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Previous release (v1)
2024-04-18 11:42:33, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_032753 2162 bp mRNA linear PRI 26-DEC-2022
DEFINITION Homo sapiens retina and anterior neural fold homeobox 2 (RAX2),
transcript variant 2, mRNA.
ACCESSION NM_032753
VERSION NM_032753.4
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 2162)
AUTHORS Yang P, Chiang PW, Weleber RG and Pennesi ME.
TITLE Autosomal Dominant Retinal Dystrophy With Electronegative Waveform
Associated With a Novel RAX2 Mutation
JOURNAL JAMA Ophthalmol 133 (6), 653-661 (2015)
PUBMED 25789692
REMARK GeneRIF: A frameshift heterozygous mutation in RAX2 inherited in an
autosomal dominant fashion was associated with mixed cone and rod
dysfunction.
REFERENCE 2 (bases 1 to 2162)
AUTHORS Davila S, Froeling FE, Tan A, Bonnard C, Boland GJ, Snippe H,
Hibberd ML and Seielstad M.
TITLE New genetic associations detected in a host response study to
hepatitis B vaccine
JOURNAL Genes Immun 11 (3), 232-238 (2010)
PUBMED 20237496
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 3 (bases 1 to 2162)
AUTHORS Vaquerizas JM, Kummerfeld SK, Teichmann SA and Luscombe NM.
TITLE A census of human transcription factors: function, expression and
evolution
JOURNAL Nat Rev Genet 10 (4), 252-263 (2009)
PUBMED 19274049
REMARK Review article
REFERENCE 4 (bases 1 to 2162)
AUTHORS Wang QL, Chen S, Esumi N, Swain PK, Haines HS, Peng G, Melia BM,
McIntosh I, Heckenlively JR, Jacobson SG, Stone EM, Swaroop A and
Zack DJ.
TITLE QRX, a novel homeobox gene, modulates photoreceptor gene expression
JOURNAL Hum Mol Genet 13 (10), 1025-1040 (2004)
PUBMED 15028672
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AC005777.1, BC018709.1 and
AY211277.1.
This sequence is a reference standard in the RefSeqGene project.
On Jun 2, 2019 this sequence version replaced NM_032753.3.
Summary: This gene encodes a homeodomain-containing protein that
plays a role in eye development. Mutation of this gene causes
age-related macular degeneration type 6, an eye disorder resulting
in accumulations of protein and lipid beneath the retinal pigment
epithelium and within the Bruch's membrane. Defects in this gene
can also cause cone-rod dystrophy type 11, a disease characterized
by the initial degeneration of cone photoreceptor cells and
resulting in loss of color vision and visual acuity, followed by
the degeneration of rod photoreceptor cells, which progresses to
night blindness and the loss of peripheral vision. Alternative
splicing results in multiple transcript variants. [provided by
RefSeq, Jan 2016].
##Evidence-Data-START##
Transcript exon combination :: AY211277.1, SRR14372080.339505.1
[ECO:0000332]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-7 AC005777.1 8911-8917 c
8-17 BC018709.1 1-10
18-1073 AY211277.1 2-1057
1074-1495 BC018709.1 1326-1747
1496-1944 AY211277.1 1481-1929
1945-2145 BC018709.1 2199-2399
2146-2157 AY211277.1 2131-2142
2158-2162 BC018709.1 2412-2416
FEATURES Location/Qualifiers
source 1..2162
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="19"
/map="19p13.3"
gene 1..2162
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/note="retina and anterior neural fold homeobox 2"
/db_xref="GeneID:84839"
/db_xref="HGNC:HGNC:18286"
/db_xref="MIM:610362"
exon 1..66
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/inference="alignment:Splign:2.1.0"
variation 4
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:150444854"
variation 5
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:370564299"
variation 8
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037275151"
variation 9
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:912749730"
variation 10
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037275085"
variation 11
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1206517243"
variation 13
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145738199"
variation 14
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1407741009"
variation 16
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:886054371"
variation 17
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037274922"
variation 18
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:959858612"
variation 19
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:576680324"
variation 25
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403744575"
variation 26
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1431138226"
variation 26
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322471973"
variation 27
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037274769"
variation 33
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037274738"
variation 35
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1234677376"
variation 36
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1372937839"
variation 37
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271892443"
variation 38
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037274587"
variation 39
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1306578133"
variation 41
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1445635462"
variation 43
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:920193014"
variation 44
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:974261994"
variation 45
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1299442229"
variation 46
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037274406"
variation 47
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1464980540"
variation 48
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:994833506"
variation 49
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:563046576"
variation 52..65
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="gggc"
/replace="gggctgccgtgggc"
/db_xref="dbSNP:572518936"
variation 53
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1436920396"
variation 54
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:182965071"
variation 55..59
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="ctgcc"
/replace="ctgcctgcc"
/db_xref="dbSNP:2037274092"
variation 55
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1178230926"
variation 56
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037274192"
variation 58
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1440609438"
variation 59
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252745152"
variation 60
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1184528094"
variation 61
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1599187718"
variation 63
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1218333531"
variation 65
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:776666200"
variation 66
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:981516220"
exon 67..291
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/inference="alignment:Splign:2.1.0"
variation 69
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:757287837"
variation 72
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1305855323"
variation 75
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444896908"
CDS 76..630
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/note="retina and anterior neural fold homeobox like 1;
Q50-type retinal homeobox protein; retina and anterior
neural fold homeobox-like protein 1"
/codon_start=1
/product="retina and anterior neural fold homeobox protein
2"
/protein_id="NP_116142.1"
/db_xref="CCDS:CCDS12112.1"
/db_xref="GeneID:84839"
/db_xref="HGNC:HGNC:18286"
/db_xref="MIM:610362"
/translation="
MFLSPGEGPATEGGGLGPGEEAPKKKHRRNRTTFTTYQLHQLERAFEASHYPDVYSREELAAKVHLPEVRVQVWFQNRRAKWRRQERLESGSGAVAAPRLPEAPALPFARPPAMSLPLEPWLGPGPPAVPGLPRLLGPGPGLQASFGPHAFAPTFADGFALEEASLRLLAKEHAQALDRAWPPA"
misc_feature 76..174
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/note="propagated from UniProtKB/Swiss-Prot (Q96IS3.1);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature order(157..171,175..177,226..228,244..246,283..285,
289..294,301..306,310..318,322..327)
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/note="DNA binding site [nucleotide binding]"
/db_xref="CDD:238039"
misc_feature order(163..165,172..174,292..294,301..306,313..315)
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/note="specific DNA base contacts [nucleotide binding];
other site"
/db_xref="CDD:238039"
misc_feature 166..324
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/note="Homeobox domain; Region: Homeobox; pfam00046"
/db_xref="CDD:425441"
variation 76
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:966492816"
variation 78
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1329692934"
variation 79
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411731808"
variation 81
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037265665"
variation 83
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1020890733"
variation 86
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398468087"
variation 87
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201416315"
variation 89
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:144065007"
variation 90
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:781275318"
variation 93
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:755028810"
variation 94
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:556179949"
variation 96..130
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="ggggccggcaaccgagggtgggggtctggggccgg"
/replace="ggggccggcaaccgagggtgggggtctggggccggcaaccgagggtgg
gggtctggggccgg"
/db_xref="dbSNP:780405331"
variation 97
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:758091449"
variation 100
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1181819192"
variation 101
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:750120142"
variation 102
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:764316452"
variation 108
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:149515429"
variation 109
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:538785333"
variation 111
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:898244077"
variation 114
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1599187028"
variation 116
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:768008187"
variation 117
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:2145737425"
variation 120
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:139127905"
variation 122
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:751619049"
variation 124
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:766488722"
variation 125
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1338805354"
variation 128
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:778194719"
variation 129
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:367658021"
variation 132
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:769403788"
variation 133
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:374434635"
variation 138
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037264626"
variation 139
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037264583"
variation 140
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1406715423"
variation 142
