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2024-04-24 15:05:03, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001257967 4142 bp mRNA linear PRI 18-APR-2013
DEFINITION Homo sapiens coiled-coil domain containing 129 (CCDC129),
transcript variant 1, mRNA.
ACCESSION NM_001257967
VERSION NM_001257967.1 GI:384081584
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 4142)
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 4142)
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
AK304387.1, AC006044.2, BC132719.1 and AK128026.1.
Transcript Variant: This variant (1) encodes the longest isoform
(1).
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 :: AK304387.1 [ECO:0000332]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-241 AK304387.1 1-241
242-242 AC006044.2 27302-27302
243-1001 BC132719.1 134-892
1002-1277 AC006044.2 52302-52577
1278-1615 AK304387.1 1278-1615
1616-1616 AC006044.2 117022-117022
1617-2572 BC132719.1 1508-2463
2573-2573 AC006044.2 117979-117979
2574-3310 AK304387.1 2574-3310
3311-3808 AK128026.1 3713-4210
3809-3809 AC006044.2 127539-127539
3810-4142 AK128026.1 4212-4544
FEATURES Location/Qualifiers
source 1..4142
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="7"
/map="7p14.3"
gene 1..4142
/gene="CCDC129"
/note="coiled-coil domain containing 129"
/db_xref="GeneID:223075"
/db_xref="HGNC:27363"
exon 1..50
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
exon 51..124
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
misc_feature 55..57
/gene="CCDC129"
/note="upstream in-frame stop codon"
variation 88
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:117297547"
CDS 118..3282
/gene="CCDC129"
/note="isoform 1 is encoded by transcript variant 1;
coiled-coil domain-containing protein 129"
/codon_start=1
/product="coiled-coil domain-containing protein 129
isoform 1"
/protein_id="NP_001244896.1"
/db_xref="GI:384081585"
/db_xref="GeneID:223075"
/db_xref="HGNC:27363"
/translation="
MSVSLQNYSPMMAQKSQGSDNLQEGQEKSKREILKCTKSAWAPLDEWLPPDPEEESQSLTIPMLEDSKQESIQQWLDSGFFVSANENFQQVIDRTVSLYEQGMVQMTVKDYMRSLHQFSETPILSRGTSFNSCYSTASVPQSIPEWLEFWEIDPVEILLDLGFGADEPDICMQIPARFLGCGSAARGINIRVFLEAQKQRMDIENPNLYGRFRQLEILDHVTNAFSSLLSDVSILPNRAEEKAGGESVQRTSVSAAKEHRRRMGKLLRRASKQNIRRDCNPEVSESFKVKDEVFVPFTKPWDCGAELAATSINHKQNHLSLSVEHQSLQACDDLLPYPPHGLLSKQWPCSSMPAKQAPPSCVSEGSVKGRTQKENLFQTNKLKSLSHLAGKGPDSFEMEEVQSFEEETGNPLDMTSGTVGARVDRANSCQSDSSGFLEEPLEPLPLQMPSLPNSQSPAENGGRKPRDQSHSLVSSQDCQLESDGPDSKSRASMSFSSQEANALEQRASVSVMEEEFLLEAMEGPPELYIPDMACAKTTTRGECPRKDSHLWQLLPMPHAEYEVTRPTATSKYDHPLGFMVTHVTEMQDSFVRPEGAGKVQSHHNESQRSPGNDHTQDKFLHVDSEAPREEESSGFCPHTNHSLLVPESSSQCIPKHSEITPYATDLAQTSEKLIPHLHKLPGDPAQVKSRSGTLGQILPGTEAEMENLPLNTGSSRSVMTQMSSSLVSAAQRAVALGTGPRGTSLECTVCDPVTATETRLGTKARQLNDASIQTSALSNKTLTHGPQPLTKSVSLDSGFSSICPMGTCHAIPAHCCICCHHHPHCHGERQSPGPEPSVCRHCLCSLTGHQEAQFMTTLKALQDTTVRELCSCTVHEMEAMKTICQSFREYLEEIEQHLMGQQALFSRDMSEEEREEAEQLQTLREALRQQVAELEFQLGDRAQQIREGILLQLEVLTAEPPEHYSNLHQYNWIEESNGQTSCSKIHPGMAPRTVFPPDDGQEAPCSGGTQLAAFTPPTLENSTRMSPSSSAWAKLGPTPLSNCPVGEKDADVFL
"
exon 125..310
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 136
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:368232809"
variation 186
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:114739660"
variation 208
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:368587451"
variation 215
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:371959143"
variation 228
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:147399119"
variation 235
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:374470226"
variation 242
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:7811042"
variation 245
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:143690079"
variation 246
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:372303441"
variation 273
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:371511395"
variation 289
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:112921112"
variation 301
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:376118062"
exon 311..359
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 336
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:200034335"
exon 360..403
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 361
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:372723381"
variation 385
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:377546776"
variation 396
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:2286711"
variation 397
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:201211575"
exon 404..455
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 413
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:149696374"
variation 438
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:145529826"
variation 449
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:374187154"
exon 456..542
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 456..457
/gene="CCDC129"
/replace=""
/replace="a"
/db_xref="dbSNP:35551867"
variation 498
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:67930674"
variation 499
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:369866067"
variation 501
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:146605019"
variation 502
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:141438918"
variation 503
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:202157240"
variation 507
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:374063664"
variation 523
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:201415095"
exon 543..745
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 544
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:370418381"
variation 550
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:372753433"
variation 571
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:200366088"
