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2024-03-29 19:21:39, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001257968            3611 bp    mRNA    linear   PRI 18-APR-2013
DEFINITION  Homo sapiens coiled-coil domain containing 129 (CCDC129),
            transcript variant 3, mRNA.
ACCESSION   NM_001257968
VERSION     NM_001257968.1  GI:384081586
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 3611)
  AUTHORS   Rose,J.E., Behm,F.M., Drgon,T., Johnson,C. and Uhl,G.R.
  TITLE     Personalized smoking cessation: interactions between nicotine dose,
            dependence and quit-success genotype score
  JOURNAL   Mol. Med. 16 (7-8), 247-253 (2010)
   PUBMED   20379614
  REMARK    GeneRIF: Clinical trial of gene-disease association and
            gene-environment interaction. (HuGE Navigator)
            Erratum:[Mol Med. 2012;18(1):729]
REFERENCE   2  (bases 1 to 3611)
  AUTHORS   Kimura,K., Wakamatsu,A., Suzuki,Y., Ota,T., Nishikawa,T.,
            Yamashita,R., Yamamoto,J., Sekine,M., Tsuritani,K., Wakaguri,H.,
            Ishii,S., Sugiyama,T., Saito,K., Isono,Y., Irie,R., Kushida,N.,
            Yoneyama,T., Otsuka,R., Kanda,K., Yokoi,T., Kondo,H., Wagatsuma,M.,
            Murakawa,K., Ishida,S., Ishibashi,T., Takahashi-Fujii,A.,
            Tanase,T., Nagai,K., Kikuchi,H., Nakai,K., Isogai,T. and Sugano,S.
  TITLE     Diversification of transcriptional modulation: large-scale
            identification and characterization of putative alternative
            promoters of human genes
  JOURNAL   Genome Res. 16 (1), 55-65 (2006)
   PUBMED   16344560
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            DA098735.1, AK295011.1 and AC006044.2.
            
            Transcript Variant: This variant (3) differs in the 5' and 3' UTRs
            and has multiple coding difference, including use of an alternate
            translation initiation site, compared to variant 1. The encoded
            isoform (3) contains a distinct N- and C-terminus.
            
            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 :: AK295011.1 [ECO:0000332]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-82                DA098735.1         1-82
            83-266              AK295011.1         1-184
            267-267             AC006044.2         27302-27302
            268-1026            AK295011.1         186-944
            1027-1302           AC006044.2         52302-52577
            1303-1640           AK295011.1         1221-1558
            1641-1641           AC006044.2         117022-117022
            1642-2597           AK295011.1         1560-2515
            2598-2598           AC006044.2         117979-117979
            2599-3611           AK295011.1         2517-3529
FEATURES             Location/Qualifiers
     source          1..3611
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="7"
                     /map="7p14.3"
     gene            1..3611
                     /gene="CCDC129"
                     /note="coiled-coil domain containing 129"
                     /db_xref="GeneID:223075"
                     /db_xref="HGNC:27363"
     exon            1..149
                     /gene="CCDC129"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    2..4
                     /gene="CCDC129"
                     /note="upstream in-frame stop codon"
     CDS             95..3283
                     /gene="CCDC129"
                     /note="isoform 3 is encoded by transcript variant 3;
                     coiled-coil domain-containing protein 129"
                     /codon_start=1
                     /product="coiled-coil domain-containing protein 129
                     isoform 3"
                     /protein_id="NP_001244897.1"
                     /db_xref="GI:384081587"
                     /db_xref="CCDS:CCDS59050.1"
                     /db_xref="GeneID:223075"
                     /db_xref="HGNC:27363"
                     /translation="
MPTTASCKTISLLKLLYSVSLQNYSPMMAQKSQGSDNLQEGQEKSKREILKCTKSAWAPLDEWLPPDPEEESQSLTIPMLEDSKQESIQQWLDSGFFVSANENFQQVIDRTVSLYEQGMVQMTVKDYMRSLHQFSETPILSRGTSFNSCYSTASVPQSIPEWLEFWEIDPVEILLDLGFGADEPDICMQIPARFLGCGSAARGINIRVFLEAQKQRMDIENPNLYGRFRQLEILDHVTNAFSSLLSDVSILPNRAEEKAGGESVQRTSVSAAKEHRRRMGKLLRRASKQNIRRDCNPEVSESFKVKDEVFVPFTKPWDCGAELAATSINHKQNHLSLSVEHQSLQACDDLLPYPPHGLLSKQWPCSSMPAKQAPPSCVSEGSVKGRTQKENLFQTNKLKSLSHLAGKGPDSFEMEEVQSFEEETGNPLDMTSGTVGARVDRANSCQSDSSGFLEEPLEPLPLQMPSLPNSQSPAENGGRKPRDQSHSLVSSQDCQLESDGPDSKSRASMSFSSQEANALEQRASVSVMEEEFLLEAMEGPPELYIPDMACAKTTTRGECPRKDSHLWQLLPMPHAEYEVTRPTATSKYDHPLGFMVTHVTEMQDSFVRPEGAGKVQSHHNESQRSPGNDHTQDKFLHVDSEAPREEESSGFCPHTNHSLLVPESSSQCIPKHSEITPYATDLAQTSEKLIPHLHKLPGDPAQVKSRSGTLGQILPGTEAEMENLPLNTGSSRSVMTQMSSSLVSAAQRAVALGTGPRGTSLECTVCDPVTATETRLGTKARQLNDASIQTSALSNKTLTHGPQPLTKSVSLDSGFSSICPMGTCHAIPAHCCICCHHHPHCHGERQSPGPEPSVCRHCLCSLTGHQEAQFMTTLKALQDTTVRELCSCTVHEMEAMKTICQSFREYLEEIEQHLMGQQALFSRDMSEEEREEAEQLQTLREALRQQVAELEFQLGDRAQQIREGILLQLEVLTAEPPEHYSNLHQYNWIEESNGQTSCSKIHPGMAPRTVFPPDDGQEAPCSGELLSAELDPFFFSSKANNSAKDEKIKSKDFLKTQDSGLL
"
     variation       140
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191095495"
     exon            150..335
                     /gene="CCDC129"
                     /inference="alignment:Splign:1.39.8"
     variation       161
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368232809"
     variation       211
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114739660"
     variation       233
                     /gene="CCDC129"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:368587451"
