"
variation 276
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1311783573"
variation 280
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328201302"
variation 282
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396348353"
variation 284
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355362274"
variation 286
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:535238556"
variation 287
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1035129104"
variation 292
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1381827628"
variation 295
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1417923146"
variation 297
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1166544818"
variation 299
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1185453944"
variation 300..307
/gene="SIX2"
/replace=""
/replace="ccggtgag"
/db_xref="dbSNP:1439285800"
variation 301
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1486519672"
variation 302..327
/gene="SIX2"
/replace="gg"
/replace="ggtgagggcgcgcgcgggcgggcggg"
/db_xref="dbSNP:1205212671"
variation 302
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1474180228"
variation 303
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1003996649"
misc_feature 304..306
/gene="SIX2"
/note="upstream in-frame stop codon"
variation 307
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1182452020"
variation 309..317
/gene="SIX2"
/replace="gcgcgcg"
/replace="gcgcgcgcg"
/db_xref="dbSNP:771892913"
variation 311
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1248189859"
variation 314
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:969590576"
variation 315
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1335789488"
variation 316
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:113836842"
variation 317
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1231607232"
variation 320
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:753012609"
variation 321..323
/gene="SIX2"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1448154178"
variation 321
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1280592680"
variation 326
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1445022111"
variation 328
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1334315848"
variation 330
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1328658014"
variation 332
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1445559796"
variation 333
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1394847488"
variation 334
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374980680"
variation 335
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:755177564"
variation 336
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1036544667"
variation 338
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1412469861"
variation 341
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:766486968"
CDS 343..1218
/gene="SIX2"
/note="sine oculis homeobox homolog 2"
/codon_start=1
/product="homeobox protein SIX2"
/protein_id="NP_058628.3"
/db_xref="CCDS:CCDS1822.1"
/db_xref="GeneID:10736"
/db_xref="HGNC:HGNC:10888"
/db_xref="MIM:604994"
/translation="
MSMLPTFGFTQEQVACVCEVLQQGGNIERLGRFLWSLPACEHLHKNESVLKAKAVVAFHRGNFRELYKILESHQFSPHNHAKLQQLWLKAHYIEAEKLRGRPLGAVGKYRVRRKFPLPRSIWDGEETSYCFKEKSRSVLREWYAHNPYPSPREKRELAEATGLTTTQVSNWFKNRRQRDRAAEAKERENNENSNSNSHNPLNGSGKSVLGSSEDEKTPSGTPDHSSSSPALLLSPPPPGLPSLHSLGHPPGPSAVPVPVPGGGGADPLQHHHGLQDSILNPMSANLVDLGS"
misc_feature 367..696
/gene="SIX2"
/note="Transcriptional regulator, SIX1, N-terminal SD
domain; Region: SIX1_SD; pfam16878"
/db_xref="CDD:318970"
misc_feature 727..882
/gene="SIX2"
/note="Homeodomain; DNA binding domains involved in the
transcriptional regulation of key eukaryotic developmental
processes; may bind to DNA as monomers or as homo- and/or
heterodimers, in a sequence-specific manner; Region:
homeodomain; cd00086"
/db_xref="CDD:238039"
misc_feature order(730..732,850..852,859..864,871..873)
/gene="SIX2"
/note="specific DNA base contacts [nucleotide binding];
other site"
/db_xref="CDD:238039"
variation 346
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471143290"
variation 349
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:760590442"
variation 350
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1572650296"
variation 355
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:773074130"
variation 357
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:767445560"
variation 360
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:761555251"
variation 363
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:774034314"
variation 364
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451062432"
variation 372
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285092172"
variation 375
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1225949527"
variation 376
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1349228254"
variation 378
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279326999"
variation 379
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1235394611"
variation 383
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:768328129"
variation 384
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:748929534"
variation 387
/gene="SIX2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201430813"
variation 390
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:745387244"
variation 395
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1348763009"
variation 399
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:778361827"
variation 401
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402361886"
variation 402
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1278038835"
variation 409
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1382783878"
variation 412
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:759005649"
variation 415
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748497053"
variation 416
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:779195505"
variation 423
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:755198683"
variation 424
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1461446076"
variation 425
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1477849344"
variation 427
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:754064188"
variation 429
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1218116448"
variation 433
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1445356095"
variation 437
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1572650203"
variation 444
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:780266512"
variation 450
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756119100"
variation 451
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1193162317"
variation 456
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750533239"
variation 459
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1350449982"
variation 461
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1170824168"
variation 463
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:767389980"
variation 465
