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Previous release (v1)
2026-10-05 18:56:50, GGRNA.v2 : RefSeq release 233 (Jan, 2026)
LOCUS NR_038198 1394 bp RNA linear PRI 21-SEP-2024 DEFINITION Homo sapiens PBX homeobox 4 (PBX4), transcript variant 2, non-coding RNA. ACCESSION NR_038198 VERSION NR_038198.2 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 1394) AUTHORS Song,Y. and Ma,R. TITLE Identifying the Potential Roles of PBX4 in Human Cancers Based on Integrative Analysis JOURNAL Biomolecules 12 (6), 822 (2022) PUBMED 35740947 REMARK GeneRIF: Identifying the Potential Roles of PBX4 in Human Cancers Based on Integrative Analysis. Publication Status: Online-Only REFERENCE 2 (bases 1 to 1394) AUTHORS Huttlin,E.L., Bruckner,R.J., Navarrete-Perea,J., Cannon,J.R., Baltier,K., Gebreab,F., Gygi,M.P., Thornock,A., Zarraga,G., Tam,S., Szpyt,J., Gassaway,B.M., Panov,A., Parzen,H., Fu,S., Golbazi,A., Maenpaa,E., Stricker,K., Guha Thakurta,S., Zhang,T., Rad,R., Pan,J., Nusinow,D.P., Paulo,J.A., Schweppe,D.K., Vaites,L.P., Harper,J.W. and Gygi,S.P. TITLE Dual proteome-scale networks reveal cell-specific remodeling of the human interactome JOURNAL Cell 184 (11), 3022-3040 (2021) PUBMED 33961781 REFERENCE 3 (bases 1 to 1394) AUTHORS Haenig,C., Atias,N., Taylor,A.K., Mazza,A., Schaefer,M.H., Russ,J., Riechers,S.P., Jain,S., Coughlin,M., Fontaine,J.F., Freibaum,B.D., Brusendorf,L., Zenkner,M., Porras,P., Stroedicke,M., Schnoegl,S., Arnsburg,K., Boeddrich,A., Pigazzini,L., Heutink,P., Taylor,J.P., Kirstein,J., Andrade-Navarro,M.A., Sharan,R. and Wanker,E.E. TITLE Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains JOURNAL Cell Rep 32 (7), 108050 (2020) PUBMED 32814053 REFERENCE 4 (bases 1 to 1394) AUTHORS Luck,K., Kim,D.K., Lambourne,L., Spirohn,K., Begg,B.E., Bian,W., Brignall,R., Cafarelli,T., Campos-Laborie,F.J., Charloteaux,B., Choi,D., Cote,A.G., Daley,M., Deimling,S., Desbuleux,A., Dricot,A., Gebbia,M., Hardy,M.F., Kishore,N., Knapp,J.J., Kovacs,I.A., Lemmens,I., Mee,M.W., Mellor,J.C., Pollis,C., Pons,C., Richardson,A.D., Schlabach,S., Teeking,B., Yadav,A., Babor,M., Balcha,D., Basha,O., Bowman-Colin,C., Chin,S.F., Choi,S.G., 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,J.N., Rangarajan,S., Rasla,J., Rayhan,A., Rolland,T., San-Miguel,A., Shen,Y., Sheykhkarimli,D., Sheynkman,G.M., Simonovsky,E., Tasan,M., Tejeda,A., Tropepe,V., Twizere,J.C., Wang,Y., Weatheritt,R.J., Weile,J., Xia,Y., Yang,X., Yeger-Lotem,E., Zhong,Q., Aloy,P., Bader,G.D., De Las Rivas,J., Gaudet,S., Hao,T., Rak,J., Tavernier,J., Hill,D.E., Vidal,M., Roth,F.P. and Calderwood,M.A. TITLE A reference map of the human binary protein interactome JOURNAL Nature 580 (7803), 402-408 (2020) PUBMED 32296183 REFERENCE 5 (bases 1 to 1394) AUTHORS Fragoza,R., Das,J., Wierbowski,S.D., Liang,J., Tran,T.N., Liang,S., Beltran,J.F., Rivera-Erick,C.A., Ye,K., Wang,T.Y., Yao,L., Mort,M., Stenson,P.D., Cooper,D.N., Wei,X., Keinan,A., Schimenti,J.C., Clark,A.G. and Yu,H. TITLE Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations JOURNAL Nat Commun 10 (1), 4141 (2019) PUBMED 31515488 REMARK Publication Status: Online-Only REFERENCE 6 (bases 1 to 1394) AUTHORS Vaquerizas,J.M., Kummerfeld,S.K., Teichmann,S.A. and Luscombe,N.M. TITLE A census of human transcription factors: function, expression and evolution JOURNAL Nat Rev Genet 10 (4), 252-263 (2009) PUBMED 19274049 REMARK Review article REFERENCE 7 (bases 1 to 1394) AUTHORS Tai,E.S., Sim,X.L., Ong,T.H., Wong,T.Y., Saw,S.M., Aung,T., Kathiresan,S., Orho-Melander,M., Ordovas,J.M., Tan,J.T. and Seielstad,M. TITLE Polymorphisms at newly identified lipid-associated loci are associated with blood lipids and cardiovascular disease in an Asian Malay population JOURNAL J Lipid Res 50 (3), 514-520 (2009) PUBMED 18987386 REMARK GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 8 (bases 1 to 1394) AUTHORS Kathiresan,S., Melander,O., Guiducci,C., Surti,A., Burtt,N.P., Rieder,M.J., Cooper,G.M., Roos,C., Voight,B.F., Havulinna,A.S., Wahlstrand,B., Hedner,T., Corella,D., Tai,E.S., Ordovas,J.M., Berglund,G., Vartiainen,E., Jousilahti,P., Hedblad,B., Taskinen,M.R., Newton-Cheh,C., Salomaa,V., Peltonen,L., Groop,L., Altshuler,D.M. and Orho-Melander,M. TITLE Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans JOURNAL Nat Genet 40 (2), 189-197 (2008) PUBMED 18193044 REMARK GeneRIF: Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) Erratum:[Nat Genet. 2008 Nov;40(11):1384] REFERENCE 9 (bases 1 to 1394) AUTHORS Laurent,A., Bihan,R., Omilli,F., Deschamps,S. and Pellerin,I. TITLE PBX proteins: much more than Hox cofactors JOURNAL Int J Dev Biol 52 (1), 9-20 (2008) PUBMED 18033668 REMARK Review article REFERENCE 10 (bases 1 to 1394) AUTHORS Wagner,K., Mincheva,A., Korn,B., Lichter,P. and Popperl,H. TITLE Pbx4, a new Pbx family member on mouse chromosome 8, is expressed during spermatogenesis JOURNAL Mech Dev 103 (1-2), 127-131 (2001) PUBMED 11335119 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from BC143588.1, AK097427.1 and CK300861.1. On Jul 12, 2019 this sequence version replaced NR_038198.1. Summary: This gene encodes a member of the pre-B cell leukemia transcription factor family. These proteins are homeobox proteins that play critical roles in embryonic development and cellular differentiation both as Hox cofactors and through Hox-independent pathways. The encoded protein contains a homeobox DNA-binding domain, but specific functions of the protein have not been determined. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, May 2011]. Transcript Variant: This variant (2) uses an alternate splice site in an internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD). 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 :: BC143588.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-1118 BC143588.1 6-1123 1119-1392 AK097427.1 1186-1459 1393-1394 CK300861.1 24-25 c FEATURES Location/Qualifiers source 1..1394 /organism="Homo sapiens" /mol_type="transcribed RNA" /db_xref="taxon:9606" /chromosome="19" /map="19p13.11" gene 1..1394 /gene="PBX4" /note="PBX homeobox 4" /db_xref="GeneID:80714" /db_xref="HGNC:HGNC:13403" /db_xref="MIM:608127" misc_RNA 1..1394 /gene="PBX4" /product="PBX homeobox 4, transcript variant 2" /db_xref="GeneID:80714" /db_xref="HGNC:HGNC:13403" /db_xref="MIM:608127" exon 1..177 /gene="PBX4" /inference="alignment:Splign:2.1.0" variation 1 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2514007266" variation 3 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2061701773" variation 5 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2514007252" variation 6 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2514007248" variation 8 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1323509832" variation 9 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1021962012" variation 10 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2514007236" variation 11 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2514007233" variation 12 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2514007229" variation 13 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1291716737" variation 14..20 /gene="PBX4" /replace="caggctc" /replace="caggctcaggctc" /db_xref="dbSNP:1284503427" variation 14 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1011518400" variation 15 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1285017089" variation 16 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2061701595" variation 17 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2061701570" variation 18 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2514007210" variation 19 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061701544" variation 20 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2061701510" variation 21 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1020429047" variation 23 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1457607774" variation 24 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1014338177" variation 25 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1599388932" variation 26 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2514007188" variation 27 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:896077777" variation 28..30 /gene="PBX4" /replace="cc" /replace="ccc" /replace="cccc" /db_xref="dbSNP:1202186623" variation 28 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061701391" variation 29 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2061701368" variation 30 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2061701332" variation 33 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2514007167" variation 37 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1250146107" variation 39 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1034596970" variation 40 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061701294" variation 41 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2514007149" variation 42 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2061701274" variation 44 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2514007139" variation 46 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1001789328" variation 47..68 /gene="PBX4" /replace="gccctgccgctcatggccgccc" /replace="gccctgccgctcatggccgccctgccgctcatggccgccc" /db_xref="dbSNP:2514007087" variation 47 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2514007129" variation 50 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2514007126" variation 51 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2061701219" variation 53 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061701210" variation 54 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:112396932" variation 55 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1304877086" variation 58 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:768977682" misc_feature 59..409 /gene="PBX4" /inference="COORDINATES: alignment:Blast2seq::RefSeq|NM_025245.3" /note="primary ORF has stop codon >50 nucleotides from the terminal splice site; nonsense-mediated decay (NMD) candidate" variation 59 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:763281601" variation 