     variation       240
                     /gene="CCDC129"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:371959143"
     variation       253
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147399119"
     variation       260
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374470226"
     variation       267
                     /gene="CCDC129"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:7811042"
     variation       270
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143690079"
     variation       271
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372303441"
     variation       298
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371511395"
     variation       314
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112921112"
     variation       326
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376118062"
     exon            336..384
                     /gene="CCDC129"
                     /inference="alignment:Splign:1.39.8"
     variation       361
                     /gene="CCDC129"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200034335"
     exon            385..428
                     /gene="CCDC129"
                     /inference="alignment:Splign:1.39.8"
     variation       386
                     /gene="CCDC129"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372723381"
     variation       410
                     /gene="CCDC129"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:377546776"
     variation       421
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2286711"
     variation       422
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201211575"
     exon            429..480
                     /gene="CCDC129"
                     /inference="alignment:Splign:1.39.8"
     variation       438
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149696374"
     variation       463
                     /gene="CCDC129"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:145529826"
     variation       474
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374187154"
     exon            481..567
                     /gene="CCDC129"
                     /inference="alignment:Splign:1.39.8"
     variation       481..482
                     /gene="CCDC129"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:35551867"
     variation       523
                     /gene="CCDC129"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:67930674"
     variation       524
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369866067"
     variation       526
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146605019"
     variation       527
                     /gene="CCDC129"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:141438918"
     variation       528
                     /gene="CCDC129"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:202157240"
     variation       532
                     /gene="CCDC129"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374063664"
     variation       548
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201415095"
     exon            568..770
                     /gene="CCDC129"
                     /inference="alignment:Splign:1.39.8"
     variation       569
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370418381"
     variation       575
                     /gene="CCDC129"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372753433"
     variation       596
                     /gene="CCDC129"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:200366088"
     variation       623
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376020926"
     variation       674
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370670531"
     variation       713
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187352726"
     variation       740
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199790271"
     variation       756
                     /gene="CCDC129"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:371060962"
     variation       764
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191694538"
     variation       765
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375679267"
     variation       769
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143370840"
     exon            771..1342
                     /gene="CCDC129"
                     /inference="alignment:Splign:1.39.8"
     variation       774
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151254328"
     variation       800
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200848834"
     variation       830
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140428776"
     variation       863
                     /gene="CCDC129"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200031625"
     variation       891
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373956174"
     variation       908
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376757677"
     variation       921
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201901788"
     variation       933
                     /gene="CCDC129"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:184653370"
     variation       951
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373138016"
     variation       961
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200960115"
     variation       971
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201177934"
     variation       972
