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2025-05-09 19:17:25, GGRNA : RefSeq release 60 (20130726)
LOCUS NR_047565 4544 bp RNA linear PRI 17-JUL-2013
DEFINITION Homo sapiens coiled-coil domain containing 129 (CCDC129),
transcript variant 4, non-coding RNA.
ACCESSION NR_047565
VERSION NR_047565.1 GI:384081588
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 4544)
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 4544)
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
AK128026.1, AC005090.2, AC006044.2 and BC132719.1.
Transcript Variant: This variant (4) uses an alternate 5' exon
structure, compared to variant 1. This variant is represented as
non-coding due to the presence of an upstream ORF that is predicted
to interfere with translation of the longest ORF; translation of
the upstream ORF renders the transcript a candidate for
nonsense-mediated mRNA decay (NMD).
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.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-234 AK128026.1 1-234
235-537 AC005090.2 107799-108101
538-1241 AK128026.1 538-1241
1242-1242 AC006044.2 29077-29077
1243-2017 AK128026.1 1243-2017
2018-2018 AC006044.2 117022-117022
2019-2974 BC132719.1 1508-2463
2975-2975 AC006044.2 117979-117979
2976-4210 AK128026.1 2976-4210
4211-4211 AC006044.2 127539-127539
4212-4544 AK128026.1 4212-4544
FEATURES Location/Qualifiers
source 1..4544
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="7"
/map="7p14.3"
gene 1..4544
/gene="CCDC129"
/note="coiled-coil domain containing 129"
/db_xref="GeneID:223075"
/db_xref="HGNC:27363"
misc_RNA 1..4544
/gene="CCDC129"
/product="coiled-coil domain containing 129, transcript
variant 4"
/db_xref="GeneID:223075"
/db_xref="HGNC:27363"
exon 1..974
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 27
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:373754732"
variation 48
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:113626631"
variation 56
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:13223005"
variation 61
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:79507561"
misc_feature 141..455
/gene="CCDC129"
/inference="COORDINATES: ab initio prediction:ORF Finder"
/note="long (>35aa) upstream ORF has strong Kozak
sequence; nonsense-mediated decay mRNA (NMD) candidate"
variation 155
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:112408760"
variation 165
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:185624605"
variation 174
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:188954217"
variation 187
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:193053302"
variation 198
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:185415228"
variation 235
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:217152"
variation 242
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:11978226"
variation 271
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:188894682"
variation 277
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:377430761"
variation 293
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:12701103"
variation 311
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:111451899"
variation 319
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:111908567"
variation 326
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:12701104"
variation 360
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:12701105"
variation 453
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:217153"
variation 463
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:183808370"
variation 537
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:217154"
variation 560
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:140494755"
variation 605
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:150418649"
variation 637
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:145196814"
variation 675
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:12701106"
variation 696
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:188188823"
variation 698
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:73305474"
variation 714
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:180736658"
variation 748
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:12701107"
variation 775
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:187303262"
variation 789
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:190773785"
variation 820
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:78623479"
variation 838
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:182067798"
exon 975..1156
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 982
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:368232809"
misc_feature 994..3684
/gene="CCDC129"
/inference="COORDINATES:
alignment:Blast2seq::RefSeq|NM_194300.3"
/note="primary ORF"
variation 1032
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:114739660"
variation 1054
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:368587451"
variation 1061
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:371959143"
variation 1074
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:147399119"
variation 1081
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:374470226"
variation 1088
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:7811042"
variation 1091
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:143690079"
variation 1092
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:372303441"
variation 1119
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:371511395"
variation 1135
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:112921112"
variation 1147
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:376118062"
exon 1157..1205
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 1182
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:200034335"
exon 1206..1249