60 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1599388882" variation 63..101 /gene="PBX4" /replace="ccgccccgc" /replace="ccgccccgccgcgccccgcgccatcgccccccgccccgc" /db_xref="dbSNP:2514007008" variation 63 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1279778130" variation 64..81 /gene="PBX4" /replace="cgccccgc" /replace="cgccccgccgcgccccgc" /db_xref="dbSNP:2514007050" variation 64 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2514007095" variation 65 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2061701066" variation 66..69 /gene="PBX4" /replace="ccc" /replace="cccc" /db_xref="dbSNP:2514007082" variation 66 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1375016353" variation 67 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2061701019" variation 68 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1048709240" variation 69..77 /gene="PBX4" /replace="cgccgcgcc" /replace="cgccgcgccgcgcc" /db_xref="dbSNP:2514007068" variation 69 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:568019117" variation 71..84 /gene="PBX4" /replace="ccgcgccccgcgcc" /replace="ccgcgccccgcgccccgcgcc" /db_xref="dbSNP:1383287800" variation 72 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1359528098" variation 74 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:375518457" variation 77 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:770173658" variation 78 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1318425041" variation 79 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:897548586" variation 80 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:746324550" variation 82 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:781667877" variation 84 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1856073161" variation 85 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2144805544" variation 89..94 /gene="PBX4" /replace="ccccc" /replace="cccccc" /replace="ccccccc" /db_xref="dbSNP:2061700688" variation 89 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1338588159" variation 90 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:548276808" variation 91 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2514007030" variation 92 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1394267453" variation 93 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1400141456" variation 94 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1568402983" variation 95 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:746589833" variation 96..99 /gene="PBX4" /replace="ccc" /replace="cccc" /db_xref="dbSNP:2514007015" variation 96 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2514007017" variation 98 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061700641" variation 99 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:938731988" variation 100 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:1454375691" variation 101 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2514007004" variation 102 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2514006999" variation 103 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2514006995" variation 105 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:868574591" variation 106 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1382336010" variation 109 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:777270741" variation 110 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1439425739" variation 113 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2514006969" variation 114 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1244178185" variation 115 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:980196490" variation 118 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2514006951" variation 119 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:758112937" variation 121 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1441256016" variation 122 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:370270980" variation 123 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2514006932" variation 125 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2514006926" variation 126 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:528628394" variation 127 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:1050357546" variation 128 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1352236053" variation 129 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:868836058" variation 131 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2061700341" variation 133 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:754837361" variation 136 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:753758616" variation 137 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:766401982" variation 139 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2514006893" variation 140 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2061700266" variation 141..142 /gene="PBX4" /replace="c" /replace="cc" /db_xref="dbSNP:2514006884" variation 141 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2061700243" variation 142 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2514006882" variation 145 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:990445099" variation 147 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1316968346" variation 148 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061700195" variation 149 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2514006863" variation 151..152 /gene="PBX4" /replace="c" /replace="cc" /replace="cccc" /db_xref="dbSNP:752859637" variation 151 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2061700173" variation 156 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061700104" variation 158 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2514006835" variation 159 /gene="PBX4" /replace="" /replace="t" /db_xref="dbSNP:2514006826" variation 159 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:761782975" variation 160 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2514006808" variation 163 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:751709419" variation 164 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1266949078" variation 165 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2514006792" variation 166 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2514006789" variation 167 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1318901772" variation 168 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2514006778" variation 168 /gene="PBX4" /replace="c" /replace="ctc" /db_xref="dbSNP:1296078947" variation 169 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061699960" variation 170 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2514006768" variation 172..173 /gene="PBX4" /replace="gg" /replace="ggg" /db_xref="dbSNP:2061699943" variation 172 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2514006766" variation 173 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:565955170" variation 174 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:763121425" variation 176 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2514006743" variation 177 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1275603834" exon 178..251 /gene="PBX4" /inference="alignment:Splign:2.1.0" variation 179..209 /gene="PBX4" /replace="aagc" /replace="aagcatgctctgaattgccatcggatgaagc" /db_xref="dbSNP:2513984461" variation 179 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2144770513" variation 180 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513984568" variation 181 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1021296680" variation 183 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061582117" variation 184 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1403905598" variation 187 /gene="PBX4" /replace="" /replace="t" /db_xref="dbSNP:754292125" variation 187 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:191905542" variation 187 /gene="PBX4" /replace="t" /replace="tt" /db_xref="dbSNP:1732010637" variation 189 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513984531" variation 192 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513984523" variation 195 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513984517" variation 197 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:778709380" variation 198 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513984506" variation 200 /gene="PBX4" /replace="" /replace="c" /db_xref="dbSNP:753564379" variation 200 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:151162080" variation 201 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1413139492" variation 204 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2061581943" variation 205 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513984469" variation 208 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1175719970" variation 209..210 /gene="PBX4" /replace="c" /replace="cc" /db_xref="dbSNP:1480485642" variation 209 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:779830144" variation 212 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513984445" variation 213..216 /gene="PBX4" /replace="ctct" /replace="ctctct" /db_xref="dbSNP:2061581748" variation 213 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513984439" variation 215 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:756115893" variation 220 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2513984426" variation 221 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:377677809" variation 222 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513984415" variation 223 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:375684730" variation 224 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:763032974" variation 226 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061581632" variation 231 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:752913335" variation 233..234 /gene="PBX4" /replace="" /replace="c" /db_xref="dbSNP:2061581499" variation 233 