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2024-04-18 12:30:30, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001080517            6827 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens SET domain containing 5 (SETD5), mRNA.
ACCESSION   NM_001080517 XM_926615
VERSION     NM_001080517.1  GI:122937491
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 6827)
  AUTHORS   Muzny,D.M., Scherer,S.E., Kaul,R., Wang,J., Yu,J., Sudbrak,R.,
            Buhay,C.J., Chen,R., Cree,A., Ding,Y., Dugan-Rocha,S., Gill,R.,
            Gunaratne,P., Harris,R.A., Hawes,A.C., Hernandez,J., Hodgson,A.V.,
            Hume,J., Jackson,A., Khan,Z.M., Kovar-Smith,C., Lewis,L.R.,
            Lozado,R.J., Metzker,M.L., Milosavljevic,A., Miner,G.R.,
            Morgan,M.B., Nazareth,L.V., Scott,G., Sodergren,E., Song,X.Z.,
            Steffen,D., Wei,S., Wheeler,D.A., Wright,M.W., Worley,K.C.,
            Yuan,Y., Zhang,Z., Adams,C.Q., Ansari-Lari,M.A., Ayele,M.,
            Brown,M.J., Chen,G., Chen,Z., Clendenning,J.,
            Clerc-Blankenburg,K.P., Chen,R., Chen,Z., Davis,C., Delgado,O.,
            Dinh,H.H., Dong,W., Draper,H., Ernst,S., Fu,G.,
            Gonzalez-Garay,M.L., Garcia,D.K., Gillett,W., Gu,J., Hao,B.,
            Haugen,E., Havlak,P., He,X., Hennig,S., Hu,S., Huang,W.,
            Jackson,L.R., Jacob,L.S., Kelly,S.H., Kube,M., Levy,R., Li,Z.,
            Liu,B., Liu,J., Liu,W., Lu,J., Maheshwari,M., Nguyen,B.V.,
            Okwuonu,G.O., Palmeiri,A., Pasternak,S., Perez,L.M., Phelps,K.A.,
            Plopper,F.J., Qiang,B., Raymond,C., Rodriguez,R.,
            Saenphimmachak,C., Santibanez,J., Shen,H., Shen,Y., Subramanian,S.,
            Tabor,P.E., Verduzco,D., Waldron,L., Wang,J., Wang,J., Wang,Q.,
            Williams,G.A., Wong,G.K., Yao,Z., Zhang,J., Zhang,X., Zhao,G.,
            Zhou,J., Zhou,Y., Nelson,D., Lehrach,H., Reinhardt,R., Naylor,S.L.,
            Yang,H., Olson,M., Weinstock,G. and Gibbs,R.A.
  TITLE     The DNA sequence, annotation and analysis of human chromosome 3
  JOURNAL   Nature 440 (7088), 1194-1198 (2006)
   PUBMED   16641997
COMMENT     PROVISIONAL REFSEQ: This record has not yet been subject to final
            NCBI review. The reference sequence was derived from AC018506.5.
            On Jan 18, 2007 this sequence version replaced gi:113414362.
            
            Sequence Note: The RefSeq transcript and protein were derived from
            genomic sequence to make the sequence consistent with the reference
            genome assembly. The genomic coordinates used for the transcript
            record were based on alignments.
