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2019-03-25 14:37:33, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001257998            5741 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens coiled-coil domain containing 132 (CCDC132),
            transcript variant 3, mRNA.
ACCESSION   NM_001257998
VERSION     NM_001257998.1  GI:384229073
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 5741)
  AUTHORS   Bailey,S.D., Xie,C., Do,R., Montpetit,A., Diaz,R., Mohan,V.,
            Keavney,B., Yusuf,S., Gerstein,H.C., Engert,J.C. and Anand,S.
  CONSRTM   DREAM investigators
  TITLE     Variation at the NFATC2 locus increases the risk of
            thiazolidinedione-induced edema in the Diabetes REduction
            Assessment with ramipril and rosiglitazone Medication (DREAM) study
  JOURNAL   Diabetes Care 33 (10), 2250-2253 (2010)
   PUBMED   20628086
  REMARK    GeneRIF: Observational study of gene-disease association,
            gene-environment interaction, and pharmacogenomic / toxicogenomic.
            (HuGE Navigator)
REFERENCE   2  (bases 1 to 5741)
  AUTHORS   Matsumoto,Y., Imai,Y., Sugita,Y., Tanaka,T., Tsujimoto,G., Saito,H.
            and Oshida,T.
  TITLE     CCDC132 is highly expressed in atopic dermatitis T cells
  JOURNAL   Mol Med Rep 3 (1), 83-87 (2010)
   PUBMED   21472204
REFERENCE   3  (bases 1 to 5741)
  AUTHORS   Talmud,P.J., Drenos,F., Shah,S., Shah,T., Palmen,J., Verzilli,C.,
            Gaunt,T.R., Pallas,J., Lovering,R., Li,K., Casas,J.P., Sofat,R.,
            Kumari,M., Rodriguez,S., Johnson,T., Newhouse,S.J., Dominiczak,A.,
            Samani,N.J., Caulfield,M., Sever,P., Stanton,A., Shields,D.C.,
            Padmanabhan,S., Melander,O., Hastie,C., Delles,C., Ebrahim,S.,
            Marmot,M.G., Smith,G.D., Lawlor,D.A., Munroe,P.B., Day,I.N.,
            Kivimaki,M., Whittaker,J., Humphries,S.E. and Hingorani,A.D.
  CONSRTM   ASCOT investigators; NORDIL investigators; BRIGHT Consortium
  TITLE     Gene-centric association signals for lipids and apolipoproteins
            identified via the HumanCVD BeadChip
  JOURNAL   Am. J. Hum. Genet. 85 (5), 628-642 (2009)
   PUBMED   19913121
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   4  (bases 1 to 5741)
  AUTHORS   Lamesch,P., Li,N., Milstein,S., Fan,C., Hao,T., Szabo,G., Hu,Z.,
            Venkatesan,K., Bethel,G., Martin,P., Rogers,J., Lawlor,S.,
            McLaren,S., Dricot,A., Borick,H., Cusick,M.E., Vandenhaute,J.,
            Dunham,I., Hill,D.E. and Vidal,M.
  TITLE     hORFeome v3.1: a resource of human open reading frames representing
            over 10,000 human genes
  JOURNAL   Genomics 89 (3), 307-315 (2007)
   PUBMED   17207965
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            BC017888.1, AK126478.1, AC002453.1, AC002379.1 and BE671517.1.
            
            Transcript Variant: This variant (3) contains an alternate exon
            compared to variant 1. The resulting isoform (c) has a shorter and
            distinct N-terminus compared to isoform a.
            
            Sequence Note: This RefSeq record was created from transcript and
            genomic sequence data to make the sequence consistent with the
            reference genome assembly. The genomic coordinates used for the
            transcript record were based on transcript alignments.
