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2025-05-09 19:01:56, 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
//
by
@meso_cacase at
DBCLS
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