            
            ##Evidence-Data-START##
            RNAseq introns :: single sample supports all introns ERS025082,
                              ERS025085 [ECO:0000348]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-259               AC018506.5         112881-113139       c
            260-319             AC018506.5         86332-86391         c
            320-506             AC018506.5         81849-82035         c
            507-612             AC018506.5         76908-77013         c
            613-764             AC018506.5         76373-76524         c
            765-823             AC018506.5         75976-76034         c
            824-1002            AC018506.5         74952-75130         c
            1003-1245           AC018506.5         70160-70402         c
            1246-1394           AC018506.5         69117-69265         c
            1395-1512           AC018506.5         68613-68730         c
            1513-1622           AC018506.5         67441-67550         c
            1623-1875           AC018506.5         65558-65810         c
            1876-1959           AC018506.5         65118-65201         c
            1960-2217           AC018506.5         63551-63808         c
            2218-2538           AC018506.5         62852-63172         c
            2539-2781           AC018506.5         62228-62470         c
            2782-2911           AC018506.5         56990-57119         c
            2912-3159           AC018506.5         46186-46433         c
            3160-3630           AC018506.5         39929-40399         c
            3631-3932           AC018506.5         37321-37622         c
            3933-4066           AC018506.5         36276-36409         c
            4067-4155           AC018506.5         35702-35790         c
            4156-6827           AC018506.5         32704-35375         c
FEATURES             Location/Qualifiers
     source          1..6827
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="3"
                     /map="3p25.3"
     gene            1..6827
                     /gene="SETD5"
                     /note="SET domain containing 5"
                     /db_xref="GeneID:55209"
                     /db_xref="HGNC:25566"
     exon            1..259
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       63
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:190589751"
     variation       139
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368108766"
     variation       247
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372009489"
     exon            260..319
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     exon            320..506
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       378
                     /gene="SETD5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:184300828"
     variation       404
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77800928"
     misc_feature    406..408
                     /gene="SETD5"
                     /note="upstream in-frame stop codon"
     variation       415
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189957277"
     variation       426
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370213013"
     variation       428
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182194074"
     CDS             436..4764
                     /gene="SETD5"
                     /codon_start=1
                     /product="SET domain-containing protein 5"
                     /protein_id="NP_001073986.1"
                     /db_xref="GI:122937492"
                     /db_xref="CCDS:CCDS46741.1"
                     /db_xref="GeneID:55209"
                     /db_xref="HGNC:25566"
                     /translation="
MSIAIPLGVTTSDTSYSDMAAGSDPESVEASPAVNEKSVYSTHNYGTTQRHGCRGLPYATIIPRSDLNGLPSPVEERCGDSPNSEGETVPTWCPCGLSQDGFLLNCDKCRGMSRGKVIRLHRRKQDNISGGDSSATESWDEELSPSTVLYTATQHTPTSITLTVRRTKPKKRKKSPEKGRAAPKTKKIKNSPSEAQNLDENTTEGWENRIRLWTDQYEEAFTNQYSADVQNALEQHLHSSKEFVGKPTILDTINKTELACNNTVIGSQMQLQLGRVTRVQKHRKILRAARDLALDTLIIEYRGKVMLRQQFEVNGHFFKKPYPFVLFYSKFNGVEMCVDARTFGNDARFIRRSCTPNAEVRHMIADGMIHLCIYAVSAITKDAEVTIAFDYEYSNCNYKVDCACHKGNRNCPIQKRNPNATELPLLPPPPSLPTIGAETRRRKARRKELEMEQQNEASEENNDQQSQEVPEKVTVSSDHEEVDNPEEKPEEEKEEVIDDQENLAHSRRTREDRKVEAIMHAFENLEKRKKRRDQPLEQSNSDVEITTTTSETPVGEETKTEAPESEVSNSVSNVTIPSTPQSVGVNTRRSSQAGDIAAEKLVPKPPPAKPSRPRPKSRISRYRTSSAQRLKRQKQANAQQAELSQAALEEGGSNSLVTPTEAGSLDSSGENRPLTGSDPTVVSITGSHVNRAASKYPKTKKYLVTEWLNDKAEKQECPVECPLRITTDPTVLATTLNMLPGLIHSPLICTTPKHYIRFGSPFIPERRRRPLLPDGTFSSCKKRWIKQALEEGMTQTSSVPQETRTQHLYQSNENSSSSSICKDNADLLSPLKKWKSRYLMEQNVTKLLRPLSPVTPPPPNSGSKSPQLATPGSSHPGEEECRNGYSLMFSPVTSLTTASRCNTPLQFELCHRKDLDLAKVGYLDSNTNSCADRPSLLNSGHSDLAPHPSLGPTSETGFPSRSGDGHQTLVRNSDQAFRTEFNLMYAYSPLNAMPRADGLYRGSPLVGDRKPLHLDGGYCSPAEGFSSRYEHGLMKDLSRGSLSPGGERACEGVPSAPQNPPQRKKVSLLEYRKRKQEAKENSAGGGGDSAQSKSKSAGAGQGSSNSVSDTGAHGVQGSSARTPSSPHKKFSPSHSSMSHLEAVSPSDSRGTSSSHCRPQENISSRWMVPTSVERLREGGSIPKVLRSSVRVAQKGEPSPTWESNITEKDSDPADGEGPETLSSALSKGATVYSPSRYSYQLLQCDSPRTESQSLLQQSSSPFRGHPTQSPGYSYRTTALRPGNPPSHGSSESSLSSTSYSSPAHPVSTDSLAPFTGTPGYFSSQPHSGNSTGSNLPRRSCPSSAASPTLQGPSDSPTSDSVSQSSTGTLSSTSFPQNSRSSLPSDLRTISLPSAGQSAVYQASRVSAVSNSQHYPHRGSGGVHQYRLQPLQGSGVKTQTGLS
"
     misc_feature    649..651
                     /gene="SETD5"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q9C0A6.2); phosphorylation site"
     misc_feature    1321..1620
                     /gene="SETD5"
                     /note="SET (Su(var)3-9, Enhancer-of-zeste, Trithorax)
                     domain; Region: SET; smart00317"
                     /db_xref="CDD:197649"
     misc_feature    2920..2922
                     /gene="SETD5"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q9C0A6.2); phosphorylation site"
     variation       447
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373289671"
     variation       449
                     /gene="SETD5"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:377000906"
     variation       468
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370087030"
     variation       470
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201510004"
