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2024-03-28 23:52:10, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_052848               3344 bp    mRNA    linear   PRI 07-JUL-2013
DEFINITION  Homo sapiens coiled-coil domain containing 97 (CCDC97), mRNA.
ACCESSION   NM_052848
VERSION     NM_052848.1  GI:16418350
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 3344)
  AUTHORS   Guey LT, Garcia-Closas M, Murta-Nascimento C, Lloreta J, Palencia
            L, Kogevinas M, Rothman N, Vellalta G, Calle ML, Marenne G, Tardon
            A, Carrato A, Garcia-Closas R, Serra C, Silverman DT, Chanock S,
            Real FX and Malats N.
  CONSRTM   EPICURO/Spanish Bladder Cancer Study investigators
  TITLE     Genetic susceptibility to distinct bladder cancer subphenotypes
  JOURNAL   Eur. Urol. 57 (2), 283-292 (2010)
   PUBMED   19692168
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
COMMENT     PROVISIONAL REFSEQ: This record has not yet been subject to final
            NCBI review. The reference sequence was derived from BC011577.1.
            
            ##Evidence-Data-START##
            Transcript exon combination :: BC011577.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025081, ERS025082 [ECO:0000348]
            ##Evidence-Data-END##
FEATURES             Location/Qualifiers
     source          1..3344
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="19"
                     /map="19q13.2"
     gene            1..3344
                     /gene="CCDC97"
                     /note="coiled-coil domain containing 97"
                     /db_xref="GeneID:90324"
                     /db_xref="HGNC:28289"
                     /db_xref="HPRD:14467"
     exon            1..168
                     /gene="CCDC97"
                     /inference="alignment:Splign:1.39.8"
     variation       1
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:183882962"
     variation       58
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61747007"
     variation       72
                     /gene="CCDC97"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:368710855"
     variation       109
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61740091"
     CDS             123..1154
                     /gene="CCDC97"
                     /codon_start=1
                     /product="coiled-coil domain-containing protein 97"
                     /protein_id="NP_443080.1"
                     /db_xref="GI:16418351"
                     /db_xref="CCDS:CCDS12578.1"
                     /db_xref="GeneID:90324"
                     /db_xref="HGNC:28289"
                     /db_xref="HPRD:14467"
                     /translation="
MEAVATATAAKEPDKGCIEPGPGHWGELSRTPVPSKPQDKVEAAEATPVALDSDTSGAENAAVSAMLHAVAASRLPVCSQQQGEPDLTEHEKVAILAQLYHEKPLVFLERFRTGLREEHLACFGHVRGDHRADFYCAEVARQGTARPRTLRTRLRNRRYAALRELIQGGEYFSDEQMRFRAPLLYEQYIGQYLTQEELSARTPTHQPPKPGSPGRPACPLSNLLLQSYEERELQQRLLQQQEEEEACLEEEEEEEDSDEEDQRSGKDSEAWVPDSEERLILREEFTSRMHQRFLDGKDGDFDYSTVDDNPDFDNLDIVARDEEERYFDEEEPEDAPSPELDGD
"
     misc_feature    261..263
                     /gene="CCDC97"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphothreonine; propagated from
                     UniProtKB/Swiss-Prot (Q96F63.1); phosphorylation site"
     misc_feature    612..>749
                     /gene="CCDC97"
                     /note="Coiled-coil domain containing protein (DUF2052);
                     Region: DUF2052; pfam09747"
                     /db_xref="CDD:204303"
     misc_feature    <918..1082
                     /gene="CCDC97"
                     /note="Coiled-coil domain containing protein (DUF2052);
                     Region: DUF2052; pfam09747"
                     /db_xref="CDD:204303"
     misc_feature    945..947
                     /gene="CCDC97"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q96F63.1); phosphorylation site"
     misc_feature    1131..1133
                     /gene="CCDC97"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q96F63.1); phosphorylation site"
     misc_feature    1131..1133
                     /gene="CCDC97"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     variation       125
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202074678"
     variation       131
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138815567"
     variation       137..138
                     /gene="CCDC97"
                     /replace=""
                     /replace="acggcg"
                     /db_xref="dbSNP:377515634"
     variation       137
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201143753"
     variation       146
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371317372"
     exon            169..624
                     /gene="CCDC97"
                     /inference="alignment:Splign:1.39.8"
     variation       194
                     /gene="CCDC97"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:34846366"
     variation       197
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200037630"
     variation       211
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200358934"
     variation       219
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199551755"
     variation       221
                     /gene="CCDC97"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:145115154"
     variation       231
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138920679"
