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2025-05-09 19:01:06, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_194300 4030 bp mRNA linear PRI 18-APR-2013
DEFINITION Homo sapiens coiled-coil domain containing 129 (CCDC129),
transcript variant 2, mRNA.
ACCESSION NM_194300 XM_167336 XM_353571
VERSION NM_194300.3 GI:384875917
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 4030)
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 4030)
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
AC006044.2, BC132719.1 and AK128026.1.
On Apr 20, 2012 this sequence version replaced gi:154937345.
Transcript Variant: This variant (2) differs in the 5' UTR and
coding region, compared to variant 1. These differences cause
translation initiation at a downstream AUG and result in an isoform
(2) with a shorter N-terminus, compared to 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##
CDS exon combination :: BC132719.1 [ECO:0000331]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-12 AC006044.2 19179-19190
13-14 AC006044.2 27185-27186
15-129 BC132719.1 18-132
130-130 AC006044.2 27302-27302
131-889 BC132719.1 134-892
890-890 AC006044.2 52302-52302
891-1164 BC132719.1 894-1167
1165-1165 AC006044.2 52577-52577
1166-1503 BC132719.1 1169-1506
1504-1504 AC006044.2 117022-117022
1505-2460 BC132719.1 1508-2463
2461-2461 AC006044.2 117979-117979
2462-3266 BC132719.1 2465-3269
3267-3696 AK128026.1 3781-4210
3697-3697 AC006044.2 127539-127539
3698-4030 AK128026.1 4212-4544
FEATURES Location/Qualifiers
source 1..4030
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="7"
/map="7p14.3"
gene 1..4030
/gene="CCDC129"
/note="coiled-coil domain containing 129"
/db_xref="GeneID:223075"
/db_xref="HGNC:27363"
exon 1..12
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 2
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:141862699"
exon 13..198
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 24
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:368232809"
CDS 36..3170
/gene="CCDC129"
/note="isoform 2 is encoded by transcript variant 2;
coiled-coil domain-containing protein 129"
/codon_start=1
/product="coiled-coil domain-containing protein 129
isoform 2"
/protein_id="NP_919276.2"
/db_xref="GI:154937346"
/db_xref="CCDS:CCDS5435.2"
/db_xref="GeneID:223075"
/db_xref="HGNC:27363"
/translation="
MMAQKSQGSDNLQEGQEKSKREILKCTKSAWAPLDEWLPPDPEEESQSLTIPMLEDSKQESIQQWLDSGFFVSANENFQQVIDRTVSLYEQGMVQMTVKDYMRSLHQFSETPILSRGTSFNSCYSTASVPQSIPEWLEFWEIDPVEILLDLGFGADEPDICMQIPARFLGCGSAARGINIRVFLEAQKQRMDIENPNLYGRFRQLEILDHVTNAFSSLLSDVSILPNRAEEKAGGESVQRTSVSAAKEHRRRMGKLLRRASKQNIRRDCNPEVSESFKVKDEVFVPFTKPWDCGAELAATSINHKQNHLSLSVEHQSLQACDDLLPYPPHGLLSKQWPCSSMPAKQAPPSCVSEGSVKGRTQKENLFQTNKLKSLSHLAGKGPDSFEMEEVQSFEEETGNPLDMTSGTVGARVDRANSCQSDSSGFLEEPLEPLPLQMPSLPNSQSPAENGGRKPRDQSHSLVSSQDCQLESDGPDSKSRASMSFSSQEANALEQRASVSVMEEEFLLEAMEGPPELYIPDMACAKTTTRGECPRKDSHLWQLLPMPHAEYEVTRPTATSKYDHPLGFMVTHVTEMQDSFVRPEGAGKVQSHHNESQRSPGNDHTQDKFLHVDSEAPREEESSGFCPHTNHSLLVPESSSQCIPKHSEITPYATDLAQTSEKLIPHLHKLPGDPAQVKSRSGTLGQILPGTEAEMENLPLNTGSSRSVMTQMSSSLVSAAQRAVALGTGPRGTSLECTVCDPVTATETRLGTKARQLNDASIQTSALSNKTLTHGPQPLTKSVSLDSGFSSICPMGTCHAIPAHCCICCHHHPHCHGERQSPGPEPSVCRHCLCSLTGHQEAQFMTTLKALQDTTVRELCSCTVHEMEAMKTICQSFREYLEEIEQHLMGQQALFSRDMSEEEREEAEQLQTLREALRQQVAELEFQLGDRAQQIREGILLQLEVLTAEPPEHYSNLHQYNWIEESNGQTSCSKIHPGMAPRTVFPPDDGQEAPCSGGTQLAAFTPPTLENSTRMSPSSSAWAKLGPTPLSNCPVGEKDADVFL
"
variation 74
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:114739660"
variation 96
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:368587451"
variation 103
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:371959143"
variation 116
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:147399119"
variation 123
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:374470226"
variation 130
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:7811042"
variation 133
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:143690079"
variation 134
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:372303441"
variation 161
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:371511395"
variation 177
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:112921112"
variation 189
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:376118062"
exon 199..247
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 224
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:200034335"
exon 248..291
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 249
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:372723381"
variation 273
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:377546776"
variation 284
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:2286711"
variation 285
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:201211575"
exon 292..343
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 301
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:149696374"
variation 326
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:145529826"
variation 337
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:374187154"
exon 344..430
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 344..345
/gene="CCDC129"
/replace=""
/replace="a"
/db_xref="dbSNP:35551867"
variation 386
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:67930674"
variation 387
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:369866067"
variation 389
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:146605019"
variation 390
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:141438918"
variation 391
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:202157240"
variation 395
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:374063664"
variation 411
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:201415095"
exon 431..633
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 432