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037264506"
variation 143
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037264468"
variation 144
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568401195"
variation 145..153
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="aagaag"
/replace="aagaagaag"
/db_xref="dbSNP:756505075"
variation 145
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:553002220"
variation 149
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037264347"
variation 151
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370364475"
variation 157
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:779669577"
variation 158
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:199546013"
variation 159
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:535943685"
variation 162
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:778633054"
variation 165
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037263919"
variation 166
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:200153795"
variation 167
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:373009969"
variation 170
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1225721432"
variation 174
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1187429141"
variation 179
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037263650"
variation 181
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:781588193"
variation 183
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:755448810"
variation 187
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056190175"
variation 191
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:752094189"
variation 192
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:766400493"
variation 195
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473615092"
variation 199
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037263387"
variation 201
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145737312"
variation 202
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:763112380"
variation 205
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761987436"
variation 206
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:370757303"
variation 207
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:768600946"
variation 208
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:760640216"
variation 209
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:775581464"
variation 210
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163670829"
variation 211
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1599186870"
variation 213
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:771416905"
variation 214
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201124970"
variation 216..217
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="at"
/replace="gg"
/db_xref="dbSNP:2145737277"
variation 216
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:778346457"
variation 217
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:770597544"
variation 219
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:748981950"
variation 220
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037262817"
variation 222
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:781498623"
variation 223
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:565566531"
variation 225..226
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="ggatgtgtacagcctg"
/db_xref="dbSNP:1283758565"
variation 225
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:752009578"
variation 226..229
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="ggatgtgtacagcctgtaca"
/replace="tacc"
/db_xref="dbSNP:1568401113"
variation 227
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1374530421"
variation 228
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1214336624"
variation 229
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1337070706"
variation 230
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:76076446"
variation 231
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:141804618"
variation 235
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1676548519"
variation 236
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:138553345"
variation 237
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037262027"
variation 240
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037261978"
variation 241
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1404557350"
variation 244
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765285304"
variation 245
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:757454259"
variation 247
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:370195708"
variation 250
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1085307700"
variation 252
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:569526421"
variation 253
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:374872032"
variation 256
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:373359134"
variation 257
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037261470"
variation 259
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:760560608"
variation 260
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409952719"
variation 261
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:775483414"
variation 263
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037261321"
variation 267
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1188584260"
variation 268
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1396257256"
variation 269..276
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="acct"
/replace="acctacct"
/db_xref="dbSNP:2037261134"
variation 269
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:767485173"
variation 270
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252557730"
variation 277
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037261098"
variation 278
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:202149846"
variation 280
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1333788576"
variation 282
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:773887682"
variation 283
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:372266287"
variation 284
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2145737149"
variation 284
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748896187"
variation 285
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1021707653"
variation 286
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:772852323"
variation 289
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1216053749"
exon 292..2162
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/inference="alignment:Splign:2.1.0"
variation 292
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:775877146"
variation 293
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:772356880"
variation 294
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1258539834"
variation 300..301
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2037251711"
variation 300
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:574101760"
variation 301
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316964484"
variation 305
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145736540"
variation 306
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1308593558"
variation 307
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:746321949"
variation 308
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:398124430"
variation 309
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1055074641"
variation 310
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1294461966"
variation 311
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:779301810"
variation 313
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039500182"
variation 316
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1599186133"
variation 317
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1359067275"
variation 318
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:757897383"
variation 319
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037251197"
variation 322
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407392654"
variation 323
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:749374386"
variation 325
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:148629445"
variation 326
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:573043030"
variation 327
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037250863"
variation 329
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037250808"
variation 330
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1474928513"
variation 333
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1417014277"
variation 334
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752883776"
variation 335
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:121908280"
variation 336
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1599186084"
variation 340
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037250401"
variation 343
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1259459969"
variation 347
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145736454"
variation 350
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:754730849"
variation 351
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:751453416"
variation 352
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037250204"
variation 353
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1262130971"
variation 354
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:952301557"
variation 355
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037250070"
variation 357
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:201021639"
variation 358
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:762922416"
variation 361
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1289584353"
variation 365
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037249905"
variation 366
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1294479513"
variation 367..368
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="cc"
/replace="cccc"
/db_xref="dbSNP:2037249841"
variation 368
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:573892963"
variation 369
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:191051622"
variation 371
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1445024391"
variation 372
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1599186035"
variation 373
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242412901"
variation 374
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295224576"
variation 375..378
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:2145736386"
variation 375
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2145736395"
variation 376
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037249630"
variation 378
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:761417697"
variation 379
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:776155252"
variation 381
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1324110061"
variation 384
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1463116025"