     variation       296
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149006709"
     variation       309
                     /gene="CCDC97"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:143841115"
     variation       326
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377395901"
     variation       327
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201218332"
     variation       335
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373386903"
     variation       336
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148083057"
     variation       337
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138157924"
     variation       343
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147264663"
     variation       382
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377096486"
     variation       410
                     /gene="CCDC97"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200453165"
     variation       419
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368463774"
     variation       425
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139158128"
     variation       435
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376802126"
     variation       450
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:75624130"
     variation       451
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199582362"
     variation       456
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142783394"
     variation       459
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368669358"
     variation       461
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150772304"
     variation       468
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201081145"
     variation       497
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149083553"
     variation       498
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375014029"
     variation       502
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200401151"
     variation       506
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149954618"
     variation       517
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200711332"
     variation       543
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144177246"
     variation       545
                     /gene="CCDC97"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:371814241"
     variation       547
                     /gene="CCDC97"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:376402988"
     variation       558
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143157411"
     variation       560
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201965455"
     variation       564
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201767377"
     variation       569
                     /gene="CCDC97"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374504882"
     variation       573
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143186733"
     variation       579
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140291750"
     variation       580
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376499375"
     exon            625..903
                     /gene="CCDC97"
                     /inference="alignment:Splign:1.39.8"
     variation       690
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201959741"
     variation       695
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369747565"
     variation       713
                     /gene="CCDC97"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:367901995"
     variation       718
                     /gene="CCDC97"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200609121"
     variation       722
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115805108"
     variation       725
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151298239"
     variation       746
                     /gene="CCDC97"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374433360"
     variation       748
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377173036"
     variation       752
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140569847"
     variation       753
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376212276"
     variation       758
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:3745294"
     variation       761
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150477178"
     variation       765
                     /gene="CCDC97"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:370690859"
     variation       779
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372944406"
     variation       806
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138340001"
     variation       836
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377330475"
     variation       897
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142324018"
     exon            904..1033
                     /gene="CCDC97"
                     /inference="alignment:Splign:1.39.8"
     variation       916
                     /gene="CCDC97"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:146376772"
     variation       929
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200306132"
     variation       935
                     /gene="CCDC97"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:374299134"
     variation       941
