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Previous release (v1)
2024-05-03 03:04:08, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_160934 1374 bp RNA linear PRI 02-OCT-2023
DEFINITION Homo sapiens arginase 1 (ARG1), transcript variant 4, non-coding
RNA.
ACCESSION NR_160934
VERSION NR_160934.1
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 1374)
AUTHORS Li Q, Wang Y, Shi L, Wang Q, Yang G, Deng L, Tian Y, Hua X and Yuan
X.
TITLE Arginase-1 promotes lens epithelial-to-mesenchymal transition in
different models of anterior subcapsular cataract
JOURNAL Cell Commun Signal 21 (1), 236 (2023)
PUBMED 37723490
REMARK GeneRIF: Arginase-1 promotes lens epithelial-to-mesenchymal
transition in different models of anterior subcapsular cataract.
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 1374)
AUTHORS Bonometti A, Borsani O, Rumi E, Ferretti VV, Dioli C, Lucato E,
Paulli M and Boveri E.
TITLE Arginase-1+ bone marrow myeloid cells are reduced in
myeloproliferative neoplasms and correlate with clinical phenotype,
fibrosis, and molecular driver
JOURNAL Cancer Med 12 (7), 7815-7822 (2023)
PUBMED 36524315
REMARK GeneRIF: Arginase-1+ bone marrow myeloid cells are reduced in
myeloproliferative neoplasms and correlate with clinical phenotype,
fibrosis, and molecular driver.
REFERENCE 3 (bases 1 to 1374)
AUTHORS Menjivar RE, Nwosu ZC, Du W, Donahue KL, Hong HS, Espinoza C, Brown
K, Velez-Delgado A, Yan W, Lima F, Bischoff A, Kadiyala P,
Salas-Escabillas D, Crawford HC, Bednar F, Carpenter E, Zhang Y,
Halbrook CJ, Lyssiotis CA and Pasca di Magliano M.
TITLE Arginase 1 is a key driver of immune suppression in pancreatic
cancer
JOURNAL Elife 12, e80721 (2023)
PUBMED 36727849
REMARK GeneRIF: Arginase 1 is a key driver of immune suppression in
pancreatic cancer.
Publication Status: Online-Only
REFERENCE 4 (bases 1 to 1374)
AUTHORS Tyrinova TV, Batorov EV, Aristova TA, Ushakova GY, Sizikova SA,
Denisova VV, Ostanin AA and Chernykh ER.
TITLE Expression of Inhibitory Molecules (Arginase-1, IDO, and PD-L1) by
Myeloid-Derived Suppressor Cells in Multiple Myeloma Patients in
Remission
JOURNAL Bull Exp Biol Med 174 (1), 71-75 (2022)
PUBMED 36437327
REMARK GeneRIF: Expression of Inhibitory Molecules (Arginase-1, IDO, and
PD-L1) by Myeloid-Derived Suppressor Cells in Multiple Myeloma
Patients in Remission.
REFERENCE 5 (bases 1 to 1374)
AUTHORS Ah Mew,N., Simpson,K.L., Gropman,A.L., Lanpher,B.C., Chapman,K.A.
and Summar,M.L.
TITLE Urea Cycle Disorders Overview
JOURNAL (in) Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW
and Amemiya A (Eds.);
GENEREVIEWS(R);
(1993)
PUBMED 20301396
REFERENCE 6 (bases 1 to 1374)
AUTHORS Sun,A., Crombez,E.A. and Wong,D.
TITLE Arginase Deficiency
JOURNAL (in) Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW
and Amemiya A (Eds.);
GENEREVIEWS(R);
(1993)
PUBMED 20301338
REFERENCE 7 (bases 1 to 1374)
AUTHORS Uchino T, Haraguchi Y, Aparicio JM, Mizutani N, Higashikawa M,
Naitoh H, Mori M and Matsuda I.
TITLE Three novel mutations in the liver-type arginase gene in three
unrelated Japanese patients with argininemia
JOURNAL Am J Hum Genet 51 (6), 1406-1412 (1992)
PUBMED 1463019
REFERENCE 8 (bases 1 to 1374)
AUTHORS Grody WW, Klein D, Dodson AE, Kern RM, Wissmann PB, Goodman BK,
Bassand P, Marescau B, Kang SS, Leonard JV et al.
TITLE Molecular genetic study of human arginase deficiency
JOURNAL Am J Hum Genet 50 (6), 1281-1290 (1992)
PUBMED 1598908
REFERENCE 9 (bases 1 to 1374)
AUTHORS Ikemoto M, Tabata M, Miyake T, Kono T, Mori M, Totani M and Murachi
T.