variation 385
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037249489"
variation 387
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037249458"
variation 389
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772425151"
variation 390
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:968835887"
variation 391
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1020556796"
variation 392
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="t"
/db_xref="dbSNP:1371131603"
variation 392
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1462895070"
variation 394
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:759806695"
variation 395
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:774846243"
variation 396
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:771534203"
variation 398
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037249056"
variation 399
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749859588"
variation 400
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1467659356"
variation 402
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273209818"
variation 403
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777949969"
variation 404
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1030315829"
variation 405..410
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="ccccc"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:1230788366"
variation 405
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037248782"
variation 406
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1251233912"
variation 409..495
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="ccggccatgtcgctgcccctggagccctggttgggccccggaccgccg
gccgtgccaggcctcccccgcctcctgggcccgggcccg"
/db_xref="dbSNP:1568400617"
variation 409
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770022976"
variation 410
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781281689"
variation 411..412
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1286946201"
variation 411
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568400696"
variation 413
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2145736261"
variation 415
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1002124313"
variation 416
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301564042"
variation 419
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:398124431"
variation 420
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:755282511"
variation 421
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037248327"
variation 422
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1599185944"
variation 424
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:900588930"
variation 425
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:751304733"
variation 426
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1184300868"
variation 429
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1409720236"
variation 430
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037248139"
variation 433
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1045743925"
variation 437
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037248055"
variation 439
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1173290478"
variation 440
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1427343992"
variation 441
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1016261221"
variation 442..459
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="ggcc"
/replace="ggccccggaccgccggcc"
/db_xref="dbSNP:2037247409"
variation 443
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:779877505"
variation 444
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1167236192"
variation 445
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1005347152"
variation 446
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037247776"
variation 447
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:888248705"
variation 448
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:950155665"
variation 450
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1412019106"
variation 451..493
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="cc"
/replace="ccgccggccgtgccaggcctcccccgcctcctgggcccgggcc"
/db_xref="dbSNP:2037246413"
variation 452..466
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="cgccggccgtgccag"
/db_xref="dbSNP:1342399719"
variation 452
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:537165398"
variation 453
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:929891283"
variation 455
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1253237453"
variation 456
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:895500531"
variation 457
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037247449"
variation 458..459
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1274933809"
variation 459
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1195021627"
variation 460
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:758285438"
variation 461
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037247242"
variation 462
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037108094"
variation 463
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250490026"
variation 465
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037247103"
variation 467
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:937125036"
variation 468
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037246975"
variation 471..475
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:2145736106"
variation 471
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:577841273"
variation 472
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1481836442"
variation 473
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278560302"
variation 475
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:941526473"
variation 476
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:910094615"
variation 478
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1305878885"
variation 483..497
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="gggcccggg"
/replace="gggcccgggcccggg"
/replace="gggcccgggcccgggcccggg"
/db_xref="dbSNP:549932754"
variation 483
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145736090"
variation 484..496
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="gg"
/replace="ggcccgggcccgg"
/db_xref="dbSNP:2037246262"
variation 484
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:121908281"
variation 486
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1248541458"
variation 488
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:978473853"
variation 489..491
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1328132335"
variation 489
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1335212510"
variation 491
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037246447"
variation 494
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750394661"
variation 495
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:947549671"
variation 497
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1391061686"
variation 498
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1431848727"
variation 499..513
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="ctgcaagcgtccttc"
/db_xref="dbSNP:1568400594"
variation 500
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2145736040"
variation 501
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1310919721"
variation 504
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:922236026"
variation 505
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:113176673"
variation 506
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:989493054"
variation 507
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:149918940"
variation 512
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037245932"
variation 513
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1468184577"
variation 514
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:957818577"
variation 516
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:761243587"
variation 517
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1183181146"
variation 518..521
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="ctca"
/db_xref="dbSNP:1256017785"
variation 519
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1439994082"
variation 521
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1230148971"
variation 522
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037245494"
variation 530
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:753446591"
variation 532
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037245396"
variation 534
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1486188826"
variation 536
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1282782912"
variation 539..550
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="t"
/replace="tcgcagatggct"
/db_xref="dbSNP:886041039"
variation 539
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203569849"
variation 540
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:923302208"
variation 541
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1280147395"
variation 543
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037245167"
variation 544
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1241272400"
variation 547..548
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1449763445"
variation 547
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352324861"
variation 551
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:2037244999"
variation 552
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:763649255"
variation 553
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:760415111"
variation 554
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016314982"
variation 555
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:906473424"
variation 562
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:534656129"
variation 565
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1335805560"
variation 566
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:771442676"
variation 567
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1014225698"
variation 569
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:112538462"
variation 570
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1165336895"
variation 574
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:771011757"
variation 575
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:202103390"
variation 576
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451579585"
variation 579
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1388641253"
variation 581
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1416399047"
variation 583
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037244369"
variation 584
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1187818180"
variation 585
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:941485794"
variation 588
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145735879"
variation 589
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:773857866"
variation 591
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1891440096"