            
            ##Evidence-Data-START##
            Transcript exon combination :: AK126478.1 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025081, ERS025083 [ECO:0000350]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-26                BC017888.1         1-26
            27-443              AK126478.1         1-417
            444-444             AC002453.1         51338-51338
            445-3518            AK126478.1         419-3492
            3519-5731           AC002379.1         86200-88412
            5732-5741           BE671517.1         1-10                c
FEATURES             Location/Qualifiers
     source          1..5741
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="7"
                     /map="7q21.3"
     gene            1..5741
                     /gene="CCDC132"
                     /note="coiled-coil domain containing 132"
                     /db_xref="GeneID:55610"
                     /db_xref="HGNC:25956"
     exon            1..161
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       9
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:76810131"
     variation       38
                     /gene="CCDC132"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:115505401"
     variation       64
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376190032"
     variation       74
                     /gene="CCDC132"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370533330"
     variation       112
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369703869"
     variation       138
                     /gene="CCDC132"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:372814646"
     exon            162..230
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       163
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377215860"
     variation       188
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143665286"
     variation       221
                     /gene="CCDC132"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:146829042"
     exon            231..258
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    232..234
                     /gene="CCDC132"
                     /note="upstream in-frame stop codon"
     CDS             247..3051
                     /gene="CCDC132"
                     /note="isoform c is encoded by transcript variant 3;
                     coiled-coil domain-containing protein 132"
                     /codon_start=1
                     /product="coiled-coil domain-containing protein 132
                     isoform c"
                     /protein_id="NP_001244927.1"
                     /db_xref="GI:384229074"
                     /db_xref="CCDS:CCDS59065.1"
                     /db_xref="GeneID:55610"
                     /db_xref="HGNC:25956"
                     /translation="
MLTLEEFRELREQPSDPQAEQELINSIEQVYFSVDSFDIVKYELEKLPPVLNLQELEAYRDKLKQQQAAVSKKVADLILEKQPAYVKELERVTSLQTGLQLAAVICTNGRRHLNIAKEGFTQASLGLLANQRKRQLLIGLLKSLRTIKTLQRTDVRLSEMLEEEDYPGAIQLCLECQKAASTFKHYSCISELNSKLQDTLEQIEEQLDVALSKICKNFDINHYTKVQQAYRLLGKTQTAMDQLHMHFTQAIHNTVFQVVLGYVELCAGNTDTKFQKLQYKDLCTHVTPDSYIPCLADLCKALWEVMLSYYRTMEWHEKHDNEDTASASEGSNMIGTEETNFDRGYIKKKLEHGLTRIWQDVQLKVKTYLLGTDLSIFKYDDFIFVLDIISRLMQVGEEFCGSKSEVLQESIRKQSVNYFKNYHRTRLDELRMFLENETWELCPVKSNFSILQLHEFKFMEQSRSPSVSPSKQPVSTSSKTVTLFEQYCSGGNPFEIQANHKDEETEDVLASNGYESDEQEKSAYQEYDSDSDVPEELKRDYVDEQTGDGPVKSVSRETLKSRKKSDYSLNKVNAPILTNTTLNVIRLVGKYMQMMNILKPIAFDVIHFMSQLFDYYLYAIYTFFGRNDSLESTGLGLSSSRLRTTLNRIQESLIDLEVSADPTATLTAAEERKEKVPSPHLSHLVVLTSGDTLYGLAERVVATESLVFLAEQFEFLQPHLDAVMPAVKKPFLQQFYSQTVSTASELRKPIYWIVAGKALDYEQMLLLMANVKWDVKEIMSQHNIYVDALLKEFEQFNRRLNEVSKRVRIPLPVSNILWEHCIRLANRTIVEGYANVKKCSNEGRALMQLDFQQFLMKLEKLTDIRPIPDKEFVETYIKAYYLTENDMERWIKEHREYSTKQLTNLVNVCLGSHINKKARQKLLAAIDDIDRPKR
"
     misc_feature    316..1191
                     /gene="CCDC132"
                     /note="Protein of unknown function N-terminal domain
                     (DUF2450); Region: DUF2450; pfam10475"
                     /db_xref="CDD:151041"
     misc_feature    2323..3030
                     /gene="CCDC132"
                     /note="Protein of unknown function C-terminus (DUF2451);
                     Region: DUF2451; pfam10474"
                     /db_xref="CDD:151040"
     variation       247
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2214098"
     exon            259..381
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       277
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368989470"
     variation       289
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371874797"
     variation       312
                     /gene="CCDC132"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372697126"
     exon            382..453
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       419
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185236240"
     variation       450
                     /gene="CCDC132"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:367996589"
     exon            454..507
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       485
                     /gene="CCDC132"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:146490784"
     exon            508..578
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       513
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17851579"
     variation       529
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140993533"