TITLE Expression of human liver arginase in Escherichia coli.
Purification and properties of the product
JOURNAL Biochem J 270 (3), 697-703 (1990)
PUBMED 2241902
REFERENCE 10 (bases 1 to 1374)
AUTHORS Haraguchi Y, Aparicio JM, Takiguchi M, Akaboshi I, Yoshino M, Mori
M and Matsuda I.
TITLE Molecular basis of argininemia. Identification of two discrete
frame-shift deletions in the liver-type arginase gene
JOURNAL J Clin Invest 86 (1), 347-350 (1990)
PUBMED 2365823
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AL121575.24.
Summary: Arginase catalyzes the hydrolysis of arginine to ornithine
and urea. At least two isoforms of mammalian arginase exist (types
I and II) which differ in their tissue distribution, subcellular
localization, immunologic crossreactivity and physiologic function.
The type I isoform encoded by this gene, is a cytosolic enzyme and
expressed predominantly in the liver as a component of the urea
cycle. Inherited deficiency of this enzyme results in argininemia,
an autosomal recessive disorder characterized by hyperammonemia.
Two transcript variants encoding different isoforms have been found
for this gene. [provided by RefSeq, Sep 2011].
Sequence Note: The RefSeq transcript was derived from the reference
genome assembly. The genomic coordinates were determined from
alignments.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: SRR5189664.106656.1,
SRR5189664.109866.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA2145122, SAMEA2145893
[ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-114 AL121575.24 73531-73644
115-289 AL121575.24 79416-79590
290-449 AL121575.24 81524-81683
450-544 AL121575.24 82926-83020
545-649 AL121575.24 83365-83469
650-786 AL121575.24 83660-83796
787-1374 AL121575.24 84047-84634
FEATURES Location/Qualifiers
source 1..1374
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="6"
/map="6q23.2"
gene 1..1374
/gene="ARG1"
/note="arginase 1"
/db_xref="GeneID:383"
/db_xref="HGNC:HGNC:663"
/db_xref="MIM:608313"
misc_RNA 1..1374
/gene="ARG1"
/product="arginase 1, transcript variant 4"
/db_xref="GeneID:383"
/db_xref="HGNC:HGNC:663"
/db_xref="MIM:608313"
exon 1..114
/gene="ARG1"
/inference="alignment:Splign:2.1.0"
variation 3
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:865842223"
variation 5
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:976317468"
variation 8
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773464123"
variation 11
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:776217305"
variation 15
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:761516831"
variation 18
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1773464293"
variation 20
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1562351309"
variation 21
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:766705948"
variation 22
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419548929"
variation 23
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1411205906"
variation 24
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1773464654"
variation 25
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:751924194"
variation 27
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:755511669"
variation 32
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:767964945"
variation 34
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:752788818"
variation 35
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114507179"
variation 37
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:370747314"
variation 38
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:777817531"
variation 44
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1270717261"
variation 50
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:987130050"
variation 52
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:749521049"
variation 54
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:757468683"
variation 55
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1257656358"
variation 56
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1335795532"
variation 57
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:778602133"
misc_feature 58..126
/gene="ARG1"
/inference="COORDINATES:
alignment:Blast2seq::RefSeq|NM_001244438.2"
/note="primary ORF has stop codon >50 nucleotides from the
terminal splice site; nonsense-mediated decay (NMD)
candidate"
variation 59
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1554249332"
variation 60
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:745624953"
variation 62
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451420493"
variation 63
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138584410"
variation 64
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:558377642"
variation 70
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:768343568"
variation 72
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1585391128"
variation 73
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1190948767"
variation 75
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1773466397"
variation 76
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:989204710"
variation 77
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422307581"
variation 78
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773466629"
variation 79
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:776185609"
variation 80
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:149310631"
variation 81
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:774603245"
variation 82
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208775075"
variation 86..87
/gene="ARG1"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1773467460"
variation 86
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1404599890"
variation 89
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:28941474"
variation 92
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:147419581"
variation 95
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1264271302"
variation 97
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1398211516"
variation 99
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:939256919"
variation 103
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1773467987"
variation 105..107
/gene="ARG1"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2114507395"
variation 105
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1585391263"
variation 108
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:753260969"
variation 110
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356179382"
variation 111
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1335826272"
variation 113
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:761148101"
variation 114
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150766204"
exon 115..289
/gene="ARG1"
/inference="alignment:Splign:2.1.0"
variation 115
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1299429729"
variation 119
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372415368"
variation 120
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773782658"
variation 121
/gene="ARG1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1486740324"
variation 122
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1260906835"
variation 123
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773783050"
variation 126
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1773783170"
variation 128
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375655714"
variation 131
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773783430"
variation 134
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1415873396"
variation 135
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232128891"
variation 137
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1320772127"
variation 138
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1773784046"
variation 141
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:188888028"
variation 143
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:535161157"
variation 144
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:752395217"
variation 145
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242421631"
variation 154