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 1207
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:372723381"
variation 1231
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:377546776"
variation 1242
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:2286711"
variation 1243
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:201211575"
exon 1250..1301
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 1259
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:149696374"
variation 1284
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:145529826"
variation 1295
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:374187154"
exon 1302..1388
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 1302..1303
/gene="CCDC129"
/replace=""
/replace="a"
/db_xref="dbSNP:35551867"
variation 1344
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:67930674"
variation 1345
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:369866067"
variation 1347
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:146605019"
variation 1348
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:141438918"
variation 1349
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:202157240"
variation 1353
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:374063664"
variation 1369
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:201415095"
exon 1389..1591
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 1390
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:370418381"
variation 1396
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:372753433"
variation 1417
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:200366088"
variation 1444
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:376020926"
variation 1495
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:370670531"
variation 1534
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:187352726"
variation 1561
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:199790271"
variation 1577
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:371060962"
variation 1585
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:191694538"
variation 1586
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:375679267"
variation 1590
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:143370840"
exon 1592..1719
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 1595
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:151254328"
variation 1621
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:200848834"
variation 1651
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:140428776"
variation 1684
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:200031625"
variation 1712
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:373956174"
exon 1720..1777
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 1744
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:188006642"
variation 1775
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:374799170"
exon 1778..1860
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 1821
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:370130726"
variation 1831
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:367919427"
variation 1839
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:373855014"
variation 1840
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:368202210"
exon 1861..3132
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 1888
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:372684457"
variation 1889
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:150398844"
variation 1890
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:185577476"
variation 1900
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:369485544"
variation 1901
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:138418545"
variation 1908
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:143912195"
variation 1948
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:201060776"
variation 1965
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:146986060"
variation 1973
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:190307572"
variation 1990
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:376801262"
variation 1991
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:138066602"
variation 1992
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:143751428"
variation 2000
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:115087893"
variation 2018
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:4141001"
variation 2024
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:182124848"
variation 2039
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:148685966"
variation 2040
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:141164020"
variation 2059
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:376345625"
variation 2060
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:200626153"
variation 2081
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:377326064"
variation 2095
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:150717357"
variation 2120
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:139246994"
variation 2135
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:144022203"
variation 2160
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:76357748"
variation 2166
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:38396"
variation 2194
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:73686905"
variation 2218
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:77197319"
variation 2240
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:371473428"
variation 2309
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:375287000"
variation 2330
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:368084998"
variation 2336
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:116406137"
variation 2338
