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Previous release (v1)
2024-11-23 01:40:20, GGRNA.v2 : RefSeq release 226 (Sep, 2024)
LOCUS XM_017013846 1772 bp mRNA linear PRI 25-AUG-2024
DEFINITION PREDICTED: Homo sapiens ring finger protein 122 (RNF122),
transcript variant X1, mRNA.
ACCESSION XM_017013846
VERSION XM_017013846.2
DBLINK BioProject: PRJNA168
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
COMMENT MODEL REFSEQ: This record is predicted by automated computational
analysis. This record is derived from a genomic sequence
(NC_000008.11) annotated using gene prediction method: Gnomon,
supported by EST evidence.
Also see:
Documentation of NCBI's Annotation Process
On Apr 5, 2022 this sequence version replaced XM_017013846.1.
##Genome-Annotation-Data-START##
Annotation Provider :: NCBI RefSeq
Annotation Status :: Updated annotation
Annotation Name :: GCF_000001405.40-RS_2024_08
Annotation Pipeline :: NCBI eukaryotic genome annotation
pipeline
Annotation Software Version :: 10.3
Annotation Method :: Best-placed RefSeq; Gnomon;
RefSeqFE; cmsearch; tRNAscan-SE
Features Annotated :: Gene; mRNA; CDS; ncRNA
Annotation Date :: 08/23/2024
##Genome-Annotation-Data-END##
FEATURES Location/Qualifiers
source 1..1772
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="8"
gene 1..1772
/gene="RNF122"
/note="ring finger protein 122; Derived by automated
computational analysis using gene prediction method:
Gnomon. Supporting evidence includes similarity to: 4
ESTs, 21 long SRA reads, and 100% coverage of the
annotated genomic feature by RNAseq alignments, including
14 samples with support for all annotated introns"
/db_xref="GeneID:79845"
/db_xref="HGNC:HGNC:21147"
/db_xref="MIM:620523"
variation 2..5
/gene="RNF122"
/replace="tcca"
/replace="tccatcca"
/db_xref="dbSNP:1243053278"
variation 3
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1195113823"
variation 4
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:577827642"
variation 5
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810615542"
variation 6
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1468642359"
variation 10
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810615475"
variation 11
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1222410610"
variation 13
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1357846515"
variation 15
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810615350"
variation 21
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:59553113"
variation 29
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:148747814"
variation 31
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810615148"
variation 35..42
/gene="RNF122"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/replace="aaaaaaaaa"
/db_xref="dbSNP:1013165069"
variation 35
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:941740863"
variation 38
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810615050"
variation 40..43
/gene="RNF122"
/replace=""
/replace="aaag"
/db_xref="dbSNP:895684364"
variation 42
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810614925"
variation 43
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128841119"
variation 44
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:746950199"
variation 45
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056458627"
variation 46
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810614747"
variation 59
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:908928146"
variation 64
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1585364099"
variation 66
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1384119206"
variation 67
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489343592"
variation 70
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1217448202"
variation 76
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810614398"
variation 78
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810614349"
variation 79
/gene="RNF122"
/replace=""
/replace="t"
/db_xref="dbSNP:1810614304"
variation 79
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1268225443"
variation 80
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810614227"
variation 81
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:544345125"
variation 82
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:2128841106"
variation 83
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201620384"
variation 84
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810614158"
variation 85
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1363891731"
variation 86
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:939459673"
variation 87
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1156507348"
variation 88
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1362080599"
variation 89
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810614002"
variation 94..96
/gene="RNF122"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1289174303"
variation 98
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810613923"
variation 99
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1404284107"
variation 101
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:897136815"
variation 103
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810613786"
variation 104
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1363596212"
variation 105
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:573729587"
variation 107
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1585364060"
variation 108
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:983616328"
variation 118
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:377587726"
variation 119
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:111742997"
variation 120
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128841097"
variation 122
/gene="RNF122"
/replace=""
/replace="a"
/db_xref="dbSNP:1371990019"
variation 122
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1585364043"
variation 123
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:992026928"
variation 125
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810613307"
variation 127
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1167968059"
variation 128
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:747810284"
variation 129
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1585364034"
variation 135
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1311102234"
variation 137
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1356123694"
variation 138
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:2128841090"
variation 139
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:185297752"
variation 142
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810613013"
variation 143
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1585364026"
variation 146
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810612935"
variation 147
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1241089146"
variation 151
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810612860"
variation 153
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810612828"
variation 154
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1291198029"
variation 155
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1585364021"
variation 158
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810612714"
variation 160
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810612643"
variation 163
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1585364018"
variation 165
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1810612561"
variation 170
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:181503826"
variation 178
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810612491"
variation 180
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:959261530"
variation 182
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1199085965"
variation 187