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1004244007"
variation 468
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:141233412"
variation 469
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:142188105"
variation 471
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432211155"
variation 473
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:761885079"
variation 475
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:762656667"
variation 480
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1435301297"
variation 484
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318978237"
variation 487
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1377023303"
variation 490
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1162669421"
variation 496
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1328060990"
variation 504
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1171585184"
variation 505
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:775227612"
variation 507
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1420407308"
variation 513
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371643533"
variation 516
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:759081313"
variation 520
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772685693"
variation 522
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189229819"
variation 529
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:748645065"
variation 531
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1476186900"
variation 533
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:541992883"
variation 534
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:768843368"
variation 538
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:749666764"
variation 542
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1308451126"
variation 546
/gene="SIX2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1273204133"
variation 547
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1323853697"
variation 549
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:780209481"
variation 552
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:948792823"
variation 555
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:756350301"
variation 564
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415307802"
variation 567
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1357359319"
variation 569
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:750476114"
variation 570
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:531931374"
variation 571
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:916070659"
variation 572
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:757211278"
variation 580
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172750431"
variation 583
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1408470316"
variation 584
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422985242"
variation 589
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:751507324"
variation 594
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:924892477"
variation 595
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:11540435"
variation 596
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1476471051"
variation 597
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1255942874"
variation 598
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:372580849"
variation 606
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:764108669"
variation 611
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1481138422"
variation 618..621
/gene="SIX2"
/replace="c"
/replace="catc"
/db_xref="dbSNP:1449178426"
variation 619
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:762591882"
variation 622
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:202091722"
variation 624
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201197395"
variation 625
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1256860344"
variation 627
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1233289347"
variation 630
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:759311436"
variation 632
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201927647"
variation 633
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:956734375"
variation 634
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:370882250"
variation 640
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:563107358"
variation 643
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1373747192"
variation 644
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1474185385"
variation 649
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:760243444"
variation 654
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387079577"
variation 655
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403498689"
variation 657
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444824729"
variation 660
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1399929699"
variation 663
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:148660332"
variation 666
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:546453073"
variation 672
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1415802630"
variation 676
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1164647831"
variation 679
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1558440805"
variation 684
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200549810"
variation 690
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1410594313"
variation 693
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1175913242"
variation 696
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1457601978"
variation 702
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1237123333"
variation 705
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213947892"
variation 708
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469386806"
variation 711
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1263210272"
variation 712
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1243948703"
variation 714
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:554460571"
variation 717
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1572649959"
variation 720
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:780441973"
variation 725
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:769968755"
variation 737
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1558440775"
variation 741
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1237609240"
variation 742
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1375897164"
variation 747
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1304382860"
variation 753
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1443425620"
variation 754
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:746152954"
variation 763
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:781233805"
variation 765
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454756698"
variation 771
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:757228133"
variation 772
