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Previous release (v1)
2024-05-03 19:09:39, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_038206 388 bp RNA linear PRI 20-JUL-2023
DEFINITION Homo sapiens CFAP418 antisense RNA 1 (CFAP418-AS1), transcript
variant 6, long non-coding RNA.
ACCESSION NR_038206
VERSION NR_038206.1
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 388)
AUTHORS Mortlock DP, Fang ZM, Chandler KJ, Hou Y, Bickford LR, de Bock CE,
Eapen V and Clarke RA.
TITLE Transcriptional Interference Regulates the Evolutionary Development
of Speech
JOURNAL Genes (Basel) 13 (7), 1195 (2022)
PUBMED 35885978
REMARK Publication Status: Online-Only
REFERENCE 2 (bases 1 to 388)
AUTHORS Fang Z, Zhao Z, Eapen V and Clarke RA.
TITLE siRNA Mediate RNA Interference Concordant with Early On-Target
Transient Transcriptional Interference
JOURNAL Genes (Basel) 12 (8), 1290 (2021)
PUBMED 34440463
REMARK Publication Status: Online-Only
REFERENCE 3 (bases 1 to 388)
AUTHORS Wade TD, Gordon S, Medland S, Bulik CM, Heath AC, Montgomery GW and
Martin NG.
TITLE Genetic variants associated with disordered eating
JOURNAL Int J Eat Disord 46 (6), 594-608 (2013)
PUBMED 23568457
REFERENCE 4 (bases 1 to 388)
AUTHORS Fernandez-Rozadilla C, Cazier JB, Tomlinson IP, Carvajal-Carmona
LG, Palles C, Lamas MJ, Baiget M, Lopez-Fernandez LA,
Brea-Fernandez A, Abuli A, Bujanda L, Clofent J, Gonzalez D, Xicola
R, Andreu M, Bessa X, Jover R, Llor X, Moreno V, Castells A,
Carracedo A, Castellvi-Bel S and Ruiz-Ponte C.
CONSRTM EPICOLON Consortium
TITLE A colorectal cancer genome-wide association study in a Spanish
cohort identifies two variants associated with colorectal cancer
risk at 1p33 and 8p12
JOURNAL BMC Genomics 14, 55 (2013)
PUBMED 23350875
REMARK Publication Status: Online-Only
REFERENCE 5 (bases 1 to 388)
AUTHORS Comuzzie AG, Cole SA, Laston SL, Voruganti VS, Haack K, Gibbs RA
and Butte NF.
TITLE Novel genetic loci identified for the pathophysiology of childhood
obesity in the Hispanic population
JOURNAL PLoS One 7 (12), e51954 (2012)
PUBMED 23251661
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
GU295159.1 and AC116154.2.
Transcript Variant: This variant (6) lacks two internal exons,
includes an alternate exon and uses two alternate splice sites,
compared to variant 1.
##Evidence-Data-START##
Transcript exon combination :: GU295159.1 [ECO:0000332]
RNAseq introns :: partial sample support SAMEA2154665,
SAMEA2159080 [ECO:0000350]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-160 GU295159.1 1-160
161-161 AC116154.2 167004-167004
162-227 GU295159.1 162-227
228-228 AC116154.2 181019-181019
229-388 GU295159.1 229-388
FEATURES Location/Qualifiers
source 1..388
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="8"
/map="8q22.1"
gene 1..388
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/note="CFAP418 antisense RNA 1"
/db_xref="GeneID:100616530"
/db_xref="HGNC:HGNC:50444"
ncRNA 1..388
/ncRNA_class="lncRNA"
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/product="CFAP418 antisense RNA 1, transcript variant 6"
/db_xref="GeneID:100616530"
/db_xref="HGNC:HGNC:50444"
exon 1..55
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/inference="alignment:Splign:2.1.0"
variation 2..22
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="gtgaagaggtgccagaatccg"
/replace="gtgaagaggtgccagaatccgtgaagaggtgccagaatccg"
/db_xref="dbSNP:1812074123"
variation 6
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1157981322"
variation 7
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:906266089"
variation 9
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1812074623"
variation 10
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:62524394"
variation 11
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1042741646"
variation 13
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1812075281"
variation 15
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace=""
/replace="a"
/db_xref="dbSNP:1812075559"
variation 15
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1466800792"
variation 16
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1812075675"
variation 18
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1812075781"
variation 19
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:900419859"
variation 20
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400431335"
variation 22
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1171433303"
variation 23
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2132170291"
variation 24
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1477029064"
variation 25
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1379268881"
variation 26
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1586041877"
variation 27
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:996463123"
variation 29
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1236075585"
variation 30
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1812076800"
variation 31
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1458356551"
variation 33
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1262638784"
variation 34
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1812077183"
variation 35
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1812077282"
variation 36
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:564636740"
variation 37
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1347825847"
variation 38
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1051618912"
variation 39
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1375151514"
variation 40
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:890264298"
variation 41
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1004656367"
variation 42
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1014994483"
variation 43
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:963425651"
variation 44..48
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="ctgcc"
/replace="ctgcctgcc"
/db_xref="dbSNP:1404343415"
variation 44
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace=""
/replace="c"
/db_xref="dbSNP:1173106677"
variation 47
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1021869263"
variation 48
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378292139"
variation 49
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:994797826"
variation 50
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1024020863"
variation 51
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1812078894"
variation 54
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1812079064"
variation 55
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:968747490"
exon 56..94
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/inference="alignment:Splign:2.1.0"
variation 60
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:897886145"
variation 64
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1820719936"
variation 67
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242039925"
variation 68
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:924937148"
variation 71..73
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1198179776"
variation 71
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1820720168"
variation 75
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1484046838"
variation 82
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:749836506"
variation 85
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1820720528"
variation 86
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:930639502"
variation 88
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049053477"
variation 89
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:985213286"
variation 90
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:912294249"
variation 91
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace=""
/replace="t"
/db_xref="dbSNP:1240850388"
variation 91
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381891040"
variation 94
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:944239745"
exon 95..204
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/inference="alignment:Splign:2.1.0"
variation 97
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1389497093"