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1490010712"
variation 192
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810612315"
variation 195
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1437699989"
variation 196
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810612240"
variation 201
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1271727006"
variation 202
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1223849863"
variation 203
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1033627910"
variation 204
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810612076"
variation 205
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1000864411"
variation 207
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810612001"
variation 208
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1480382010"
variation 209
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1439943971"
variation 211
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1162508015"
variation 212
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:868206166"
variation 216
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:903857024"
variation 217
/gene="RNF122"
/replace=""
/replace="c"
/db_xref="dbSNP:1810611770"
variation 217
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810611739"
variation 219
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810611703"
variation 220
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810611660"
variation 222
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:941586542"
variation 224
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810611577"
variation 225
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810611540"
variation 230
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1021002888"
variation 233
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1229891117"
variation 236
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810611398"
variation 238..251
/gene="RNF122"
/replace="ttc"
/replace="ttctaagttagttc"
/db_xref="dbSNP:1333151006"
variation 238..239
/gene="RNF122"
/replace=""
/replace="tt"
/db_xref="dbSNP:1810611313"
variation 238
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:910128792"
variation 240
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810611267"
variation 241..250
/gene="RNF122"
/replace="t"
/replace="taagttagtt"
/db_xref="dbSNP:1810611171"
variation 243..250
/gene="RNF122"
/replace="agtt"
/replace="agttagtt"
/db_xref="dbSNP:1810611131"
variation 243
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1010079068"
variation 248
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1389532379"
variation 254
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810611045"
variation 255
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:891270855"
variation 256
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810610965"
variation 257
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810610918"
variation 265
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051688344"
variation 266..270
/gene="RNF122"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1447851062"
variation 266
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1585363975"
variation 279
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1810610747"
variation 280
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:932793915"
variation 281
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:922789571"
variation 290
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810610598"
variation 293
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810610567"
variation 296
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810610520"
variation 298
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1810610484"
variation 299
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:976475012"
variation 305
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:2128841051"
variation 306
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810610400"
variation 307
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:369611888"
variation 310
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810610297"
variation 312
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810610266"
variation 313
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810610223"
variation 314
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:900091836"
variation 315
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810610116"
variation 317
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:978839186"
variation 320
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1240467923"
variation 328
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810609981"
variation 331
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1402439692"
variation 332
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1799650336"
variation 342
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1338873611"
variation 343
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745685003"
variation 348
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415246669"
variation 349
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1404530136"
variation 351
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1171047073"
variation 352
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1469314860"
variation 353
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1402936608"
variation 354
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:778092147"
variation 355
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:756336836"
variation 358
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:748357167"
variation 362
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1478792342"
variation 367
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1240130576"
variation 376
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:781326193"
variation 377
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:755028263"
CDS 378..773
/gene="RNF122"
/codon_start=1
/product="RING finger protein 122 isoform X1"
/protein_id="XP_016869335.1"
/db_xref="GeneID:79845"
/db_xref="HGNC:HGNC:21147"
/db_xref="MIM:620523"
/translation="
MPPISFQDLPLNIYMVIFGTGIFVFMLSLIFCCYFISKLRNQAQSERYGYKEVVLKGDAKKLQLYGQTCAVCLEDFKGKDELGVLPCQHAFHRKCLVKWLEVRCVCPMCNKPIASPSEATQNIGILLDELV"
misc_feature 576..716
/gene="RNF122"
/note="RING finger, H2 subclass, found in RING finger
protein 122 (RNF122) and similar proteins; Region:
RING-H2_RNF122; cd16676"
/db_xref="CDD:438338"
misc_feature order(582..584,591..593,636..638,642..644,651..653,
660..662,693..695,702..704)
/gene="RNF122"
/note="Zn binding site [ion binding]; other site"
/db_xref="CDD:438338"
variation 379
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810494274"
variation 381
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:929125683"
variation 382
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:751997578"
variation 383
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:111889159"
variation 384
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201419677"
variation 388
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:984112683"
variation 394
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:372043460"
variation 395
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277263596"
variation 398
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:3735951"
variation 399
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:75557466"
variation 400
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1290866282"
variation 401
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:765564449"
variation 406
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:866871197"
variation 407
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:377115228"
variation 408
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:146246424"
variation 411
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:201319122"
variation 414
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1332392799"
variation 415
