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Previous release (v1)
2024-11-23 01:43:35, GGRNA.v2 : RefSeq release 226 (Sep, 2024)
LOCUS NM_024787 1872 bp mRNA linear PRI 03-APR-2024
DEFINITION Homo sapiens ring finger protein 122 (RNF122), mRNA.
ACCESSION NM_024787
VERSION NM_024787.3
KEYWORDS RefSeq; MANE Select.
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 1872)
AUTHORS Luck,K., Kim,D.K., Lambourne,L., Spirohn,K., Begg,B.E., Bian,W.,
Brignall,R., Cafarelli,T., Campos-Laborie,F.J., Charloteaux,B.,
Choi,D., Cote,A.G., Daley,M., Deimling,S., Desbuleux,A., Dricot,A.,
Gebbia,M., Hardy,M.F., Kishore,N., Knapp,J.J., Kovacs,I.A.,
Lemmens,I., Mee,M.W., Mellor,J.C., Pollis,C., Pons,C.,
Richardson,A.D., Schlabach,S., Teeking,B., Yadav,A., Babor,M.,
Balcha,D., Basha,O., Bowman-Colin,C., Chin,S.F., Choi,S.G.,
Colabella,C., Coppin,G., D'Amata,C., De Ridder,D., De Rouck,S.,
Duran-Frigola,M., Ennajdaoui,H., Goebels,F., Goehring,L., Gopal,A.,
Haddad,G., Hatchi,E., Helmy,M., Jacob,Y., Kassa,Y., Landini,S.,
Li,R., van Lieshout,N., MacWilliams,A., Markey,D., Paulson,J.N.,
Rangarajan,S., Rasla,J., Rayhan,A., Rolland,T., San-Miguel,A.,
Shen,Y., Sheykhkarimli,D., Sheynkman,G.M., Simonovsky,E., Tasan,M.,
Tejeda,A., Tropepe,V., Twizere,J.C., Wang,Y., Weatheritt,R.J.,
Weile,J., Xia,Y., Yang,X., Yeger-Lotem,E., Zhong,Q., Aloy,P.,
Bader,G.D., De Las Rivas,J., Gaudet,S., Hao,T., Rak,J.,
Tavernier,J., Hill,D.E., Vidal,M., Roth,F.P. and Calderwood,M.A.
TITLE A reference map of the human binary protein interactome
JOURNAL Nature 580 (7803), 402-408 (2020)
PUBMED 32296183
REFERENCE 2 (bases 1 to 1872)
AUTHORS Garcia-Martinez,I., Sanchez-Mora,C., Soler Artigas,M., Rovira,P.,
Pagerols,M., Corrales,M., Calvo-Sanchez,E., Richarte,V.,
Bustamante,M., Sunyer,J., Cormand,B., Casas,M., Ramos-Quiroga,J.A.
and Ribases,M.
TITLE Gene-wide Association Study Reveals RNF122 Ubiquitin Ligase as a
Novel Susceptibility Gene for Attention Deficit Hyperactivity
Disorder
JOURNAL Sci Rep 7 (1), 5407 (2017)
PUBMED 28710364
REMARK GeneRIF: Findings indicate genetic association between E3 ubiquitin
ligase RNF122 and Attention Deficit Disorders with Hyperactivity
(ADHD).
Publication Status: Online-Only
REFERENCE 3 (bases 1 to 1872)
AUTHORS Peng,Z., Shi,T. and Ma,D.
TITLE RNF122: a novel ubiquitin ligase associated with calcium-modulating
cyclophilin ligand
JOURNAL BMC Cell Biol 11, 41 (2010)
PUBMED 20553626
REMARK Publication Status: Online-Only
REFERENCE 4 (bases 1 to 1872)
AUTHORS Wang,L., Gao,X., Gao,P., Deng,W., Yu,P., Ma,J., Guo,J., Wang,X.,
Cheng,H., Zhang,C., Yu,C., Ma,X., Lv,B., Lu,Y., Shi,T. and Ma,D.
TITLE Cell-based screening and validation of human novel genes associated
with cell viability
JOURNAL J Biomol Screen 11 (4), 369-376 (2006)
PUBMED 16751333
REFERENCE 5 (bases 1 to 1872)
AUTHORS Saurin,A.J., Borden,K.L., Boddy,M.N. and Freemont,P.S.
TITLE Does this have a familiar RING?
JOURNAL Trends Biochem Sci 21 (6), 208-214 (1996)
PUBMED 8744354
REFERENCE 6 (bases 1 to 1872)
AUTHORS Koyama,K., Sudo,K. and Nakamura,Y.
TITLE Isolation of 115 human chromosome 8-specific expressed-sequence
tags by exon amplification
JOURNAL Genomics 26 (2), 245-253 (1995)
PUBMED 7601449
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DA610129.1, DA904646.1,
BC093884.1 and AC013603.17.
On Jul 19, 2013 this sequence version replaced NM_024787.2.
Summary: The encoded protein contains a RING finger, a motif
present in a variety of functionally distinct proteins and known to
be involved in protein-protein and protein-DNA interactions. The
encoded protein is localized to the endoplasmic reticulum and golgi
apparatus, and may be associated with cell viability. [provided by
RefSeq, Jul 2013].