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147146526"
variation 155
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486118722"
variation 160
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:763960889"
variation 161..164
/gene="ARG1"
/replace="t"
/replace="taat"
/db_xref="dbSNP:1773785398"
variation 161
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:753347547"
variation 164
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1488015922"
variation 165
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773785683"
variation 167
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114530488"
variation 169
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:111640755"
variation 171..173
/gene="ARG1"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1562356664"
variation 171
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756825623"
variation 173
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2114530548"
variation 176
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773786267"
variation 180
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:778376916"
variation 182
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114530584"
variation 184
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1562356680"
variation 190
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1422422629"
variation 191
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1554250510"
variation 194
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:745580041"
variation 195
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:956942732"
variation 196
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757959356"
variation 200
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:748414362"
variation 202
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:867223787"
variation 208
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1289634469"
variation 211
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773787835"
variation 214
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1296916689"
variation 215
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369393679"
variation 216
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:547122192"
variation 218
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:571619062"
variation 221
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:148619575"
variation 225
/gene="ARG1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:142107090"
variation 226
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256715205"
variation 227
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773789074"
variation 229
/gene="ARG1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:774273532"
variation 234
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1459752618"
variation 235
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1311659158"
variation 237
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1022874044"
variation 239
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114530857"
variation 240
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1063493"
variation 241
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773789976"
variation 246..250
/gene="ARG1"
/replace="a"
/replace="aagaa"
/db_xref="dbSNP:1773790103"
variation 247
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242167030"
variation 249
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2114530900"
variation 250
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:759832639"
variation 254
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:34504481"
variation 255..256
/gene="ARG1"
/replace="g"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:796051923"
variation 255
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374676787"
variation 259
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1211764471"
variation 260
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1773791337"
variation 265
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:34724840"
variation 266
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1239300546"
variation 267
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114531019"
variation 268
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2114531029"
variation 273
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:760319794"
variation 275
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114531053"
variation 276..280
/gene="ARG1"
/replace="ggcgg"
/replace="ggcggcgg"
/db_xref="dbSNP:772521719"
variation 276
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1251633225"
variation 278
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:763868954"
variation 279
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:753829097"
variation 281
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2114531110"
variation 285
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1380298803"
variation 287
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1338975137"
exon 290..449
/gene="ARG1"
/inference="alignment:Splign:2.1.0"
variation 291
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1585419602"
variation 292
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:761773853"
variation 293
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:749043086"
variation 296
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:995938048"
variation 297
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:749966465"
variation 298..301
/gene="ARG1"
/replace="atgc"
/replace="ttgg"
/db_xref="dbSNP:2114539256"
variation 298
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762306280"
variation 301
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1441486160"
variation 305
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1290471714"
variation 306
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773905930"
variation 307..311
/gene="ARG1"
/replace="tct"
/replace="tctct"
/db_xref="dbSNP:1276600622"
variation 308..320
/gene="ARG1"
/replace="c"
/replace="ctctggccatgcc"
/db_xref="dbSNP:2114539307"
variation 311
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1365543098"
variation 314..315
/gene="ARG1"
/replace=""
/replace="cc"
/db_xref="dbSNP:1218794954"
variation 314
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296548302"
variation 315
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1320194930"
variation 317
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200458963"
variation 319..327
/gene="ARG1"
/replace=""
/replace="ccagggtcc"
/db_xref="dbSNP:1257775697"
variation 319..320
/gene="ARG1"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1773906992"
variation 320
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1585419820"
variation 323
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773907379"
variation 326
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:751231138"
variation 328
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1773907667"
variation 329..330
/gene="ARG1"
/replace=""
/replace="t"
/db_xref="dbSNP:1224399418"
variation 331
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1773907918"
variation 332
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1245522728"
variation 333
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:754655577"
variation 335
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:754205928"
variation 337
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:757852473"
variation 338
/gene="ARG1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1585419917"
variation 339
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1478575616"
variation 341
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1585419946"
variation 342
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773909219"
variation 344
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:779219793"
variation 346
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:746381302"
variation 347
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1585419999"
variation 349
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:104893947"
variation 350
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114539596"
variation 351
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:780157621"
variation 352
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:913575060"