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370395768"
     variation       974
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372951947"
     variation       976
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111332081"
     variation       996
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186789215"
     variation       1027
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6945679"
     variation       1042
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368881766"
     variation       1043
                     /gene="CCDC129"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:111510506"
     variation       1053
                     /gene="CCDC129"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:371421598"
     variation       1101
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373943918"
     variation       1138
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200119465"
     variation       1175
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368169623"
     variation       1200
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372420153"
     variation       1236
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192536493"
     variation       1245
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375575625"
     variation       1247
                     /gene="CCDC129"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:369963496"
     variation       1264
                     /gene="CCDC129"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372373590"
     variation       1302
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10252720"
     variation       1324
                     /gene="CCDC129"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368760577"
     exon            1343..1400
                     /gene="CCDC129"
                     /inference="alignment:Splign:1.39.8"
     variation       1367
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188006642"
     variation       1398
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374799170"
     exon            1401..1483
                     /gene="CCDC129"
                     /inference="alignment:Splign:1.39.8"
     variation       1444
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370130726"
     variation       1454
                     /gene="CCDC129"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:367919427"
     variation       1462
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373855014"
     variation       1463
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368202210"
     exon            1484..2755
                     /gene="CCDC129"
                     /inference="alignment:Splign:1.39.8"
     variation       1511
                     /gene="CCDC129"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:372684457"
     variation       1512
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150398844"
     variation       1513
                     /gene="CCDC129"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:185577476"
     variation       1523
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369485544"
     variation       1524
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138418545"
     variation       1531
                     /gene="CCDC129"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:143912195"
     variation       1571
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201060776"
     variation       1588
                     /gene="CCDC129"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:146986060"
     variation       1596
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190307572"
     variation       1613
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376801262"
     variation       1614
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138066602"
     variation       1615
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143751428"
     variation       1623
                     /gene="CCDC129"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:115087893"
     variation       1641
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:4141001"
     variation       1647
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182124848"
     variation       1662
                     /gene="CCDC129"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:148685966"
     variation       1663
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141164020"
     variation       1682
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376345625"
     variation       1683
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200626153"
     variation       1704
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377326064"
     variation       1718
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150717357"
     variation       1743
                     /gene="CCDC129"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:139246994"
     variation       1758
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144022203"
     variation       1783
                     /gene="CCDC129"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:76357748"
     variation       1789
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:38396"
     variation       1817
                     /gene="CCDC129"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:73686905"
     variation       1841
                     /gene="CCDC129"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:77197319"
     variation       1863