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2061581547" variation 235 /gene="PBX4" /replace="g" /replace="gcgtgctctg" /db_xref="dbSNP:2061581462" variation 236 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:1388222933" variation 241 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2061581418" variation 242 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1599373105" variation 243 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:765501853" variation 247 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513984339" variation 249 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513984335" variation 250 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2061581347" variation 251 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1257358020" exon 252..398 /gene="PBX4" /inference="alignment:Splign:2.1.0" variation 253 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513942878" variation 255 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2061378546" variation 256 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:752825609" variation 257 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513942870" variation 258 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061378503" variation 259 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:148760242" variation 262..263 /gene="PBX4" /replace="cc" /replace="ccc" /db_xref="dbSNP:2513942854" variation 262 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513942862" variation 263 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:755156215" variation 264 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:754031746" variation 264 /gene="PBX4" /replace="g" /replace="gg" /db_xref="dbSNP:2513942839" variation 267 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:766712556" variation 268 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:760954860" variation 269 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:202136740" variation 272 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513942806" variation 273 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1309061872" variation 275 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513942794" variation 276 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:761382733" variation 277 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:774041383" variation 278 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:147300531" variation 280 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513942773" variation 282 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:144094318" variation 283 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:775018508" variation 284..288 /gene="PBX4" /replace="cccc" /replace="ccccc" /db_xref="dbSNP:749987427" variation 284 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:151268425" variation 285 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1056130210" variation 286 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:377023999" variation 288..289 /gene="PBX4" /replace="" /replace="ct" /db_xref="dbSNP:1163908546" variation 288 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2513942720" variation 289 /gene="PBX4" /replace="" /replace="t" /db_xref="dbSNP:2061378058" variation 289 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513942706" variation 290 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2061378037" variation 292 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:112528821" variation 293 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:746982264" variation 294 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1181241653" variation 295 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2061377927" variation 296 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1472489068" variation 297 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513942665" variation 298 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:778918344" variation 299 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513942657" variation 301 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1219051558" variation 304 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1381811621" variation 307..326 /gene="PBX4" /replace="gctggataacatgctgctgg" /replace="gctggataacatgctgctggataacatgctgctgg" /db_xref="dbSNP:2513942541" variation 307 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513942638" variation 308 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2513942627" variation 309 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2061377806" variation 310 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:200752601" variation 311 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:754029172" variation 312 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513942596" variation 314 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1222703145" variation 316 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513942583" variation 317 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513942577" variation 318..325 /gene="PBX4" /replace="tgctgctg" /replace="tgctgctgctg" /db_xref="dbSNP:766903302" variation 320 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1323906550" variation 322 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2513942557" variation 323 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513942554" variation 325 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:766581133" variation 328 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2061377625" variation 333 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513942527" variation 334 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:140225945" variation 335 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:570261973" variation 336 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:768104532" variation 337 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:972035858" variation 338 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1303401630" variation 341 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:375963844" variation 342 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513942486" variation 344 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2061377460" variation 345 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:550438529" variation 346 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:763640323" variation 347..349 /gene="PBX4" /replace="" /replace="gag" /db_xref="dbSNP:1479284662" variation 347 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:550752634" variation 348 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513942458" variation 352 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513942455" variation 355..360 /gene="PBX4" /replace="ag" /replace="aggaag" /db_xref="dbSNP:2513942436" variation 356 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:775195749" variation 358 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061377331" variation 359 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1195856369" variation 360..368 /gene="PBX4" /replace="gaggag" /replace="gaggaggag" /db_xref="dbSNP:2513942405" variation 361 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2061377281" variation 362 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513942422" variation 364 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513942419" variation 366 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:769381097" variation 368 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513942400" variation 369 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:372958240" variation 370..374 /gene="PBX4" /replace="ggtgg" /replace="ggtggtgg" /db_xref="dbSNP:2061377134" variation 370 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:776372370" variation 371 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513942393" variation 373 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:770737826" variation 374 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513942380" variation 375 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:746893120" variation 376 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:369260221" variation 379 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1319294451" variation 380 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:768779861" variation 381 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513942348" variation 382 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:749382075" variation 383 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:748095342" variation 385 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513942339" variation 395 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:756328917" variation 396 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2513942329" variation 397 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:750702081" variation 398 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513942316" exon 399..589 /gene="PBX4" /inference="alignment:Splign:2.1.0" variation 399 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513941160" variation 400 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1157161103" variation 401 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2144712710" variation 403 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2513941131" variation 405 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:761605001" variation 406 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1369505191" variation 410 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513941106" variation 411 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513941096" variation 414 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2144712670" variation 415 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513941077" variation 418 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:113788698" variation 419 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:567856973" variation 420 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513941061" variation 422 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:769694481" variation 423 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:201625234" variation 