     variation       547
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111678071"
     exon            579..696
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       585
                     /gene="CCDC132"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375674244"
     variation       607
                     /gene="CCDC132"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:143512538"
     variation       608
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370247072"
     variation       646
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374485392"
     variation       647
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201400427"
     exon            697..732
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       712
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145621721"
     exon            733..815
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       753
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200949909"
     variation       805
                     /gene="CCDC132"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:372089506"
     exon            816..858
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       840
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375400119"
     exon            859..957
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       870
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377185723"
     variation       889
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148835608"
     variation       938
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370126178"
     exon            958..1098
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       978
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202242070"
     variation       1008
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375006121"
     variation       1022
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368851885"
     variation       1062
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200883111"
     exon            1099..1231
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       1134
                     /gene="CCDC132"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:188742733"
     variation       1162
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200944614"
     variation       1188
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138784387"
     variation       1210
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369737684"
     variation       1216
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202155789"
     variation       1223
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199896068"
     exon            1232..1323
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       1246
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377270059"
     variation       1260
                     /gene="CCDC132"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:199714930"
     variation       1266
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200187082"
     variation       1274
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371166383"
     variation       1299
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373817251"
     variation       1315
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375780858"
     variation       1322..1323
                     /gene="CCDC132"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:140810598"
     exon            1324..1418
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       1327
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201054996"
     variation       1347
                     /gene="CCDC132"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200434482"
     variation       1372
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374290264"
     variation       1415
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368241812"
     exon            1419..1517
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       1440
                     /gene="CCDC132"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:371633008"
     variation       1468
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376939967"
     variation       1471
                     /gene="CCDC132"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369316514"
     variation       1517
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11540025"
     exon            1518..1608
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       1558
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:137879844"
     variation       1592
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200751674"
     variation       1602
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369067607"
     exon            1609..1785
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       1634
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146809545"
     variation       1741
                     /gene="CCDC132"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:200076275"
     variation       1748
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371073974"
     exon            1786..1904
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       1869
                     /gene="CCDC132"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:368505711"
     variation       1884
                     /gene="CCDC132"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:141252888"