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371473428"
     variation       1932
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375287000"
     variation       1953
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368084998"
     variation       1959
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116406137"
     variation       1961
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147656859"
     variation       2011
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143660819"
     variation       2024
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199508649"
     variation       2032
                     /gene="CCDC129"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201778549"
     variation       2035
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200300960"
     variation       2041
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:38397"
     variation       2074
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186727343"
     variation       2075
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375104335"
     variation       2086
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138128234"
     variation       2096
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148074341"
     variation       2115
                     /gene="CCDC129"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:150134204"
     variation       2191
                     /gene="CCDC129"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:200026024"
     variation       2224
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181108787"
     variation       2242
                     /gene="CCDC129"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:117782044"
     variation       2314
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377002952"
     variation       2326
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185363516"
     variation       2353
                     /gene="CCDC129"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372213107"
     variation       2362
                     /gene="CCDC129"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:375422464"
     variation       2428
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149320755"
     variation       2439
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141868591"
     variation       2456
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200809374"
     variation       2479
                     /gene="CCDC129"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:137859522"
     variation       2519
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146267805"
     variation       2535
                     /gene="CCDC129"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369385676"
     variation       2555
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189731201"
     variation       2561
                     /gene="CCDC129"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:202078186"
     variation       2570
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145959636"
     variation       2596
                     /gene="CCDC129"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:139858209"
     variation       2598
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10247620"
     variation       2620
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:76733226"
     variation       2621
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139431992"
     variation       2656
                     /gene="CCDC129"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:150049545"
     variation       2709
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147673017"
     variation       2749
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377331865"
     variation       2754
                     /gene="CCDC129"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:142323942"
     exon            2756..2883
                     /gene="CCDC129"
                     /inference="alignment:Splign:1.39.8"
     variation       2760
                     /gene="CCDC129"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201917207"
     variation       2787
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200617855"
     variation       2804
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142885665"
     variation       2805
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144601428"
     variation       2831
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:7799540"
     variation       2836
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148953571"
     variation       2864
                     /gene="CCDC129"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370201894"
     exon            2884..2995
                     /gene="CCDC129"
                     /inference="alignment:Splign:1.39.8"
     variation       2893
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374114030"
     variation       2895
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143151561"
     variation       2903
                     /gene="CCDC129"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201354762"
     variation       2912
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148236609"
     variation       2913
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:80081783"
     variation       2938
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141259951"
     exon            2996..3161
                     /gene="CCDC129"
                     /inference="alignment:Splign:1.39.8"