     exon            507..612
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     exon            613..764
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       615
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374396895"
     STS             620..697
                     /gene="SETD5"
                     /standard_name="G66214"
                     /db_xref="UniSTS:230202"
     variation       626
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368353953"
     variation       634
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200031380"
     variation       648
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371515878"
     variation       665
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:41387348"
     variation       683
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367751379"
     variation       698
                     /gene="SETD5"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:371529347"
     variation       747
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376494447"
     variation       749
                     /gene="SETD5"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:185408508"
     exon            765..823
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       791
                     /gene="SETD5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:11720526"
     exon            824..1002
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     STS             833..1843
                     /gene="SETD5"
                     /standard_name="Setd5"
                     /db_xref="UniSTS:507217"
     variation       934
                     /gene="SETD5"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:370291812"
     variation       939
                     /gene="SETD5"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:370585538"
     variation       956
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375122657"
     exon            1003..1245
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       1044
                     /gene="SETD5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201728851"
     variation       1119
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368771701"
     variation       1122
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371218876"
     variation       1151
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375003888"
     variation       1210
                     /gene="SETD5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:367686844"
     exon            1246..1394
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       1284
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17050347"
     exon            1395..1512
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       1463
                     /gene="SETD5"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:371439647"
     variation       1503
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375926486"
     exon            1513..1622
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       1527
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374226733"
     variation       1545
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77664997"
     variation       1597
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200900982"
     exon            1623..1875
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       1635
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181539866"
     variation       1661
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200411830"
     variation       1701
                     /gene="SETD5"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201331854"
     variation       1708
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372257643"
     variation       1715
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375321317"
     variation       1721
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184437226"
     variation       1775
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200137965"
     variation       1808
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371491667"
     exon            1876..1959
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       1880
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187196435"
     variation       1894
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369459846"
     variation       1899
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199524842"
     variation       1901
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374542281"
     variation       1925
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377747511"
     variation       1950
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:117265865"
     exon            1960..2217
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       1981
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147867570"
     variation       2035
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200917280"
     variation       2074
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370512198"
     variation       2163
                     /gene="SETD5"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:191615401"
     variation       2188
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368383990"
     exon            2218..2538
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       2224
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371738111"
     variation       2229
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376761696"
     variation       2237
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369117880"
     variation       2298
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374237333"
     variation       2334
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373096622"
     variation       2345
                     /gene="SETD5"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201561587"
     variation       2347
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145659084"
     variation       2414
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183864096"
     variation       2441