variation 354
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1773910245"
variation 355
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773910389"
variation 356
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:866733989"
variation 356
/gene="ARG1"
/replace="t"
/replace="tt"
/db_xref="dbSNP:776939220"
variation 360
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:747268449"
variation 362
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114539679"
variation 364
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773910941"
variation 365
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114539712"
variation 366
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298811632"
variation 367
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140549609"
variation 368
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1216971255"
variation 370
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:771165013"
variation 371
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773911699"
variation 372
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1773911841"
variation 374
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:774535167"
variation 376
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:574320679"
variation 377
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:747883555"
variation 381
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:769778089"
variation 386
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1288330812"
variation 388
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1451472748"
variation 390
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:535456448"
variation 391
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:765859028"
variation 392
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:773968554"
variation 395
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:759282838"
variation 397
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:104893943"
variation 400..403
/gene="ARG1"
/replace="actt"
/replace="acttactt"
/db_xref="dbSNP:762633715"
variation 400
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1562359055"
variation 401
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:946323935"
variation 404
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1472997422"
variation 405
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1585420271"
variation 406
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1554250849"
variation 407
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114539979"
variation 408..409
/gene="ARG1"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1585420294"
variation 409
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:767219084"
variation 412
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:754259099"
variation 413
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:757762475"
variation 415
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773915079"
variation 417
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:765617697"
variation 418
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1773915383"
variation 419..421
/gene="ARG1"
/replace="atc"
/replace="atcatc"
/db_xref="dbSNP:1554250852"
variation 431
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:750937576"
variation 434
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398269910"
variation 435
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114540101"
variation 438
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1562359129"
variation 440
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1585420412"
variation 444
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1297815353"
variation 445
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773916416"
variation 446..448
/gene="ARG1"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1773916575"
variation 447
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:927479708"
exon 450..544
/gene="ARG1"
/inference="alignment:Splign:2.1.0"
variation 451
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200319835"
variation 453
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773984847"
variation 455
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:766853875"
variation 456
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:751647696"
variation 457
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114545404"
variation 458
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144403253"
variation 459
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1270108834"
variation 461
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114545447"
variation 462
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:894163186"
variation 465
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1773986191"
variation 466
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201484132"
variation 470
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:752966614"
variation 475..477
/gene="ARG1"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1239789338"
variation 475
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773986769"
variation 476
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146625637"
variation 477
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1773987315"
variation 478
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1437673274"
variation 481
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773987627"
variation 484
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773987980"
variation 485
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1773988131"
variation 487
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1177962638"
variation 488
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773988483"
variation 489
/gene="ARG1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:949681378"
variation 490..494
/gene="ARG1"
/replace="tatct"
/replace="tatctatct"
/db_xref="dbSNP:1773988852"
variation 494
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:756330677"
variation 495
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1773989211"
variation 497
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1171036648"
variation 500
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773989636"
variation 503
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773989815"
variation 504
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:777462361"
variation 505
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:903693189"
variation 506
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370289649"
variation 508
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:770776974"
variation 509
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:779060814"
variation 511
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773991045"
variation 512
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446631328"
variation 514
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302642207"
variation 515
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114545822"
variation 517
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1251635812"
variation 518
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114545840"
variation 521
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201926198"
variation 522
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1773992117"
variation 523
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410564479"
variation 524
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773992475"
variation 525
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1472741630"
variation 527
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:745787043"
variation 528
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:771753283"
variation 530
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773993378"
variation 531..533
/gene="ARG1"
/replace=""
/replace="gac"
/db_xref="dbSNP:2114545947"
variation 531
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1033631011"
variation 532
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1322321449"
variation 533..536
/gene="ARG1"
/replace=""
/replace="ccct"
/db_xref="dbSNP:1562360285"
variation 533
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773993991"