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:188335747"
     variation       951
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368555031"
     variation       961
                     /gene="CCDC97"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:371069696"
     variation       962
                     /gene="CCDC97"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:374291353"
     variation       966
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200959788"
     variation       984
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200201804"
     variation       987
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367824945"
     variation       997
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372224178"
     variation       1017
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377111574"
     exon            1034..3322
                     /gene="CCDC97"
                     /inference="alignment:Splign:1.39.8"
     variation       1043
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143105404"
     variation       1059
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:35135271"
     variation       1067
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367678386"
     variation       1073
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374346202"
     variation       1074
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201740650"
     variation       1081
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200507915"
     variation       1127
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143731020"
     variation       1151
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148029589"
     variation       1160
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199680363"
     variation       1189
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201969844"
     variation       1197
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115799186"
     variation       1212
                     /gene="CCDC97"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374173286"
     variation       1229
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187996888"
     variation       1287
                     /gene="CCDC97"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:371298760"
     variation       1294
                     /gene="CCDC97"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:3810173"
     variation       1307
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143835604"
     variation       1333
                     /gene="CCDC97"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:79896976"
     variation       1359
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:192497317"
     variation       1427
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185328033"
     variation       1516
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189816469"
     variation       1598
                     /gene="CCDC97"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373940297"
     variation       1618
                     /gene="CCDC97"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:35587298"
     variation       1695
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372300436"
     variation       1726..1728
                     /gene="CCDC97"
                     /replace=""
                     /replace="ctt"
                     /db_xref="dbSNP:375897465"
     variation       1751
                     /gene="CCDC97"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:192961107"
     variation       1760
                     /gene="CCDC97"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:146330354"
     variation       1805..1808
                     /gene="CCDC97"
                     /replace=""
                     /replace="gtct"
                     /db_xref="dbSNP:371846519"
     variation       1813
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139650824"
     variation       1843
                     /gene="CCDC97"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:2241720"
     variation       1937..1938
                     /gene="CCDC97"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:34327670"
     variation       1991
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:75820821"
     variation       2035..2036
                     /gene="CCDC97"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:35525566"
     variation       2115
                     /gene="CCDC97"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:2241719"
     variation       2140
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2241718"
     variation       2222
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184612357"
     variation       2227
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:9282870"
     variation       2241
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:188484237"
     variation       2288
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:180951246"
     variation       2353
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116785413"
     variation       2438..2439
                     /gene="CCDC97"
                     /replace=""
                     /replace="ct"
                     /db_xref="dbSNP:144441501"
     variation       2465
                     /gene="CCDC97"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:144300220"
     variation       2541..2565
