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
gctcagagactcacgcagccccagtcccgccagtccgccaacacagtagtgccggcccccctctttccctggccctgccccccctccccgcctttggctcgctccgcctttctgccccccacccccacctcacgggtacgggccattcccggccaggaaacgccgtggcgccgcgttgggcctaactcgagtcctgccgcctcccgggagtgccgtgcgccgcagcccgggcccaggccccggcagcgcctgggacaaggtcttcagaactactagcagataatttggggggacttcatattcagaagtctatataaaggattcctcatgtccataacatgttggatgaggctctgcagctcacccccactctcagagtggtcagtctccattaattggaccccgtgatttccaatctctgctgtgttggacgtcatgagcattgcaatccctctgggagtcaccacatcagatacatcctactcagatatggctgctggatcagaccctgaatctgtggaggctagtccagcagttaatgagaagagcgtgtattccactcataattatgggaccactcagaggcatgggtgtcgaggactgccttatgctacgatcatccctcgttctgacctgaatggcctgccgtcgcctgtagaggaacgctgtggagacagcccgaactctgaaggagaaactgtacctacctggtgtccttgtggtctttctcaggatggcttccttctcaactgtgacaagtgcaggggaatgagcagggggaaggttattagacttcatcggcggaagcaggacaacatatcaggtggggatagcagtgcaacagaaagctgggatgaggagctttctccttccactgtgttgtatacagcaacacagcacacacctacaagcatcaccttaactgttagaagaaccaaacccaagaagcggaaaaagagtccagaaaagggtcgtgcagcaccaaagacgaagaaaatcaagaattctccctctgaagcacagaatttagatgagaatacaactgagggctgggaaaatcggataagactatggactgaccagtatgaagaagctttcactaatcagtacagtgcagatgtacagaacgcgcttgaacaacacctacattctagcaaggaatttgtgggcaaacctactattttagacactattaataagactgaattggcctgtaataacacagttattggttcccaaatgcagttacagctgggaagagtcactcgtgttcaaaagcaccggaagatcctgagggctgcaagagatttggctttggacactcttataatagagtatcgtgggaaagtcatgttacgacagcaatttgaggtcaatgggcatttcttcaaaaaaccatacccctttgtgctcttctactcaaaattcaatggtgtagagatgtgtgtggatgcccgtactttcggtaatgatgctcggttcatcagaagatcatgtacaccaaatgcagaggtgcgacacatgattgcagatgggatgattcacctgtgcatctatgctgtgtctgccatcaccaaggatgctgaggtcaccatagcatttgattatgagtatagtaactgtaattataaagtggactgtgcctgtcacaagggaaaccggaattgtcctatacaaaaaaggaatcctaatgctacagaactgccactcctaccacctcctccaagcctacccaccattggagcagagactagacgtagaaaagcacgacggaaagagctagagatggagcagcagaatgaggcttcagaggagaataatgaccagcaatcacaagaagttccagaaaaagtaactgtatccagtgatcatgaggaagtagacaatccagaagaaaaaccagaagaagagaaagaagaggttatagatgaccaggagaacctagctcatagcaggaggaccagggaagatagaaaggtagaagccatcatgcatgcttttgaaaacttagagaaaagaaagaagcggcgggatcagcccttggaacagagcaactctgatgtagagattactacaaccacctcagagactcctgttggtgaagagacaaaaactgaagcccctgaatctgaagttagcaactctgtttcaaatgttaccatcccaagcaccccacagagtgttggtgtgaatacccggaggtcttcccaagcaggggatattgctgcagaaaaactagtccccaagccacctccagcaaagccttctaggccccggccgaagagtcgaatttctcggtacaggaccagttcagcccaaagactaaagcgtcagaagcaggccaatgcacagcaggcagaattgtcacaagctgccttggaagagggaggaagtaacagtttagtaactcctactgaagctggaagtctagacagttcaggagaaaacaggccattaacagggtctgacccaactgtggtgtcaattactggatcccatgtcaaccgtgctgcatctaaataccccaaaaccaaaaagtatctagttacagaatggttgaatgacaaagcagagaagcaagagtgccctgttgagtgccctttacgtatcacaacggatccaactgtactggcaacgaccctaaacatgttaccaggtcttatccattccccgttaatttgcaccacccccaaacactacattcgctttggctcaccctttatccctgagagacgtcgaaggccccttctgcctgatggcacattcagctcctgtaagaagcgctggataaaacaagccttagaagaagggatgactcaaacatcatctgtaccccaagagactagaactcagcacctataccaaagcaatgagaatagtagctcttctagtatctgcaaagacaatgcagacttgttgagcccattaaagaaatggaagtctcgctatctgatggagcagaatgtcaccaagttacttcggcctctgtctccagtcacaccaccccctcccaattcaggctcaaagagtccccagctggccacacctggctcatctcacccaggagaagaggagtgtcgaaatggatacagcctcatgttttcaccagtcacatctcttactactgctagtcgctgcaacactcctctacagtttgagctttgtcaccgaaaagacctggatttggcaaaagtaggataccttgactccaacactaacagctgtgctgatagaccttccctactcaactcaggtcattctgacctggctcctcatccctccctcggacccacttctgagactggtttcccaagcagaagtggagatggacatcagaccctcgtgagaaactcagaccaggcatttcggacagagttcaacttgatgtatgcctactcccctttgaatgctatgcctcgagcagatggactgtatcgaggatctcctctagtgggggataggaagcctttacatttggatgggggatattgttcccctgcagaaggattttccagcagatatgaacatggcttaatgaaagacctctctcgtggatccttgtcacctggtggtgaaagggcctgtgaaggagtcccatctgccccccagaacccaccacagaggaaaaaagtatccctgctggagtaccgaaaacggaaacaagaagctaaggaaaattctgctggtgggggaggtgactctgcacagagcaaaagcaagtctgcaggagctgggcaaggcagcagtaactccgtttccgacactggtgcccatggtgtgcagggatcctcagcccgaactccatcttcccctcacaaaaaattctccccatctcattcctctatgtcccatttggaggcggtaagcccatcagattccagaggcacttcttcatctcactgcagacctcaagagaatatcagcagtaggtggatggttcccacatcagtagaacgactccgagaaggagggagcatccccaaggtcctccgaagcagcgtgagggtggcccaaaagggagagccctctcccacatgggagagtaacatcacagagaaagactcagaccctgcagatggagaaggcccagagacattaagctcagcactctctaaaggagcaacagtttacagcccttccagatacagctaccagctcctgcagtgtgatagtcctcggacagaatcacaaagcctccttcagcagagttcctcccccttcagaggacatcctacacagtctccaggatacagttatcgaactactgcactgagacctggaaaccccccctctcacggttcttcagaatcatccctctcttccacgtcctattccagccccgcccaccctgtgtccacagactcgttggccccatttacggggacaccagggtattttagcagccagccacattctggaaacagcactggcagcaatcttccaaggaggagctgcccttctagtgctgctagccctaccctgcagggaccctcagactcgccaacctcagattcagtttctcagtccagcacaggaactctgagttccacctcctttcctcagaactctaggtcgtcattgccatcagacttacggactatcagtctgcccagtgctgggcagtcagctgtctaccaggcctccagggtatctgcggtttccaattcacagcactacccacaccgtgggagtgggggtgtgcaccagtaccgactccagccactgcaagggtcaggagtcaagactcagacgggactttcctagggcttctggatttgggcaaacagaactgaatgagcccatagctgcttccttccagctgcctctggaacctaggccgagcatattgctgaggaacggggggtacaaggtgccagaggattgggtctggtggacaagaaacaagacttgtggtcacaattggcctctggccttggagaaagctgtaaatcttgtctgaagcagagactataaagaagtttctccctgctgtcaagggtacattgttgacaagcaaatggtgtttcggttagtaacggttctaagtgcaatgagttgtgttgaagcctccgtctcccatccttgcctgtagcccgtagtcacttgtgcagtgaggacatctttttaaatttaaaaaaaaaaaaaaaaaaagttttcaaaggaaaaaaagttaaaagagccaatctcaaagccccaagccatctgagtactgttagggttttatgcacttaagaaaaaaggtaggtatgtaaatgttcatcctaagacaaccattccaaaagcaggtatctggccaatgtgtgtccaccaagaatactgtttatctttgtcttaagatcaccaagaaataggcaaggatagtaaagcttggaacctgcaccaactggagggtgcctggctctttgaagaaaagctcatggtcagctcttgattattcgggagcagattatttgagtagattgtctgagcctccaactgttaccatcctactcccccttcccaagctatttcacagctcagtaacccatgaagtaagtagacaagaaaaggaggaatgagacatgatataggccaattgcattgctacttaccagcttttggcaataaatttcattaggaaggataccgagtggtttgggaatgcttcgaattttattttttctactcccaattaatcaggagttgatgatcccatgagcaggaccgcctccatgattggggagcatgcacttgtgactgcagggtaagagtgggaagataggtttgtggagtggcaccgacaggactgtgattgtgtgtgggcctgccccacatttctctgggggatgcttatgtgagagtgggcccagtgaaagagttaccaagccacccacacccctaacactgttctggatgagagatgagagcagaccggcttctccccatcagtgcattgtgcctgttgtacacccctggaggagccctggagccagcccaggtggggtacacaatctttttaaattccatatggttgccagcttatttctttcacttgtttactgtaatatctggcgtgtttttatttatctaattttgtattcagttataaccatggtaggggtagtgaatatatgacaggtgtaatccctggtgctgcagtggaccttcttttcttttggacaagataatactgtgagtttccctccttccttccctctaatttgttttccttttttccccagcctcttgcatccccttcttttctaccctgtcctacaactatcatatgcacagtcttctctctttgtgtgtgactgttacaaaatttcacttttcaaaatcgaaatcaggtgtttgctcaaatgaggggagattttttttttttttttttttttaaatgctgagacctcagcagagtacttttctttttgttgtttcccccacaaacccatcagtctgggagagcattgggagtggaaatcatgttgcctgggatgctggtttctttgtatattatataaaacgtatgtaaatgtctctccatttgggctggggtttgcattctccccttggctatttaaccaaggggagaggccagcgggcaggcggccctcaccctgcctggcacgtgcagagaccccagccactctgtgtgggcagggtgctgtcaagaccagacctcttgggggggtaggggcgggggggtggggggaactcttggaagggaagaagtatcacttctttctcaagtggagtgtttacaccttgctgtaacatttgaactttcacaagagatgtaataattttgataataaaattcttaaccataataatcataaagttgagaa
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