variation 594
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2145735870"
variation 595
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1239523974"
variation 599
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1191315157"
variation 601
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037244164"
variation 604
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1599185610"
variation 610
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1025462223"
variation 613
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:567006348"
variation 618
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145735857"
variation 619
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285206637"
variation 620
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1207025589"
variation 621
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:769934766"
variation 622
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1271231378"
variation 627
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1291600031"
variation 637
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781395665"
variation 638
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:778410291"
variation 639
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285669869"
variation 643
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1428380234"
variation 644
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1325548103"
variation 645
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1318540795"
variation 646..648
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1429367131"
variation 646
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1458393430"
variation 648
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:747281291"
variation 649
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1391595572"
variation 651
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1160479173"
variation 652
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:922852315"
variation 653
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037243492"
variation 655
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1462366807"
variation 656
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1416590311"
variation 657
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1185206434"
variation 658
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:756545759"
variation 659
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748592898"
variation 661..663
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1190712383"
variation 664
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037243231"
variation 668
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1026466064"
variation 669
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1252389963"
variation 675
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:139146360"
variation 676
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:989221840"
variation 678
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:745749097"
variation 681
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1291917539"
variation 682
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:536413590"
variation 686
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1467312373"
variation 690
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1424440320"
variation 700
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:112751250"
variation 701
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037242823"
variation 703
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568400427"
variation 704
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1483737658"
variation 705
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037242699"
variation 706
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037242650"
variation 707
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037242582"
variation 709
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1431974527"
variation 717
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1255859869"
variation 718
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:886054369"
variation 719
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1033493718"
variation 724
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:980576702"
variation 727
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488585056"
variation 728
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037242305"
variation 729
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037242269"
variation 734..735
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1362646101"
variation 735
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1237258627"
variation 736
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:970979540"
variation 738
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:905498355"
variation 740
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037242174"
variation 741
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037242129"
variation 745
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:781429367"
variation 748
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145735707"
variation 749
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1599185447"
variation 750..759
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="ccaccac"
/replace="ccaccaccac"
/db_xref="dbSNP:1308390277"
variation 757
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1413987028"
variation 759
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1042846985"
variation 764
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:947103494"
variation 765
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037241810"
variation 767
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:866964205"
variation 768
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:913433357"
variation 769
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037241606"
variation 770
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1053284032"
variation 772
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:933609200"
variation 774..780
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="agaga"
/replace="agagaga"
/db_xref="dbSNP:765073500"
variation 775
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:993823380"
variation 777
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:923552826"
variation 781
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1254402355"
variation 787
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037241315"
variation 788
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:567541177"
variation 793
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1599185405"
variation 798
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037241179"
variation 799
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:897149979"
variation 800
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1232391378"
variation 803
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1177076931"
variation 804
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037241011"
variation 809
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1310390260"
variation 810
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:964698261"
variation 812
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:550787935"
variation 813
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1599185384"
variation 816
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1392935828"
variation 817
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1599185381"
variation 818
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037240729"
variation 821
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:150808899"
variation 823
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1599185373"
variation 824
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:11883056"
variation 825
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1449281671"
variation 831
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:565417258"
variation 832
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:551480253"
variation 837
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1388634597"
variation 838
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1599185352"
variation 840
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037240245"
variation 845
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:994017656"
variation 846
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568400336"
variation 850
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1599185347"
variation 857..858
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="ca"
/db_xref="dbSNP:1041298455"
variation 858
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037240014"
variation 861
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:960109331"
variation 864
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037239954"
variation 869
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:528491190"
variation 870
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1361448002"
variation 874
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1599185338"
variation 877
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1177239922"
variation 878
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1418917467"
variation 881
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037239787"
variation 887
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1001431049"
variation 889
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037239745"
variation 893
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568400313"
variation 894
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037239680"
variation 896
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:913557579"
variation 897
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037239612"
variation 898
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1599185323"
variation 900
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378865918"
variation 901..904
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1176327693"
variation 901
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:142875968"
variation 903
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:764972815"
variation 906
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:936340074"
variation 907
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037239419"
variation 910
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:374701207"
variation 918
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037239366"
variation 923
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1421413127"
variation 928
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037239315"
variation 930
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2145735532"
variation 932..938
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="tcctgtc"
/replace="tcctgtcctgtc"
/db_xref="dbSNP:2037239249"
variation 933
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1426473530"
variation 934
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037239290"
variation 939
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:905552147"
variation 940..943
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="gtta"
/db_xref="dbSNP:2037239155"
variation 940
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037239189"