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199595728"
     variation       2454
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373778653"
     variation       2458
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376201066"
     variation       2469
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:145375575"
     variation       2485
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369259948"
     exon            2539..2781
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       2553
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372906360"
     variation       2569
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376053762"
     variation       2580
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370407483"
     variation       2583
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192681161"
     variation       2641
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368466781"
     variation       2683
                     /gene="SETD5"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:371116757"
     variation       2734
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183911558"
     variation       2742
                     /gene="SETD5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200540210"
     variation       2745
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371870672"
     exon            2782..2911
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       2783
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201499833"
     variation       2809
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369830364"
     variation       2823
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372628120"
     variation       2842
                     /gene="SETD5"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:375673884"
     variation       2848
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200111947"
     variation       2856
                     /gene="SETD5"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:370594564"
     variation       2863
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200515261"
     variation       2887
                     /gene="SETD5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372699100"
     variation       2897
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376767548"
     exon            2912..3159
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       2922
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374208065"
     variation       2946
                     /gene="SETD5"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201547519"
     variation       2967
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376710019"
     variation       2979
                     /gene="SETD5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:147128913"
     variation       3036
                     /gene="SETD5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:371224058"
     variation       3049
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375015539"
     variation       3050
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200413331"
     variation       3080
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200142019"
     variation       3088
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:117354149"
     variation       3133
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113593115"
     variation       3140
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375109664"
     exon            3160..3630
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     STS             3170..3343
                     /gene="SETD5"
                     /standard_name="SHGC-76694"
                     /db_xref="UniSTS:34436"
     variation       3201
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375509474"
     variation       3209
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370208992"
     variation       3243
                     /gene="SETD5"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:372223844"
     variation       3253
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374753079"
     variation       3287
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147163116"
     variation       3301
                     /gene="SETD5"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:201868415"
     variation       3326
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372894361"
     variation       3359
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199509254"
     variation       3362
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138685269"
     variation       3437
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369238798"
     variation       3448
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190068083"
     STS             3449..3531
                     /gene="SETD5"
                     /standard_name="G66213"
                     /db_xref="UniSTS:230201"
     variation       3501
                     /gene="SETD5"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:11543057"
     variation       3551
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201568605"
     variation       3572
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371265278"
     exon            3631..3932
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       3695
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202119930"
     variation       3744
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371680000"
     variation       3753
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375375084"
     variation       3759
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144324726"
     variation       3765
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73026975"
     variation       3772
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375325655"
     variation       3773
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200143538"
     variation       3776
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201189533"
     variation       3844
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:13327456"
