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Previous release (v1)
2024-04-20 07:36:55, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_046365 496 bp RNA linear PRI 19-APR-2022
DEFINITION Homo sapiens family with sequence similarity 90 member A27,
pseudogene (FAM90A27P), non-coding RNA.
ACCESSION NR_046365
VERSION NR_046365.1
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 496)
AUTHORS Grimwood J, Gordon LA, Olsen A, Terry A, Schmutz J, Lamerdin J,
Hellsten U, Goodstein D, Couronne O, Tran-Gyamfi M, Aerts A,
Altherr M, Ashworth L, Bajorek E, Black S, Branscomb E, Caenepeel
S, Carrano A, Caoile C, Chan YM, Christensen M, Cleland CA,
Copeland A, Dalin E, Dehal P, Denys M, Detter JC, Escobar J,
Flowers D, Fotopulos D, Garcia C, Georgescu AM, Glavina T, Gomez M,
Gonzales E, Groza M, Hammon N, Hawkins T, Haydu L, Ho I, Huang W,
Israni S, Jett J, Kadner K, Kimball H, Kobayashi A, Larionov V,
Leem SH, Lopez F, Lou Y, Lowry S, Malfatti S, Martinez D, McCready
P, Medina C, Morgan J, Nelson K, Nolan M, Ovcharenko I, Pitluck S,
Pollard M, Popkie AP, Predki P, Quan G, Ramirez L, Rash S, Retterer
J, Rodriguez A, Rogers S, Salamov A, Salazar A, She X, Smith D,
Slezak T, Solovyev V, Thayer N, Tice H, Tsai M, Ustaszewska A, Vo
N, Wagner M, Wheeler J, Wu K, Xie G, Yang J, Dubchak I, Furey TS,
DeJong P, Dickson M, Gordon D, Eichler EE, Pennacchio LA,
Richardson P, Stubbs L, Rokhsar DS, Myers RM, Rubin EM and Lucas
SM.
TITLE The DNA sequence and biology of human chromosome 19
JOURNAL Nature 428 (6982), 529-535 (2004)
PUBMED 15057824
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AC092070.2 and DN930351.1.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
##Evidence-Data-START##
Transcript exon combination :: DN930351.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA2148874, SAMEA2158188
[ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-28 AC092070.2 140627-140654
29-496 DN930351.1 29-496
FEATURES Location/Qualifiers
source 1..496
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="19"
/map="19q13.42"
gene 1..496
/gene="FAM90A27P"
/note="family with sequence similarity 90 member A27,
pseudogene"
/pseudo
/db_xref="GeneID:646508"
/db_xref="HGNC:HGNC:43617"
misc_RNA 1..496
/gene="FAM90A27P"
/product="family with sequence similarity 90 member A27,
pseudogene"
/pseudo
/db_xref="GeneID:646508"
/db_xref="HGNC:HGNC:43617"
exon 1..37
/gene="FAM90A27P"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 4
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1235910180"
variation 5
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1343541691"
variation 7
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:778027940"
variation 8
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1269264764"
variation 14
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:2091405871"
variation 15..19
/gene="FAM90A27P"
/replace="aga"
/replace="agaga"
/db_xref="dbSNP:1464510707"
variation 15
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1206826518"
variation 25
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:2091405911"
variation 27
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1255199194"
variation 28
/gene="FAM90A27P"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1452390262"
variation 31
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1239511107"
variation 33
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:2091405959"
exon 38..146
/gene="FAM90A27P"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 39
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309001535"
variation 40
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:377311935"
variation 42..53
/gene="FAM90A27P"
/replace="cagcagcag"
/replace="cagcagcagcag"
/replace="cagcagcagcagcag"
/db_xref="dbSNP:759085687"
variation 47
/gene="FAM90A27P"
/replace="g"
/replace="t"
/db_xref="dbSNP:183063727"
variation 50..51
/gene="FAM90A27P"
/replace=""
/replace="aa"
/db_xref="dbSNP:1315387075"
variation 51
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760539380"
variation 53
/gene="FAM90A27P"
/replace="g"
/replace="t"
/db_xref="dbSNP:2091407772"
variation 54..61
/gene="FAM90A27P"
/replace="agc"
/replace="agcgaagc"
/db_xref="dbSNP:1244075721"
variation 55
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:201240639"
variation 56..57
/gene="FAM90A27P"
/replace=""
/replace="a"
/db_xref="dbSNP:1599942932"
variation 56
/gene="FAM90A27P"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:188231618"
variation 57
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:199718400"
variation 58
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200669069"
variation 59
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1202852629"
variation 60
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1273613632"
variation 61
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201604006"
variation 63
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1481927689"
variation 64
/gene="FAM90A27P"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1395839560"
variation 65
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:568377059"
variation 66
/gene="FAM90A27P"
/replace="a"
/replace="t"
/db_xref="dbSNP:529660154"
variation 67
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:112045296"
variation 68
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:192951984"
variation 69
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:1224096510"
variation 71
/gene="FAM90A27P"
/replace="g"
/replace="t"
/db_xref="dbSNP:1374491429"
variation 72
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:2091407976"
variation 73
/gene="FAM90A27P"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1382476039"
variation 74
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:2091407998"
variation 78
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:2091408009"
variation 79
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:1388518786"
variation 80
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1024538345"
variation 81
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:906054880"
variation 82
/gene="FAM90A27P"
/replace="g"
/replace="t"
/db_xref="dbSNP:2091408047"
variation 83
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:2146998369"
variation 84
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:2146998371"
variation 87
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:2091408060"
variation 88
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:1385979841"
variation 89
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:2091408077"
variation 90
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169663217"
variation 92
/gene="FAM90A27P"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:757760237"
variation 93
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1468406573"
variation 95
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:781760463"
variation 96
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1305120252"
variation 97
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568712461"
variation 98
/gene="FAM90A27P"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403534945"
variation 100
/gene="FAM90A27P"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:746423936"
variation 101
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:957484741"
variation 102
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367672849"