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1353506423"
variation 773
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:774627372"
variation 774
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:747117944"
variation 775
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:777532216"
variation 781
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758383352"
variation 783
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1291660988"
variation 785
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1572649912"
variation 793..796
/gene="SIX2"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1558440737"
variation 794
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:752521871"
variation 795
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:765167749"
variation 796
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1208795514"
variation 797
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369994485"
variation 799
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1485912555"
variation 808
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:753606261"
variation 814
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:17856709"
variation 816
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1248702754"
variation 818
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1214390648"
variation 819
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352666591"
variation 820
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:4143307"
variation 821
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:766057817"
variation 824
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1365366403"
variation 825
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:760060428"
variation 827
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1329630486"
variation 828
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1162921750"
variation 833
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:772796826"
variation 834
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:764482147"
variation 836
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1382789688"
variation 837
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1364194158"
variation 842
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:763491151"
variation 844
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419665425"
variation 847
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:775827253"
variation 849
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1175981095"
variation 852
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:770200234"
variation 856
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1375503887"
variation 864
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1558440685"
variation 866
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1426004280"
variation 879
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:746242850"
variation 880
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:776652900"
variation 881
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263265447"
variation 883
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1191384463"
variation 885
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1487951253"
variation 886
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1280768384"
variation 888
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:149963762"
variation 889
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:777958524"
variation 896
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:758241331"
variation 898
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1391568042"
variation 901
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:748167157"
exon 903..2206
/gene="SIX2"
/inference="alignment:Splign:2.1.0"
variation 907..912
/gene="SIX2"
/replace="aac"
/replace="aacaac"
/db_xref="dbSNP:748324030"
variation 907
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200344733"
variation 910
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1194969033"
variation 911
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356335988"
variation 912
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:754121582"
variation 913
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:766837477"
variation 916
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1241543297"
variation 918
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:760797511"
variation 921
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400896843"
variation 923
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1572648555"
variation 924
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1306574028"
variation 925
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:773427889"
variation 929
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200287647"
variation 930
/gene="SIX2"
/replace="c"
/replace="ccccccc"
/db_xref="dbSNP:142902677"
variation 931
/gene="SIX2"
/replace=""
/replace="a"
/db_xref="dbSNP:1325017131"
variation 936
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1403529250"
variation 938
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:761932667"
variation 940
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1389842225"
variation 941
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:768678682"
variation 942
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:749314865"
variation 944
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:779699277"
variation 947
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1301911629"
variation 948
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1572648511"
variation 950
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313834146"
variation 951
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:769572731"
variation 953
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274235733"
variation 954
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368466313"
variation 955..956
/gene="SIX2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:781427073"
variation 955
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:780785395"
variation 956..975
/gene="SIX2"
/replace="gc"
/replace="gcaagtcggtgttaggcagc"
/db_xref="dbSNP:754988977"
variation 956
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1353780152"
variation 962
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:756926148"
variation 963
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:142758861"
variation 964
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1190926704"
variation 968
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:777305156"
variation 971
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:755475328"
variation 973
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1351919311"
variation 976
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285812583"
variation 977
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:375228554"
variation 978
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:371909390"
variation 979
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276252658"
variation 984
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1441777211"
variation 985
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:202035375"