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:370418381"
variation 438
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:372753433"
variation 459
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:200366088"
variation 486
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:376020926"
variation 537
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:370670531"
variation 576
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:187352726"
variation 603
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:199790271"
variation 619
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:371060962"
variation 627
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:191694538"
variation 628
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:375679267"
variation 632
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:143370840"
exon 634..1205
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 637
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:151254328"
variation 663
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:200848834"
variation 693
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:140428776"
variation 726
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:200031625"
variation 754
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:373956174"
variation 771
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:376757677"
variation 784
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:201901788"
variation 796
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:184653370"
variation 814
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:373138016"
variation 824
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:200960115"
variation 834
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:201177934"
variation 835
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:370395768"
variation 837
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:372951947"
variation 839
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:111332081"
variation 859
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:186789215"
variation 890
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:6945679"
variation 905
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:368881766"
variation 906
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:111510506"
variation 916
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:371421598"
variation 964
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:373943918"
variation 1001
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:200119465"
variation 1038
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:368169623"
variation 1063
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:372420153"
variation 1099
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:192536493"
variation 1108
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:375575625"
variation 1110
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:369963496"
variation 1127
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:372373590"
variation 1165
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:10252720"
variation 1187
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:368760577"
exon 1206..1263
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 1230
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:188006642"
variation 1261
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:374799170"
exon 1264..1346
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 1307
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:370130726"
variation 1317
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:367919427"
variation 1325
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:373855014"
variation 1326
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:368202210"
exon 1347..2618
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 1374
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:372684457"
variation 1375
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:150398844"
variation 1376
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:185577476"
variation 1386
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:369485544"
variation 1387
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:138418545"
variation 1394
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:143912195"
variation 1434
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:201060776"
variation 1451
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:146986060"
variation 1459
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:190307572"
variation 1476
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:376801262"
variation 1477
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:138066602"
variation 1478
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:143751428"
variation 1486
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:115087893"
variation 1504
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:4141001"
variation 1510
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:182124848"
variation 1525
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:148685966"
variation 1526
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:141164020"
variation 1545
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:376345625"
variation 1546
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:200626153"
variation 1567
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:377326064"
variation 1581
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:150717357"
variation 1606
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:139246994"
variation 1621
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:144022203"
variation 1646
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:76357748"
variation 1652
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:38396"
variation 1680