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1810493365"
variation 416
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1355781275"
variation 418
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1452396640"
variation 420
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:760103544"
variation 422
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231260955"
variation 423
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:926628460"
variation 426
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:775524296"
variation 430
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471161893"
variation 431
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:3735950"
variation 432
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:759595318"
variation 436
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:902940567"
variation 439
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:774256289"
variation 440
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:770697160"
variation 446
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810492433"
variation 450..451
/gene="RNF122"
/replace=""
/replace="tt"
/db_xref="dbSNP:1810492370"
variation 453
/gene="RNF122"
/replace=""
/replace="a"
/db_xref="dbSNP:1810492328"
variation 453
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128839897"
variation 454
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1021366227"
variation 457
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:748345907"
variation 458
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1181346051"
variation 461
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1460641245"
variation 466
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1238243120"
variation 468..469
/gene="RNF122"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1810492013"
variation 468
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810492057"
variation 469
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:781277434"
variation 476..485
/gene="RNF122"
/replace="c"
/replace="ctattttatc"
/db_xref="dbSNP:1585360334"
variation 478
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1021035689"
variation 484
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810491846"
variation 485
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1272858769"
variation 491
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191341937"
variation 492
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:778248944"
variation 493
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1265239476"
variation 494
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:3735949"
variation 495
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1222433414"
variation 496
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:760602508"
variation 497
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:767120987"
variation 500
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:944300241"
variation 503
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:754541267"
variation 504
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316621739"
variation 505
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:751476229"
variation 509
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:150818390"
variation 513
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187595782"
variation 516
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:762998431"
variation 517
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:267601903"
variation 519
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044770908"
variation 520
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810372423"
variation 521
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:184889708"
variation 522
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:760876481"
variation 523
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451177555"
variation 524
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:775706522"
variation 525
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810372140"
variation 526
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:772070372"
variation 528
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:946228557"
variation 530
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1585356340"
variation 531
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1054030786"
variation 534
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810367108"
variation 536
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1389469080"
variation 537
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:775647291"
variation 540
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428246648"
variation 547
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:141431566"
variation 551
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1183796982"
variation 555
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:759848649"
variation 562
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810366735"
variation 566
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242608260"
variation 569
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810366623"
variation 570
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1585356161"
variation 574
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1319221619"
variation 575
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199283976"
variation 577
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1240469190"
variation 581
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810339378"
variation 584
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:763096507"
variation 585
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:773808716"
variation 586
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:770404193"
variation 587
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1392002976"
variation 588..596
/gene="RNF122"
/replace="gtctg"
/replace="gtctgtctg"
/db_xref="dbSNP:1457579520"
variation 588
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1055023182"
variation 592
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:762450024"
variation 593
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:777132335"
variation 609
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810338886"
variation 611
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:373090081"
variation 613
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:925952170"
variation 620
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128837964"
variation 626
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:148302412"
variation 627
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:115346711"
variation 629
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1212488068"
variation 630
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771445709"
variation 632
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810338436"
variation 634
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:144271550"
variation 635
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:778441882"
variation 636
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810338222"
variation 644
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:143915374"
variation 645
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:753839300"
variation 647
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:777531296"
variation 651
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1205337660"
variation 653
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:2128837946"
variation 654
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:917531496"
variation 655
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:755948110"
variation 656
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1270561628"
variation 659
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761131128"
variation 661
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:574382545"
variation 663
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1192003202"
variation 666