variation 987
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:767822221"
variation 989..998
/gene="SIX2"
/replace="agactccatc"
/replace="agactccatcagactccatc"
/db_xref="dbSNP:1558439864"
variation 990
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:762163556"
variation 991
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:199560829"
variation 993
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1358368001"
variation 994
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:267599390"
variation 995
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:267599389"
variation 996
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1435570189"
variation 998
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:762954429"
variation 999
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:150846320"
variation 1001
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:368309754"
variation 1003
/gene="SIX2"
/replace=""
/replace="a"
/db_xref="dbSNP:751621252"
variation 1004
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:929368932"
variation 1005
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:899341905"
variation 1006
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:770541388"
variation 1013
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1572648392"
variation 1019
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1196438825"
variation 1020
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1553342116"
variation 1029
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:746731462"
variation 1030
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:777256147"
variation 1032
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:938159059"
variation 1033
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:757871683"
variation 1034
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:747619226"
variation 1036
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:148356487"
variation 1037
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374628970"
variation 1042
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:750781834"
variation 1044
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1572648360"
variation 1045
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278334054"
variation 1046
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:143323460"
variation 1047..1065
/gene="SIX2"
/replace="gccgccccctgggctgccg"
/replace="gccgccccctgggctgccgccccctgggctgccg"
/db_xref="dbSNP:1476883933"
variation 1047
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:146943650"
variation 1048
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:751772244"
variation 1049
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:372153489"
variation 1051
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:763047709"
variation 1053
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1572648338"
variation 1055
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:74473757"
variation 1056
/gene="SIX2"
/replace=""
/replace="t"
/db_xref="dbSNP:1174176185"
variation 1056
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:78925885"
variation 1057
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1178977297"
variation 1058
/gene="SIX2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:368542610"
variation 1062..1078
/gene="SIX2"
/replace="gccgtccctgcacagcc"
/replace="gccgtccctgcacagccgtccctgcacagcc"
/db_xref="dbSNP:1481942706"
variation 1064
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:147806994"
variation 1065
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:776407664"
variation 1071
/gene="SIX2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1423461915"
variation 1072
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:955789502"
variation 1073
/gene="SIX2"
/replace="a"
/replace="agga"
/db_xref="dbSNP:1189298257"
variation 1075
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:770774500"
variation 1080
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:748746905"
variation 1081
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:267599388"
variation 1083
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1209865352"
variation 1086
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1207562028"
variation 1087
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:772787033"
variation 1091
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258142065"
variation 1092
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:771656233"
variation 1093
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:747669139"
variation 1094
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1558439771"
variation 1095
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1400875587"
variation 1099
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1558439766"
variation 1101
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:191828218"
variation 1102
/gene="SIX2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756635283"
variation 1103
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201764520"
variation 1104
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:781767774"
variation 1105..1123
/gene="SIX2"
/replace="gtgccag"
/replace="gtgccagtgccggtgccag"
/db_xref="dbSNP:780245216"
variation 1106
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:140763514"
variation 1109
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:752002260"
variation 1111
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:764326435"
variation 1113
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1353037134"
variation 1115
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:373961258"
variation 1116
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:150988696"
variation 1122
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1166247596"
variation 1123
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1426126643"
variation 1125
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371349704"
variation 1126
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:766312512"
variation 1129
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1182666595"
variation 1131
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:760424819"
variation 1133
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:146753226"
variation 1134
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1476728744"
variation 1135
/gene="SIX2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:771722023"
variation 1136
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761435514"
variation 1137
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:76298925"
variation 1138
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1038178246"
variation 1139
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1323497287"
variation 1140
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:767993033"
variation 1148
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1227471715"
variation 1149
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:552099678"
variation 1152
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:938226527"
variation 1155
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:781749684"
variation 1156