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:73686905"
variation 1704
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:77197319"
variation 1726
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:371473428"
variation 1795
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:375287000"
variation 1816
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:368084998"
variation 1822
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:116406137"
variation 1824
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:147656859"
variation 1874
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:143660819"
variation 1887
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:199508649"
variation 1895
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:201778549"
variation 1898
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:200300960"
variation 1904
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:38397"
variation 1937
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:186727343"
variation 1938
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:375104335"
variation 1949
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:138128234"
variation 1959
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:148074341"
variation 1978
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:150134204"
variation 2054
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:200026024"
variation 2087
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:181108787"
variation 2105
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:117782044"
variation 2177
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:377002952"
variation 2189
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:185363516"
variation 2216
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:372213107"
variation 2225
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:375422464"
variation 2291
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:149320755"
variation 2302
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:141868591"
variation 2319
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:200809374"
variation 2342
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:137859522"
variation 2382
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:146267805"
variation 2398
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:369385676"
variation 2418
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:189731201"
variation 2424
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:202078186"
variation 2433
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:145959636"
variation 2459
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:139858209"
variation 2461
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:10247620"
variation 2483
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:76733226"
variation 2484
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:139431992"
variation 2519
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:150049545"
variation 2572
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:147673017"
variation 2612
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:377331865"
variation 2617
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:142323942"
exon 2619..2746
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 2623
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:201917207"
variation 2650
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:200617855"
variation 2667
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:142885665"
variation 2668
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:144601428"
variation 2694
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:7799540"
variation 2699
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:148953571"
variation 2727
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:370201894"
exon 2747..2858
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 2756
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:374114030"
variation 2758
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:143151561"
variation 2766
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:201354762"
variation 2775
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:148236609"
variation 2776
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:80081783"
variation 2801
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:141259951"
exon 2859..4030
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 2869
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:186386347"
variation 2908
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:137892596"
variation 2971
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:142389938"
variation 2973
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:377589498"
variation 2978
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:145933301"
variation 2996
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:368179579"
variation 2997
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:111514975"
variation 3011
/gene="CCDC129"
/replace=""
/replace="g"
/db_xref="dbSNP:371362733"
variation 3031
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:149268880"
variation 3035
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:371944763"
variation 3036
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:115873834"
variation 3054
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:201005039"
variation 3059
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:200065011"
variation 3070
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:77915580"
variation 3073
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:374464304"
variation 3084
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:148552563"
variation 3109
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:183033798"
variation 3118