                     /gene="CCDC97"
                     /replace=""
                     /replace="ctctgggtcaaccagaattagagcc"
                     /db_xref="dbSNP:371928610"
     variation       2542
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11555004"
     variation       2670
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:16959007"
     variation       2772
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145153226"
     variation       2951
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185069483"
     variation       2970
                     /gene="CCDC97"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:11668308"
     variation       2989
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:116628885"
     variation       2993
                     /gene="CCDC97"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:142205256"
     variation       3035
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11555003"
     variation       3054
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:79057735"
     variation       3131
                     /gene="CCDC97"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:71816054"
     variation       3140
                     /gene="CCDC97"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6957"
     STS             3154..3285
                     /gene="CCDC97"
                     /standard_name="WI-14864"
                     /db_xref="UniSTS:19327"
     variation       3172..3175
                     /gene="CCDC97"
                     /replace=""
                     /replace="ctgt"
                     /db_xref="dbSNP:147793830"
     variation       3237..3238
                     /gene="CCDC97"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:36082857"
     variation       3277
                     /gene="CCDC97"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11304"
     variation       3286
                     /gene="CCDC97"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:189479725"
ORIGIN      
gcctgggcgcagcggtgcacccggacccggaacattctcaggcgaaagtgtctcttgcgtgcgtgggccggaggttagtgtgcggggcccgccgggcggttgaaaagtccgagagaatcaggatggaggccgtggcgacggcgacggcggcgaaggaacccgataagggctgcatagagcctggacctgggcactggggtgagctgagccggacaccagtcccatctaaaccccaggacaaagtggaagcagctgaggcaacaccagtggccctggacagtgacacctccggggctgaaaatgcagcagtgagtgctatgctgcacgctgtagccgccagccgcctgcctgtttgcagccagcagcagggtgaacccgacttgacagagcatgagaaagtggccatcctggcccagctgtaccacgagaagccactggtgttcctggagcgcttccgcacaggcctccgtgaggagcatctggcctgctttggccacgtgcgtggcgaccaccgtgcagacttctactgtgctgaggtggcccggcagggcactgcccggccccgcaccctgcgtacccgcctgcgtaaccggcgctatgctgccctgcgagagctgatccaagggggcgagtacttcagtgatgagcagatgcggttccgggcccccctgctatatgagcagtacatcgggcagtatctcacccaggaggagctcagtgcccgcaccccaacccaccagccccccaagcccgggtcccccgggagacctgcttgcccgctctccaacttgctgctccagtcctacgaggagcgggagctacagcagcgtctgctccaacagcaggaggaggaggaggcctgcttggaggaagaggaagaggaggaggacagtgacgaggaagaccagaggtcaggcaaggactcggaggcctgggttcccgactcggaggagaggctgatcctgcgagaggagttcaccagccgcatgcaccagcgcttcctagatggcaaggacggggactttgactacagcacagtagacgacaaccccgacttcgacaacctcgacatcgtggcacgggatgaggaggagaggtactttgatgaggaagaacctgaggatgcgcccagcccagagctggatggggactgatggccgccacccttcccaccgcctgccccatccccatccccaacaaggcagctgattccaggcctgctcagtgaccctttctctagggggacatcagggcagtgccccacaacccacacacaccaccatctcactgggtctagtctcatctcagacaacccccacccccactgtttctggggttccctttctcatctctcccaccctgtctcctgcctctgtctttcttggtgtctgtctgggcttctttctgtctctttctgtctttctgtctctctccctacccccgctccctctttccagtgctctggctggctgtctctccctttctccccctctctctctgccttaggctctgtctccaccgcagggcccaaggtgaaagtcctccccttgccggaggccagctggcagggcctttcgtggctggaagtggccagtttggttccggtgctgacccctaggccccagcgcagctgcctcccgtgctgtctgtctccccctctctgtttatgtctgcgctgtgtctcacactcagagcctccttgcttctgttaggttcccatctctccttctgcctcactctgggcctcttctttctacttgtacatttccacctctctaggcctctgctctcactgtccctctctgtctgtctctcagcctttatctctgggttttgatcccccactccaggctctgggccccttcttcccccttccctcaaacctggctgctataggcagcagaaccctgaccactgagtaatacagccccaggggagggaggagaccccaggcagggaggatgggggcagctctcttctctccccaggacccaggctgtggatcacggggcctgccagcttgagtgtagagggaggggggactctacccttctcagccccaccagcccccctctgcccaaccacaattttcccttcctccgccttcctctccctctcctgtttacactccccaaatgcgcacaggctgttatcatgggtcctgagtcatcccacacacagcctgccccagcgtccctgcccccagctggccgcagggcccgccccatggagccccctgccgccctgggctaatgggagccagatggccgcctggtgactcagccaccgggcctgtgggaacccaggcgtcccgccttcccatgcccccacacccggctcctgctcccccagcagacacacacaggagggcctggccactgttgagggggcacacagggcaagggtcaccaagtcggggcctagggactcctcatgcctctgagatggaatggtggtatcctgccgtggccaagcctgaaggaccctcaaaactgcctcctggagtccacggttcctgacctccgagcctcagctatgccctctgggtcaaccagaattagagccagacagggaaagtgagagctggatggaggcagacaagatgctcagagcgactattaaagaacgaaagcctctgctacggagcgcttctgtcctctgtcaggcccgagcgaagtgcctgacaccgggttggatcctcagatggccccatgaactagtgaagtgggtcaaaggaggcctggaaagatgttgcttcctcaaggccactcggccatcagaggcagaaatgaaacaggaacccaggcctagaatcacaaaggtcctagaaaccacttggctgtctggcctctcaggtgtcagggccatccagagtgagacagcattggagggacaagtgtgcatgcagatgtcctcagacgggaaggtttgagaagggtcagatggtaggcgggcctaacaagggctccgtgctagccactgtcccgcacacagacaggatcaggtcatcttgatatggagatcagtccccaaatcactgaattgtcccagcagtgctatgccctaggtactaccaatatcactcctctatttcccagaggaggaagcagcagctagactccaggaccttggggtcatatctctcagaaagccaagagtgcaggatgagagctgtctgtctcttacctgcctgtatttgtgccccatttttaaagagcagagggcctgggccacaggaaaggtatcagcccttggtgataggcacattttttaccagtctatcatttggtcattaaatttgtttacaatatactttgctataaaaaaaaaaaaaaaaaaaaaaa
//

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