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 :: AK022588.1, BC093884.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMN03267760 [ECO:0000348]
##Evidence-Data-END##
##RefSeq-Attributes-START##
MANE Ensembl match :: ENST00000256257.2/ ENSP00000256257.1
RefSeq Select criteria :: based on conservation, expression,
longest protein
##RefSeq-Attributes-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-2 DA610129.1 1-2
3-382 DA904646.1 1-380
383-896 BC093884.1 1-514
897-1872 AC013603.17 37158-38133 c
FEATURES Location/Qualifiers
source 1..1872
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="8"
/map="8p12"
gene 1..1872
/gene="RNF122"
/note="ring finger protein 122"
/db_xref="GeneID:79845"
/db_xref="HGNC:HGNC:21147"
/db_xref="MIM:620523"
exon 1..430
/gene="RNF122"
/inference="alignment:Splign:2.1.0"
variation 10
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:145119071"
variation 11
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1407631295"
variation 12
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810640527"
variation 13
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1585364864"
variation 14
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1337052772"
variation 15
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810640404"
variation 17
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810640366"
variation 18
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810640331"
variation 19
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:973483179"
variation 20
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:2128841397"
variation 21
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:141376008"
variation 22
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1054105199"
variation 23
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1200449236"
variation 25..26
/gene="RNF122"
/replace="aa"
/replace="tc"
/db_xref="dbSNP:797004755"
variation 25
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:116343092"
variation 26
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:114018657"
variation 27
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:543468973"
variation 28
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1389893385"
variation 29
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1426369451"
variation 30
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1041509707"
variation 31
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1446570008"
variation 33
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:944501506"
variation 34
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:890301081"
variation 35
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810639689"
variation 36
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1354668897"
variation 37
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1465103584"
variation 40
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1810639585"
variation 43
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1585364822"
variation 44
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1050739309"
variation 46
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1408183097"
variation 47
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1453227746"
variation 50..62
/gene="RNF122"
/replace="c"
/replace="ccgagcctccggc"
/db_xref="dbSNP:2128841386"
variation 52
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1296637621"
variation 54
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1362683511"
variation 58..87
/gene="RNF122"
/replace="ccggc"
/replace="ccggcaaaggtttttccctcctcccccggc"
/db_xref="dbSNP:1485089385"
variation 59
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:576129053"
variation 60
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1297984713"
variation 64
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810639211"
variation 68..72
/gene="RNF122"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:929637144"
variation 68
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1585364806"
variation 71
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1308225954"
variation 73
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810639057"
variation 74
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261279487"
variation 76
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810638974"
variation 78
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1206622959"
variation 80..84
/gene="RNF122"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1247809427"
variation 80
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810638878"
variation 83
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810638838"
variation 84
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1351349425"
variation 88
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810638650"
variation 89
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810638605"
variation 90
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810638567"
variation 93
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:920534256"
variation 94
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810638499"
variation 97
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810638458"
variation 100
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810638421"
variation 101
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:3735952"
variation 102
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:536056690"
variation 103
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1432140927"
variation 106
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:907948566"
variation 109
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1727400782"
variation 111..115
/gene="RNF122"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:1343279195"
variation 111
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1173666113"
variation 113
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1430743133"
variation 115
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1470258740"
variation 116
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1319741680"
variation 118
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:974381036"
variation 122..132
/gene="RNF122"
/replace="cggcgccccac"
/replace="cggcgccccacggcgccccac"
/db_xref="dbSNP:1386383293"
variation 125
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810637895"
variation 126
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:982220711"
variation 127
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1315058442"
variation 128
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:971275012"
variation 129
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810637705"
variation 130
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810637666"
variation 131
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1362898118"
variation 133
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1281457423"
variation 135
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810637490"
variation 136
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:565949201"
variation 137
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:991010831"
variation 138
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:570284142"
variation 140
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243009511"
variation 142
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1585364744"
variation 143..145
/gene="RNF122"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1810637230"
variation 143
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810637258"
variation 145
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:911020040"
variation 146..149
/gene="RNF122"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1270429123"
variation 149
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1196752286"
variation 150
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1563371991"
variation 151
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1320732729"
variation 152
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:986657609"
variation 153
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:954735347"
variation 157
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402284195"
variation 160
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1032630931"
variation 161
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1349019287"
variation 163
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1404578439"
variation 164
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1030416354"
variation 165
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:2128841362"
variation 166
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:999861151"
variation 169
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:902854257"
variation 170
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:988256580"
variation 172
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1020421650"
variation 173
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:956677424"
variation 174
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810636393"
variation 177
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:2128841357"
variation 178
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1032366451"
variation 182
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:2128841355"
variation 184
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810636335"
variation 186
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1427102320"
variation 187
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:538625311"
variation 190
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810636182"
variation 191..201
/gene="RNF122"
/replace="tttgttt"
/replace="tttgtttgttt"
/db_xref="dbSNP:1024185383"
variation 191
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810636147"
variation 193
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1219872856"
variation 195..201
/gene="RNF122"
/replace="tt"
/replace="tttgttt"
/db_xref="dbSNP:905456259"
variation 202
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:890259345"
variation 203
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:571194972"