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307761697"
variation 668
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:372733449"
variation 671
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:138443534"
variation 675
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:954422456"
variation 677
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810328542"
variation 685
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:147098542"
variation 686
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:774004086"
variation 688
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1230304691"
variation 690
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:770361600"
variation 692
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273558292"
variation 696
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1274271909"
variation 699
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1030624533"
variation 705
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1216865663"
variation 708
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810327802"
variation 712
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1337829210"
variation 713
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1270039445"
variation 714
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:748826742"
variation 716..717
/gene="RNF122"
/replace=""
/replace="a"
/db_xref="dbSNP:1385178766"
variation 722
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772648276"
variation 723..725
/gene="RNF122"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1009495800"
variation 727
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810327387"
variation 731
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451945660"
variation 732
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810327291"
variation 733
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769741086"
variation 736
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:374015683"
variation 737
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:781028541"
variation 738
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:754837343"
variation 740
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1032174469"
variation 744
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:746024052"
variation 745
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:191195067"
variation 746
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810326805"
variation 749
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386652559"
variation 753
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:867483600"
variation 754
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:757367341"
variation 755
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810326587"
variation 756
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:534605036"
variation 763
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:764116179"
variation 764
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:370863263"
variation 769
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:570071398"
variation 772
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753198887"
variation 776
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201892068"
variation 777
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284112265"
variation 781
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:536719453"
variation 782
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:186427620"
variation 786
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762635625"
variation 787
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:199638006"
variation 789
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1281407641"
variation 790
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:529550015"
variation 791
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810325759"
variation 794
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1247224353"
variation 795
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:761753833"
variation 796
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1179494356"
variation 799
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:899462737"
variation 803
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:776440869"
variation 805
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1425013339"
variation 806
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367253173"
variation 807
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810325365"
variation 808
/gene="RNF122"
/replace=""
/replace="c"
/db_xref="dbSNP:775944008"
variation 811
/gene="RNF122"
/replace="g"
/replace="gg"
/db_xref="dbSNP:770316527"
variation 812..813
/gene="RNF122"
/replace="c"
/replace="cc"
/db_xref="dbSNP:745334318"
variation 816
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:562270803"
variation 817
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1216581922"
variation 818
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1178361895"
variation 819
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810324953"
variation 820
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:768533446"
variation 822
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1232760812"
variation 824
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:746826629"
variation 826
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:139140077"
variation 829
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339985495"
variation 833
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810324623"
variation 840
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1563367291"
variation 842
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:775461036"
variation 844
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810324484"
variation 846
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:150227192"
variation 847
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1253431848"
variation 858
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:545523708"
variation 859
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810324312"
variation 862
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810324265"
variation 863
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:769508303"
variation 864
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810324162"
variation 868..872
/gene="RNF122"
/replace="ga"
/replace="gacga"
/db_xref="dbSNP:1810324009"
variation 870
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:908333473"
variation 871
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:759278666"
variation 875
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:973531310"
variation 877
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810323911"
variation 878
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:982564371"
variation 882
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172548601"
variation 890
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:942217461"
variation 893
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810323565"
variation 894
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:776193930"
variation 895
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1416725836"
variation 898
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:778213224"
variation 899
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:917097761"
variation 902
/gene="RNF122"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1810323128"
variation 906
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128837772"
variation 907
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810323075"
variation 909
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:2128837771"
variation 916
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1244883306"
variation 918
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:564298303"
variation 919
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810322926"
variation 920
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1380572676"
variation 922