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1399615363"
variation 1157
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332096871"
variation 1158
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:905364797"
variation 1160
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370231701"
variation 1162
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1459896408"
variation 1164
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:747357830"
variation 1167
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200867142"
variation 1168
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201675842"
variation 1171
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:752920874"
variation 1172
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:779212821"
variation 1176
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1437494866"
variation 1177
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:754988790"
variation 1180
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:751880162"
variation 1181
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:753952589"
variation 1183
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1156338487"
variation 1186
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1489182063"
variation 1193
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:766259257"
variation 1195
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1572648156"
variation 1196
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:544354787"
variation 1197
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:750226051"
variation 1200
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:767269171"
variation 1201
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773807534"
variation 1203
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1421332463"
variation 1205
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:768385373"
variation 1206
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1278011609"
variation 1208
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1302254296"
variation 1210
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1388536611"
variation 1214
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:988414365"
variation 1222
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:762501206"
variation 1224
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:775188449"
variation 1225
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1362829026"
variation 1226
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:934304430"
variation 1236
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1277040930"
variation 1237
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:771534603"
variation 1242
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1211622314"
variation 1243
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1419483689"
variation 1255
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1362798887"
variation 1257
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:377630153"
variation 1260
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:778187471"
variation 1262
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:889588075"
variation 1263
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1053608184"
variation 1265
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:772268991"
variation 1266
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:748554219"
variation 1267
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:778967739"
variation 1268
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:923861384"
variation 1269
/gene="SIX2"
/replace=""
/replace="t"
/db_xref="dbSNP:1170749332"
variation 1273
/gene="SIX2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:978911179"
variation 1274
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174929041"
variation 1277
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:964615164"
variation 1278..1279
/gene="SIX2"
/replace="gg"
/replace="ggggg"
/db_xref="dbSNP:370801335"
variation 1278
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:149640128"
variation 1280
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1572648084"
variation 1281
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244478341"
variation 1283
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1327458294"
variation 1285
/gene="SIX2"
/replace=""
/replace="a"
/db_xref="dbSNP:1382645360"
variation 1290
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:992839609"
variation 1291
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:551787454"
variation 1293
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1273600779"
variation 1295
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1558439542"
variation 1296
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:954585720"
variation 1301
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1572648059"
variation 1303
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1034520440"
variation 1304
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1572648056"
variation 1306
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282623527"
variation 1308
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:535011890"
variation 1310
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1572648051"
variation 1313
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1216246166"
variation 1315
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285140111"
variation 1316
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1572648044"
variation 1318
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327844717"
variation 1320
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:993541518"
variation 1326
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1448535237"
variation 1328
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:899153734"
variation 1329
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1016386689"
variation 1330
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1002658879"
variation 1335
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378012195"
variation 1339
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:905376170"
variation 1340
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386615006"
variation 1342
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402835353"
variation 1350
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1161407477"
variation 1351
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1046518675"
variation 1352
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385726088"
variation 1353
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1184292215"
variation 1354
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1239445839"
variation 1356
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1572648009"
variation 1358..1360
/gene="SIX2"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1558439497"
variation 1360
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1572648006"
variation 1365
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261553188"
variation 1374
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:565977038"
variation 1380..1388
/gene="SIX2"
/replace="gtt"
/replace="gttcttgtt"