variation 204
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810635877"
variation 205
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810635833"
variation 206
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810635800"
variation 208
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1046786216"
variation 209
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810635714"
variation 212
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:929753129"
variation 213
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810635638"
variation 214
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810635604"
variation 218
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:2128841351"
variation 219
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810635562"
variation 220
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1422506839"
variation 222
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128841350"
misc_feature 226..228
/gene="RNF122"
/note="upstream in-frame stop codon"
variation 226
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1161946715"
variation 231
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810635453"
variation 232
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:549760705"
variation 235
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:531388417"
variation 236
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1425481960"
variation 239
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1038055851"
variation 240
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1458728732"
variation 242
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:899078669"
variation 246
/gene="RNF122"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1810635177"
variation 247..252
/gene="RNF122"
/replace="cccccc"
/replace="ccccccc"
/replace="cccccccc"
/db_xref="dbSNP:141701554"
variation 247
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810635131"
variation 248
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1445008408"
variation 249
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810635039"
variation 251
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810634985"
variation 252
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037621900"
variation 253
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1359742887"
variation 258
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:567393712"
variation 259
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1203909730"
variation 261
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:940656930"
variation 262
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128841338"
variation 264
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1447424805"
variation 266
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810634623"
variation 269
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1205211865"
variation 279
/gene="RNF122"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1810634530"
variation 282
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1288875140"
variation 284
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1236798617"
variation 285
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:907884550"
variation 287
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1185219391"
variation 294
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810634341"
variation 296
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810634298"
variation 301
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810634265"
variation 303
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810634230"
variation 304
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1479297406"
variation 305
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1585364652"
variation 306
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:907809657"
variation 307
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810634065"
variation 308
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:982581362"
variation 310
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1167498149"
variation 313
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1417533890"
variation 314
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810633946"
variation 315
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:933803362"
variation 316
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810633828"
variation 317
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810633784"
variation 318
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810633752"
variation 319
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810633717"
variation 320
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810633675"
variation 321
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1330198150"
variation 323
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:913096767"
variation 324
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810633570"
variation 328
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339145051"
variation 329
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:949479370"
variation 330
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1585364631"
variation 331
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:548767834"
variation 332
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:916682134"
variation 333
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:767001151"
variation 334
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810633313"
variation 336
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810633278"
variation 338
/gene="RNF122"
/replace=""
/replace="t"
/db_xref="dbSNP:1032728362"
variation 339
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:958233673"
variation 342
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:983236767"
variation 343
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1336849740"
variation 345
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1261912198"
variation 346
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1271622727"
variation 347
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:969833896"
variation 348
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810632890"
variation 350
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1023882253"
variation 352
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810632808"
variation 358
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810632765"
variation 359
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:753074215"
variation 360
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335623555"
variation 362
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:768100824"
variation 364
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:774754275"
variation 366
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1032558935"
variation 367
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810632502"
variation 368
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810632470"
variation 369
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:201541006"
variation 369
/gene="RNF122"
/replace="g"
/replace="ggg"
/db_xref="dbSNP:1369487913"
variation 371
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810632367"
variation 373
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:762582712"
variation 376
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1167549243"
variation 377
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1371526827"
variation 378
/gene="RNF122"
/replace="c"
/replace="cacc"
/db_xref="dbSNP:1242955170"
variation 378
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422386549"
variation 379
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1175753934"
variation 380
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810632065"
variation 381
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:769228600"
variation 383
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810631973"
variation 390
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:896642859"
variation 391
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:375506076"
variation 392
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1198014423"
variation 393
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1363250775"
variation 394
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1357157352"
variation 395
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:776387869"
variation 396
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1246939141"
variation 403..404
/gene="RNF122"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1810631545"
variation 403
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:559977595"
CDS 406..873
/gene="RNF122"
/codon_start=1
/product="RING finger protein 122"
/protein_id="NP_079063.2"
/db_xref="CCDS:CCDS6091.1"
/db_xref="GeneID:79845"
/db_xref="HGNC:HGNC:21147"
/db_xref="MIM:620523"
/translation="
MHPFQWCNGCFCGLGLVSTNKSCSMPPISFQDLPLNIYMVIFGTGIFVFMLSLIFCCYFISKLRNQAQSERYGYKEVVLKGDAKKLQLYGQTCAVCLEDFKGKDELGVLPCQHAFHRKCLVKWLEVRCVCPMCNKPIASPSEATQNIGILLDELV"
misc_feature 523..585
/gene="RNF122"
/note="propagated from UniProtKB/Swiss-Prot (Q9H9V4.2);
transmembrane region"
misc_feature 676..816
/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(682..684,691..693,736..738,742..744,751..753,
760..762,793..795,802..804)
/gene="RNF122"
/note="Zn binding site [ion binding]; other site"
/db_xref="CDD:438338"
variation 406
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810631186"
variation 407
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1314170756"
variation 408
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1447040765"
variation 409
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:898255137"
variation 411
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1378733657"
variation 412
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1328883264"
variation 414
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:746962930"
variation 417
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:779988456"
variation 418
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810630676"
variation 423