429 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1426591034" variation 430 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:149342353" variation 431..438 /gene="PBX4" /replace="cctcc" /replace="cctcctcc" /db_xref="dbSNP:2513940999" variation 431 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:200663780" variation 432 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:747266166" variation 433 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513941013" variation 435 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:375549686" variation 437 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:777951740" variation 439 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513940996" variation 442 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513940989" variation 443 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513940982" variation 447 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513940971" variation 450 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:758805133" variation 452 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1331476043" variation 455 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1338758902" variation 456 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513940949" variation 457 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1292820941" variation 459 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:748538995" variation 460 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513940933" variation 461 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:8108088" variation 462 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:8108180" variation 463 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1051983057" variation 464 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061373034" variation 466..469 /gene="PBX4" /replace="cccc" /replace="ccccc" /db_xref="dbSNP:2061372918" variation 466 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:754474387" variation 467 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:765980884" variation 468 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:755719972" variation 471 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513940858" variation 472 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513940853" variation 474 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2061372899" variation 477 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513940840" variation 478 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:750109733" variation 479 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:767156757" variation 480 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:370646681" variation 482 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1193676183" variation 483 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:761671883" variation 484 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:370844553" variation 486 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:8108981" variation 487 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:900644001" variation 488 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1451942331" variation 490..512 /gene="PBX4" /replace="tcggcgccattcacggcaagttc" /replace="tcggcgccattcacggcaagttcggcgccattcacggcaagttc" /db_xref="dbSNP:2061372346" variation 490 /gene="PBX4" /replace="" /replace="t" /db_xref="dbSNP:2061372643" variation 490 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:776813089" variation 491 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1291827256" variation 492 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:771158415" variation 493 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1355471395" variation 494 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:150208525" variation 495 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:773490862" variation 496 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1342487644" variation 498 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061372468" variation 502 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2144712260" variation 503 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:141893181" variation 504 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:748607444" variation 505 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:374756898" variation 507 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513940674" variation 509 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513940667" variation 511 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513940665" variation 512 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513940653" variation 513 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:755515419" variation 515 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:749821697" variation 516 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:370372588" variation 517 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513940621" variation 521 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1172043422" variation 522 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:755632077" variation 523 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1420897889" variation 525 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:749975594" variation 526 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:780963018" variation 527 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:756988671" variation 529 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:148245498" variation 531 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1248098876" variation 533 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513940569" variation 534 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:751419097" variation 536 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1387131041" variation 538 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1383451944" variation 541 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513940546" variation 547 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513940541" variation 553 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:375600193" variation 554 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2061371963" variation 556 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:762936282" variation 559 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1200498335" variation 560 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:752697263" variation 561 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1256302332" variation 562 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513940479" variation 567 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:766502529" variation 568 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:372535392" variation 571 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:762057005" variation 572 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:774733792" variation 573 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:144820446" variation 574 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:749734718" variation 575 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061371677" variation 576 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2061371648" variation 577 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513940381" variation 578 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2061371624" variation 579 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513940366" variation 580 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513940353" variation 581 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:780542097" variation 582 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:769287977" variation 583 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513940319" variation 584 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1327522011" variation 585 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513940299" variation 586 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:745439866" variation 587 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:780686279" variation 588 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:756893868" variation 589 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513940276" exon 590..725 /gene="PBX4" /inference="alignment:Splign:2.1.0" variation 591 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:537816731" variation 592 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:778958942" variation 593 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:754899562" variation 595 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:369430064" variation 597 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:757291376" variation 598 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:750891971" variation 599 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513938925" variation 600 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:764359924" variation 601 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:35516996" variation 602 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513938891" variation 604 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1413636360" variation 607 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1600397650" variation 610 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:567185157" variation 613 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1044494570" variation 615 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513938852" variation 616 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513938838" variation 617 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2513938824" variation 618 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2061367384" variation 619 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:199673541" variation 620 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:777007324" variation 621 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513938796" variation 622 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:549163642" variation 623 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:746573169" variation 624 