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1279842549"
variation 923
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:546210261"
variation 932
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1326855688"
variation 944
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:575635538"
variation 946
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:78623242"
variation 947
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1254206830"
variation 951
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1338608637"
variation 952
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128837766"
variation 953
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810322461"
variation 956
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:563847242"
variation 969
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:991389797"
variation 971
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1487097693"
variation 972
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1195464487"
variation 973
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1264265272"
variation 974
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810322156"
variation 985
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429514747"
variation 986
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810322072"
variation 989
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810322026"
variation 991
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810321971"
variation 993
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810321924"
variation 994
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810321882"
variation 1000
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:78523626"
variation 1003
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810321772"
variation 1004
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:574244724"
variation 1007
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1286567251"
variation 1009
/gene="RNF122"
/replace=""
/replace="c"
/db_xref="dbSNP:1810321635"
variation 1010
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810321597"
variation 1011
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1436586439"
variation 1012
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810321520"
variation 1017
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810321468"
variation 1019
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:770417238"
variation 1023
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810321350"
variation 1024
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1418072156"
variation 1025
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:2128837749"
variation 1029
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:552756699"
variation 1032
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810321214"
variation 1034
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1585354672"
variation 1035
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810321120"
variation 1037
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810321075"
variation 1038
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:2128837745"
variation 1043
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1362346514"
variation 1048
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810320956"
variation 1049
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386025785"
variation 1052..1054
/gene="RNF122"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1032289134"
variation 1056
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810320809"
variation 1058
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810320762"
variation 1062
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1363954575"
variation 1063
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235005993"
variation 1064
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810320566"
variation 1065
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1033014834"
variation 1067
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:905044684"
variation 1071
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1218290726"
variation 1076
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810320418"
variation 1079
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1023014277"
variation 1080
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1443150150"
variation 1086
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1486365602"
variation 1087
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:534567871"
variation 1090
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1209623818"
variation 1098
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265789629"
variation 1099
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128837736"
variation 1102
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1387692523"
variation 1106
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:979207409"
variation 1107
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1585354629"
variation 1108
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1455954412"
variation 1113
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810319956"
variation 1114
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:967442964"
variation 1115
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1449354285"
variation 1116
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1161487486"
variation 1118
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810319745"
variation 1122
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810319688"
variation 1125
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810319643"
variation 1127
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1346022708"
variation 1129
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1020404729"
variation 1135
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1291561360"
variation 1140
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1810319389"
variation 1144
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1057128048"
variation 1145
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:747521864"
variation 1148
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:954832439"
variation 1153
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330627961"
variation 1157
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:929328919"
variation 1158
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:368203935"
variation 1159
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810319049"
variation 1167
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810319015"
variation 1170
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:558245136"
variation 1171
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1320737531"
variation 1172
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:71512677"
variation 1173
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:2128837714"
variation 1174..1189
/gene="RNF122"
/replace="acaaccttccctcccc"
/replace="acaaccttccctccccacaaccttccctcccc"
/db_xref="dbSNP:1585354564"
variation 1174
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1221543408"
variation 1175
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1222621027"
variation 1177
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:140283198"
variation 1178
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:996403395"
variation 1179
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1470140989"
variation 1183
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1214817001"
variation 1186..1189
/gene="RNF122"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1810318414"
variation 1187
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810318516"
variation 1189
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1238122007"
variation 1190..1191
/gene="RNF122"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:2128837708"
variation 1193
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:529978164"
variation 1194
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810318311"