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:142016406"
variation 3136
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:34177136"
variation 3142
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:201675506"
variation 3150
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:140998733"
variation 3179
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:368704382"
variation 3181
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:201768075"
variation 3208
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:371845154"
variation 3210
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:371968855"
variation 3212
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:138001179"
variation 3221
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:369807067"
variation 3223
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:143478742"
variation 3287
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:187942842"
variation 3323
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:374773487"
variation 3392
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:60432519"
variation 3406
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:147140713"
variation 3420
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:140268517"
variation 3496
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:371842462"
variation 3618
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:77503219"
variation 3697
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:2159513"
variation 3707
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:376168188"
variation 3793
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:182206184"
variation 3836
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:202091748"
ORIGIN
tgccttccaggattagtttgcagaattactctcctatgatggcacagaaatcacaaggatctgacaaccttcaggaaggccaggaaaagagcaagagagagatcctgaagtgcaccaaaagcgcgtgggctccgctggatgagtggctgccccctgaccctgaggaggaaagccagagtctcaccatccccatgctggaagattccaagcaagaaagtattcagcagtggctggactctggattctttgtctctgcaaatgaaaactttcaacaagtcattgaccgcactgtttctttgtatgaacaagggatggttcaaatgactgtgaaagactacatgagatctttgcatcagttttcagaaactcccatcctatccagagggaccagtttcaactcttgctattctactgcaagtgtaccacaaagcattcctgaatggctggaattttgggagatagatccagtggagattctcttggatctggggtttggtgctgatgagccagacatctgcatgcaaatcccagccagattccttggttgtggctcagcagccagaggaatcaacatccgtgtttttcttgaagctcaaaagcagcgaatggacattgagaaccccaacttgtacggtcgtttccgacagctggaaatcctggaccatgtgaccaatgccttctcatctctgctgagtgatgtcagcatcctgccaaacagagctgaagagaaagctggaggagagagtgtgcaaagaacctcagtgagtgccgccaaagagcatcgaagaagaatgggtaaactcttaaggagagcttccaaacagaacatcaggcgggattgtaacccagaggtatcagagtccttcaaggtgaaggatgaagtttttgttccctttacaaaaccatgggattgtggagcagagctagcagcaacctcaatcaaccacaagcaaaatcatttgtctctgtcagtagaacatcagtctctccaagcctgtgatgatttgctaccttatcctcctcatggtcttctgagcaagcagtggccttgctcatctatgccggccaagcaggctcctccttcctgtgtgtctgaggggtcagtcaagggcagaactcagaaggagaacttatttcagactaacaagctcaagagcttgtctcatcttgcaggcaaaggaccagactcatttgaaatggaagaggtccaaagctttgaagaagagactggtaatcctcttgacatgacttcaggaactgtaggtgccagggtggacagagcaaatagctgccagtctgacagcagcgggttcctggaggagccgctggaaccgctgcccctccagatgccttccttgccaaacagccagagtcctgctgagaatggaggtagaaagccaagagatcagagccacagcttagtatcatcccaggactgtcagctagagtcggatgggccagattccaaaagtagggcgagcatgtctttttcaagccaagaagcgaatgccttggaacaaagggcctcagtatctgtgatggaggaagagtttctgcttgaggccatggaggggccaccagagctgtatatcccagacatggcctgtgccaagaccaccacgaggggagaatgcccaaggaaagacagccatctgtggcagcttctgccaatgccccatgctgagtatgaggtcaccagacccacagccacttccaaatatgatcatcctctggggtttatggtaacccacgtcacagaaatgcaggacagttttgtgaggcctgagggagctggcaaagtgcaaagccaccacaatgagtctcaaaggtcacctggaaatgatcatactcaagacaagttccttcatgttgactctgaggccccacgagaagaggaaagcagtggattctgtcctcacaccaaccacagcttactcgtaccagaaagctcatcacagtgtatccccaagcacagtgaaatcacaccttatgcaactgaccttgctcaaacatctgaaaagctcattccccacctccataaactgcctggagatcctgcccaggtgaagtcaaggtctggtactttgggtcagatactacctgggacagaagctgagatggaaaaccttcctctaaatactggcagctccaggtctgtaatgacccagatgtcctccagcctggtgtcggctgctcagagggctgtggccttggggactggtcccagaggaacatctttagaatgcactgtgtgtgatcctgttaccgcaacagaaacaagactggggacaaaagcaagacagttaaatgatgcttccattcagacttcagctctaagcaacaagaccttgacacatgggccccagcccctcaccaaatccgtctctctagactcaggcttctctagtatctgcccaatgggcacctgccatgctatacctgcccactgctgcatctgctgtcatcaccaccctcactgccacggggagaggcaaagccctggccctgaaccctcagtctgtaggcactgcctgtgttcactaactggtcaccaggaagcccagttcatgacgactttgaaagcccttcaggacactacagtgagggagctatgttcctgcacagtccatgagatggaagccatgaagacgatatgccaaagtttccgggagtatttagaagaaattgaacagcaccttatgggacagcaggccctcttttccagggacatgtcagaggaggaaagggaggaggccgagcaactgcaaacgttacgtgaggccctgaggcagcaggtggcagagttggaatttcagttaggagaccgggctcagcaaatcagagaagggattttactgcagctggaggttctcacagcagagccacctgaacactattcaaatctgcatcaatataactggatagaagaaagcaatgggcagacttcatgttctaaaatccacccaggcatggccccgaggactgtgtttcctcccgatgatggccaggaggctccctgttcaggtgggacccagttggctgccttcactccacccaccttggagaacagcaccaggatgtctccttcatcatcagcttgggcaaagttaggtccaacccctttgtcaaattgtcctgttggagaaaaggatgcagatgtcttcctctagatcagagcaggtttgttaaccttcatacaaaatataaaggcccagaacagatgtagcaaggaaatttcaattttccccaaggagaagggtctgccaacccattgtcagctatatctctcatattctaccctttggttaaacccaagaggagtttagaatactctaatactcattcagtatagaataactgagcacctagtatgtgcctggcacagagtatgcaacagtgactaaatagtatacggtctctgccctgctagaacttacagtgtagtgggggagatagaattgcaaacaaaaagtatctgagacagacctcagtcaatatagaagtttattttgccaaggttaaggatacacacccagaagacaggtctgtgcctttctccaaagatgattttgaggccttcaacatttagtggggaaagggtgctaatggggaaagaggtgtgggtacataggaggcaaacagttgcatttttttgagtctgatcagcttttctcatgagagaaggggtagaggaactgtcacttatgcattcacctagctcagtggatctgcacttttacagaaggtaaaataaacatagggcagaggaagcaatcagatatgcatttgtctcgggggagcagagggatggctttgagttctgttctttgtcctgtacctattaagagaagctatcaatatactttgtcaggataaaattcaacagaactgttttagactaaagattttagggaccacaaggaatttcccagtgggcaaattgtgagggaggtatttagcttttaaaaaaatctttgtagctatctcatttagaaataaaatgggaggcagattgcctgatgcagctcct
//
by
@meso_cacase at
DBCLS
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