/db_xref="dbSNP:1288943753"
variation 1380
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208256820"
variation 1386
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1572647992"
variation 1404
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1468743151"
variation 1406
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:892745927"
variation 1408
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:900799435"
variation 1412
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1438561711"
variation 1422
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231240255"
variation 1429
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1364993486"
variation 1436
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:549480240"
variation 1439
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1471632055"
variation 1440
/gene="SIX2"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1162269075"
variation 1443
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390547054"
variation 1452
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1053105528"
variation 1453
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1006676401"
variation 1461
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1204155428"
variation 1473
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1438582273"
variation 1475
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446172892"
variation 1480
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1572647967"
variation 1485..1494
/gene="SIX2"
/replace="tctctc"
/replace="tctctctc"
/replace="tctctctctc"
/db_xref="dbSNP:1234850291"
variation 1487
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:61203820"
variation 1490
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1242965817"
variation 1494
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:563791208"
variation 1496..1499
/gene="SIX2"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1359362660"
variation 1496
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1572647951"
variation 1502
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316261626"
variation 1504
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1558439431"
variation 1507
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:936504015"
variation 1511
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:902441582"
variation 1512
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1252119530"
variation 1513..1514
/gene="SIX2"
/replace=""
/replace="ac"
/db_xref="dbSNP:1440191521"
variation 1517
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1186405824"
variation 1521..1522
/gene="SIX2"
/replace=""
/replace="tt"
/db_xref="dbSNP:1418051994"
variation 1523
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:550756140"
variation 1534
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1167502902"
variation 1535
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1421896998"
variation 1537
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:530623156"
variation 1540
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:753012009"
variation 1541
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1278421692"
variation 1547
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1572647912"
variation 1550
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1442537119"
variation 1560
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1356290933"
variation 1562
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1371978004"
variation 1563
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:563778918"
variation 1564
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:545015870"
variation 1565
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:937451294"
variation 1571..1576
/gene="SIX2"
/replace="tttttt"
/replace="ttttttt"
/db_xref="dbSNP:1317053837"
variation 1579
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1228147435"
variation 1580..1585
/gene="SIX2"
/replace="ct"
/replace="ctttct"
/db_xref="dbSNP:927369814"
variation 1583..1589
/gene="SIX2"
/replace="tct"
/replace="tctgtct"
/db_xref="dbSNP:560138698"
variation 1585
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:572780563"
variation 1586
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:984268679"
variation 1592
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:987324522"
variation 1594
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:954513960"
variation 1596
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:919209803"
variation 1597
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1257827796"
variation 1600
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:972978295"
variation 1601
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:966003346"
variation 1606
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:759715907"
variation 1614
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:963410309"
variation 1625
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:376367697"
variation 1629
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1171739611"
variation 1634
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1417217218"
variation 1638
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:542236271"
variation 1639
/gene="SIX2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:867265685"
variation 1644
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1032064619"
variation 1647
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1001124272"
variation 1651..1655
/gene="SIX2"
/replace="ct"
/replace="cttct"
/db_xref="dbSNP:1558439356"
variation 1652
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1470650026"
variation 1656
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1296576915"
variation 1657
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339600463"
variation 1660
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:776735982"
variation 1664
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:902304080"
variation 1665
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1254172921"
variation 1673
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:969420662"
variation 1675..1679
/gene="SIX2"
/replace="ct"
/replace="cttct"
/db_xref="dbSNP:1220721133"
variation 1677..1681
/gene="SIX2"
/replace="tct"
/replace="tctct"
/db_xref="dbSNP:543337097"
variation 1687
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1572647828"
variation 1689..1700
/gene="SIX2"
/replace="ctctc"
/replace="ctctcttctctc"
/db_xref="dbSNP:1224491039"
variation 1689..1694
/gene="SIX2"
/replace="ctct"
/replace="ctctct"
/db_xref="dbSNP:1013543149"
variation 1699
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2290029"
variation 1700
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1349403100"
variation 1701
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1214088555"
variation 1703
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1013737980"
variation 1705
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:937315559"
variation 1712
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:892629854"
variation 1717
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1572647808"
variation 1720..1724
/gene="SIX2"
/replace="tgtgt"
/replace="tgtgtgt"