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:373548259"
variation 424
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:200835272"
variation 425
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1456877367"
variation 429
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:749460188"
exon 431..587
/gene="RNF122"
/inference="alignment:Splign:2.1.0"
variation 431
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1402439692"
variation 432
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1799650336"
variation 442
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1338873611"
variation 443
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745685003"
variation 448
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415246669"
variation 449
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1404530136"
variation 451
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1171047073"
variation 452
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1469314860"
variation 453
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1402936608"
variation 454
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:778092147"
variation 455
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:756336836"
variation 458
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:748357167"
variation 462
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1478792342"
variation 467
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1240130576"
variation 476
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:781326193"
variation 477
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:755028263"
variation 479
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810494274"
variation 481
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:929125683"
variation 482
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:751997578"
variation 483
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:111889159"
variation 484
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201419677"
variation 488
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:984112683"
variation 494
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:372043460"
variation 495
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277263596"
variation 498
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:3735951"
variation 499
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:75557466"
variation 500
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1290866282"
variation 501
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:765564449"
variation 506
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:866871197"
variation 507
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:377115228"
variation 508
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:146246424"
variation 511
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:201319122"
variation 514
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1332392799"
variation 515
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1810493365"
variation 516
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1355781275"
variation 518
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1452396640"
variation 520
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:760103544"
variation 522
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231260955"
variation 523
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:926628460"
variation 526
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:775524296"
variation 530
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471161893"
variation 531
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:3735950"
variation 532
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:759595318"
variation 536
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:902940567"
variation 539
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:774256289"
variation 540
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:770697160"
variation 546
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810492433"
variation 550..551
/gene="RNF122"
/replace=""
/replace="tt"
/db_xref="dbSNP:1810492370"
variation 553
/gene="RNF122"
/replace=""
/replace="a"
/db_xref="dbSNP:1810492328"
variation 553
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128839897"
variation 554
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1021366227"
variation 557
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:748345907"
variation 558
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1181346051"
variation 561
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1460641245"
variation 566
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1238243120"
variation 568..569
/gene="RNF122"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1810492013"
variation 568
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810492057"
variation 569
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:781277434"
variation 576..585
/gene="RNF122"
/replace="c"
/replace="ctattttatc"
/db_xref="dbSNP:1585360334"
variation 578
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1021035689"
variation 584
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810491846"
variation 585
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1272858769"
exon 588..633
/gene="RNF122"
/inference="alignment:Splign:2.1.0"
variation 591
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191341937"
variation 592
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:778248944"
variation 593
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1265239476"
variation 594
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:3735949"
variation 595
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1222433414"
variation 596
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:760602508"
variation 597
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:767120987"
variation 600
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:944300241"
variation 603
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:754541267"
variation 604
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316621739"
variation 605
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:751476229"
variation 609
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:150818390"
variation 613
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187595782"
variation 616
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:762998431"
variation 617
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:267601903"
variation 619
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044770908"
variation 620
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810372423"
variation 621
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:184889708"
variation 622
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:760876481"
variation 623
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451177555"
variation 624
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:775706522"
variation 625
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810372140"
variation 626
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:772070372"
variation 628
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:946228557"
variation 630
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1585356340"
variation 631
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1054030786"
exon 634..675
/gene="RNF122"
/inference="alignment:Splign:2.1.0"
variation 634
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810367108"
variation 636
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1389469080"
variation 637
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:775647291"
variation 640
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428246648"
variation 647
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:141431566"
variation 651
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1183796982"
variation 655
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:759848649"
variation 662
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810366735"
variation 666
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242608260"
variation 669
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810366623"
variation 670
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1585356161"
variation 674
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1319221619"
variation 675
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199283976"
exon 676..758
/gene="RNF122"
/inference="alignment:Splign:2.1.0"
variation 677
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1240469190"
variation 681
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810339378"
variation 684
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:763096507"
variation 685
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:773808716"
variation 686
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:770404193"
variation 687
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1392002976"
variation 688..696
/gene="RNF122"
/replace="gtctg"
/replace="gtctgtctg"
/db_xref="dbSNP:1457579520"
variation 688
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1055023182"
variation 692
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:762450024"
variation 693
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:777132335"
variation 709
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810338886"
variation 711
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:373090081"
variation 713
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:925952170"
variation 720
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128837964"
variation 726
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:148302412"
variation 727
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:115346711"
variation 729
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1212488068"
variation 730
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771445709"
variation 732
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810338436"
variation 734
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:144271550"
variation 735