variation 534
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775104877"
variation 535
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1773994839"
variation 537
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768303250"
variation 538
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:536659345"
variation 539
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114546024"
variation 540
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1773995607"
variation 542
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:773465984"
variation 544..547
/gene="ARG1"
/replace="acta"
/replace="actatataataaaaactctgggaattaacta"
/db_xref="dbSNP:1773995902"
variation 544
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114546062"
exon 545..649
/gene="ARG1"
/inference="alignment:Splign:2.1.0"
variation 545
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774017438"
variation 546
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:934942148"
variation 548
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376378819"
variation 550
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:886061061"
variation 553
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1774018016"
variation 559..562
/gene="ARG1"
/replace="ct"
/replace="ctct"
/replace="ctctct"
/db_xref="dbSNP:766868484"
variation 559..561
/gene="ARG1"
/replace="ctc"
/replace="ctcctc"
/db_xref="dbSNP:1554251136"
variation 563
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1774018427"
variation 564
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174556768"
variation 566
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429174075"
variation 567..570
/gene="ARG1"
/replace="atta"
/replace="attatta"
/db_xref="dbSNP:750397270"
variation 567
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:761361984"
variation 568
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:936518459"
variation 570
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1774019249"
variation 572
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1774019394"
variation 573
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:771334658"
variation 574
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1299638170"
variation 575
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114547822"
variation 576..579
/gene="ARG1"
/replace="tttt"
/replace="tttttt"
/db_xref="dbSNP:1337890012"
variation 578
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149496218"
variation 579
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1313116151"
variation 580
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1774020295"
variation 582..585
/gene="ARG1"
/replace="a"
/replace="atga"
/db_xref="dbSNP:1562360814"
variation 582
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:760069095"
variation 586
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482393038"
variation 587..588
/gene="ARG1"
/replace=""
/replace="tg"
/db_xref="dbSNP:2114547911"
variation 587
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:767964970"
variation 590
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1013928443"
variation 596
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:775435820"
variation 598
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2114547946"
variation 599
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114547956"
variation 600
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:896852725"
variation 603
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1218958661"
variation 605
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1028447199"
variation 607
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:993784608"
variation 611
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2114548020"
variation 614
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:760873925"
variation 615
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1280581278"
variation 616
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:764066842"
variation 617
/gene="ARG1"
/replace=""
/replace="g"
/db_xref="dbSNP:1774022406"
variation 619
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258641833"
variation 620
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:891212218"
variation 622..627
/gene="ARG1"
/replace="aagaaa"
/replace="aagaaagaaa"
/db_xref="dbSNP:1554251158"
variation 624
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200496725"
variation 625
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:952443355"
variation 628..633
/gene="ARG1"
/replace="ca"
/replace="cactca"
/db_xref="dbSNP:756080885"
variation 629
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2114548129"
variation 630
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:757518422"
variation 631
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:985150840"
variation 637
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1205047507"
variation 641
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1159865595"
variation 646
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358115389"
variation 647
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1452547824"
variation 648
/gene="ARG1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1303114569"
variation 649
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145177175"
exon 650..786
/gene="ARG1"
/inference="alignment:Splign:2.1.0"
variation 652
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1360594253"
variation 654..657
/gene="ARG1"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1464239857"
variation 657
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:894974293"
variation 662..663
/gene="ARG1"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1774036379"
variation 663
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1400801659"
variation 665
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138705915"
variation 668
/gene="ARG1"
/replace=""
/replace="t"
/db_xref="dbSNP:2114549176"
variation 668
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774036796"
variation 669
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:538034569"
variation 671
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:780770809"
variation 673
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307053782"
variation 674..677
/gene="ARG1"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1554251191"
variation 674
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774037326"
variation 678
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1487873106"
variation 682
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1372696715"
variation 683
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1250527571"
variation 684
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1478297270"
variation 686
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148939143"
variation 687
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:104893948"
variation 688..690
/gene="ARG1"
/replace=""
/replace="gac"
/db_xref="dbSNP:773118188"
variation 692
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1303519696"
variation 693
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:764273304"
variation 696
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:776530369"
variation 698
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274386174"
variation 699
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1259059245"
variation 700
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774039822"
variation 704
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:762145115"
variation 708
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:765495464"
variation 710
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:750244366"
variation 714
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:758338836"
variation 719
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1774040468"
variation 723
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:981570531"
variation 724
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:766077763"
variation 725
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774040997"
variation 726
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:751567681"
variation 728
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:556756212"
variation 729