variation 1195
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1456453871"
variation 1196
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810318240"
variation 1198
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:867219030"
variation 1203
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:899451633"
variation 1204
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:569640266"
variation 1214
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163003199"
variation 1220..1231
/gene="RNF122"
/replace="ggaaggaaggaa"
/replace="ggaaggaaggaaggaa"
/db_xref="dbSNP:1810317928"
variation 1224
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419714590"
variation 1232
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1325728352"
variation 1234
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810317834"
variation 1236
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1038031560"
variation 1244
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810317767"
variation 1246
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128837700"
variation 1247..1250
/gene="RNF122"
/replace="gc"
/replace="gcgc"
/db_xref="dbSNP:1444375489"
variation 1248
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:576930981"
variation 1249
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:986295956"
variation 1253
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1292831009"
variation 1256
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:886838183"
variation 1257
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:923037559"
variation 1263
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046774895"
variation 1264
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:554603743"
variation 1266..1268
/gene="RNF122"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1810317268"
variation 1268
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:949814966"
variation 1270
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1306261642"
variation 1273
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1207307798"
variation 1274
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:956584977"
variation 1276
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810317031"
variation 1278
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:917043712"
variation 1285..1287
/gene="RNF122"
/replace="a"
/replace="aga"
/db_xref="dbSNP:1810316889"
variation 1286
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1032237125"
variation 1292
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:979345947"
variation 1293
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810316859"
variation 1296
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810316821"
variation 1297
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1810316780"
variation 1299
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1475375851"
variation 1301
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810316671"
variation 1302
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056073738"
variation 1305
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128837680"
variation 1308
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:536362653"
variation 1310
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1023463555"
variation 1314
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810316394"
variation 1315
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810316354"
variation 1316
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810316313"
variation 1317
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810316270"
variation 1323
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:937268922"
variation 1324
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423178959"
variation 1329
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:181768653"
variation 1332
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810316070"
variation 1333
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:2128837674"
variation 1336
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810316022"
variation 1338
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:758914485"
variation 1339
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1461930757"
variation 1342
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:547236738"
variation 1349
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:528775770"
variation 1350
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:3735948"
variation 1351
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1036198684"
variation 1353
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:114804489"
variation 1354
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:779252145"
variation 1355
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:530983401"
variation 1357
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810315348"
variation 1358
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810315306"
variation 1361
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810315266"
variation 1362
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274355365"
variation 1363
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429181557"
variation 1365
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810315147"
variation 1366
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810315112"
variation 1367
/gene="RNF122"
/replace=""
/replace="a"
/db_xref="dbSNP:1810315070"
variation 1367
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:897835525"
variation 1369
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810314960"
variation 1370
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810314911"
variation 1372..1373
/gene="RNF122"
/replace=""
/replace="aa"
/db_xref="dbSNP:1810314824"
variation 1372
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810314866"
variation 1373..1378
/gene="RNF122"
/replace="agag"
/replace="agagag"
/replace="agagagag"
/db_xref="dbSNP:1486114412"
variation 1376
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1282648366"
variation 1379
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:151187022"
variation 1380
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:534619590"
variation 1382
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016949899"
variation 1384..1385
/gene="RNF122"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1476288680"
variation 1385
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810314462"
variation 1386
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810314431"
variation 1388
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424386605"
variation 1392
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810314329"
variation 1393
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:2128837660"
variation 1395
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810314283"
variation 1396
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810314247"
variation 1400
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1430880296"
variation 1402
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1005107988"
variation 1403
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:886744845"
variation 1405
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810314092"
variation 1406
/gene="RNF122"
/replace=""
/replace="g"
/db_xref="dbSNP:1810314063"
variation 1406
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1375580294"
variation 1409
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:541877847"
variation 1413
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:889406556"
variation 1416
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1197496824"
variation 1418
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:189877271"
variation 1420
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810313791"
variation 1437
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1293697598"
variation 1438
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1433344061"
variation 1439
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:559090739"