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513938773" variation 625 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513938768" variation 626 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2061367240" variation 628 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2513938746" variation 629 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2061367208" variation 631 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513938728" variation 632 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513938718" variation 633..634 /gene="PBX4" /replace="a" /replace="aa" /db_xref="dbSNP:1350344478" variation 634 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:200360885" variation 636 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:771887948" variation 638 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2061367096" variation 639..643 /gene="PBX4" /replace="t" /replace="tattt" /db_xref="dbSNP:1458206956" variation 639 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:893139411" variation 641..645 /gene="PBX4" /replace="ttt" /replace="tttt" /replace="ttttt" /replace="tttttt" /db_xref="dbSNP:2513938658" variation 641 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:75799973" variation 646 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1600397549" variation 647 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:371731150" variation 649 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2061366948" variation 650 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:766263116" variation 652 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061366897" variation 653 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513938614" variation 654 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513938608" variation 656 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2061366875" variation 658 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1199326906" variation 659 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1474933646" variation 660 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2061366830" variation 661 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1600397525" variation 662..664 /gene="PBX4" /replace="cc" /replace="ccc" /db_xref="dbSNP:1196167241" variation 662 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2144710198" variation 663 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:778805645" variation 665 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061366708" variation 666 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513938524" variation 667 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1600397500" variation 668..671 /gene="PBX4" /replace="ccc" /replace="cccc" /db_xref="dbSNP:1181521760" variation 668 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1485083799" variation 670 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513938494" variation 674 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:754746946" variation 675 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:749186272" variation 676 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513938462" variation 679 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513938451" variation 681 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1323959579" variation 685..691 /gene="PBX4" /replace="aaga" /replace="aagaaga" /db_xref="dbSNP:2513938406" variation 685 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:779925886" variation 686 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513938433" variation 687 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:367886261" variation 689 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513938414" variation 691 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1414890336" variation 692 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:751688787" variation 693 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513938388" variation 695 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513938380" variation 696 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:201537948" variation 697 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:866931015" variation 699 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513938345" variation 701 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:145584999" variation 702 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513938327" variation 704..706 /gene="PBX4" /replace="gg" /replace="ggg" /db_xref="dbSNP:2513938301" variation 704 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2061366332" variation 705 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2513938310" variation 707 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:765570036" variation 708 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:200171479" variation 710 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2061366278" variation 711 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:372436008" variation 713 /gene="PBX4" /replace="c" /replace="cc" /db_xref="dbSNP:2513938272" variation 713 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1438358713" variation 714 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:547605373" variation 715 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513938254" variation 716 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1164164050" variation 717 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2144709910" variation 718 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513938231" variation 719 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:1460955886" variation 721 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513938211" variation 722 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513938200" variation 723 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:866348308" variation 725 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513938185" exon 726..882 /gene="PBX4" /inference="alignment:Splign:2.1.0" variation 726 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:769599693" variation 727 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:1600391721" variation 728 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2061333662" variation 730..735 /gene="PBX4" /replace="ct" /replace="ctaact" /db_xref="dbSNP:2513930893" variation 730 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2061333637" variation 731 /gene="PBX4" /replace="t" /replace="tt" /db_xref="dbSNP:1256191522" variation 732 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513930898" variation 734 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:371142377" variation 735 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:1018838985" variation 737 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513930878" variation 739 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:1345452499" variation 743 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1009244067" variation 744 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2061333498" variation 747 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:772125392" variation 748 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061333446" variation 749 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061333414" variation 750 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2144698595" variation 751 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:62137777" variation 752 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513930823" variation 755 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:114083358" variation 756 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:779161815" variation 757 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:148814820" variation 758 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1218061912" variation 759 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513930791" variation 760 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513930781" variation 762 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1389706617" variation 763 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061333219" variation 764 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:1395916029" variation 765 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513930759" variation 767 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:926735805" variation 768 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2061333152" variation 769 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513930740" variation 771 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:761236400" variation 772 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:754108921" variation 775 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2061333057" variation 776 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:780220611" variation 777 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061333001" variation 778 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:756556827" variation 779 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513930700" variation 780..782 /gene="PBX4" /replace="tt" /replace="ttt" /db_xref="dbSNP:2061332923" variation 787 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513930685" variation 790 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1178008041" variation 793 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1440719062" variation 797 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:750965127" variation 798 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1180336620" variation 799 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2061332745" variation 805 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:376647012" variation 806 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:145467560" variation 807 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1183232898" variation 808 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1484447906" variation 810 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513930622" variation 812 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513930619" variation 814 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:550466530" variation 815 