/db_xref="dbSNP:1264260785"
variation 1720
/gene="SIX2"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1282980933"
variation 1729
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:369709057"
variation 1732
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1223806666"
variation 1735
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395836732"
variation 1736
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1351955762"
variation 1737
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1052743031"
variation 1740
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:760603263"
variation 1743..1744
/gene="SIX2"
/replace="ac"
/replace="acac"
/db_xref="dbSNP:1403939113"
variation 1743
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1572647789"
variation 1747..1748
/gene="SIX2"
/replace=""
/replace="ct"
/db_xref="dbSNP:150971507"
variation 1748
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1345970516"
variation 1754
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1365198497"
variation 1755
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295042211"
variation 1766
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:77492481"
variation 1770
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304067119"
variation 1771
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1372547829"
variation 1773
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1344489445"
variation 1783..1786
/gene="SIX2"
/replace="c"
/replace="ctac"
/db_xref="dbSNP:1572647764"
variation 1790
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:904197908"
variation 1791
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1572647749"
variation 1792
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1401287298"
variation 1798
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1308111988"
variation 1799
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043087734"
variation 1801
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1414268068"
variation 1803
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1197603581"
variation 1805
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048427800"
variation 1806
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1480219064"
variation 1808
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:942997245"
variation 1812..1816
/gene="SIX2"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:931484268"
variation 1818
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:918794201"
variation 1829
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1254109565"
variation 1835..1840
/gene="SIX2"
/replace="a"
/replace="agaaaa"
/db_xref="dbSNP:1572647699"
variation 1841..1842
/gene="SIX2"
/replace=""
/replace="ttag"
/db_xref="dbSNP:965680025"
variation 1841
/gene="SIX2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2290030"
variation 1844
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:912803911"
variation 1845
/gene="SIX2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:576383890"
variation 1846
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:985137336"
variation 1847
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:182325607"
variation 1853
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:953668789"
variation 1860
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1032096705"
variation 1861
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1572647669"
variation 1864
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:541416230"
variation 1871
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:966859968"
variation 1877..1880
/gene="SIX2"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:751291798"
variation 1883
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1443978582"
variation 1885
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:747914560"
variation 1886
/gene="SIX2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:919043710"
variation 1888
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1225180677"
variation 1893
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1310048511"
variation 1894
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:566401400"
variation 1907
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:963595066"
variation 1912
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1558439231"
variation 1913
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1572647656"
variation 1922
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:774012414"
variation 1926
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:909231612"
variation 1931
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:980763721"
variation 1933
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1197279369"
variation 1934
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1232434132"
variation 1937..1938
/gene="SIX2"
/replace=""
/replace="c"
/db_xref="dbSNP:760856738"
variation 1938..1943
/gene="SIX2"
/replace="a"
/replace="aagtga"
/db_xref="dbSNP:1179177970"
variation 1944
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1558439215"
variation 1948
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1054944033"
variation 1952
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1474773255"
variation 1953
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1165333050"
variation 1954
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:969348883"
variation 1959
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:80289874"
variation 1965
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1328093899"
variation 1968
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1354614380"
variation 1969
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:535861305"
variation 1974
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:905839922"
variation 1976
/gene="SIX2"
/replace="a"
/replace="atta"
/db_xref="dbSNP:1294343348"
variation 1977
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:570118117"
variation 1978
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213400640"
variation 1981
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1272842003"
variation 1982..2004
/gene="SIX2"
/replace="cct"
/replace="cctcgtcatacgcccctcctcct"
/db_xref="dbSNP:1374297673"
variation 1982..1999
/gene="SIX2"
/replace="cctc"
/replace="cctcgtcatacgcccctc"
/db_xref="dbSNP:1411183078"
variation 1983
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1308169729"
variation 1985
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1361185618"
variation 1986
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235981177"
variation 1988
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:112423728"
variation 1992
/gene="SIX2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:77956519"
variation 1993
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:530722485"
variation 1996..2004
/gene="SIX2"
/replace="cctcct"
/replace="cctcctcct"
/db_xref="dbSNP:1435012573"
variation 1996
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1390982995"
variation 1997
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1018514277"
variation 2001
/gene="SIX2"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1173391978"
variation 2003..2007
/gene="SIX2"
/replace="ct"