variation 947
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1042733352"
variation 948
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1199440183"
variation 950
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482220318"
variation 951
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:926331334"
variation 953
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037238969"
variation 954
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:980936242"
variation 955
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1011366370"
variation 956
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:559347055"
variation 957
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037238854"
variation 962
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025265039"
variation 963
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:971995911"
variation 964
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037238790"
variation 969
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1053243121"
variation 970
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1306842943"
variation 973
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:542961923"
variation 974
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1016156373"
variation 975
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037238581"
variation 977
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377984760"
variation 978
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:573855282"
variation 979
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1243525279"
variation 988
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1474208449"
variation 989
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037238282"
variation 991
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037238222"
variation 992
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145735438"
variation 993
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:540904191"
variation 994
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:563450780"
variation 995
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039283695"
variation 997
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037238032"
variation 998..999
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2037237914"
variation 998
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:756898228"
variation 999
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:543676430"
variation 1000
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:984751573"
variation 1004
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:929269038"
variation 1005..1008
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:2037237743"
variation 1005
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037237776"
variation 1009
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:771616343"
variation 1011
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:73531473"
variation 1012
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:992623473"
variation 1013
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="g"
/db_xref="dbSNP:1430276600"
variation 1013
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1818087698"
variation 1016
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037237609"
variation 1022
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1303799978"
variation 1024
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:2037237557"
variation 1025..1031
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="tctct"
/replace="tctctct"
/db_xref="dbSNP:2037237518"
variation 1028
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037237533"
variation 1036..1040
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="ct"
/replace="ctcct"
/db_xref="dbSNP:1381728838"
variation 1045
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1421119688"
variation 1048
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145735383"
variation 1060
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:959918734"
variation 1061
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:945630878"
variation 1062
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:892698318"
variation 1067
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037237372"
variation 1077
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:147235958"
variation 1082..1085
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:2037237258"
variation 1082
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568400222"
variation 1083
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:370569469"
variation 1085
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037237227"
variation 1087
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037237201"
variation 1088
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1444989966"
variation 1092
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1214548921"
variation 1093..1097
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="aa"
/replace="aacaa"
/db_xref="dbSNP:2145735350"
variation 1099
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037237114"
variation 1100..1108
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="agcagc"
/replace="agcagcagc"
/db_xref="dbSNP:926277551"
variation 1103
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:1237853883"
variation 1107
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="g"
/db_xref="dbSNP:753823753"
variation 1107
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037237008"
variation 1109
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1229209654"
variation 1111..1121
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="ccgcgagcctg"
/db_xref="dbSNP:1176991714"
variation 1112
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035915540"
variation 1113
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:980045637"
variation 1114
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:534280724"
variation 1115
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:753371180"
variation 1117
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1405801682"
variation 1120
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:1011252751"
variation 1121
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1400360122"
variation 1122
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037236534"
variation 1124..1129
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="ctc"
/replace="ctcctc"
/db_xref="dbSNP:1377680439"
variation 1126
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037236488"
variation 1127
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037236443"
variation 1131
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:891425007"
variation 1133
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037236313"
variation 1134
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037236280"
variation 1135
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1312626875"
variation 1138
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037236207"
variation 1139
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:917743185"
variation 1142
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:764144252"
variation 1143
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1280789566"
variation 1147..1150
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="tgtg"
/replace="tgtgtg"
/db_xref="dbSNP:2037235930"
variation 1147
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:542850364"
variation 1149
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037235969"
variation 1152
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037235897"
variation 1154
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:961867623"
variation 1157
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1242900798"
variation 1158
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1342272741"
variation 1165
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:573611356"
variation 1166
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:997655392"
variation 1167..1168
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1208537861"
variation 1167
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037235623"
variation 1168
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1399881648"
variation 1169
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037235497"
variation 1171
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037235459"
variation 1172
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:984676271"
variation 1176
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1483346450"
variation 1178
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1599185088"
variation 1180
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1599185083"
variation 1182
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:760554835"
variation 1183
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:902037235"
variation 1184
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1469652297"
variation 1185
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037235078"
variation 1187
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037235037"
variation 1200
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037234991"
variation 1205
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037234945"
variation 1207
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1191809118"
variation 1209
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:747650052"
variation 1210
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037234819"
variation 1212
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037234779"
variation 1213
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1039169289"
variation 1214
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037234698"
variation 1216
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397168431"
variation 1220
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1401066152"
variation 1221
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:558372260"
variation 1223
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037234546"
variation 1224
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1385213687"
variation 1227
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037234469"
variation 1231
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1878296029"
variation 1235
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1028777617"
variation 1243
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037234368"
variation 1248..1250
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:2037234277"
variation 1249
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1371486734"
variation 1251
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1412143938"
variation 1253
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:775459770"
variation 1254
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:886054368"
variation 1255
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037234163"
variation 1257
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:965869191"
variation 1258
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:888032282"
variation 1260
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:572021504"
variation 1262
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:929336441"