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:200643734" variation 816 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:1355627152" variation 817 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513930595" variation 818 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2513930589" variation 819 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:769573106" variation 820 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:1600391535" variation 822 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2513930574" variation 823 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513930567" variation 825 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061332369" variation 826 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1600391532" variation 827 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:149681009" variation 829 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:139542458" variation 830 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:147715000" variation 831 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:746995103" variation 833 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513930510" variation 835 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:774242734" variation 837..840 /gene="PBX4" /replace="gggg" /replace="ggggg" /db_xref="dbSNP:2513930491" variation 839 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513930499" variation 840 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513930482" variation 841 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:1600391489" variation 842 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2513930465" variation 846 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:768790018" variation 849 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1420656020" variation 851 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:369823420" variation 854 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:377739787" variation 855 /gene="PBX4" /replace="" /replace="g" /db_xref="dbSNP:777095711" variation 855 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:116791423" variation 856 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061332035" variation 857 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061332004" variation 859 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:1600391432" variation 860 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513930386" variation 861 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513930379" variation 863 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:781756177" variation 864 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2061331893" variation 865 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:559098874" variation 868 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513930356" variation 871 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:752130197" variation 872 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513930347" variation 873 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:763456034" variation 876 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1489137480" variation 880 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:545565884" variation 881 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:201219684" variation 882 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:753559018" exon 883..989 /gene="PBX4" /inference="alignment:Splign:2.1.0" variation 883 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2061322175" variation 884 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2144695039" variation 886..911 /gene="PBX4" /replace="" /replace="cctctggacccttcccgctgcccagc" /db_xref="dbSNP:2513927684" variation 886..887 /gene="PBX4" /replace="cc" /replace="ccc" /db_xref="dbSNP:2513927854" variation 887 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513927845" variation 888 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513927837" variation 892..899 /gene="PBX4" /replace="" /replace="gacccttc" /db_xref="dbSNP:2513927778" variation 892..894 /gene="PBX4" /replace="" /replace="gac" /db_xref="dbSNP:1218668039" variation 893 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513927831" variation 894 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1370532538" variation 895..927 /gene="PBX4" /replace="ccttcc" /replace="ccttcccgctgcccagcgctggggacgccttcc" /db_xref="dbSNP:2513927607" variation 895 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513927816" variation 896 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1278371971" variation 897 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1448139309" variation 898 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:1289570851" variation 899 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:1489867288" variation 900 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2061322007" variation 901..902 /gene="PBX4" /replace="" /replace="tggaa" /db_xref="dbSNP:2061321965" variation 901 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1037751245" variation 902 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:372278117" variation 903 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513927751" variation 904 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513927742" variation 906 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:770018670" variation 907 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2061321894" variation 908 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513927719" variation 909 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2144694934" variation 910 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2513927695" variation 911 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1360985986" variation 912 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:368764630" variation 913 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1398950489" variation 915..918 /gene="PBX4" /replace="ggg" /replace="gggg" /db_xref="dbSNP:2513927648" variation 915 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513927660" variation 917 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:374485381" variation 918 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2513927638" variation 919 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513927634" variation 920 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:770188527" variation 921 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:370342583" variation 922 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513927616" variation 927 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061321720" variation 929 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1009294838" variation 930 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1600389275" variation 932 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513927580" variation 933 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513927568" variation 936 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:747449194" variation 937 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:141765874" variation 938 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513927536" variation 939 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1197101347" variation 944 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061321604" variation 945 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1439568685" variation 946 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:772590168" variation 949 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513927496" variation 953 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061321544" variation 955 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513927484" variation 956 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1243122199" variation 957 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:199666197" variation 958 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513927454" variation 959 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:561205164" variation 960 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061321469" variation 962 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513927431" variation 963 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513927420" variation 964 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513927409" variation 966 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513927399" variation 967 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1315590848" variation 968 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513927381" variation 969 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1050467693" variation 970 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:867567047" variation 972 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:1233321590" variation 974 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:932153564" variation 976 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1291035642" variation 977 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513927333" variation 978 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513927326" variation 979 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513927319" variation 980 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513927309" variation 981..989 /gene="PBX4" /replace="cagtcccag" /replace="cagtcccagtcccag" /db_xref="dbSNP:2513927268" variation 981 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1377338622" variation 982 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1413853053" variation 983 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061321248" variation 986 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1340894853" variation 987 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1290348283" variation 989 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513927258" exon 990..1394 /gene="PBX4" /inference="alignment:Splign:2.1.0" variation 990 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:771225104" variation 991 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2061310594" variation 992 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1600387250" variation 