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:147656859"
variation 2388
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:143660819"
variation 2401
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:199508649"
variation 2409
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:201778549"
variation 2412
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:200300960"
variation 2418
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:38397"
variation 2451
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:186727343"
variation 2452
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:375104335"
variation 2463
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:138128234"
variation 2473
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:148074341"
variation 2492
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:150134204"
variation 2568
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:200026024"
variation 2601
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:181108787"
variation 2619
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:117782044"
variation 2691
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:377002952"
variation 2703
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:185363516"
variation 2730
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:372213107"
variation 2739
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:375422464"
variation 2805
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:149320755"
variation 2816
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:141868591"
variation 2833
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:200809374"
variation 2856
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:137859522"
variation 2896
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:146267805"
variation 2912
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:369385676"
variation 2932
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:189731201"
variation 2938
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:202078186"
variation 2947
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:145959636"
variation 2973
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:139858209"
variation 2975
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:10247620"
variation 2997
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:76733226"
variation 2998
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:139431992"
variation 3033
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:150049545"
variation 3086
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:147673017"
variation 3126
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:377331865"
variation 3131
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:142323942"
exon 3133..3260
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 3137
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:201917207"
variation 3164
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:200617855"
variation 3181
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:142885665"
variation 3182
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:144601428"
variation 3208
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:7799540"
variation 3213
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:148953571"
variation 3241
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:370201894"
exon 3261..3372
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 3270
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:374114030"
variation 3272
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:143151561"
variation 3280
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:201354762"
variation 3289
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:148236609"
variation 3290
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:80081783"
variation 3315
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:141259951"
exon 3373..4544
/gene="CCDC129"
/inference="alignment:Splign:1.39.8"
variation 3383
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:186386347"
variation 3422
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:137892596"
variation 3485
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:142389938"
variation 3487
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:377589498"
variation 3492
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:145933301"
variation 3510
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:368179579"
variation 3511
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:111514975"
variation 3525
/gene="CCDC129"
/replace=""
/replace="g"
/db_xref="dbSNP:371362733"
variation 3545
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:149268880"
variation 3549
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:371944763"
variation 3550
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:115873834"
variation 3568
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:201005039"
variation 3573
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:200065011"
variation 3584
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:77915580"
variation 3587
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:374464304"
variation 3598
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:148552563"
variation 3623
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:183033798"
variation 3632
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:142016406"
variation 3650
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:34177136"
variation 3656
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:201675506"
variation 3664
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:140998733"
variation 3693
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:368704382"
variation 3695
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:201768075"
variation 3722