variation 1264
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1279361854"
variation 1265
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1339777439"
variation 1266
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1197510704"
variation 1268
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037233929"
variation 1269
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1599185028"
variation 1271
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:767221990"
variation 1276
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:992280356"
variation 1277
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:112369501"
variation 1280
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1254957896"
variation 1284
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010119724"
variation 1288
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037233742"
variation 1292
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:892645756"
variation 1296
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037233685"
variation 1297
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1477435359"
variation 1304
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:778568577"
variation 1305
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568400098"
variation 1306
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:928487890"
variation 1309
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:576669713"
variation 1310
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:28673245"
variation 1311
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1447305599"
variation 1313
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1001154925"
variation 1315
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037233410"
variation 1317
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208248243"
variation 1318
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037233364"
variation 1319
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:115071988"
variation 1320
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:949142739"
variation 1331..1337
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="gagag"
/replace="gagagag"
/db_xref="dbSNP:1326625879"
variation 1333
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037233188"
variation 1335
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1599184967"
variation 1337..1339
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1229405773"
variation 1337
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302183750"
variation 1345
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037232967"
variation 1346
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1218137292"
variation 1347
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316593410"
variation 1348..1350
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1467155450"
variation 1348
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:990041035"
variation 1349
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145735087"
variation 1350..1354
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="gccag"
/db_xref="dbSNP:138512126"
variation 1350
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:917547"
variation 1351
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037232626"
variation 1352
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1031739378"
variation 1353
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1599184940"
variation 1355
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037232443"
variation 1356
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:2037232410"
variation 1362
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037232377"
variation 1366
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037232357"
variation 1367
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1448942088"
variation 1372
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1322007235"
variation 1375
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037232261"
variation 1376
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037232235"
variation 1377
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037232202"
variation 1380
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:571601214"
variation 1381
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:901586216"
variation 1384
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473418462"
variation 1386
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1167665146"
variation 1387
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:2037232091"
variation 1388
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1419425408"
variation 1389
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037232027"
variation 1390
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1459454439"
variation 1391
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037231986"
variation 1392
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1324612320"
variation 1394
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037231954"
variation 1395
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1599184907"
variation 1396
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1325985778"
variation 1398..1403
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="gtc"
/replace="gtcgtc"
/db_xref="dbSNP:1315969232"
variation 1400
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1017267736"
variation 1401
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1007689446"
variation 1404
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:1568400025"
variation 1406
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:887917665"
variation 1407
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:551864984"
variation 1409
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1332561160"
variation 1412
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2145734996"
variation 1413
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1232812430"
variation 1414
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:929531306"
variation 1415
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:917546"
variation 1418
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1203554366"
variation 1419
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2145734989"
variation 1421
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2145734986"
variation 1422
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="a"
/db_xref="dbSNP:2037231540"
variation 1423
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:965420416"
variation 1424
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1486178205"
variation 1425
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190471891"
variation 1428
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037231431"
variation 1431
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037231391"
variation 1432
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037231354"
variation 1433
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145734973"
variation 1434
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1196540731"
variation 1435..1438
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1163670662"
variation 1435
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056861754"
variation 1436
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256086044"
variation 1437
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:939491559"
variation 1441
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037231069"
variation 1442
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1020082058"
variation 1443
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1455038195"
variation 1444
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037230915"
variation 1445
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:926699833"
variation 1449
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009656822"
variation 1450
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037230774"
variation 1451
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1415213441"
variation 1453
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:143706741"
variation 1455
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037230632"
variation 1458
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037230591"
variation 1460
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:956854433"
variation 1463
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1414019055"
variation 1465
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1307810901"
variation 1466
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1032544180"
variation 1467
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037230377"
variation 1468
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1456459740"
variation 1469
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037230284"
variation 1470
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1237193177"
variation 1473
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037230179"
variation 1477
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037230143"
variation 1483
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037230122"
variation 1485
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037230092"
variation 1487
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037230066"
variation 1491
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037230036"
variation 1492
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037230014"
variation 1494..1495
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="tc"
/db_xref="dbSNP:2037229967"
variation 1494
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1260399047"
variation 1496
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:917545"
variation 1497
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:948551826"
variation 1498..1501
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="gcat"
/db_xref="dbSNP:2037229738"
variation 1498
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037229835"
variation 1499
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037229800"
variation 1500
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:914387817"
variation 1501
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037229718"
variation 1502..1503
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="aaga"
/db_xref="dbSNP:2037229660"
variation 1502
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037229683"
variation 1503
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:148990863"
variation 1505
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2145734881"
variation 1509
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145734874"
variation 1512
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:956141720"
variation 1514
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037229559"
variation 1516
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:924339003"
variation 1518
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:773142284"
variation 1523
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037229475"
variation 1524
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:940480224"
variation 1525
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:887600199"
variation 1526
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1434048965"