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:182650447"
variation 730
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:755779260"
variation 733
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:777467993"
variation 735
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114549524"
variation 736
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1301274210"
variation 737
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1585428624"
variation 741
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:756108043"
variation 742
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:748924712"
variation 746
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:777639743"
variation 749..753
/gene="ARG1"
/replace="ag"
/replace="agaag"
/db_xref="dbSNP:1554251236"
variation 750
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2114549604"
variation 753
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:372489226"
variation 754
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:772473981"
variation 758
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:770834693"
variation 761
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:775687110"
variation 764
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114549662"
variation 771
/gene="ARG1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:747579073"
variation 773
/gene="ARG1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:541871489"
variation 776
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1279130152"
variation 778
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774043950"
variation 780
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:776782905"
variation 781
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:761914559"
variation 782
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:111253965"
variation 784
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:773629257"
exon 787..1374
/gene="ARG1"
/inference="alignment:Splign:2.1.0"
variation 788
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:747275658"
variation 789..795
/gene="ARG1"
/replace="ct"
/replace="ctactct"
/db_xref="dbSNP:1562361751"
variation 790
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1700711482"
variation 792..796
/gene="ARG1"
/replace="ctc"
/replace="ctctc"
/db_xref="dbSNP:1585429783"
variation 798..799
/gene="ARG1"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1774059448"
variation 800
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1230505073"
variation 802..807
/gene="ARG1"
/replace="tagata"
/replace="tagatagata"
/db_xref="dbSNP:1562361762"
variation 802
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1288396873"
variation 803
/gene="ARG1"
/replace=""
/replace="a"
/db_xref="dbSNP:2114551021"
variation 804
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774060019"
variation 806
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353394805"
variation 807
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774060317"
variation 808
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:769207030"
variation 809
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:781780752"
variation 811
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395352972"
variation 812
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1165610556"
variation 815
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:748654016"
variation 816
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:770050608"
variation 817
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1190609964"
variation 819
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:773398169"
variation 820
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774061694"
variation 821..823
/gene="ARG1"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2114551140"
variation 822
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172085840"
variation 823
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473029048"
variation 824
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1585429947"
variation 825
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:763302987"
variation 826..828
/gene="ARG1"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1562361837"
variation 827
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:771010341"
variation 828
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423942491"
variation 831
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:774211424"
variation 833
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774062925"
variation 836
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1774063052"
variation 840
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370022660"
variation 841
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190531585"
variation 842..849
/gene="ARG1"
/replace="agaag"
/replace="agaagaag"
/db_xref="dbSNP:1399124034"
variation 842
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114551265"
variation 843
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774063642"
variation 846
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:932875709"
variation 848
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1585430092"
variation 853
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:104893942"
variation 854
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1317961968"
variation 855
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:104893940"
variation 856
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:760574009"
variation 857..858
/gene="ARG1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:771395982"
variation 859
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2114551376"
variation 861
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:763625573"
variation 862
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1585430178"
variation 863
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:532943866"
variation 866
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:756944730"
variation 867
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:778360659"
variation 868
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1332603898"
variation 869
/gene="ARG1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:750083218"
variation 875
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2114551460"
variation 876
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:755359126"
variation 880
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781676090"
variation 882
/gene="ARG1"
/replace="a"
/replace="atgtaatttataaaatagttga"
/db_xref="dbSNP:1774066189"
variation 883..884
/gene="ARG1"
/replace=""
/replace="cc"
/db_xref="dbSNP:1585430273"
variation 883
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774066324"
variation 885
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:748708936"
variation 885
/gene="ARG1"
/replace="t"
/replace="tgtaatttataaaatagt"
/db_xref="dbSNP:1585430285"
variation 887
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114551538"
variation 889
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:770387974"
variation 891
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:148113697"
variation 896
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373480378"
variation 897
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:866970619"
variation 899
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:771190594"
variation 901
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1461329572"
variation 904
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:774505525"
variation 906
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:897222563"
variation 907
/gene="ARG1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:377280518"
variation 908
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:370831108"
variation 909
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373491227"
variation 910
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:775225648"
variation 912
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:760628925"
variation 914
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1585430449"
variation 916
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403109925"
variation 918
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:763958621"
variation 920