variation 103
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1599942986"
variation 104
/gene="FAM90A27P"
/replace="g"
/replace="t"
/db_xref="dbSNP:1229453750"
variation 105
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1297079743"
variation 108
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:768174660"
variation 109
/gene="FAM90A27P"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:988877243"
variation 110
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:1264832053"
variation 111
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:2091408225"
variation 116
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1599943002"
variation 119
/gene="FAM90A27P"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:114262625"
variation 120
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:1268299952"
variation 121
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:182874367"
variation 122
/gene="FAM90A27P"
/replace="a"
/replace="t"
/db_xref="dbSNP:2091408281"
variation 124
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:2146998403"
variation 125..130
/gene="FAM90A27P"
/replace="aga"
/replace="agaaga"
/db_xref="dbSNP:1482878104"
variation 125
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:80039192"
variation 129
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:1314444732"
variation 130
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:1568712491"
variation 131..139
/gene="FAM90A27P"
/replace="ttgtt"
/replace="ttgtttgtt"
/db_xref="dbSNP:1450802861"
variation 131
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:557949717"
variation 132
/gene="FAM90A27P"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1449496000"
variation 133
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187560009"
variation 134
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:760451119"
variation 136
/gene="FAM90A27P"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1448125294"
variation 137
/gene="FAM90A27P"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1178676374"
variation 141
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:770762545"
variation 142
/gene="FAM90A27P"
/replace="g"
/replace="t"
/db_xref="dbSNP:576344564"
variation 143
/gene="FAM90A27P"
/replace="g"
/replace="t"
/db_xref="dbSNP:1301563642"
variation 145
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390955688"
exon 147..496
/gene="FAM90A27P"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 153
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2091412654"
variation 155
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:2091412664"
variation 157
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386785712"
variation 164
/gene="FAM90A27P"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1438835277"
variation 169
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:2146998952"
variation 171
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295542915"
variation 172
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1294296596"
variation 173
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:2091412701"
variation 175
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:2146998955"
variation 176
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:2091412715"
variation 178
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:2146998956"
variation 180..186
/gene="FAM90A27P"
/replace="aaga"
/replace="aagaaga"
/db_xref="dbSNP:2091412726"
variation 182
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1334710929"
variation 190
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:2091412752"
variation 194
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1345026172"
variation 196
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1366669346"
variation 197
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:2091412774"
variation 199
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:2091412785"
variation 200
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1599943593"
variation 202
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:2084838516"
variation 203
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:2091412799"
variation 205
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1384802286"
variation 209
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1459287952"
variation 212
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1413267923"
variation 214
/gene="FAM90A27P"
/replace="g"
/replace="t"
/db_xref="dbSNP:1290215132"
variation 217
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:2091412843"
variation 218
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:1329765382"
variation 220
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:751884107"
variation 221
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:552087071"
variation 222
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:2091412880"
variation 223
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:2091412889"
variation 234
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1264627527"
variation 236
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322959853"
variation 237
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:570090675"
variation 239
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1245710030"
variation 240
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1599943615"
variation 241
/gene="FAM90A27P"
/replace="g"
/replace="t"
/db_xref="dbSNP:2146998987"
variation 243
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1046373196"
variation 249
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1197708121"
variation 250
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1254661079"
variation 251
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:2091412973"
variation 254
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473191488"
variation 255
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1158568806"
variation 256
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1405921069"
variation 259
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407102458"
variation 260
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1165761850"
variation 266
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1349516430"
variation 268
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469317287"
variation 269
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:111531670"
variation 270
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1351075937"
variation 273
/gene="FAM90A27P"
/replace="g"
/replace="t"
/db_xref="dbSNP:747607056"
variation 274
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:549537629"
variation 281
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:567615637"
variation 287
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380728228"
variation 288
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:1054890698"
variation 289
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1361448754"
variation 290
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:534822239"
variation 292
/gene="FAM90A27P"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568713022"
variation 293
/gene="FAM90A27P"
/replace="g"
/replace="t"
/db_xref="dbSNP:2091413124"
variation 294
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318977257"
variation 295
/gene="FAM90A27P"
/replace="g"
/replace="t"
/db_xref="dbSNP:1319539254"
variation 296