variation 1527
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037229349"
variation 1529
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298636383"
variation 1531
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1375397350"
variation 1532
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:10405125"
variation 1533
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1332448820"
variation 1534..1537
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1301722451"
variation 1534
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:921814565"
variation 1536
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037229151"
variation 1539
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:181573768"
variation 1540
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:372452808"
variation 1542
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037229022"
variation 1547
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1017319851"
variation 1548
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:748630795"
variation 1552
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037228909"
variation 1553
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1479931544"
variation 1555
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1193642513"
variation 1557
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1236961921"
variation 1558
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1007241070"
variation 1565..1574
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="cggctggccc"
/db_xref="dbSNP:1332818881"
variation 1565
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1195058130"
variation 1566
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1397448144"
variation 1579
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:886054367"
variation 1585
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1410443397"
variation 1587
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037228616"
variation 1588
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1599184695"
variation 1589
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:912603253"
variation 1591
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037228533"
variation 1593
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1170592457"
variation 1599
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145734797"
variation 1601
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:988214081"
variation 1602
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:886054366"
variation 1604
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:866962886"
variation 1607
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:956803181"
variation 1614
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1478922343"
variation 1616
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037228320"
variation 1617
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037228291"
variation 1619
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1324090700"
variation 1620
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037228244"
variation 1625
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1032491752"
variation 1626
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1395475559"
variation 1627
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037228146"
variation 1633
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2145734777"
variation 1635
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037228121"
variation 1636
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:979570262"
variation 1637
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145734769"
variation 1641
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145734766"
variation 1645
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037228063"
variation 1647
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:969593840"
variation 1648
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306273569"
variation 1649
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:543639717"
variation 1650
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1256894327"
variation 1653
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037227954"
variation 1654
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1468504582"
variation 1655
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037227892"
variation 1656
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1214979146"
variation 1663
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1487944852"
variation 1665
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:533160062"
variation 1666
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2145734734"
variation 1668
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:896134547"
variation 1670
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1426676688"
variation 1683
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1014572912"
variation 1684
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:368356816"
variation 1685
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1442343282"
variation 1692
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037227691"
variation 1694
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037227661"
variation 1701
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037227637"
variation 1702..1722
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="cccagatcac"
/replace="cccagatcactcccagatcac"
/db_xref="dbSNP:143816706"
variation 1704
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037227605"
variation 1706
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1277188766"
variation 1707
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:898071508"
variation 1710
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1348964458"
variation 1712
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037227495"
variation 1713..1723
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="cccagatcacc"
/db_xref="dbSNP:945501026"
variation 1717
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037227462"
variation 1723
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037227362"
variation 1727
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037227331"
variation 1734
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1056680876"
variation 1739
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037227266"
variation 1741
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037227239"
variation 1743
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1003963778"
variation 1744
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:865777598"
variation 1748
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037227133"
variation 1749
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1442389569"
variation 1755
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037227070"
variation 1760
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:905167387"
variation 1764
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1332048126"
variation 1768
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1045194428"
variation 1774
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:781672239"
variation 1775
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:886054365"
variation 1776..1779
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1476139623"
variation 1776
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:541141934"
variation 1778..1782
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="cc"
/replace="ccgcc"
/db_xref="dbSNP:2037226830"
variation 1778
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192631064"
variation 1779
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1860322"
variation 1780
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1162883673"
variation 1781
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037226859"
variation 1782
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1413091180"
variation 1787
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1401523830"
variation 1791
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1054691513"
variation 1792
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1343621605"
variation 1793
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419530134"
variation 1795
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037226627"
variation 1796
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037226600"
variation 1798
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:934470760"
variation 1799
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:554924169"
variation 1802
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1413407200"
variation 1807
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1418058981"
variation 1809
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1377751315"
variation 1811
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1382467055"
variation 1812
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:778752074"
variation 1814
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1177835874"
variation 1815
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037226301"
variation 1816
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037226268"
variation 1819
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145734589"
variation 1820
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1472474640"
variation 1821
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235809993"
variation 1824
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:965701181"
variation 1830
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:910201278"
variation 1832
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190171660"
variation 1835
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:886054364"
variation 1839
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:935335961"
variation 1840..1842
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="att"
/db_xref="dbSNP:1185647890"
variation 1840
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="a"
/db_xref="dbSNP:2037225995"
variation 1840
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:2037225967"
variation 1841..1851
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="tttttttttt"
/replace="ttttttttttt"
/replace="tttttttttttt"
/db_xref="dbSNP:969959848"
variation 1842
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:925325878"
variation 1851
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:541461753"
variation 1852..1854
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:2037225786"
variation 1852
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1406131291"
variation 1855
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1023841184"
variation 1856
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037225728"
variation 1863
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174657273"
variation 1866
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1377596244"
variation 1867
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:992808097"
variation 1869
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:951791249"
variation 1872
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037225601"
variation 1873
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751574450"
variation 1874
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442366753"