variation 598
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:376020926"
variation 649
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:370670531"
variation 688
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:187352726"
variation 715
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:199790271"
variation 731
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:371060962"
variation 739
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:191694538"
variation 740
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:375679267"
variation 744
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:143370840"
exon 746..1317
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 749
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:151254328"
variation 775
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:200848834"
variation 805
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:140428776"
variation 838
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:200031625"
variation 866
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:373956174"
variation 883
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:376757677"
variation 896
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:201901788"
variation 908
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:184653370"
variation 926
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:373138016"
variation 936
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:200960115"
variation 946
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:201177934"
variation 947
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:370395768"
variation 949
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:372951947"
variation 951
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:111332081"
variation 971
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:186789215"
variation 1002
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:6945679"
variation 1017
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:368881766"
variation 1018
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:111510506"
variation 1028
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:371421598"
variation 1076
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:373943918"
variation 1113
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:200119465"
variation 1150
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:368169623"
variation 1175
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:372420153"
variation 1211
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:192536493"
variation 1220
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:375575625"
variation 1222
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:369963496"
variation 1239
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:372373590"
variation 1277
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:10252720"
variation 1299
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:368760577"
exon 1318..1375
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 1342
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:188006642"
variation 1373
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:374799170"
exon 1376..1458
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 1419
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:370130726"
variation 1429
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:367919427"
variation 1437
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:373855014"
variation 1438
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:368202210"
exon 1459..2730
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 1486
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:372684457"
variation 1487
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:150398844"
variation 1488
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:185577476"
variation 1498
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:369485544"
variation 1499
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:138418545"
variation 1506
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:143912195"
variation 1546
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:201060776"
variation 1563
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:146986060"
variation 1571
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:190307572"
variation 1588
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:376801262"
variation 1589
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:138066602"
variation 1590
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:143751428"
variation 1598
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:115087893"
variation 1616
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:4141001"
variation 1622
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:182124848"
variation 1637
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:148685966"
variation 1638
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:141164020"
variation 1657
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:376345625"
variation 1658
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:200626153"
variation 1679
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:377326064"
variation 1693
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:150717357"
variation 1718
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:139246994"
variation 1733
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:144022203"
variation 1758
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:76357748"
variation 1764
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:38396"
variation 1792
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:73686905"
variation 1816
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:77197319"
variation 1838