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:778441882"
variation 736
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810338222"
variation 744
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:143915374"
variation 745
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:753839300"
variation 747
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:777531296"
variation 751
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1205337660"
variation 753
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:2128837946"
variation 754
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:917531496"
variation 755
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:755948110"
variation 756
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1270561628"
exon 759..1872
/gene="RNF122"
/inference="alignment:Splign:2.1.0"
variation 759
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761131128"
variation 761
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:574382545"
variation 763
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1192003202"
variation 766
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307761697"
variation 768
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:372733449"
variation 771
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:138443534"
variation 775
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:954422456"
variation 777
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810328542"
variation 785
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:147098542"
variation 786
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:774004086"
variation 788
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1230304691"
variation 790
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:770361600"
variation 792
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273558292"
variation 796
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1274271909"
variation 799
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1030624533"
variation 805
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1216865663"
variation 808
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810327802"
variation 812
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1337829210"
variation 813
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1270039445"
variation 814
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:748826742"
variation 816..817
/gene="RNF122"
/replace=""
/replace="a"
/db_xref="dbSNP:1385178766"
variation 822
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772648276"
variation 823..825
/gene="RNF122"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1009495800"
variation 827
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810327387"
variation 831
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451945660"
variation 832
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810327291"
variation 833
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769741086"
variation 836
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:374015683"
variation 837
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:781028541"
variation 838
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:754837343"
variation 840
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1032174469"
variation 844
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:746024052"
variation 845
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:191195067"
variation 846
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810326805"
variation 849
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386652559"
variation 853
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:867483600"
variation 854
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:757367341"
variation 855
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810326587"
variation 856
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:534605036"
variation 863
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:764116179"
variation 864
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:370863263"
variation 869
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:570071398"
variation 872
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753198887"
variation 876
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201892068"
variation 877
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284112265"
variation 881
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:536719453"
variation 882
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:186427620"
variation 886
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762635625"
variation 887
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:199638006"
variation 889
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1281407641"
variation 890
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:529550015"
variation 891
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810325759"
variation 894
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1247224353"
variation 895
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:761753833"
variation 896
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1179494356"
variation 899
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:899462737"
variation 903
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:776440869"
variation 905
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1425013339"
variation 906
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367253173"
variation 907
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810325365"
variation 908
/gene="RNF122"
/replace=""
/replace="c"
/db_xref="dbSNP:775944008"
variation 911
/gene="RNF122"
/replace="g"
/replace="gg"
/db_xref="dbSNP:770316527"
variation 912..913
/gene="RNF122"
/replace="c"
/replace="cc"
/db_xref="dbSNP:745334318"
variation 916
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:562270803"
variation 917
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1216581922"
variation 918
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1178361895"
variation 919
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810324953"
variation 920
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:768533446"
variation 922
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1232760812"
variation 924
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:746826629"
variation 926
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:139140077"
variation 929
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339985495"
variation 933
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810324623"
variation 940
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1563367291"
variation 942
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:775461036"
variation 944
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810324484"
variation 946
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:150227192"
variation 947
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1253431848"
variation 958
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:545523708"
variation 959
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810324312"
variation 962
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810324265"
variation 963
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:769508303"
variation 964
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810324162"
variation 968..972
/gene="RNF122"
/replace="ga"
/replace="gacga"
/db_xref="dbSNP:1810324009"
variation 970
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:908333473"
variation 971
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:759278666"
variation 975
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:973531310"
variation 977
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810323911"
variation 978
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:982564371"
variation 982
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172548601"
variation 990
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:942217461"
variation 993
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810323565"
variation 994
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:776193930"
variation 995
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1416725836"
variation 998
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:778213224"
variation 999
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:917097761"
variation 1002
/gene="RNF122"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1810323128"
variation 1006
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128837772"
variation 1007
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810323075"
variation 1009
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:2128837771"
variation 1016
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1244883306"
variation 1018
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:564298303"
variation 1019
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810322926"
variation 1020
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1380572676"
variation 1022
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1279842549"
variation 1023
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:546210261"
variation 1032
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1326855688"
variation 1044
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:575635538"
variation 1046
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:78623242"
variation 1047
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1254206830"
variation 1051
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1338608637"
variation 1052
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128837766"
variation 1053
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810322461"
variation 1056
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:563847242"
variation 1069
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:991389797"
variation 1071
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1487097693"
variation 1072
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1195464487"
variation 1073