993 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1202071338" variation 995 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061310531" variation 996 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:914478462" variation 997 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513924993" variation 998 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:760836249" variation 1001 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:1167423827" variation 1005 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1280691706" variation 1006 /gene="PBX4" /replace="a" /replace="aa" /db_xref="dbSNP:772034081" variation 1006 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1600387204" variation 1007..1011 /gene="PBX4" /replace="gggg" /replace="ggggg" /db_xref="dbSNP:1368762457" variation 1007 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:377365977" variation 1009 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061310352" variation 1010 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:989249024" variation 1011 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:1236235757" variation 1012..1013 /gene="PBX4" /replace="c" /replace="cc" /db_xref="dbSNP:1302550442" variation 1012 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513924910" variation 1013 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513924896" variation 1014 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1600387183" variation 1015..1020 /gene="PBX4" /replace="ccc" /replace="ccccc" /replace="cccccc" /replace="ccccccc" /db_xref="dbSNP:748202447" variation 1015 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513924887" variation 1016 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2513924875" variation 1017 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1386314532" variation 1018 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513924867" variation 1019 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:773575047" variation 1020 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513924839" variation 1021 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2144691476" variation 1022 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1299457982" variation 1023 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:35913871" variation 1024 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513924809" variation 1025 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:1300128117" variation 1026 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1460596653" variation 1028 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2061309993" variation 1029 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:374029974" variation 1030 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513924782" variation 1032 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061309944" variation 1034 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:772334586" variation 1035 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513924759" variation 1036 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:567459353" variation 1038 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:777072275" variation 1040 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2061309840" variation 1041 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:768144971" variation 1044 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513924725" variation 1048 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513924719" variation 1049 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513924710" variation 1051 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:748850883" variation 1052 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513924691" variation 1053 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:779543575" variation 1054 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513924677" variation 1055 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1174972745" variation 1056 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:755755192" variation 1059 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513924656" variation 1060 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513924651" variation 1062 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:963919830" variation 1063 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2061309604" variation 1064 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2144691304" variation 1065 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1280572392" variation 1066 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:750067213" variation 1067 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513924608" variation 1068 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:780985151" variation 1069 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:934671282" variation 1070 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1199039530" variation 1072 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:757122658" variation 1074 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:376094794" variation 1075 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1482229926" variation 1076 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513924565" variation 1079 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1199872774" variation 1080 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2144691211" variation 1081 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1255524421" variation 1083 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513924538" variation 1084 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:751538631" variation 1085 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:769057071" variation 1086 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:371587486" variation 1087 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513924512" variation 1088 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513924508" variation 1089 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:753913371" variation 1090 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513924499" variation 1091 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2144691165" variation 1092 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513924492" variation 1093 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:766390616" variation 1096 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1313676179" variation 1098..1104 /gene="PBX4" /replace="ag" /replace="aggaaag" /db_xref="dbSNP:2513924469" variation 1100..1105 /gene="PBX4" /replace="ga" /replace="gaaaga" /db_xref="dbSNP:779008785" variation 1100 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2061309108" variation 1105 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513924460" variation 1106 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:369459162" variation 1107 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:970227358" variation 1108 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:760890336" variation 1110 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2513924444" variation 1111 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:773308630" variation 1112 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:373886682" variation 1113 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:762219907" variation 1115 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513924419" variation 1117 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513924416" variation 1118 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061308947" variation 1119 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513924410" variation 1120 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:547648306" variation 1121 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1417970882" variation 1122 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2144691066" variation 1123 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1257826349" variation 1124 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1295888879" variation 1125 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513924391" variation 1126 /gene="PBX4" /replace="t" /replace="tt" /db_xref="dbSNP:755156391" variation 1127 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513924385" variation 1129 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1329865370" variation 1130 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:369021002" variation 1131 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1205497179" variation 1132 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513924366" variation 1135 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513924358" variation 1136 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:769196000" variation 1137 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:749827879" variation 1141 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513924343" variation 1143 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513924336" variation 1145 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:886064172" variation 1147 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061308653" variation 1149 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513924318" variation 1151 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:534059373" variation 1152 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513924313" variation 1154 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2061308604" variation 1155 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:746041669" variation 1158 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513924305" variation 1159 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:571531014" variation 1160 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061308566" variation 1161 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:997195662" variation 1162 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1187369790" variation 1163 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:551394672" variation 1164 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1038867805" variation 1165 