variation 1879
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037225495"
variation 1880
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1027862612"
variation 1882
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1374286742"
variation 1886
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:994076896"
variation 1887
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:756949675"
variation 1888
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:753483270"
variation 1895
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037225326"
variation 1896
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037225301"
variation 1897
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1004477347"
variation 1898
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037225248"
variation 1899
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1836121217"
variation 1900
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1599184445"
variation 1903
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037225177"
variation 1906
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208421186"
variation 1908
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037225128"
variation 1912
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1661045396"
variation 1915
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:879270537"
variation 1921
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:887452255"
variation 1922
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037225040"
variation 1924
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1206792435"
variation 1925
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1599184427"
variation 1928
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037224953"
variation 1930
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568399751"
variation 1933
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:796661165"
variation 1938
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037224875"
variation 1943
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037224852"
variation 1945
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1439336622"
variation 1946
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1281958115"
variation 1947
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397310167"
variation 1948
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1450074262"
variation 1950
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:995978121"
variation 1952
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037224684"
variation 1954
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:138882802"
variation 1956
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1420924451"
variation 1957..1960
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1412126974"
variation 1958
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:556680562"
variation 1959
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:2037224560"
variation 1963
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397971978"
variation 1966
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1362231528"
variation 1968
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:905221601"
variation 1969..1971
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:533827006"
variation 1970
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1009209788"
variation 1972
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1405019314"
variation 1973
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:557232331"
variation 1979
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:8103165"
variation 1981
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037224253"
variation 1988
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:537209342"
variation 1989
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1274021560"
variation 1990
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1339993241"
variation 1991
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145734404"
variation 1994
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:893896630"
variation 1996
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:6510769"
variation 1998
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:557945632"
variation 2002
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037224006"
variation 2003
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037223979"
variation 2006
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037223940"
variation 2016
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037223907"
variation 2020
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1457343900"
variation 2021
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:2037223839"
variation 2040
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:925315867"
variation 2041
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:1043827967"
variation 2052
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:948193256"
variation 2058
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:934501930"
variation 2061
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373931425"
variation 2064
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:535098347"
variation 2065
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1166622663"
variation 2072
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1263184456"
variation 2075
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:902992031"
variation 2076
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1040718133"
variation 2082
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="g"
/replace="t"
/db_xref="dbSNP:1599184327"
variation 2086
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:1164987642"
variation 2090
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2037223551"
variation 2091
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2145734341"
variation 2096
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:566212226"
variation 2097
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1599184322"
variation 2098
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037223491"
variation 2099
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1599184316"
variation 2101
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2145734325"
variation 2103
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1489443433"
variation 2104
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:2037223416"
variation 2105
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:992317695"
variation 2107
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1322664820"
variation 2110
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2145734306"
variation 2111
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037223256"
variation 2113
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:886054363"
variation 2115
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145734295"
variation 2119
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1326759579"
variation 2120
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:1432848167"
variation 2121
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="g"
/db_xref="dbSNP:1599184296"
variation 2123
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1276277511"
variation 2124
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037223014"
variation 2131
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037222984"
variation 2132
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:961173478"
variation 2134
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:2145734270"
variation 2141..2146
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="aaaaaa"
/db_xref="dbSNP:1234040876"
variation 2141
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2145734266"
variation 2144..2150
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="aaa"
/replace="aaacaaa"
/db_xref="dbSNP:1450710786"
variation 2144
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="t"
/db_xref="dbSNP:2037222907"
variation 2147
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1275122025"
variation 2149
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/db_xref="dbSNP:2037222774"
variation 2150
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:908101133"
variation 2152
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace=""
/replace="c"
/db_xref="dbSNP:2037222640"
variation 2152
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287089282"
variation 2153
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:775609621"
variation 2155..2161
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="aaa"
/replace="aaacaaa"
/db_xref="dbSNP:1449135227"
variation 2158
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="c"
/replace="t"
/db_xref="dbSNP:1262903125"
variation 2159..2162
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="aa"
/replace="aaaa"
/db_xref="dbSNP:983670157"
variation 2159
/gene="RAX2"
/gene_synonym="ARMD6; CORD11; QRX; RAXL1; RP95"
/replace="a"
/replace="g"
/db_xref="dbSNP:2037222473"
ORIGIN
agacgcagcgccaggcccgctggggcaggtgtcccgtggaaatcgacggaggggctgccgtgggcggtgggagccatgttcctgagcccgggcgaggggccggcaaccgagggtgggggtctggggccgggcgaggaggcccccaagaagaagcaccggaggaaccgcaccaccttcaccacctaccagctgcaccagctggagcgggcgttcgaggcctctcactacccggatgtgtacagccgtgaggagctggcagccaaggtgcacctacctgaggtgcgcgtgcaggtgtggttccagaaccgccgggccaagtggcgccgccaggagcggctggagtcaggctcgggtgccgtggcagctccgagactccccgaggccccagcgctgccgttcgcccgccccccggccatgtcgctgcccctggagccctggttgggccccggaccgccggccgtgccaggcctcccccgcctcctgggcccgggcccggggctgcaagcgtccttcgggcctcatgcctttgctcccaccttcgcagatggcttcgccctggaggaggcgtccctgcggctgctggccaaggaacatgcacaggctctggacagggcctggccgccagcctgagcctgccgccctcccgggccccctcctcggcccaacccgagaaccggggacgtgccctggtgacagccaccacgccttggcctaggccgaggtcatggagcaaccgtggtcaggccaggccaccaccactggggagcgggaccagagagacaggctgctgggttccctgcccccatcccgtctcccaccccatcgccacccgtcctgctggcagcggactggcccccagtgtcaggcaggaggtgacccaagtattctcaggccaggtgcggggacctcctcccctcctggggcctcagtctcctgtctgttaattgggcgtgggggcctccgaggttcgagggctgcgaggctgtgggtggcgggaccgctgactctgtaagatgagtgtaaatctctctgcttctcctaatccccatcagcagagctgcccactctccaggctcccagtcccctggaaataacaaatagcagcagctcccgcgagcctggtctcctctcaccgtgtgctcgccatgtgagcactcccctctccgttgtgccctggacctcgggcacagctgtcagcccattctatagagagggaaaccggggcttaggcaggaagccaggtccccaaagtcgcacggccaggagtggatggagctgcctttcagacccatcaccggtcctaccgtccggggcacagcgacaggttctggagagagggtgggtcccgggccaggtgctggtgggcctccaggtggaggcgggctgatgctgggtgtgtcgtcatcgtcagaccgttcctcacgtccccacagaccccaggccctgtgcatgtccccagtggaggcatggccagcatctgctctgtccaacccagccgcatcgcccaagagctctgagcaaggaggctgtcgcggggccgagaacccgctgggactggcaagcacggctggcccagtgcagcaggagggggccctgaggcatgggatgggacagtctgggccagcgccacctcccgggacagaagtgcggcaccagggcaggagctgcagtagctaccctccccgtctccagcctgggctccccagatcactcccagatcaccaggtcaccccatctctaggcggcacctcacacaccagtcctgtggtccaacgccccgccatcacccaatgtcaccgcacaccaggcagtggggacacggcagtaagcacaagaaagatttttttttttaaagctaaaccaggccaggtgcggtggctcatgcctgtaatcccagtgctttgggaggctgaggtgggaggattgcttgagaccagcctgggtgacacagcaagaccccatctccacaaacgtttttaaaatgtgccgggtgtactggtgcacacctgtcatcccagctacccaagaagctgaggcaagaggatcacttgagcccagaaggtcgaggctgcagggagctgtgatcacactgctgcactccagcctgtgcaacagagccagaccctgactcaatacaaataaaaaacaaatctaaaacaaaa
//
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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