     variation       3861
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146583836"
     variation       3874
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374898000"
     exon            3933..4066
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       3983
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377349853"
     variation       3999
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6779961"
     variation       4035
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376334779"
     exon            4067..4155
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       4103
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373191662"
     exon            4156..6827
                     /gene="SETD5"
                     /inference="alignment:Splign:1.39.8"
     variation       4181
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372283291"
     variation       4206
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:202098816"
     variation       4208
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367569965"
     variation       4239
                     /gene="SETD5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:373046266"
     variation       4268
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201663969"
     variation       4288
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372152804"
     variation       4289
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376768374"
     variation       4290
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369121817"
     variation       4326
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199989217"
     variation       4342
                     /gene="SETD5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:377060727"
     variation       4358
                     /gene="SETD5"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:11542009"
     variation       4364
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201582360"
     variation       4376
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377008740"
     variation       4379
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202179816"
     variation       4433
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373417594"
     variation       4448
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376057899"
     variation       4489
                     /gene="SETD5"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201224440"
     variation       4497
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370412797"
     variation       4509
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200296385"
     variation       4535
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374412039"
     variation       4550
                     /gene="SETD5"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:62246321"
     variation       4566
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17747739"
     variation       4575
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374462952"
     variation       4595
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:80044089"
     variation       4603
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367768112"
     variation       4637
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371489622"
     variation       4642
                     /gene="SETD5"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:376512544"
     variation       4650
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:183053371"
     variation       4685
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368126889"
     variation       4688
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372048733"
     variation       4691
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188493095"
     variation       4715
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199797835"
     variation       4792
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377088655"
     variation       4805
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369475282"
     variation       4862
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146711037"
     variation       4883
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:192905198"
     variation       4937
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184678645"
     STS             4985..5114
                     /gene="SETD5"
                     /standard_name="RH12737"
                     /db_xref="UniSTS:64710"
     variation       4992
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:76610781"
     variation       5013
                     /gene="SETD5"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:189465678"
     variation       5072
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142730352"
     variation       5095
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11928554"
     variation       5130
                     /gene="SETD5"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:62246322"
     variation       5133
                     /gene="SETD5"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:5846639"
     variation       5133
                     /gene="SETD5"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:62964260"
     variation       5215
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:116540535"
     variation       5319
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147980693"
     variation       5348
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191204680"
     variation       5437
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:74981768"
     variation       5496
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141809438"
     variation       5500
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2279440"
     variation       5628
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:79402583"
     variation       5647
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150583070"
     variation       5796
                     /gene="SETD5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:17081119"
     variation       5913
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139957215"