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:776119677"
variation 921..922
/gene="ARG1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1554251356"
variation 923
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1774069461"
variation 925
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774069594"
variation 927
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114551786"
variation 928..929
/gene="ARG1"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1420954130"
variation 928
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202219126"
variation 930
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:929906801"
variation 935
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1405840831"
variation 936
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:764788600"
variation 937
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:73544627"
variation 940..946
/gene="ARG1"
/replace="acc"
/replace="acccacc"
/db_xref="dbSNP:1554251368"
variation 940
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147409787"
variation 942
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236330989"
variation 943
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278453710"
variation 946
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1338971763"
variation 947
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114551913"
variation 955
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774071718"
variation 956
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1345200446"
variation 959
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1224996446"
variation 965
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774072137"
variation 966..967
/gene="ARG1"
/replace="c"
/replace="cc"
/db_xref="dbSNP:777029258"
variation 966
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1460741759"
variation 967
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:768028958"
variation 968
/gene="ARG1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1240654191"
variation 970
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:556580014"
variation 971
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302005911"
variation 972
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1039895471"
variation 975
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:778359686"
variation 976
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1003113919"
variation 977
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:749799579"
variation 980
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1479102307"
variation 981
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:757327323"
variation 988
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428993393"
variation 991
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:779017704"
variation 992
/gene="ARG1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746107017"
variation 993..998
/gene="ARG1"
/replace="taatta"
/replace="taattaatta"
/db_xref="dbSNP:1774074616"
variation 993
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1384782370"
variation 1000
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774074760"
variation 1001
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1394888884"
variation 1002
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:998785714"
variation 1006
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774075099"
variation 1008
/gene="ARG1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1020469542"
variation 1015
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1471251940"
variation 1022
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1381185470"
variation 1024
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774075562"
variation 1026..1030
/gene="ARG1"
/replace="agtta"
/replace="agttagtta"
/db_xref="dbSNP:1774075801"
variation 1026
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:886061062"
variation 1027..1029
/gene="ARG1"
/replace="gtt"
/replace="gttgtt"
/db_xref="dbSNP:1774076053"
variation 1027
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774075934"
variation 1033
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774076176"
variation 1035
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193053345"
variation 1038..1040
/gene="ARG1"
/replace="aaa"
/replace="aaaaa"
/db_xref="dbSNP:1031460462"
variation 1043
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1774076591"
variation 1044
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114552326"
variation 1049
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774076708"
variation 1056..1060
/gene="ARG1"
/replace="aaaa"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:1774076854"
variation 1060
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:967511482"
variation 1062
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1000451954"
variation 1063..1067
/gene="ARG1"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1490701827"
variation 1068
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1033260259"
variation 1069
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774077627"
variation 1075
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1803151"
variation 1077
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174907667"
variation 1078
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774078007"
variation 1082..1085
/gene="ARG1"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1774078280"
variation 1082
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1281815681"
variation 1083
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1774078413"
variation 1085
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406817942"
variation 1087
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:958728303"
variation 1089
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774078853"
variation 1091
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1419278786"
variation 1092
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1161780198"
variation 1095
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1279216962"
variation 1097
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2114552516"
variation 1098..1099
/gene="ARG1"
/replace=""
/replace="tt"
/db_xref="dbSNP:1774079535"
variation 1098
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774079388"
variation 1103
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774079660"
variation 1111
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367079499"
variation 1115
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1372612653"
variation 1116
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306266187"
variation 1120
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1437727554"
variation 1126..1131
/gene="ARG1"
/replace="ct"
/replace="ctaact"
/db_xref="dbSNP:1774080314"
variation 1126
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1326381254"
variation 1131..1136
/gene="ARG1"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1562362355"
variation 1137
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316628197"
variation 1140
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402847913"
variation 1141
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1774080821"
variation 1142
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:991492256"
variation 1144..1172
/gene="ARG1"
/replace="aaa"
/replace="aaaagcttatattttctaacttggcaaaa"
/db_xref="dbSNP:1774081067"
variation 1148
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:917342667"
variation 1149
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021313033"
variation 1152
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774081567"
variation 1154
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1475016426"
variation 1155..1158
/gene="ARG1"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1774081931"
variation 1155
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:971523115"
variation 1159..1164
/gene="ARG1"
/replace="ctaact"
/replace="ctaactaact"
/db_xref="dbSNP:1195028170"
variation 1169
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774082229"
variation 1173
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1774082351"
variation 1175..1184
/gene="ARG1"
/replace="ctta"
/replace="cttatcctta"