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1175921804" variation 1166..1174 /gene="PBX4" /replace="ga" /replace="gacctcaga" /db_xref="dbSNP:2513924268" variation 1166 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1487532543" variation 1171 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2513924269" variation 1175 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513924262" variation 1176 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513924252" variation 1177 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513924247" variation 1178..1180 /gene="PBX4" /replace="cc" /replace="ccc" /db_xref="dbSNP:2513924241" variation 1179 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2061308434" variation 1181 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513924235" variation 1183 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513924229" variation 1184 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513924224" variation 1186..1195 /gene="PBX4" /replace="ggtggtggtg" /replace="ggtggtggtggtg" /db_xref="dbSNP:894663533" variation 1186 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1295801249" variation 1187 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2061308408" variation 1188 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2513924211" variation 1189 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513924208" variation 1191 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513924204" variation 1192 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513924199" variation 1193 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513924194" variation 1196..1198 /gene="PBX4" /replace="cc" /replace="ccc" /db_xref="dbSNP:2513924177" variation 1199 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1288368063" variation 1200 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:1217683247" variation 1204..1207 /gene="PBX4" /replace="cccc" /replace="ccccc" /db_xref="dbSNP:2513924140" variation 1204 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513924155" variation 1206 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2513924148" variation 1209 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:947210147" variation 1210 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2061308329" variation 1211 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061308309" variation 1212 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:531290499" variation 1213 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513924106" variation 1218 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2144690793" variation 1219 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1055995665" variation 1223 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1386039495" variation 1225 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1301816154" variation 1226 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:893076685" variation 1229 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:2513924075" variation 1230 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061308179" variation 1231 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:562390443" variation 1232 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2144690722" variation 1233 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1242499016" variation 1234 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1053039836" variation 1235 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513924047" variation 1237 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513924043" variation 1238 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1216707925" variation 1239 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2061308092" variation 1241 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1313350716" variation 1242 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513924027" variation 1249 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:934665337" variation 1251 /gene="PBX4" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:928624617" variation 1252 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:981541477" variation 1253 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513924008" variation 1254 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513924002" variation 1255 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513923997" variation 1256 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1299624397" variation 1257 /gene="PBX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:569370125" variation 1258 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2061307940" variation 1259 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1157429320" variation 1260 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:1379134704" variation 1267 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513923962" variation 1269 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2144690622" variation 1270 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2061307890" variation 1271 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1400805387" variation 1272 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:963823354" variation 1274 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2061307821" variation 1276 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:2513923916" variation 1278..1287 /gene="PBX4" /replace="cattctccca" /replace="cattctcccattctccca" /db_xref="dbSNP:2513923907" variation 1285 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1018045361" variation 1287 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:770996395" variation 1288 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:948804977" variation 1289 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:2513923886" variation 1291 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:983949889" variation 1292 /gene="PBX4" /replace="" /replace="a" /db_xref="dbSNP:2061307718" variation 1292 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:952457661" variation 1296 /gene="PBX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1025434173" variation 1297 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:549050854" variation 1301 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:1308474356" variation 1302 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:1372645457" variation 1308 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513923851" variation 1309 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:867228314" variation 1315 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2061307565" variation 1317 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513923832" variation 1319 /gene="PBX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:906209559" variation 1320 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:144960029" variation 1322..1323 /gene="PBX4" /replace="a" /replace="aa" /db_xref="dbSNP:894756371" variation 1322 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1320124759" variation 1323 /gene="PBX4" /replace="a" /replace="t" /db_xref="dbSNP:184567636" variation 1324 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:540396999" variation 1325 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1265845876" variation 1328 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:936192700" variation 1333 /gene="PBX4" /replace="g" /replace="t" /db_xref="dbSNP:1238133807" variation 1335 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513923773" variation 1337 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:1470140786" variation 1338 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2144690440" variation 1340 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:904567520" variation 1342 /gene="PBX4" /replace="" /replace="c" /db_xref="dbSNP:2061307296" variation 1342 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2061307272" variation 1344 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513923746" variation 1348 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1194651011" variation 1354 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:2513923730" variation 1357 /gene="PBX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1041813548" variation 1358 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:2513923715" variation 1362 /gene="PBX4" /replace="a" /replace="g" /db_xref="dbSNP:2513923708" variation 1367 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1451310563" variation 1368 /gene="PBX4" /replace="a" /replace="c" /db_xref="dbSNP:1600386547" variation 1378 /gene="PBX4" /replace="c" /replace="t" /db_xref="dbSNP:1600386543" variation 1385 /gene="PBX4" /replace="c" /replace="g" /db_xref="dbSNP:946009374" ORIGIN
agtggtagtgctccaggctcgacggcaccctcacagcgcccgcccggccctgccgctcatggccgccccgccgcgccccgcgccatcgccccccgccccgcggcgcctcgacacgagcgacgtcctgcagcagatcatggccatcaccgaccagagcctggacgaggcacaggccagaaagcatgctctgaattgccatcggatgaagcctgctctgttcagcgtgctctgtgagatcaaggaaaagacagtggtaagcatccgtggcattcaagacgaagatccccctgacgcccagctcctgaggctggataacatgctgctggctgagggcgtgtgcaggcccgagaagagaggaagaggaggagcggtggccagggccggcacagcaacaccaggcctgtcgtgagttcaccacgcacgtcaccaacctcctccaggagcagagcaggatgaggcctgtctcccctaaggagattgagcgcatggtcggcgccattcacggcaagttcagcgccatccagatgcagttgaagcagagcacctgtgaggcagtgatgaccctgcgttcgcggctgctcgatgccaggcgcaagcggcggaatttcagcaagcaggcgacggaagtgctgaatgagtatttttactcccatctgaacaacccttaccccagcgaagaagccaaagaagagctggccaggaagggcggcctcaccatctcccaggtctctaactggtttggcaacaaaagaatccggtataaaaagaacatggggaagtttcaagaagaggctaccatttacacgggtaaaacggctgtggataccacggaagttggggtcccagggaaccacgccagctgcctgtcaacacctagctccggctcctctggacccttcccgctgcccagcgctggggacgccttcctcaccctgcggactctggcctctctccagcctcctcctgggggaggctgcctgcagtcccaggcccagggtagctggcagggggccaccccccaacctgcaactgcctcacctgctggagaccctggcagcatcaactccagtacatctaattaagtttgggggataagcaggaaagagcgctgcgtgagctgccatgtatcgccagccgttgctttgttactgaacgtgccgccgacgacctcagaaaacccagatgggtggtggtgcccatgagcccctgctcctcagccaggcccgtggcgccggctcatgtgtctgctgcgactcgagatggcctgaaacgccactcattctcccacttcagttcgtttttttgacagtaattttatggtaacgctatgaattgaattgtctgttctaggactgggcacagattttcccattaaaatttttgacttattttaa
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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