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1264265272"
variation 1074
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810322156"
variation 1085
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429514747"
variation 1086
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810322072"
variation 1089
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810322026"
variation 1091
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810321971"
variation 1093
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810321924"
variation 1094
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810321882"
variation 1100
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:78523626"
variation 1103
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810321772"
variation 1104
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:574244724"
variation 1107
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1286567251"
variation 1109
/gene="RNF122"
/replace=""
/replace="c"
/db_xref="dbSNP:1810321635"
variation 1110
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810321597"
variation 1111
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1436586439"
variation 1112
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810321520"
variation 1117
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810321468"
variation 1119
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:770417238"
variation 1123
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810321350"
variation 1124
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1418072156"
variation 1125
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:2128837749"
variation 1129
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:552756699"
variation 1132
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810321214"
variation 1134
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1585354672"
variation 1135
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810321120"
variation 1137
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810321075"
variation 1138
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:2128837745"
variation 1143
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1362346514"
variation 1148
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810320956"
variation 1149
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386025785"
variation 1152..1154
/gene="RNF122"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1032289134"
variation 1156
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810320809"
variation 1158
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810320762"
variation 1162
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1363954575"
variation 1163
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235005993"
variation 1164
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810320566"
variation 1165
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1033014834"
variation 1167
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:905044684"
variation 1171
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1218290726"
variation 1176
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810320418"
variation 1179
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1023014277"
variation 1180
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1443150150"
variation 1186
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1486365602"
variation 1187
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:534567871"
variation 1190
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1209623818"
variation 1198
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265789629"
variation 1199
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128837736"
variation 1202
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1387692523"
variation 1206
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:979207409"
variation 1207
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1585354629"
variation 1208
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1455954412"
variation 1213
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810319956"
variation 1214
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:967442964"
variation 1215
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1449354285"
variation 1216
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1161487486"
variation 1218
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810319745"
variation 1222
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810319688"
variation 1225
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810319643"
variation 1227
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1346022708"
variation 1229
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1020404729"
variation 1235
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1291561360"
variation 1240
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1810319389"
variation 1244
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1057128048"
variation 1245
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:747521864"
variation 1248
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:954832439"
variation 1253
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330627961"
variation 1257
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:929328919"
variation 1258
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:368203935"
variation 1259
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810319049"
variation 1267
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810319015"
variation 1270
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:558245136"
variation 1271
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1320737531"
variation 1272
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:71512677"
variation 1273
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:2128837714"
variation 1274..1289
/gene="RNF122"
/replace="acaaccttccctcccc"
/replace="acaaccttccctccccacaaccttccctcccc"
/db_xref="dbSNP:1585354564"
variation 1274
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1221543408"
variation 1275
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1222621027"
variation 1277
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:140283198"
variation 1278
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:996403395"
variation 1279
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1470140989"
variation 1283
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1214817001"
variation 1286..1289
/gene="RNF122"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1810318414"
variation 1287
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810318516"
variation 1289
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1238122007"
variation 1290..1291
/gene="RNF122"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:2128837708"
variation 1293
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:529978164"
variation 1294
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810318311"
variation 1295
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1456453871"
variation 1296
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810318240"
variation 1298
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:867219030"
variation 1303
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:899451633"
variation 1304
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:569640266"
variation 1314
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163003199"
variation 1320..1331
/gene="RNF122"
/replace="ggaaggaaggaa"
/replace="ggaaggaaggaaggaa"
/db_xref="dbSNP:1810317928"
variation 1324
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419714590"
variation 1332
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1325728352"
variation 1334
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810317834"
variation 1336
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1038031560"
variation 1344
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810317767"
variation 1346
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128837700"
variation 1347..1350
/gene="RNF122"
/replace="gc"
/replace="gcgc"
/db_xref="dbSNP:1444375489"
variation 1348
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:576930981"
variation 1349
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:986295956"
variation 1353
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1292831009"
variation 1356
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:886838183"
variation 1357
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:923037559"
variation 1363
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046774895"
variation 1364
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:554603743"
variation 1366..1368
/gene="RNF122"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1810317268"
variation 1368
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:949814966"
variation 1370
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1306261642"
variation 1373
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1207307798"
variation 1374
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:956584977"
variation 1376
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810317031"
variation 1378
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:917043712"
variation 1385..1387
/gene="RNF122"
/replace="a"
/replace="aga"
/db_xref="dbSNP:1810316889"
variation 1386
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1032237125"
variation 1392
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:979345947"
variation 1393
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810316859"
variation 1396
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810316821"
variation 1397
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1810316780"
variation 1399
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1475375851"
variation 1401
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810316671"
variation 1402
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056073738"
variation 1405
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128837680"
variation 1408