/db_xref="dbSNP:1774082495"
variation 1176..1177
/gene="ARG1"
/replace=""
/replace="tt"
/db_xref="dbSNP:1774082880"
variation 1176..1177
/gene="ARG1"
/replace="tt"
/replace="tttt"
/db_xref="dbSNP:1774082739"
variation 1176
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1488524612"
variation 1180
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774083001"
variation 1181
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256353263"
variation 1183
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1774083272"
variation 1184..1190
/gene="ARG1"
/replace="aga"
/replace="agaaaga"
/db_xref="dbSNP:1367932520"
variation 1190
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774083531"
variation 1194
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1585431190"
variation 1195
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774083780"
variation 1196
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1585431197"
variation 1200
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:972527136"
variation 1201
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774084136"
variation 1203
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1408114429"
variation 1205
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114552870"
variation 1207
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1585431238"
variation 1208
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:918425492"
variation 1211
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114552890"
variation 1212
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114552900"
variation 1214..1218
/gene="ARG1"
/replace="aaa"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1774084693"
variation 1217
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1585431258"
variation 1218
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:953667116"
variation 1222
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774085109"
variation 1224
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1585431279"
variation 1225
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:568284407"
variation 1231
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1774085475"
variation 1232
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213508983"
variation 1236
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774085715"
variation 1240..1244
/gene="ARG1"
/replace="cac"
/replace="cacac"
/db_xref="dbSNP:1339268659"
variation 1241
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1048340568"
variation 1242
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402223512"
variation 1243..1248
/gene="ARG1"
/replace="acttac"
/replace="acttacttac"
/db_xref="dbSNP:912772679"
variation 1247
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:909797455"
variation 1249
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114553041"
variation 1254
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:944253301"
variation 1255
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1413098328"
variation 1256
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774086545"
variation 1257
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:973308077"
variation 1259
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114553078"
variation 1262
/gene="ARG1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334875942"
variation 1263
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142812031"
variation 1266
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1417275513"
variation 1268
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1774087722"
variation 1277
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114553128"
variation 1279
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1039354514"
variation 1280
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1478024159"
variation 1283
/gene="ARG1"
/replace=""
/replace="t"
/db_xref="dbSNP:1416815139"
variation 1290
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1292418691"
variation 1300
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486424679"
variation 1306
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:554233544"
variation 1308
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:553833088"
variation 1310
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1435629575"
variation 1312
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1271492978"
variation 1313..1324
/gene="ARG1"
/replace=""
/replace="gtactatgtgtc"
/db_xref="dbSNP:1035699012"
variation 1313
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1319225383"
variation 1318
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:572234646"
variation 1319
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1293008170"
variation 1321
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231880386"
variation 1324
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774089744"
variation 1326
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1381580463"
variation 1327
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303695682"
variation 1329
/gene="ARG1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779162184"
variation 1331
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1044356580"
variation 1335..1340
/gene="ARG1"
/replace="aaaaaa"
/replace="aaaaaaa"
/db_xref="dbSNP:2114553332"
variation 1339
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:997958923"
variation 1341
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774090625"
variation 1342
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1774090763"
variation 1344
/gene="ARG1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1585431631"
variation 1345
/gene="ARG1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1466025813"
variation 1346..1351
/gene="ARG1"
/replace="tttttt"
/replace="ttttttt"
/db_xref="dbSNP:1178561779"
variation 1347
/gene="ARG1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1774091198"
variation 1351
/gene="ARG1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1774091319"
variation 1355
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1393674371"
variation 1361..1365
/gene="ARG1"
/replace="t"
/replace="tcttt"
/db_xref="dbSNP:1240820800"
variation 1362
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1585431684"
variation 1363
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774091891"
variation 1365
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774092024"
variation 1367
/gene="ARG1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774092145"
variation 1370
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:537322176"
variation 1371
/gene="ARG1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1774092393"
variation 1373
/gene="ARG1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1041819461"
ORIGIN
gtcactgagggttgactgactggagagctcaagtgcagcaaagagaagtgtcagagcatgagcgccaagtccagaaccatagggattattggagctcctttctcaaagggacagagtgtgatgtgaaggattatggggacctgccctttgctgacatccctaatgacagtccctttcaaattgtgaagaatccaaggtctgtgggaaaagcaagcgagcagctggctggcaaggtggcagaagtcaagaagaacggaagaatcagcctggtgctgggcggagaccacagtttggcaattggaagcatctctggccatgccagggtccaccctgatcttggagtcatctgggtggatgctcacactgatatcaacactccactgacaaccacaagtggaaacttgcatggacaacctgtatctttcctcctgaaggaactaaaaggaaagattcccgatgtgccaggattctcctgggtgactccctgtatatctgccaaggatattgtgtatattggcttgagagacgtggaccctggggaacactacattttgaaaactctaggcattaaatacttttcaatgactgaagtggacagactaggaattggcaaggtgatggaagaaacactcagctatctactaggaagaaagaaaaggccaattcatctaagttttgatgttgacggactggacccatctttcacaccagctactggcacaccagtcgtgggaggtctgacatacagagaaggtctctacatcacagaagaaatctacaaaacagggctactctcaggattagatataatggaagtgaacccatccctggggaagacaccagaagaagtaactcgaacagtgaacacagcagttgcaataaccttggcttgtttcggacttgctcgggagggtaatcacaagcctattgactaccttaacccacctaagtaaatgtggaaacatccgatataaatctcatagttaatggcataattagaaagctaatcattttcttaagcatagagttatccttctaaagacttgttctttcagaaaaatgtttttccaattagtataaactctacaaattccctcttggtgtaaaattcaagatgtggaaattctaacttttttgaaatttaaaagcttatattttctaacttggcaaaagacttatccttagaaagagaagtgtacattgatttccaattaaaaatttgctggcattaaaaataagcacacttacataagcccccatacatagagtgggactcttggaatcaggagacaaagctaccacatgtggaaaggtactatgtgtccatgtcattcaaaaaatgtgattttttataataaactctttataacaaga
//
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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