     exon            1905..2011
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       1951
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374860561"
     exon            2012..2133
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       2043
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367596092"
     variation       2047
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199629360"
     variation       2094
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371808024"
     exon            2134..2214
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       2145
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375083734"
     exon            2215..2363
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       2252
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373349963"
     variation       2321
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376216197"
     variation       2322
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200975765"
     variation       2323
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2106432"
     variation       2344
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377166540"
     exon            2364..2460
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       2388
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371325624"
     variation       2406
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376064331"
     exon            2461..2619
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       2473
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191341151"
     variation       2529
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377259320"
     variation       2603
                     /gene="CCDC132"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:368046857"
     exon            2620..2741
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       2703
                     /gene="CCDC132"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373044128"
     exon            2742..2931
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       2747
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200136574"
     variation       2750
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:61741161"
     variation       2791
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2374639"
     variation       2833
                     /gene="CCDC132"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:377675568"
     variation       2844
                     /gene="CCDC132"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:3764799"
     variation       2886
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148888740"
     variation       2905
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377485014"
     variation       2911
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200300253"
     exon            2932..5738
                     /gene="CCDC132"
                     /inference="alignment:Splign:1.39.8"
     variation       2942
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61745719"
     variation       2976
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370500282"
     variation       3019
                     /gene="CCDC132"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:373958295"
     variation       3028
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368407161"
     variation       3056
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371906960"
     variation       3074
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144266211"
     variation       3076
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192787205"
     variation       3086
                     /gene="CCDC132"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368865634"
     variation       3090
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372156123"
     variation       3099
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146571220"
     variation       3119
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184288073"
     variation       3121
                     /gene="CCDC132"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:140043089"
     variation       3123
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142268872"
     variation       3137
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151222457"
     variation       3162
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140358038"
     variation       3208
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:75758985"
     variation       3249..3250
                     /gene="CCDC132"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:34521532"
     variation       3280
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370407683"
     variation       3302
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17165292"
     variation       3339
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372037711"
     variation       3340
                     /gene="CCDC132"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:189188031"
     variation       3367
                     /gene="CCDC132"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:182276909"
     variation       3376
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:77206719"
     STS             3386..3499
                     /gene="CCDC132"
                     /standard_name="RH44310"
                     /db_xref="UniSTS:81088"