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:2146999022"
variation 300
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:1220781101"
variation 303
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:1277172995"
variation 305
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:71363324"
variation 306
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1176385781"
variation 307
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770670429"
variation 309
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:893602998"
variation 311
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473818184"
variation 314
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:1182511246"
variation 315
/gene="FAM90A27P"
/replace=""
/replace="a"
/db_xref="dbSNP:1177524374"
variation 315
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:3091271"
variation 320
/gene="FAM90A27P"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1010631516"
variation 321
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1442977043"
variation 323
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1170677930"
variation 329
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:1248381767"
variation 332
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1021097158"
variation 335
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:759459051"
variation 336
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1326775593"
variation 343
/gene="FAM90A27P"
/replace="a"
/replace="t"
/db_xref="dbSNP:199940440"
variation 346
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:2091413340"
variation 347
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448195234"
variation 352
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1283063416"
variation 356
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295627688"
variation 359
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:2091413374"
variation 360
/gene="FAM90A27P"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:538581423"
variation 363
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:2091413401"
variation 364
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1029328224"
variation 367
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:762925449"
variation 369
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:2091413443"
variation 370
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:1343331371"
variation 373
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1204797739"
variation 376
/gene="FAM90A27P"
/replace="g"
/replace="t"
/db_xref="dbSNP:764279444"
variation 382
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1444618392"
variation 386
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1210965948"
variation 395
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1237011974"
variation 399
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:1355221154"
variation 400
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:2091413498"
variation 403
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:2091413507"
variation 405
/gene="FAM90A27P"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:986342307"
variation 407
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442807520"
variation 409
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1190772280"
variation 415
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:2091413541"
variation 416
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:774681541"
variation 418
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:2091413558"
variation 423
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:556817022"
variation 424
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1599943699"
variation 425
/gene="FAM90A27P"
/replace="c"
/replace="g"
/db_xref="dbSNP:574942351"
variation 426
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:963510391"
variation 427
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:1390625174"
variation 428
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:973583859"
variation 429
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1165925480"
variation 430
/gene="FAM90A27P"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1427241458"
variation 433
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:919357260"
variation 434
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:542208217"
variation 435
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258119237"
variation 436
/gene="FAM90A27P"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:929401901"
variation 437
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:554245503"
variation 438
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1436567982"
variation 440
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:756573657"
variation 442
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:927933760"
variation 443
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1227223122"
variation 445
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:2146999130"
variation 454
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:937934167"
variation 461
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243007878"
variation 471
/gene="FAM90A27P"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1268759534"
variation 473
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:766783556"
variation 474
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:1220341162"
variation 475
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1409731411"
variation 476
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:142963909"
variation 477
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:893656753"
variation 482
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1474094012"
variation 483
/gene="FAM90A27P"
/replace="a"
/replace="c"
/db_xref="dbSNP:541627927"
variation 484
/gene="FAM90A27P"
/replace="a"
/replace="g"
/db_xref="dbSNP:200901810"
variation 486
/gene="FAM90A27P"
/replace="c"
/replace="t"
/db_xref="dbSNP:1248942219"
variation 487
/gene="FAM90A27P"
/replace="a"
/replace="t"
/db_xref="dbSNP:2091413842"
variation 488
/gene="FAM90A27P"
/replace="a"
/replace="t"
/db_xref="dbSNP:2091413855"
variation 490
/gene="FAM90A27P"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1464594307"
variation 491
/gene="FAM90A27P"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:777298913"
variation 492
/gene="FAM90A27P"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1042205681"
variation 493..494
/gene="FAM90A27P"
/replace="ac"
/replace="tt"
/db_xref="dbSNP:71337404"
variation 493
/gene="FAM90A27P"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1478203655"
variation 494
/gene="FAM90A27P"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:902300971"
variation 495
/gene="FAM90A27P"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201904782"
ORIGIN
ttacgacgaatgacagagaaaaggagcgaagtccaagtccccagcagcagcagagcgaagctccgacgcagacatttcccagaactccccaagagaaaatgcaggaagcctggaaggagccagcagaagattgtttgttcctgaggcatcctaccatgccactgcctgtccacaccaccaagaagagatctgtcctgggccctgtgtccacaggtccaccgcctgtcaacaaacccgagatgagattactctgcccttcgggtcacaacgattcacctcaactgagcacctgtggacccaccaaaggacatggcagggacgttactgcctccctgctccctgttctgaagagctcccaccagacccccactctcagtgccaggctgccagccaacaggcctgacatgtcctcccatggtgctctccagcctgccatgcaggcgcttgccctgggtcctggccttaaatcccaggcagaaatcaaacatcccgacgc
//
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]