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:371473428"
variation 1907
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:375287000"
variation 1928
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:368084998"
variation 1934
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:116406137"
variation 1936
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:147656859"
variation 1986
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:143660819"
variation 1999
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:199508649"
variation 2007
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:201778549"
variation 2010
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:200300960"
variation 2016
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:38397"
variation 2049
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:186727343"
variation 2050
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:375104335"
variation 2061
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:138128234"
variation 2071
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:148074341"
variation 2090
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:150134204"
variation 2166
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:200026024"
variation 2199
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:181108787"
variation 2217
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:117782044"
variation 2289
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:377002952"
variation 2301
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:185363516"
variation 2328
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:372213107"
variation 2337
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:375422464"
variation 2403
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:149320755"
variation 2414
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:141868591"
variation 2431
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:200809374"
variation 2454
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:137859522"
variation 2494
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:146267805"
variation 2510
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:369385676"
variation 2530
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:189731201"
variation 2536
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:202078186"
variation 2545
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:145959636"
variation 2571
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:139858209"
variation 2573
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:10247620"
variation 2595
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:76733226"
variation 2596
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:139431992"
variation 2631
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:150049545"
variation 2684
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:147673017"
variation 2724
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:377331865"
variation 2729
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:142323942"
exon 2731..2858
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 2735
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:201917207"
variation 2762
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:200617855"
variation 2779
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:142885665"
variation 2780
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:144601428"
variation 2806
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:7799540"
variation 2811
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:148953571"
variation 2839
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:370201894"
exon 2859..2970
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 2868
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:374114030"
variation 2870
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:143151561"
variation 2878
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:201354762"
variation 2887
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:148236609"
variation 2888
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:80081783"
variation 2913
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:141259951"
exon 2971..4142
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 2981
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:186386347"
variation 3020
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:137892596"
variation 3083
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:142389938"
variation 3085
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:377589498"
variation 3090
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:145933301"
variation 3108
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:368179579"
variation 3109
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:111514975"
variation 3123
/gene="CCDC129"
/replace=""
/replace="g"
/db_xref="dbSNP:371362733"
variation 3143
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:149268880"
variation 3147
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:371944763"
variation 3148
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:115873834"
variation 3166
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:201005039"
variation 3171
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:200065011"
variation 3182
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:77915580"
variation 3185
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:374464304"
variation 3196
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:148552563"
variation 3221
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:183033798"
variation 3230
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:142016406"
variation 3248
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:34177136"