/replace="cttct"
/db_xref="dbSNP:1357765727"
variation 2005
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1314328091"
variation 2008
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1007265379"
variation 2009
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174326067"
variation 2013..2014
/gene="SIX2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1363229259"
variation 2016
/gene="SIX2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1469509496"
variation 2019
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:960840340"
variation 2024
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:564968120"
variation 2026..2030
/gene="SIX2"
/replace="cac"
/replace="cacac"
/db_xref="dbSNP:912836008"
variation 2028
/gene="SIX2"
/replace=""
/replace="c"
/db_xref="dbSNP:1378373658"
variation 2028
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:944157748"
variation 2031..2035
/gene="SIX2"
/replace="cgcgc"
/replace="cgcgcgc"
/db_xref="dbSNP:1476378907"
variation 2031
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:369025364"
variation 2032
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:888780857"
variation 2033
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051512760"
variation 2034
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242455822"
variation 2045
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:933020381"
variation 2054
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1572647552"
variation 2060
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1394022009"
variation 2068
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:897669398"
variation 2069
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1434726981"
variation 2070
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1175143966"
variation 2076
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1358184460"
variation 2078
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:985670004"
variation 2079
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1036579508"
variation 2080..2085
/gene="SIX2"
/replace="ccccc"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:1261453257"
variation 2084
/gene="SIX2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:941853958"
variation 2085
/gene="SIX2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:909152479"
variation 2088
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235046612"
variation 2091
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:932313110"
variation 2093
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:980649322"
variation 2094
/gene="SIX2"
/replace=""
/replace="g"
/db_xref="dbSNP:1284764801"
variation 2094
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204750628"
variation 2095
/gene="SIX2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1448516603"
variation 2099
/gene="SIX2"
/replace=""
/replace="g"
/db_xref="dbSNP:1466616697"
variation 2101
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1240765994"
variation 2102
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:748751565"
variation 2104
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1252237131"
variation 2106
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1454353211"
variation 2109
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:190846424"
variation 2115
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368144979"
variation 2123
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:956978159"
variation 2129
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1469357200"
variation 2132
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1158777989"
variation 2136
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1031189106"
variation 2141
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:979489379"
variation 2149
/gene="SIX2"
/replace="c"
/replace="g"
/db_xref="dbSNP:980036426"
variation 2150
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:878866616"
variation 2152
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1018981666"
variation 2158
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:559236812"
variation 2161
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:542175339"
variation 2167
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1572647483"
variation 2170
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1394336237"
variation 2172
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021095615"
variation 2173..2175
/gene="SIX2"
/replace="aaa"
/replace="aaaaa"
/db_xref="dbSNP:573717307"
variation 2176
/gene="SIX2"
/replace="c"
/replace="t"
/db_xref="dbSNP:888789102"
variation 2186
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1029971434"
variation 2189
/gene="SIX2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1033566925"
variation 2200
/gene="SIX2"
/replace="g"
/replace="t"
/db_xref="dbSNP:773144593"
variation 2204
/gene="SIX2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1352591037"
ORIGIN
aagaaagctgagagccagctagacgggagggagaacgagtgagaagcgagcgagggaacggcgggcgggcgcggagcatgcggagcggcgccccgggcggcccccgggcttgggcgagggcttgggccaggcgcgcgggccgttggggttcggagcttcgtgggacccgcggccggcgcggggacgtacggcagtgactcggggctcaccgggggccagtgccgggccagggggccagccccgcccgcgtctcggcccggacggcccggcgaggaagctcccatgcgggaccgcgcggcccggtgagggcgcgcgcgggcgggcggggacgcagccggcaccatgtccatgctgcccaccttcggcttcacgcaggagcaagtggcgtgcgtgtgcgaggtgctgcagcagggcggcaacatcgagcggctgggccgcttcctgtggtcgctgcccgcctgcgagcaccttcacaagaatgaaagcgtgctcaaggccaaggccgtggtggccttccaccgcggcaacttccgcgagctctacaagatcctggagagccaccagttctcgccgcacaaccacgccaagctgcagcagctgtggctcaaggcacactacatcgaggcggagaagctgcgcggccgacccctgggcgccgtgggcaaataccgcgtgcgccgcaaattcccgctgccgcgctccatctgggacggcgaggagaccagctactgcttcaaggaaaagagtcgcagcgtgctgcgcgagtggtacgcgcacaacccctacccttcaccccgcgagaagcgtgagctggcggaggccacgggcctcaccaccacacaggtcagcaactggttcaagaaccggcggcagcgcgaccgggcggccgaggccaaggaaagggagaacaacgagaactccaattctaacagccacaacccgctgaatggcagcggcaagtcggtgttaggcagctcggaggatgagaagactccatcggggacgccagaccactcatcatccagccccgcactgctcctcagcccgccgccccctgggctgccgtccctgcacagcctgggccaccctccgggccccagcgcagtgccagtgccggtgccaggcggaggtggagcggacccactgcaacaccaccatggcctgcaggactccatcctcaaccccatgtcagccaacctcgtggacctgggctcctagaacccatttgccttgatgagcttgccttttgtgacttgacactggggacgtggagtggcggtgtccaggggcgccccgcccctgcggccccaccaggtactgaaagacccgcaggctgagcgggtagaacagccgggtagggcagatagctgtctatgttggttcttgtttgggatttattttcaacaagttacttttaggatccttttggggctggagactgagtcttgaaccacagaagggaataaattatacaccactgtcattctctctctccctctgtctcttccttttaccctctcttgtcttgccttttccccctttcctcttcctttcccttccttctcttttcttttttctgctttctgtctttctccctctccttgtattgctttccttctagatttctagcttgccaccgttcattctctccttctgtctctccctttctctctccttctctgtttctcctctcttctctcctgccagtctcttgtactctgtgtcctggtccctccgtatgtacccctgtctttctcctcctgactggtggtctatctgcccctacctctggccctcgctttaccggagtagggggtgggagagggaagaggagagaaaatacagggactttgaacctaggccatctcctgaggccttttccctcgcccatgtgggtcagtgggagctgcaggtgtcagcttttcgtctagtaacttaagtgagagagaaagggcagcgccacagaagcccctaaacgccgcctcgtcatacgcccctcctccttctctcttggcgaggccccgccacaccgcgctcttcctcccgggactgtgactacagcgctcccggctgagcgcgccccccgagccgccgacttgccgtctccccgtaatgccctcatgtgaatgttcttcgggaaatatttctgcttttattttataataaaattagaaatcataaatatataaatggttatatgccacaa
//
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]