variation 1440
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:2128837651"
variation 1445
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810313498"
variation 1446
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810313413"
variation 1457..1500
/gene="RNF122"
/replace="tt"
/replace="ttgaggtttgtgggcccctctagaggagggctagttctatactt"
/db_xref="dbSNP:1810312845"
variation 1457
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046721678"
variation 1467
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:114355002"
variation 1474
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1232816872"
variation 1480
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:577047481"
variation 1481..1482
/gene="RNF122"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1810313200"
variation 1483
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2128837644"
variation 1487..1495
/gene="RNF122"
/replace="cta"
/replace="ctagttcta"
/db_xref="dbSNP:934973256"
variation 1489
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:923015716"
variation 1490
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810313107"
variation 1491
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810313059"
variation 1493
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:2128837643"
variation 1495
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1052631865"
variation 1498
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:2128837640"
variation 1499
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:895591763"
variation 1502
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1216237837"
variation 1503
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1055620955"
variation 1504
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:937195781"
variation 1506
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810312690"
variation 1507
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1810312645"
variation 1508
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810312612"
variation 1510
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:759286177"
variation 1512
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810312512"
variation 1513
/gene="RNF122"
/replace=""
/replace="a"
/db_xref="dbSNP:1810312468"
variation 1513
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1249531350"
variation 1514..1517
/gene="RNF122"
/replace="ggg"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1409713774"
variation 1514
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:925827533"
variation 1516
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1229039844"
variation 1517..1518
/gene="RNF122"
/replace=""
/replace="gtt"
/db_xref="dbSNP:1810312168"
variation 1517
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:868437879"
variation 1518..1519
/gene="RNF122"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1402745924"
variation 1518
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1156400090"
variation 1519..1525
/gene="RNF122"
/replace=""
/replace="ctttttt"
/db_xref="dbSNP:1439301784"
variation 1519..1520
/gene="RNF122"
/replace=""
/replace="ct"
/db_xref="dbSNP:1810311999"
variation 1519..1520
/gene="RNF122"
/replace=""
/replace="ct"
/db_xref="dbSNP:1585354336"
variation 1519
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:867878085"
variation 1520..1545
/gene="RNF122"
/replace="tttttttttt"
/replace="tttttttttttt"
/replace="ttttttttttttt"
/replace="tttttttttttttt"
/replace="ttttttttttttttt"
/replace="tttttttttttttttt"
/replace="ttttttttttttttttt"
/replace="tttttttttttttttttt"
/replace="ttttttttttttttttttt"
/replace="tttttttttttttttttttt"
/replace="ttttttttttttttttttttt"
/replace="tttttttttttttttttttttt"
/replace="ttttttttttttttttttttttt"
/replace="tttttttttttttttttttttttt"
/replace="ttttttttttttttttttttttttt"
/replace="tttttttttttttttttttttttttt"
/replace="ttttttttttttttttttttttttttt"
/replace="tttttttttttttttttttttttttttt"
/replace="ttttttttttttttttttttttttttttt"
/replace="tttttttttttttttttttttttttttttt"
/replace="ttttttttttttttttttttttttttttttt"
/replace="tttttttttttttttttttttttttttttttt"
/replace="ttttttttttttttttttttttttttttttttt"
/replace="tttttttttttttttttttttttttttttttttt"
/replace="ttttttttttttttttttttttttttttttttttt"
/replace="tttttttttttttttttttttttttttttttttttt"
/replace="ttttttttttttttttttttttttttttttttttttt"
/replace="tttttttttttttttttttttttttttttttttttttt"
/replace="ttttttttttttttttttttttttttttttttttttttt"
/db_xref="dbSNP:rs35370120"
variation 1520..1521
/gene="RNF122"
/replace=""
/replace="c"
/replace="g"
/db_xref="dbSNP:2128837620"
variation 1520
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810311892"
variation 1520
/gene="RNF122"
/replace="t"
/replace="tgttttttttt"
/db_xref="dbSNP:1810311924"
variation 1521
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810311845"
variation 1523
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810311818"
variation 1524..1525
/gene="RNF122"
/replace=""
/replace="c"
/db_xref="dbSNP:1349714991"
variation 1525
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810311707"
variation 1529
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810311674"
variation 1538..1539
/gene="RNF122"
/replace=""
/replace="c"
/db_xref="dbSNP:1328553890"
variation 1539
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810311587"
variation 1540..1546
/gene="RNF122"
/replace=""
/replace="ttttttg"
/db_xref="dbSNP:1810310834"
variation 1541..1548
/gene="RNF122"
/replace="t"
/replace="tttttgat"
/db_xref="dbSNP:1810310224"
variation 1541
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1043337853"
variation 1543..1546
/gene="RNF122"
/replace=""
/replace="tttg"
/db_xref="dbSNP:1810310790"
variation 1544..1546
/gene="RNF122"
/replace=""
/replace="ttg"
/db_xref="dbSNP:1317210658"
variation 1545..1548
/gene="RNF122"
/replace="t"
/replace="tgat"
/db_xref="dbSNP:1810310184"
variation 1545..1546
/gene="RNF122"
/replace=""
/replace="tg"
/replace="tga"
/replace="ttg"
/db_xref="dbSNP:1810310874"
variation 1545..1546
/gene="RNF122"
/replace=""
/replace="tg"
/db_xref="dbSNP:1810310663"
variation 1545
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1346937738"
variation 1546..1549
/gene="RNF122"
/replace=""
/replace="gatc"
/db_xref="dbSNP:374520435"
variation 1546..1547
/gene="RNF122"
/replace=""
/replace="t"
/replace="tt"
/db_xref="dbSNP:1491279506"
variation 1546..1547
/gene="RNF122"
/replace=""
/replace="ga"
/db_xref="dbSNP:1491578426"
variation 1546
/gene="RNF122"
/replace=""
/replace="g"
/db_xref="dbSNP:1810310627"
variation 1546
/gene="RNF122"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1554531516"
variation 1546
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1193613836"
variation 1547
/gene="RNF122"
/replace=""
/replace="a"
/db_xref="dbSNP:1810310364"
variation 1547
/gene="RNF122"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1810310323"
variation 1547
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252010924"
variation 1548
/gene="RNF122"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1810310146"
variation 1549..1550
/gene="RNF122"
/replace=""
/replace="t"
/db_xref="dbSNP:1810309983"
variation 1549
/gene="RNF122"
/replace=""
/replace="c"
/db_xref="dbSNP:1810310073"
variation 1549
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1186338413"
variation 1550
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810309930"
variation 1553
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810309888"
variation 1555
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810309860"
variation 1556
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:74630292"
variation 1557
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810309746"
variation 1558
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1474392550"
variation 1559
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128837596"
variation 1560
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:2128837594"
variation 1562
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1419100305"
variation 1563