     variation       6374
                     /gene="SETD5"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:58994037"
     variation       6677
                     /gene="SETD5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:7635794"
     variation       6678
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:77085802"
     variation       6678
                     /gene="SETD5"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:372452647"
     variation       6681
                     /gene="SETD5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:77280788"
     variation       6682
                     /gene="SETD5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75718126"
     variation       6698
                     /gene="SETD5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:13085737"
     variation       6735
                     /gene="SETD5"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:13085756"
     variation       6738
                     /gene="SETD5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:13085758"
ORIGIN      
gctcagagactcacgcagccccagtcccgccagtccgccaacacagtagtgccggcccccctctttccctggccctgccccccctccccgcctttggctcgctccgcctttctgccccccacccccacctcacgggtacgggccattcccggccaggaaacgccgtggcgccgcgttgggcctaactcgagtcctgccgcctcccgggagtgccgtgcgccgcagcccgggcccaggccccggcagcgcctgggacaaggtcttcagaactactagcagataatttggggggacttcatattcagaagtctatataaaggattcctcatgtccataacatgttggatgaggctctgcagctcacccccactctcagagtggtcagtctccattaattggaccccgtgatttccaatctctgctgtgttggacgtcatgagcattgcaatccctctgggagtcaccacatcagatacatcctactcagatatggctgctggatcagaccctgaatctgtggaggctagtccagcagttaatgagaagagcgtgtattccactcataattatgggaccactcagaggcatgggtgtcgaggactgccttatgctacgatcatccctcgttctgacctgaatggcctgccgtcgcctgtagaggaacgctgtggagacagcccgaactctgaaggagaaactgtacctacctggtgtccttgtggtctttctcaggatggcttccttctcaactgtgacaagtgcaggggaatgagcagggggaaggttattagacttcatcggcggaagcaggacaacatatcaggtggggatagcagtgcaacagaaagctgggatgaggagctttctccttccactgtgttgtatacagcaacacagcacacacctacaagcatcaccttaactgttagaagaaccaaacccaagaagcggaaaaagagtccagaaaagggtcgtgcagcaccaaagacgaagaaaatcaagaattctccctctgaagcacagaatttagatgagaatacaactgagggctgggaaaatcggataagactatggactgaccagtatgaagaagctttcactaatcagtacagtgcagatgtacagaacgcgcttgaacaacacctacattctagcaaggaatttgtgggcaaacctactattttagacactattaataagactgaattggcctgtaataacacagttattggttcccaaatgcagttacagctgggaagagtcactcgtgttcaaaagcaccggaagatcctgagggctgcaagagatttggctttggacactcttataatagagtatcgtgggaaagtcatgttacgacagcaatttgaggtcaatgggcatttcttcaaaaaaccatacccctttgtgctcttctactcaaaattcaatggtgtagagatgtgtgtggatgcccgtactttcggtaatgatgctcggttcatcagaagatcatgtacaccaaatgcagaggtgcgacacatgattgcagatgggatgattcacctgtgcatctatgctgtgtctgccatcaccaaggatgctgaggtcaccatagcatttgattatgagtatagtaactgtaattataaagtggactgtgcctgtcacaagggaaaccggaattgtcctatacaaaaaaggaatcctaatgctacagaactgccactcctaccacctcctccaagcctacccaccattggagcagagactagacgtagaaaagcacgacggaaagagctagagatggagcagcagaatgaggcttcagaggagaataatgaccagcaatcacaagaagttccagaaaaagtaactgtatccagtgatcatgaggaagtagacaatccagaagaaaaaccagaagaagagaaagaagaggttatagatgaccaggagaacctagctcatagcaggaggaccagggaagatagaaaggtagaagccatcatgcatgcttttgaaaacttagagaaaagaaagaagcggcgggatcagcccttggaacagagcaactctgatgtagagattactacaaccacctcagagactcctgttggtgaagagacaaaaactgaagcccctgaatctgaagttagcaactctgtttcaaatgttaccatcccaagcaccccacagagtgttggtgtgaatacccggaggtcttcccaagcaggggatattgctgcagaaaaactagtccccaagccacctccagcaaagccttctaggccccggccgaagagtcgaatttctcggtacaggaccagttcagcccaaagactaaagcgtcagaagcaggccaatgcacagcaggcagaattgtcacaagctgccttggaagagggaggaagtaacagtttagtaactcctactgaagctggaagtctagacagttcaggagaaaacaggccattaacagggtctgacccaactgtggtgtcaattactggatcccatgtcaaccgtgctgcatctaaataccccaaaaccaaaaagtatctagttacagaatggttgaatgacaaagcagagaagcaagagtgccctgttgagtgccctttacgtatcacaacggatccaactgtactggcaacgaccctaaacatgttaccaggtcttatccattccccgttaatttgcaccacccccaaacactacattcgctttggctcaccctttatccctgagagacgtcgaaggccccttctgcctgatggcacattcagctcctgtaagaagcgctggataaaacaagccttagaagaagggatgactcaaacatcatctgtaccccaagagactagaactcagcacctataccaaagcaatgagaatagtagctcttctagtatctgcaaagacaatgcagacttgttgagcccattaaagaaatggaagtctcgctatctgatggagcagaatgtcaccaagttacttcggcctctgtctccagtcacaccaccccctcccaattcaggctcaaagagtccccagctggccacacctggctcatctcacccaggagaagaggagtgtcgaaatggatacagcctcatgttttcaccagtcacatctcttactactgctagtcgctgcaacactcctctacagtttgagctttgtcaccgaaaagacctggatttggcaaaagtaggataccttgactccaacactaacagctgtgctgatagaccttccctactcaactcaggtcattctgacctggctcctcatccctccctcggacccacttctgagactggtttcccaagcagaagtggagatggacatcagaccctcgtgagaaactcagaccaggcatttcggacagagttcaacttgatgtatgcctactcccctttgaatgctatgcctcgagcagatggactgtatcgaggatctcctctagtgggggataggaagcctttacatttggatgggggatattgttcccctgcagaaggattttccagcagatatgaacatggcttaatgaaagacctctctcgtggatccttgtcacctggtggtgaaagggcctgtgaaggagtcccatctgccccccagaacccaccacagaggaaaaaagtatccctgctggagtaccgaaaacggaaacaagaagctaaggaaaattctgctggtgggggaggtgactctgcacagagcaaaagcaagtctgcaggagctgggcaaggcagcagtaactccgtttccgacactggtgcccatggtgtgcagggatcctcagcccgaactccatcttcccctcacaaaaaattctccccatctcattcctctatgtcccatttggaggcggtaagcccatcagattccagaggcacttcttcatctcactgcagacctcaagagaatatcagcagtaggtggatggttcccacatcagtagaacgactccgagaaggagggagcatccccaaggtcctccgaagcagcgtgagggtggcccaaaagggagagccctctcccacatgggagagtaacatcacagagaaagactcagaccctgcagatggagaaggcccagagacattaagctcagcactctctaaaggagcaacagtttacagcccttccagatacagctaccagctcctgcagtgtgatagtcctcggacagaatcacaaagcctccttcagcagagttcctcccccttcagaggacatcctacacagtctccaggatacagttatcgaactactgcactgagacctggaaaccccccctctcacggttcttcagaatcatccctctcttccacgtcctattccagccccgcccaccctgtgtccacagactcgttggccccatttacggggacaccagggtattttagcagccagccacattctggaaacagcactggcagcaatcttccaaggaggagctgcccttctagtgctgctagccctaccctgcagggaccctcagactcgccaacctcagattcagtttctcagtccagcacaggaactctgagttccacctcctttcctcagaactctaggtcgtcattgccatcagacttacggactatcagtctgcccagtgctgggcagtcagctgtctaccaggcctccagggtatctgcggtttccaattcacagcactacccacaccgtgggagtgggggtgtgcaccagtaccgactccagccactgcaagggtcaggagtcaagactcagacgggactttcctagggcttctggatttgggcaaacagaactgaatgagcccatagctgcttccttccagctgcctctggaacctaggccgagcatattgctgaggaacggggggtacaaggtgccagaggattgggtctggtggacaagaaacaagacttgtggtcacaattggcctctggccttggagaaagctgtaaatcttgtctgaagcagagactataaagaagtttctccctgctgtcaagggt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