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:536362653"
variation 1410
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1023463555"
variation 1414
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810316394"
variation 1415
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810316354"
variation 1416
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810316313"
variation 1417
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810316270"
variation 1423
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:937268922"
variation 1424
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423178959"
variation 1429
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:181768653"
variation 1432
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810316070"
variation 1433
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:2128837674"
variation 1436
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810316022"
variation 1438
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:758914485"
variation 1439
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1461930757"
variation 1442
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:547236738"
variation 1449
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:528775770"
variation 1450
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:3735948"
variation 1451
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1036198684"
variation 1453
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:114804489"
variation 1454
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:779252145"
variation 1455
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:530983401"
variation 1457
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810315348"
variation 1458
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810315306"
variation 1461
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810315266"
variation 1462
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274355365"
variation 1463
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429181557"
variation 1465
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810315147"
variation 1466
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810315112"
variation 1467
/gene="RNF122"
/replace=""
/replace="a"
/db_xref="dbSNP:1810315070"
variation 1467
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:897835525"
variation 1469
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810314960"
variation 1470
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810314911"
variation 1472..1473
/gene="RNF122"
/replace=""
/replace="aa"
/db_xref="dbSNP:1810314824"
variation 1472
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810314866"
variation 1473..1478
/gene="RNF122"
/replace="agag"
/replace="agagag"
/replace="agagagag"
/db_xref="dbSNP:1486114412"
variation 1476
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1282648366"
variation 1479
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:151187022"
variation 1480
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:534619590"
variation 1482
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016949899"
variation 1484..1485
/gene="RNF122"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1476288680"
variation 1485
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810314462"
variation 1486
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810314431"
variation 1488
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424386605"
variation 1492
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810314329"
variation 1493
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:2128837660"
variation 1495
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810314283"
variation 1496
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810314247"
variation 1500
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1430880296"
variation 1502
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1005107988"
variation 1503
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:886744845"
variation 1505
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810314092"
variation 1506
/gene="RNF122"
/replace=""
/replace="g"
/db_xref="dbSNP:1810314063"
variation 1506
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1375580294"
variation 1509
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:541877847"
variation 1513
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:889406556"
variation 1516
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1197496824"
variation 1518
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:189877271"
variation 1520
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810313791"
variation 1537
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1293697598"
variation 1538
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1433344061"
variation 1539
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:559090739"
variation 1540
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:2128837651"
variation 1545
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810313498"
variation 1546
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810313413"
variation 1557..1600
/gene="RNF122"
/replace="tt"
/replace="ttgaggtttgtgggcccctctagaggagggctagttctatactt"
/db_xref="dbSNP:1810312845"
variation 1557
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046721678"
variation 1567
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:114355002"
variation 1574
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1232816872"
variation 1580
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:577047481"
variation 1581..1582
/gene="RNF122"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1810313200"
variation 1583
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2128837644"
variation 1587..1595
/gene="RNF122"
/replace="cta"
/replace="ctagttcta"
/db_xref="dbSNP:934973256"
variation 1589
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:923015716"
variation 1590
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810313107"
variation 1591
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810313059"
variation 1593
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:2128837643"
variation 1595
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1052631865"
variation 1598
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:2128837640"
variation 1599
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:895591763"
variation 1602
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1216237837"
variation 1603
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1055620955"
variation 1604
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:937195781"
variation 1606
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810312690"
variation 1607
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1810312645"
variation 1608
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810312612"
variation 1610
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:759286177"
variation 1612
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810312512"
variation 1613
/gene="RNF122"
/replace=""
/replace="a"
/db_xref="dbSNP:1810312468"
variation 1613
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1249531350"
variation 1614..1617
/gene="RNF122"
/replace="ggg"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1409713774"
variation 1614
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:925827533"
variation 1616
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1229039844"
variation 1617..1618
/gene="RNF122"
/replace=""
/replace="gtt"
/db_xref="dbSNP:1810312168"
variation 1617
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:868437879"
variation 1618..1619
/gene="RNF122"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1402745924"
variation 1618
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1156400090"
variation 1619..1625
/gene="RNF122"
/replace=""
/replace="ctttttt"
/db_xref="dbSNP:1439301784"
variation 1619..1620
/gene="RNF122"
/replace=""
/replace="ct"
/db_xref="dbSNP:1810311999"
variation 1619..1620
/gene="RNF122"
/replace=""
/replace="ct"
/db_xref="dbSNP:1585354336"
variation 1619
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:867878085"
variation 1620..1645
/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 1620..1621
/gene="RNF122"
/replace=""
/replace="c"
/replace="g"
/db_xref="dbSNP:2128837620"
variation 1620
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810311892"
variation 1620
/gene="RNF122"
/replace="t"
/replace="tgttttttttt"
/db_xref="dbSNP:1810311924"
variation 1621
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810311845"
variation 1623
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810311818"
variation 1624..1625
/gene="RNF122"
/replace=""
/replace="c"
/db_xref="dbSNP:1349714991"
variation 1625
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810311707"
variation 1629
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810311674"
variation 1638..1639
/gene="RNF122"
/replace=""
/replace="c"
/db_xref="dbSNP:1328553890"
variation 1639
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810311587"
variation 1640..1646
/gene="RNF122"
/replace=""
/replace="ttttttg"
/db_xref="dbSNP:1810310834"
variation 1641..1648
/gene="RNF122"
/replace="t"
/replace="tttttgat"
/db_xref="dbSNP:1810310224"
variation 1641
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1043337853"
variation 1643..1646
/gene="RNF122"
/replace=""
/replace="tttg"
/db_xref="dbSNP:1810310790"
variation 1644..1646
/gene="RNF122"
/replace=""
/replace="ttg"
/db_xref="dbSNP:1317210658"
variation 1645..1648
/gene="RNF122"
/replace="t"
/replace="tgat"
/db_xref="dbSNP:1810310184"
variation 1645..1646
/gene="RNF122"
/replace=""
/replace="tg"
/replace="tga"
/replace="ttg"
/db_xref="dbSNP:1810310874"
variation 1645..1646
/gene="RNF122"
/replace=""
/replace="tg"
/db_xref="dbSNP:1810310663"
variation 1645
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1346937738"
variation 1646..1649
/gene="RNF122"
/replace=""
/replace="gatc"
/db_xref="dbSNP:374520435"
variation 1646..1647
/gene="RNF122"
/replace=""
/replace="t"
/replace="tt"