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1461898850"
variation 1565
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1166702038"
variation 1566
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:2128837592"
variation 1570
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810309541"
variation 1571
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1395035700"
variation 1572
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1410620470"
variation 1575
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:2128837589"
variation 1577
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1333682953"
variation 1578
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1170124920"
variation 1579
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416920086"
variation 1581..1582
/gene="RNF122"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1810309269"
variation 1593
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810309222"
variation 1594
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1585354271"
variation 1595
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:924946326"
variation 1598
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810309117"
variation 1599
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:945955516"
variation 1603
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:2128837584"
variation 1612
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:979123721"
variation 1613
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:913196344"
variation 1617
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:987507650"
variation 1623
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1585354256"
variation 1626
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810308848"
variation 1629
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1225100095"
variation 1632
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1253027980"
variation 1633
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810308760"
variation 1635
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:377093527"
variation 1636
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:559692491"
variation 1638..1639
/gene="RNF122"
/replace=""
/replace="a"
/db_xref="dbSNP:1810308577"
variation 1638
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1269865680"
variation 1642
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1199381962"
variation 1644
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:954769080"
variation 1648
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258614705"
variation 1653
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:780174103"
variation 1655
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:143143677"
variation 1656
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:372536535"
variation 1657..1659
/gene="RNF122"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1373761768"
variation 1657
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1016444141"
variation 1659
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:536325525"
variation 1660
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810307816"
variation 1661
/gene="RNF122"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1810307782"
variation 1666
/gene="RNF122"
/replace=""
/replace="g"
/db_xref="dbSNP:1810307746"
variation 1666
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:35048552"
variation 1674..1678
/gene="RNF122"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1563366978"
variation 1675
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1339943854"
variation 1676
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1436785490"
variation 1680
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:983632364"
variation 1684
/gene="RNF122"
/replace=""
/replace="a"
/db_xref="dbSNP:1810307513"
variation 1685
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035741649"
variation 1686
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810307416"
variation 1690
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810307369"
variation 1692..1693
/gene="RNF122"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1383907306"
variation 1696
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810307289"
variation 1698
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:951009152"
variation 1700
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1455060429"
variation 1702
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810307153"
variation 1706..1708
/gene="RNF122"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1283506474"
variation 1707
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:112905687"
variation 1712
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326949410"
variation 1716
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:962135739"
variation 1717
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810306869"
variation 1727
/gene="RNF122"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1211104850"
variation 1727
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1300593587"
variation 1728
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1013906649"
variation 1729
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:28666638"
variation 1735
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810306579"
variation 1750
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810306549"
variation 1752
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810306511"
variation 1754
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810306460"
variation 1756
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:889354066"
variation 1757..1758
/gene="RNF122"
/replace=""
/replace="aa"
/db_xref="dbSNP:1810306350"
variation 1763
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176955021"
variation 1764
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810306227"
variation 1765
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810306181"
variation 1769
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1585354156"
variation 1770
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1392499435"
variation 1772
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810306009"
ORIGIN
ctccagcctgggcaacaagagcgaaactccatctaaaaaaaagccgttttcctgagttgataaaccctcgcagagagctccgcgcccggctgtccctggggtgcgaggctggcctggcgggagccgtgtttctggccacaaggccagattagggtgtctgctcctgagcccaagtgaaggccacacctccagacgcgacaacccctcgccccatttctccccaggcctgggtgatgcttctaagttagttcatttcacctgaggctttttggaggttcaggtgatactgggttaggctggagtctgattcctcagcgagctacctgaaagggtgtttctgtggcctgggactggttagcaccaacaagtcctgctcgatgccacccatcagtttccaggaccttccgctcaacatctatatggtcatcttcggcacaggcatctttgtcttcatgctcagccttatcttctgctgctattttatcagcaaactgcggaaccaggcacagagtgagcgatacggatataaggaggtggtgcttaaaggtgatgccaagaagttacaattatatgggcagacctgcgcagtctgtctggaagacttcaaggggaaggatgagttaggcgtgctcccgtgccaacacgcctttcaccgcaagtgtctggtgaaatggctggaagttcgctgtgtctgccccatgtgtaacaagcccattgctagtccctcagaggccacgcagaacattgggattctattggatgagctggtgtgagtgctgccgctacaccgagacctggagaagacctcttgcctcatggatgtctggtccctctgcacagctccaaccaacaggactgtagggtgatgacgatcactttcccagtgatgagaagggtggtctaggactgggcttctaccctcagtgcaagaccagtgccagatgtgcccccacttcctgcctcctgaagccttcttccctgctactccatgctggtggcctcacccatcaagaccactgtctcctggtactggactatctacctgccttgtccctgttctgggggaaggtgtccaccccgatcaagaacatggagaaagtcctctttcaaggctcccattaggaggatgagctgccttgacccagaagggatgagacgggctcttacctctctacaaccttccctccccttcccactccttccggagtaaggttagaagggaaggaaggaaagatcaaggaaccaagcgcctccacgggaggcgagggaggctctgtatgaaacagaagagcagggacataaaggaaaatgtcagtgtttacatgggacctatggaaacaaaggctggcgggcgccagctgactccagagtaagagagggcccttcccctgccaggacccacggtgctatccattcagtctcttcctcagttaatctcggagcttcctattccatgttgaggtttgtgggcccctctagaggagggctagttctatacttaaattgattcccaggggccttttttttttttttttttttttttttgatcaaaaggggtgtggggatgggggtgtctacggttaagcaacagatacctccttccctttgtaaatagtatttttatacttcatcctcgcctctcaggctttagatacgaaatctccagaatggaagggggtggggattttctgttcctccctggagtgggtgagggtgggagaaagttacatatttaaagaaaaataaatttaataacaagtttctctaaccta
//
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]