variation 3254
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:201675506"
variation 3262
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:140998733"
variation 3291
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:368704382"
variation 3293
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:201768075"
variation 3320
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:371845154"
variation 3322
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:371968855"
variation 3324
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:138001179"
variation 3333
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:369807067"
variation 3335
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:143478742"
variation 3399
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:187942842"
variation 3435
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:374773487"
variation 3504
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:60432519"
variation 3518
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:147140713"
variation 3532
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:140268517"
variation 3608
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:371842462"
variation 3730
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:77503219"
variation 3809
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:2159513"
variation 3819
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:376168188"
variation 3905
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:182206184"
variation 3948
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:202091748"
ORIGIN
gtttccttcaggaactttcagatggctcaggagtggagcttttgtggcagttcctgacaggataaggacaagaagcaacacacagaagagaaggaaaaagaaagaaaactgaccaatatgagtgttagtttgcagaattactctcctatgatggcacagaaatcacaaggatctgacaaccttcaggaaggccaggaaaagagcaagagagagatcctgaagtgcaccaaaagcgcgtgggctccgctggatgagtggctgccccctgaccctgaggaggaaagccagagtctcaccatccccatgctggaagattccaagcaagaaagtattcagcagtggctggactctggattctttgtctctgcaaatgaaaactttcaacaagtcattgaccgcactgtttctttgtatgaacaagggatggttcaaatgactgtgaaagactacatgagatctttgcatcagttttcagaaactcccatcctatccagagggaccagtttcaactcttgctattctactgcaagtgtaccacaaagcattcctgaatggctggaattttgggagatagatccagtggagattctcttggatctggggtttggtgctgatgagccagacatctgcatgcaaatcccagccagattccttggttgtggctcagcagccagaggaatcaacatccgtgtttttcttgaagctcaaaagcagcgaatggacattgagaaccccaacttgtacggtcgtttccgacagctggaaatcctggaccatgtgaccaatgccttctcatctctgctgagtgatgtcagcatcctgccaaacagagctgaagagaaagctggaggagagagtgtgcaaagaacctcagtgagtgccgccaaagagcatcgaagaagaatgggtaaactcttaaggagagcttccaaacagaacatcaggcgggattgtaacccagaggtatcagagtccttcaaggtgaaggatgaagtttttgttccctttacaaaaccatgggattgtggagcagagctagcagcaacctcaatcaaccacaagcaaaatcatttgtctctgtcagtagaacatcagtctctccaagcctgtgatgatttgctaccttatcctcctcatggtcttctgagcaagcagtggccttgctcatctatgccggccaagcaggctcctccttcctgtgtgtctgaggggtcagtcaagggcagaactcagaaggagaacttatttcagactaacaagctcaagagcttgtctcatcttgcaggcaaaggaccagactcatttgaaatggaagaggtccaaagctttgaagaagagactggtaatcctcttgacatgacttcaggaactgtaggtgccagggtggacagagcaaatagctgccagtctgacagcagcgggttcctggaggagccgctggaaccgctgcccctccagatgccttccttgccaaacagccagagtcctgctgagaatggaggtagaaagccaagagatcagagccacagcttagtatcatcccaggactgtcagctagagtcggatgggccagattccaaaagtagggcgagcatgtctttttcaagccaagaagcgaatgccttggaacaaagggcctcagtatctgtgatggaggaagagtttctgcttgaggccatggaggggccaccagagctgtatatcccagacatggcctgtgccaagaccaccacgaggggagaatgcccaaggaaagacagccatctgtggcagcttctgccaatgccccatgctgagtatgaggtcaccagacccacagccacttccaaatatgatcatcctctggggtttatggtaacccacgtcacagaaatgcaggacagttttgtgaggcctgagggagctggcaaagtgcaaagccaccacaatgagtctcaaaggtcacctggaaatgatcatactcaagacaagttccttcatgttgactctgaggccccacgagaagaggaaagcagtggattctgtcctcacaccaaccacagcttactcgtaccagaaagctcatcacagtgtatccccaagcacagtgaaatcacaccttatgcaactgaccttgctcaaacatctgaaaagctcattccccacctccataaactgcctggagatcctgcccaggtgaagtcaaggtctggtactttgggtcagatactacctgggacagaagctgagatggaaaaccttcctctaaatactggcagctccaggtctgtaatgacccagatgtcctccagcctggtgtcggctgctcagagggctgtggccttggggactggtcccagaggaacatctttagaatgcactgtgtgtgatcctgttaccgcaacagaaacaagactggggacaaaagcaagacagttaaatgatgcttccattcagacttcagctctaagcaacaagaccttgacacatgggccccagcccctcaccaaatccgtctctctagactcaggcttctctagtatctgcccaatgggcacctgccatgctatacctgcccactgctgcatctgctgtcatcaccaccctcactgccacggggagaggcaaagccctggccctgaaccctcagtctgtaggcactgcctgtgttcactaactggtcaccaggaagcccagttcatgacgactttgaaagcccttcaggacactacagtgagggagctatgttcctgcacagtccatgagatggaagccatgaagacgatatgccaaagtttccgggagtatttagaagaaattgaacagcaccttatgggacagcaggccctcttttccagggacatgtcagaggaggaaagggaggaggccgagcaactgcaaacgttacgtgaggccctgaggcagcaggtggcagagttggaatttcagttaggagaccgggctcagcaaatcagagaagggattttactgcagctggaggttctcacagcagagccacctgaacactattcaaatctgcatcaatataactggatagaagaaagcaatgggcagacttcatgttctaaaatccacccaggcatggccccgaggactgtgtttcctcccgatgatggccaggaggctccctgttcaggtgggacccagttggctgccttcactccacccaccttggagaacagcaccaggatgtctccttcatcatcagcttgggcaaagttaggtccaacccctttgtcaaattgtcctgttggagaaaaggatgcagatgtcttcctctagatcagagcaggtttgttaaccttcatacaaaatataaaggcccagaacagatgtagcaaggaaatttcaattttccccaaggagaagggtctgccaacccattgtcagctatatctctcatattctaccctttggttaaacccaagaggagtttagaatactctaatactcattcagtatagaataactgagcacctagtatgtgcctggcacagagtatgcaacagtgactaaatagtatacggtctctgccctgctagaacttacagtgtagtgggggagatagaattgcaaacaaaaagtatctgagacagacctcagtcaatatagaagtttattttgccaaggttaaggatacacacccagaagacaggtctgtgcctttctccaaagatgattttgaggccttcaacatttagtggggaaagggtgctaatggggaaagaggtgtgggtacataggaggcaaacagttgcatttttttgagtctgatcagcttttctcatgagagaaggggtagaggaactgtcacttatgcattcacctagctcagtggatctgcacttttacagaaggtaaaataaacatagggcagaggaagcaatcagatatgcatttgtctcgggggagcagagggatggctttgagttctgttctttgtcctgtacctattaagagaagctatcaatatactttgtcaggataaaattcaacagaactgttttagactaaagattttagggaccacaaggaatttcccagtgggcaaattgtgagggaggtatttagcttttaaaaaaatctttgtagctatctcatttagaaataaaatgggaggcagattgcctgatgcagctcct
//
by
@meso_cacase at
DBCLS
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