     variation       3006
                     /gene="CCDC129"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:186386347"
     variation       3045
                     /gene="CCDC129"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:137892596"
     variation       3108
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142389938"
     variation       3110
                     /gene="CCDC129"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:377589498"
     variation       3115
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145933301"
     variation       3133
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368179579"
     variation       3134
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111514975"
     variation       3148
                     /gene="CCDC129"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:371362733"
     exon            3162..3611
                     /gene="CCDC129"
                     /inference="alignment:Splign:1.39.8"
     variation       3190..3191
                     /gene="CCDC129"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:35589779"
     variation       3190
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201037213"
     variation       3200
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113645776"
     variation       3315
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:7791685"
     variation       3323
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192959503"
     variation       3335
                     /gene="CCDC129"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149244251"
     variation       3376
                     /gene="CCDC129"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185225383"
     variation       3398
                     /gene="CCDC129"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:188142862"
ORIGIN      
atagttctgcagtcacaagggctttgtagtcagtcttagctgctggaacattcaaggagacaaaaaggcacagaagatctccacacatactttgatgccaactacagcaagttgcaagaccatttctctgctgaaactcctttattctgttagtttgcagaattactctcctatgatggcacagaaatcacaaggatctgacaaccttcaggaaggccaggaaaagagcaagagagagatcctgaagtgcaccaaaagcgcgtgggctccgctggatgagtggctgccccctgaccctgaggaggaaagccagagtctcaccatccccatgctggaagattccaagcaagaaagtattcagcagtggctggactctggattctttgtctctgcaaatgaaaactttcaacaagtcattgaccgcactgtttctttgtatgaacaagggatggttcaaatgactgtgaaagactacatgagatctttgcatcagttttcagaaactcccatcctatccagagggaccagtttcaactcttgctattctactgcaagtgtaccacaaagcattcctgaatggctggaattttgggagatagatccagtggagattctcttggatctggggtttggtgctgatgagccagacatctgcatgcaaatcccagccagattccttggttgtggctcagcagccagaggaatcaacatccgtgtttttcttgaagctcaaaagcagcgaatggacattgagaaccccaacttgtacggtcgtttccgacagctggaaatcctggaccatgtgaccaatgccttctcatctctgctgagtgatgtcagcatcctgccaaacagagctgaagagaaagctggaggagagagtgtgcaaagaacctcagtgagtgccgccaaagagcatcgaagaagaatgggtaaactcttaaggagagcttccaaacagaacatcaggcgggattgtaacccagaggtatcagagtccttcaaggtgaaggatgaagtttttgttccctttacaaaaccatgggattgtggagcagagctagcagcaacctcaatcaaccacaagcaaaatcatttgtctctgtcagtagaacatcagtctctccaagcctgtgatgatttgctaccttatcctcctcatggtcttctgagcaagcagtggccttgctcatctatgccggccaagcaggctcctccttcctgtgtgtctgaggggtcagtcaagggcagaactcagaaggagaacttatttcagactaacaagctcaagagcttgtctcatcttgcaggcaaaggaccagactcatttgaaatggaagaggtccaaagctttgaagaagagactggtaatcctcttgacatgacttcaggaactgtaggtgccagggtggacagagcaaatagctgccagtctgacagcagcgggttcctggaggagccgctggaaccgctgcccctccagatgccttccttgccaaacagccagagtcctgctgagaatggaggtagaaagccaagagatcagagccacagcttagtatcatcccaggactgtcagctagagtcggatgggccagattccaaaagtagggcgagcatgtctttttcaagccaagaagcgaatgccttggaacaaagggcctcagtatctgtgatggaggaagagtttctgcttgaggccatggaggggccaccagagctgtatatcccagacatggcctgtgccaagaccaccacgaggggagaatgcccaaggaaagacagccatctgtggcagcttctgccaatgccccatgctgagtatgaggtcaccagacccacagccacttccaaatatgatcatcctctggggtttatggtaacccacgtcacagaaatgcaggacagttttgtgaggcctgagggagctggcaaagtgcaaagccaccacaatgagtctcaaaggtcacctggaaatgatcatactcaagacaagttccttcatgttgactctgaggccccacgagaagaggaaagcagtggattctgtcctcacaccaaccacagcttactcgtaccagaaagctcatcacagtgtatccccaagcacagtgaaatcacaccttatgcaactgaccttgctcaaacatctgaaaagctcattccccacctccataaactgcctggagatcctgcccaggtgaagtcaaggtctggtactttgggtcagatactacctgggacagaagctgagatggaaaaccttcctctaaatactggcagctccaggtctgtaatgacccagatgtcctccagcctggtgtcggctgctcagagggctgtggccttggggactggtcccagaggaacatctttagaatgcactgtgtgtgatcctgttaccgcaacagaaacaagactggggacaaaagcaagacagttaaatgatgcttccattcagacttcagctctaagcaacaagaccttgacacatgggccccagcccctcaccaaatccgtctctctagactcaggcttctctagtatctgcccaatgggcacctgccatgctatacctgcccactgctgcatctgctgtcatcaccaccctcactgccacggggagaggcaaagccctggccctgaaccctcagtctgtaggcactgcctgtgttcactaactggtcaccaggaagcccagttcatgacgactttgaaagcccttcaggacactacagtgagggagctatgttcctgcacagtccatgagatggaagccatgaagacgatatgccaaagtttccgggagtatttagaagaaattgaacagcaccttatgggacagcaggccctcttttccagggacatgtcagaggaggaaagggaggaggccgagcaactgcaaacgttacgtgaggccctgaggcagcaggtggcagagttggaatttcagttaggagaccgggctcagcaaatcagagaagggattttactgcagctggaggttctcacagcagagccacctgaacactattcaaatctgcatcaatataactggatagaagaaagcaatgggcagacttcatgttctaaaatccacccaggcatggccccgaggactgtgtttcctcccgatgatggccaggaggctccctgttcaggtgaattattgtctgcagagctggatcccttttttttttcttcaaaagcaaataactctgctaaagatgaaaaaataaaatcaaaagactttctgaagacacaagactctggtctgttgtaattgtttttctttgttgagaaaataatcagtttccagagtataacacatgtcgaacaaaatagaacatttgtaaagaggttagagtatcaaagtggtgcccctttgagaagaaaaagttttagagtgttttcatgtggaatggtgggttgcatacgtaatttcaaattgtaatttaaaacaacaaattgttcatgatgtgcgagaattgtaggttattaaaagccttgttaaattgtttttcttgaaaattgagagaacaggaacagaagccaaaatatggacggcacctttctctagcccaaactcagcctctaattgcctgatctta
//

Annotations:



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