     variation       3519
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11540024"
     variation       3536
                     /gene="CCDC132"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:186327200"
     variation       3681
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142147490"
     variation       3701
                     /gene="CCDC132"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:3735650"
     variation       3772
                     /gene="CCDC132"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:145899579"
     variation       3779
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111634740"
     variation       3847
                     /gene="CCDC132"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:2285506"
     variation       4029
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17165299"
     variation       4079
                     /gene="CCDC132"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138716693"
     variation       4160
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142722832"
     variation       4162
                     /gene="CCDC132"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376781675"
     variation       4198
                     /gene="CCDC132"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:58383093"
     variation       4253
                     /gene="CCDC132"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:114980211"
     variation       4272
                     /gene="CCDC132"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:143421699"
     variation       4290
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148379408"
     variation       4367
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:116637828"
     variation       4387
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:77226429"
     variation       4422
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189459808"
     variation       4442
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141557557"
     variation       4482
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181458400"
     variation       4517
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186046386"
     variation       4531
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2285507"
     variation       4553
                     /gene="CCDC132"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:191376387"
     variation       4600
                     /gene="CCDC132"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:118115946"
     variation       4660
                     /gene="CCDC132"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:150883928"
     variation       4681
                     /gene="CCDC132"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:183038785"
     variation       4718
                     /gene="CCDC132"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:375123175"
     variation       4811
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:74713513"
     variation       4821
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374654008"
     variation       5023..5024
                     /gene="CCDC132"
                     /replace=""
                     /replace="t"
                     /replace="tt"
                     /db_xref="dbSNP:35020495"
     variation       5023
                     /gene="CCDC132"
                     /replace=""
                     /replace="ttt"
                     /db_xref="dbSNP:200289887"
     variation       5032
                     /gene="CCDC132"
                     /replace=""
                     /replace="tt"
                     /db_xref="dbSNP:10546852"
     variation       5044
                     /gene="CCDC132"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:10238215"
     variation       5212
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17165300"
     variation       5221
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142943490"
     variation       5398
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17165301"
     variation       5404
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146104663"
     variation       5426
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376377612"
     variation       5430
                     /gene="CCDC132"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201022056"
     variation       5500
                     /gene="CCDC132"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:117491408"
     variation       5557
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185887518"
     variation       5564
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:73712852"
     variation       5594
                     /gene="CCDC132"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:73219929"
     variation       5629
                     /gene="CCDC132"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:369169965"
     variation       5734
                     /gene="CCDC132"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190856711"
ORIGIN      