variation 104
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2130855015"
variation 108
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1814014302"
variation 121
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402683086"
variation 126
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1050684100"
variation 127
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1814014751"
variation 128
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:931536546"
variation 130
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1451138368"
variation 136
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390508298"
variation 138
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1814015274"
variation 139
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1395173240"
variation 140
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1814015529"
variation 142
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1814015664"
variation 144
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1814015803"
variation 145
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1332133298"
variation 148
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1814016086"
variation 149
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:567138929"
variation 150
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328118794"
variation 161
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:16892130"
variation 162
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:942428310"
variation 164
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:556426608"
variation 166
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274591837"
variation 167
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1226771420"
variation 173
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1814017133"
variation 175
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2130855095"
variation 179
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1814017222"
variation 190
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1298760400"
variation 199
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232165050"
exon 205..263
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/inference="alignment:Splign:2.1.0"
variation 209
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2130873406"
variation 210
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469483992"
variation 217
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:536148559"
variation 219..222
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="aata"
/replace="aataata"
/db_xref="dbSNP:1284433148"
variation 219..220
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace=""
/replace="aa"
/db_xref="dbSNP:1814661214"
variation 220
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1214099601"
variation 221
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1045704875"
variation 223
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:905471049"
variation 227
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2130873425"
variation 228
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:3107035"
variation 230
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1814662097"
variation 232
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:949418889"
variation 234
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1178852370"
variation 237
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1814662485"
variation 238
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2130873450"
variation 240
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1814662603"
variation 252..255
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1814662710"
variation 261
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390062645"
variation 263
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:184430875"
exon 264..388
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/inference="alignment:Splign:2.1.0"
variation 264
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1815024619"
variation 265..267
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:1815024688"
variation 272
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1263343361"
variation 274
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace=""
/replace="t"
/db_xref="dbSNP:1218469059"
variation 275
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1815024892"
variation 277
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1815024959"
variation 278..282
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="aca"
/replace="acaca"
/db_xref="dbSNP:1815025031"
variation 279
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318018129"
variation 284
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2130884677"
variation 285..322
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="ctgaagctctcctggca"
/replace="ctgaagctctcctggcatactctgaagctctcctggca"
/replace="ctgaagctctcctggcatactctgaagctctcctggcatactctgaag
ctctcctggca"
/db_xref="dbSNP:997294015"
variation 285
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1815025166"
variation 286
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1563739280"
variation 290
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1446366623"
variation 291
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1027512549"
variation 294
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2130884690"
variation 295
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1815025515"
variation 300
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1358601613"
variation 311
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1815025867"
variation 314
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:79951318"
variation 318
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1815026017"
variation 319
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:544466088"
variation 320
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1456437969"
variation 321
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:77667067"
variation 327
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:970522064"
variation 330
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:545624382"
variation 333
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1349179330"
variation 335
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1321539185"
variation 338
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:999369197"
variation 339
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1815026729"
variation 342
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1815026795"
variation 343
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1385323319"
variation 344
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:907868196"
variation 346
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030718981"
variation 350
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1815027154"
variation 357
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1815027231"
variation 360
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:966444146"
variation 361
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1815027367"
variation 363
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1188636602"
variation 372
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:533475518"
variation 374
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1586800155"
variation 380
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1815027678"
variation 381
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1815027740"
variation 386..388
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1815027869"
variation 386
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:989662603"
variation 387
/gene="CFAP418-AS1"
/gene_synonym="C8orf37-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1815027927"
ORIGIN
agtgaagaggtgccagaatccgcgaagagggtcgacgaatgcgctgccgcggaggcaacaatggccatgagggattcaaggattatgcggtaagaaccagtggaactgaggctgcttggaatatcccttctctttgccatccacttgacctgactagtctcgattggttctttgggagcccttcaagatcccttcaaaaccaggtctctgcaccctacaatacaccaactggcagttccatcatttgaaagaaaatcttcaaggtttaagacctgtgacacagactgaagctctcctggcatactctgaagctctcctggcaccctcccctttatgcttcacaggtgtttctcctaataaatttcttgtatgtctcatcccatctggg
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
[Full Text]