/db_xref="dbSNP:1491279506"
variation 1646..1647
/gene="RNF122"
/replace=""
/replace="ga"
/db_xref="dbSNP:1491578426"
variation 1646
/gene="RNF122"
/replace=""
/replace="g"
/db_xref="dbSNP:1810310627"
variation 1646
/gene="RNF122"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1554531516"
variation 1646
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1193613836"
variation 1647
/gene="RNF122"
/replace=""
/replace="a"
/db_xref="dbSNP:1810310364"
variation 1647
/gene="RNF122"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1810310323"
variation 1647
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252010924"
variation 1648
/gene="RNF122"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1810310146"
variation 1649..1650
/gene="RNF122"
/replace=""
/replace="t"
/db_xref="dbSNP:1810309983"
variation 1649
/gene="RNF122"
/replace=""
/replace="c"
/db_xref="dbSNP:1810310073"
variation 1649
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1186338413"
variation 1650
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810309930"
variation 1653
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810309888"
variation 1655
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810309860"
variation 1656
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:74630292"
variation 1657
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810309746"
variation 1658
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1474392550"
variation 1659
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:2128837596"
variation 1660
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:2128837594"
variation 1662
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1419100305"
variation 1663
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1461898850"
variation 1665
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1166702038"
variation 1666
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:2128837592"
variation 1670
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810309541"
variation 1671
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1395035700"
variation 1672
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1410620470"
variation 1675
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:2128837589"
variation 1677
/gene="RNF122"
/replace="a"
/replace="t"
/db_xref="dbSNP:1333682953"
variation 1678
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1170124920"
variation 1679
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416920086"
variation 1681..1682
/gene="RNF122"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1810309269"
variation 1693
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810309222"
variation 1694
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1585354271"
variation 1695
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:924946326"
variation 1698
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810309117"
variation 1699
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:945955516"
variation 1703
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:2128837584"
variation 1712
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:979123721"
variation 1713
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:913196344"
variation 1717
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:987507650"
variation 1723
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1585354256"
variation 1726
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1810308848"
variation 1729
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1225100095"
variation 1732
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1253027980"
variation 1733
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810308760"
variation 1735
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:377093527"
variation 1736
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:559692491"
variation 1738..1739
/gene="RNF122"
/replace=""
/replace="a"
/db_xref="dbSNP:1810308577"
variation 1738
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1269865680"
variation 1742
/gene="RNF122"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1199381962"
variation 1744
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:954769080"
variation 1748
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258614705"
variation 1753
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:780174103"
variation 1755
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:143143677"
variation 1756
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:372536535"
variation 1757..1759
/gene="RNF122"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1373761768"
variation 1757
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1016444141"
variation 1759
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:536325525"
variation 1760
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810307816"
variation 1761
/gene="RNF122"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1810307782"
variation 1766
/gene="RNF122"
/replace=""
/replace="g"
/db_xref="dbSNP:1810307746"
variation 1766
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:35048552"
variation 1774..1778
/gene="RNF122"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1563366978"
variation 1775
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1339943854"
variation 1776
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1436785490"
variation 1780
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:983632364"
variation 1784
/gene="RNF122"
/replace=""
/replace="a"
/db_xref="dbSNP:1810307513"
variation 1785
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035741649"
variation 1786
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810307416"
variation 1790
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810307369"
variation 1792..1793
/gene="RNF122"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1383907306"
variation 1796
/gene="RNF122"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810307289"
variation 1798
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:951009152"
variation 1800
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1455060429"
variation 1802
/gene="RNF122"
/replace="c"
/replace="g"
/db_xref="dbSNP:1810307153"
variation 1806..1808
/gene="RNF122"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1283506474"
variation 1807
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:112905687"
variation 1812
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326949410"
variation 1816
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:962135739"
variation 1817
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810306869"
variation 1827
/gene="RNF122"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1211104850"
variation 1827
/gene="RNF122"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1300593587"
variation 1828
/gene="RNF122"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1013906649"
variation 1829
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:28666638"
variation 1835
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810306579"
regulatory 1842..1847
/regulatory_class="polyA_signal_sequence"
/gene="RNF122"
/note="hexamer: AATAAA"
variation 1850
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810306549"
variation 1852
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810306511"
variation 1854
/gene="RNF122"
/replace="a"
/replace="g"
/db_xref="dbSNP:1810306460"
variation 1856
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:889354066"
variation 1857..1858
/gene="RNF122"
/replace=""
/replace="aa"
/db_xref="dbSNP:1810306350"
variation 1863
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176955021"
variation 1864
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810306227"
variation 1865
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1810306181"
variation 1869
/gene="RNF122"
/replace="a"
/replace="c"
/db_xref="dbSNP:1585354156"
variation 1870
/gene="RNF122"
/replace="c"
/replace="t"
/db_xref="dbSNP:1392499435"
polyA_site 1872
/gene="RNF122"
/note="major polyA site"
variation 1872
/gene="RNF122"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1810306009"
ORIGIN
gtcagtttcggaaccccagccagctcacctctgcgccgctgaacccgatccgagcctccggcaaaggtttttccctcctcccccggccgagggcttctgcagcccgggcacccccgccccgcggcgccccacattcccccagcccggggcccttggcgcgtgcgctccgtgcggctgtgctccgcgggactttgtttgtttcctcctcgtccctctttgttgggctgaacaccagcctcgtcaaagccccccactccggagggagttcggcttctccagcagggcggctgcagcgcgctgccccgaccccgcctgcggcccctcacgccgctagtgctcccaccccgccctcctggcaccccgcctgcgtccgttcgcccgaggaagccaaccgcgacttcattgatgcacccattccagtggtgtaacgggtgtttctgtggcctgggactggttagcaccaacaagtcctgctcgatgccacccatcagtttccaggaccttccgctcaacatctatatggtcatcttcggcacaggcatctttgtcttcatgctcagccttatcttctgctgctattttatcagcaaactgcggaaccaggcacagagtgagcgatacggatataaggaggtggtgcttaaaggtgatgccaagaagttacaattatatgggcagacctgcgcagtctgtctggaagacttcaaggggaaggatgagttaggcgtgctcccgtgccaacacgcctttcaccgcaagtgtctggtgaaatggctggaagttcgctgtgtctgccccatgtgtaacaagcccattgctagtccctcagaggccacgcagaacattgggattctattggatgagctggtgtgagtgctgccgctacaccgagacctggagaagacctcttgcctcatggatgtctggtccctctgcacagctccaaccaacaggactgtagggtgatgacgatcactttcccagtgatgagaagggtggtctaggactgggcttctaccctcagtgcaagaccagtgccagatgtgcccccacttcctgcctcctgaagccttcttccctgctactccatgctggtggcctcacccatcaagaccactgtctcctggtactggactatctacctgccttgtccctgttctgggggaaggtgtccaccccgatcaagaacatggagaaagtcctctttcaaggctcccattaggaggatgagctgccttgacccagaagggatgagacgggctcttacctctctacaaccttccctccccttcccactccttccggagtaaggttagaagggaaggaaggaaagatcaaggaaccaagcgcctccacgggaggcgagggaggctctgtatgaaacagaagagcagggacataaaggaaaatgtcagtgtttacatgggacctatggaaacaaaggctggcgggcgccagctgactccagagtaagagagggcccttcccctgccaggacccacggtgctatccattcagtctcttcctcagttaatctcggagcttcctattccatgttgaggtttgtgggcccctctagaggagggctagttctatacttaaattgattcccaggggccttttttttttttttttttttttttttgatcaaaaggggtgtggggatgggggtgtctacggttaagcaacagatacctccttccctttgtaaatagtatttttatacttcatcctcgcctctcaggctttagatacgaaatctccagaatggaagggggtggggattttctgttcctccctggagtgggtgagggtgggagaaagttacatatttaaagaaaaataaatttaataacaagtttctctaaccta
//
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.
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