aggataccctgggtcggctcctccacgtgaccacccactatggcttcctagtgtcagggccagctgtgtagtggctcggtgtgatttgttagctctttgaggcagggtaccctcctcaggatttcgatatgcaaaaaatcaaatctctcatgacccgacagggtctgaaaagccctcaagaaagcctcagtgatcttggtgccatagagagtctccgggtccctggaaagttagagccctaacgtgatgttaactttggaagaattcagggaacttcgagaacagccaagtgaccctcaagctgaacaagagcttattaatagtattgaacaagtatatttttctgtggattcatttgatattgttaaatatgagctggagaagcttccacctgttctcaatttgcaagaattagaggcgtatagagacaaattgaaacaacagcaagctgcagtatctaaaaaagtggcagatttaatccttgaaaaacagcctgcttatgtaaaggaacttgaaagagttacctcattgcagacaggtcttcaattagctgctgttatctgtacaaatgggagaagacacttgaatattgcaaaggaaggttttactcaagctagtttaggccttcttgcaaatcaaaggaaacgtcagttgctgattggacttctgaaatctctgagaactataaaaacattgcaaagaacagatgtacggttaagtgaaatgctggaggaggaagattatccaggagctattcagttgtgccttgaatgtcaaaaagctgccagcacttttaaacattacagttgtataagtgaactgaattcaaagctgcaagatactttggaacagattgaggaacagctggacgtagctctttccaaaatctgcaagaattttgacattaaccattataccaaggttcaacaagcttatcgacttcttggaaaaacacagacagcaatggatcaacttcatatgcacttcacccaagccattcacaacaccgtgtttcaagttgttcttggttatgtggaactatgtgcaggaaacacagacacaaaattccaaaagctgcaatataaggatctctgtacacatgttacaccagacagctatattccatgccttgcagacctgtgcaaagcactatgggaagttatgctcagctattataggactatggaatggcatgaaaagcatgacaatgaggatactgcttcagcttctgaagggagtaatatgataggtactgaagaaactaattttgatcgtggctacataaaaaagaaattagaacatggacttacacgaatatggcaggatgttcagctaaaagtaaaaacctacttgcttggaactgatttgtctatattcaaatatgatgatttcatctttgttttggatataatcagcaggttgatgcaagttggagaagaattttgtggtagcaagtctgaagttttacaggaatctattagaaaacaaagtgtcaattatttcaagaattaccatagaacacggctcgatgaactgagaatgttcttagagaatgagacttgggaactttgtcctgttaagtcaaatttcagcatcttgcaacttcatgaatttaaattcatggaacagtctcgctccccatcagtttcacctagtaaacagccagtctcaacttcttcaaaaacagtgaccttgtttgagcagtactgtagtggtgggaatccatttgaaattcaggccaaccacaaagatgaagaaacagaagatgtcttagcttctaatgggtatgaatctgatgaacaagaaaagagtgcctatcaagagtatgacagtgacagtgatgttcctgaggaactcaaacgagactatgtggatgagcagacaggagatggtcctgtgaaaagtgtttctcgggaaactctaaaaagcaggaagaaatcagattacagtctaaataaagtgaatgcacctatcttaacaaatacaacattgaacgtcataagacttgttggaaaatatatgcagatgatgaacattcttaagccaattgcctttgatgttattcatttcatgtctcaactatttgattattacttgtatgcaatatataccttttttggtcggaatgattcattggaatcaactggactcggccttagtagtagtagactaagaacaactctaaacagaatacaagaaagccttattgatctagaagtttcagctgatcctactgccacactcacagcagcagaagaaagaaaggagaaggtgccaagtccacacctcagtcacctagtggttttgacatctggggatacgctgtatgggttggcagaaagagtggtagccacggaatccttggtattcttggctgaacagtttgagttccttcagccacatctggatgctgtgatgcctgcagtcaaaaagccctttcttcagcagttctattctcagacagtctcaaccgccagtgaactacggaaaccaatttactggattgtagctggtaaagcccttgattatgaacagatgctgcttctcatggctaatgtgaaatgggatgtaaaagaaattatgtcacagcacaacatatatgtagatgcactattaaaggaatttgagcagtttaacaggaggctaaatgaagtttctaagagagttcgcatacccttgcctgtgtctaatatactttgggaacattgtatacgattggctaatcgaactattgtagaaggatatgccaatgtcaagaaatgcagtaatgagggtcgtgccctgatgcaattggattttcaacagtttttaatgaaacttgaaaaactaacagatattagacccattcctgataaagaatttgtagaaacttatattaaagcttattacctaactgagaatgacatggaacggtggatcaaagagcacagggaatattcaacgaagcagctgaccaatctggtgaatgtttgcctgggatcccatatcaataagaaagcaagacaaaaacttctagcagctatagatgatatagacagacctaaaagataatgaacacagctctctttcctcaatggcattgatcctcactcaacatatatgacctgaaagccagtttttttatgcacttctgacaactatctgctaagaaaactttgtgcatgtttttttgactggaaagtggaaaatattgaaatgtgtgtggtgttctcatgacttttatatgctgtggtctcttcaacttttggtctcatttgttgtaatctgaaatgatgttgccgccttgtcataacaatggttatgtgactacagttatacattttacagaagaatgtaccataagtatataattagaagaacagtggcttaatatatgtatgggaagtttatggaaaatgaagttggcacttttctaccctctgagcttggttcttaataagcataatgtgagggtgaatatgtagtatctcctaattatgagcactgcatgagaattaaaaaacacatgtaagtaaaatagttgaaaaatcagtatgttctctgtttttaaaatgtcaaagtttatgtcagggttaatttagttataacaaagtgatcataatggtgaaatttaataaatatactctagtatgatcagcctatgtgagactacattttgattttttgtgtggcatgcagatgtcatgaactatagtgcagcttttagtgtgttctaattttaattgttttatatcctgaaaccaatggtgaaaagtaatttcattgagggtaccttttcaatgcctgagtagcatacagaatcatgattatgagactttcttttatctttctttataaaaatatgtggtttttttgttgaaagttttggtctctttaaattcagattttgtcttaggacagtaaaacccaggttgactgactcaggaaacagttgtctgctagtcactcataaatgtacggtcatatgttcactcttcttaaatatccaccttttataacacaaatgtaaaatagtatcagtctagccaatgatgaactctggaatccacttagtcttcagtaagtatgtgctgttcctctaaactttgccctgaagccagggatcttctcctaatgtatgtgacataaaaatccattttccatgtactcttgccaactgtctgataaggaattttgtgtgtgttctttctgactggagagtggaggacatctaagcttgtgtggcattggtccaatgattgccatgcatgacctgtaacatcaacagctcacagaatcctaaggaatcatgtgagaaacaggccttgggtcttatgagtcttctgggacctaaggtgataaaatggatggcacagaatggcatgtgatcaagcatggaggtgataaggaaacaattgctactctgtgtccatcagtccctgcgatgtctgtaaatgcacagtgtaatgtgaagcactttcagaatatgtttgtgtgtgtctgtatgctgagtgttttcttttcatcctctcatgtcggagttcatttactgtcaatttaaaactttcctcttgtaaaaaggtatgagtttggtgccattatgatttggttgtggctagattatatacttgtgaagtagattctgcctgtagccattatttatatgcagccacttgaagaaaacaaacatgagataagcttggtccttgagtttaaatggcatatttagctgggcacataaagagctaatcaatcttttaaaatttgcagttgatgaagagctgcttatttttctcttctacatggattttatagttggtttcctttaatttctactttagttggccctagataatatgaacaggaatcacctgcctggtagagcccagtgttttccaaggtaataggaattgatacaaaagaattacttatcttgttagagactcgaccatgcaatctgacagaccttttaacctacccttactttgctttctccatcttcaaaatgaaatggtggatctttttaatgctttttgaaaaaggttttttttttttttttttttcattaaaaggtagcttaataagtgctagctagcatcaaaacagtaacaggaggtttgagtcatgaagttacctaatcacaagagagttaccagacatttctcaaatactttatacagtaatattgagttataaccatgtaacattttatgaaactaattttcagataaatacaattgaaaagctgagaatgtaaatggaattatacgtgttccaaaaactatcattaccaaaaatttattatttttgagtctaaactttccttaactttgacattttccatgaaagtttcctgtagaatttaccatgggagcatggtaaattagcattccctgagaaagaatgatcatttctacaaatacattgtcttgcatttaaaaatgctaggggggcacatagcaattcaaatgaactagtttgctttggtttataaaaccaacagagattttgtaagttcactttaactaataaactcatttacacaacttattaaatgaatttctcttgaaaccagggccatatggtattttatcatatctttaaataaaatttcgaaatttctatttagctgagtgctaaagtgaaactttgttagattaaatagctttttcttaactcaccaaaaagtagtaaaaggcttgtaattcaattcaccttgtaagcatagttgtcttttgtaataaaaaactagatctgaaaaa
//

Annotations:



by @meso_cacase at DBCLS
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