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:371845154"
variation 3724
/gene="CCDC129"
/replace="g"
/replace="t"
/db_xref="dbSNP:371968855"
variation 3726
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:138001179"
variation 3735
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:369807067"
variation 3737
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:143478742"
variation 3801
/gene="CCDC129"
/replace="c"
/replace="g"
/db_xref="dbSNP:187942842"
variation 3837
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:374773487"
variation 3906
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:60432519"
variation 3920
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:147140713"
variation 3934
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:140268517"
variation 4010
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:371842462"
variation 4132
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:77503219"
variation 4211
/gene="CCDC129"
/replace="a"
/replace="t"
/db_xref="dbSNP:2159513"
variation 4221
/gene="CCDC129"
/replace="a"
/replace="g"
/db_xref="dbSNP:376168188"
variation 4307
/gene="CCDC129"
/replace="a"
/replace="c"
/db_xref="dbSNP:182206184"
variation 4350
/gene="CCDC129"
/replace="c"
/replace="t"
/db_xref="dbSNP:202091748"
ORIGIN
atcctcccagaaacccagccggcttcacctctcaccaacagtggctgcgggactttccagcacctagcctgggcattcccacagcccagagggagctcgtcccagacaaccaagaggaaaagaagggaaacaagaaagagatggagacccatcattgtggccaacgaccccacgaagagggaatagcggtccacgcacgggacccagcctccgatcaagcccagcaggcgccgggtgcgcctgtgctgggaggcagagcccacgcccacccggaaccgcgccggccagcgaggtccgtgcgcagccccggctgccgcctgcgcttctccctccacacctcaccgttagcagagggagccggctccggcctcagccagccccagagacaggcccccacagcacagcggcgggctgaagggctcctcgagcgtggccagagcagacgccgaggctaaggaggtgccgagagacagcgagggctgctagcacattgtcacctctcaatactggaactcagaataagaggtctccactgttctgagttatgggagaaagatgggtgtatggtagacagaatagtgcctccccacaacaaagatgtcaacatgttactgtgtgtgttaaaagggactttgtaggtgtgagtaagttgaagatcttgagaagaaaagattatcctgggttttttgggtggggccaatgtcataaaaaggtccagataagaaagaggcagaagagtcagggtcagaggaggagccatcatgataggagcagagaagcagagtcaggagagttgatgctacactgctaactttgaagatgaagaagccacgagctatggaatggagacagcctctgaaaggcaaggagatggatttcctttagagcttccaggaaggagtgcaggcctgctaacagatacgttttagcccagtgagactaatttttagacttctgacttccaggaccgtaagtttgcagaattactctcctatgatggcacagaaatcacaaggatctgacaaccttcaggaaggccaggaaaagagcaagagagagatcctgaagtgcaccaaaagcgcgtgggctccgctggatgagtggctgccccctgaccctgaggaggaaagccagagtctcaccatccccatgctggaagattccaagcaagaaagtattcagcagtggctggactctggattctttgtctctgcaaatgaaaactttcaacaagtcattgaccgcactgtttctttgtatgaacaagggatggttcaaatgactgtgaaagactacatgagatctttgcatcagttttcagaaactcccatcctatccagagggaccagtttcaactcttgctattctactgcaagtgtaccacaaagcattcctgaatggctggaattttgggagatagatccagtggagattctcttggatctggggtttggtgctgatgagccagacatctgcatgcaaatcccagccagattccttggttgtggctcagcagccagaggaatcaacatccgtgtttttcttgaagctcaaaagcagcgaatggacattgagaaccccaacttgtacggtcgtttccgacagctggaaatcctggaccatgtgaccaatgccttctcatctctgctgagtgatgtcagcatcctgccaaacagagctgaagagaaagctggaggagagagtgtgcaaagaacctcagtccaaagctttgaagaagagactggtaatcctcttgacatgacttcaggaactgtaggtgccagggtggacagagcaaatagctgccagtctgacagcagcgggttcctggaggagccgctggaaccgctgcccctccagatgccttccttgccaaacagccagagtcctgctgagaatggaggtagaaagccaagagatcagagccacagcttagtatcatcccaggactgtcagctagagtcggatgggccagattccaaaagtagggcgagcatgtctttttcaagccaagaagcgaatgccttggaacaaagggcctcagtatctgtgatggaggaagagtttctgcttgaggccatggaggggccaccagagctgtatatcccagacatggcctgtgccaagaccaccacgaggggagaatgcccaaggaaagacagccatctgtggcagcttctgccaatgccccatgctgagtatgaggtcaccagacccacagccacttccaaatatgatcatcctctggggtttatggtaacccacgtcacagaaatgcaggacagttttgtgaggcctgagggagctggcaaagtgcaaagccaccacaatgagtctcaaaggtcacctggaaatgatcatactcaagacaagttccttcatgttgactctgaggccccacgagaagaggaaagcagtggattctgtcctcacaccaaccacagcttactcgtaccagaaagctcatcacagtgtatccccaagcacagtgaaatcacaccttatgcaactgaccttgctcaaacatctgaaaagctcattccccacctccataaactgcctggagatcctgcccaggtgaagtcaaggtctggtactttgggtcagatactacctgggacagaagctgagatggaaaaccttcctctaaatactggcagctccaggtctgtaatgacccagatgtcctccagcctggtgtcggctgctcagagggctgtggccttggggactggtcccagaggaacatctttagaatgcactgtgtgtgatcctgttaccgcaacagaaacaagactggggacaaaagcaagacagttaaatgatgcttccattcagacttcagctctaagcaacaagaccttgacacatgggccccagcccctcaccaaatccgtctctctagactcaggcttctctagtatctgcccaatgggcacctgccatgctatacctgcccactgctgcatctgctgtcatcaccaccctcactgccacggggagaggcaaagccctggccctgaaccctcagtctgtaggcactgcctgtgttcactaactggtcaccaggaagcccagttcatgacgactttgaaagcccttcaggacactacagtgagggagctatgttcctgcacagtccatgagatggaagccatgaagacgatatgccaaagtttccgggagtatttagaagaaattgaacagcaccttatgggacagcaggccctcttttccagggacatgtcagaggaggaaagggaggaggccgagcaactgcaaacgttacgtgaggccctgaggcagcaggtggcagagttggaatttcagttaggagaccgggctcagcaaatcagagaagggattttactgcagctggaggttctcacagcagagccacctgaacactattcaaatctgcatcaatataactggatagaagaaagcaatgggcagacttcatgttctaaaatccacccaggcatggccccgaggactgtgtttcctcccgatgatggccaggaggctccctgttcaggtgggacccagttggctgccttcactccacccaccttggagaacagcaccaggatgtctccttcatcatcagcttgggcaaagttaggtccaacccctttgtcaaattgtcctgttggagaaaaggatgcagatgtcttcctctagatcagagcaggtttgttaaccttcatacaaaatataaaggcccagaacagatgtagcaaggaaatttcaattttccccaaggagaagggtctgccaacccattgtcagctatatctctcatattctaccctttggttaaacccaagaggagtttagaatactctaatactcattcagtatagaataactgagcacctagtatgtgcctggcacagagtatgcaacagtgactaaatagtatacggtctctgccctgctagaacttacagtgtagtgggggagatagaattgcaaacaaaaagtatctgagacagacctcagtcaatatagaagtttattttgccaaggttaaggatacacacccagaagacaggtctgtgcctttctccaaagatgattttgaggccttcaacatttagtggggaaagggtgctaatggggaaagaggtgtgggtacataggaggcaaacagttgcatttttttgagtctgatcagcttttctcatgagagaaggggtagaggaactgtcacttatgcattcacctagctcagtggatctgcacttttacagaaggtaaaataaacatagggcagaggaagcaatcagatatgcatttgtctcgggggagcagagggatggctttgagttctgttctttgtcctgtacctattaagagaagctatcaatatactttgtcaggataaaattcaacagaactgttttagactaaagattttagggaccacaaggaatttcccagtgggcaaattgtgagggaggtatttagcttttaaaaaaatctttgtagctatctcatttagaaataaaatgggaggcagattgcctgatgcagctcct
//
by
@meso_cacase at
DBCLS
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