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2025-05-09 19:06:13, 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
//
by
@meso_cacase at
DBCLS
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