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Previous release (v1)
2024-04-26 23:56:49, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_152227 2099 bp mRNA linear PRI 10-APR-2023
DEFINITION Homo sapiens sorting nexin 5 (SNX5), transcript variant 1, mRNA.
ACCESSION NM_152227
VERSION NM_152227.3
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 2099)
AUTHORS Tornero-Ecija A, Zapata-Del-Bano A, Anton-Esteban L, Vincent O and
Escalante R.
TITLE The association of lipid transfer protein VPS13A with endosomes is
mediated by sorting nexin SNX5
JOURNAL Life Sci Alliance 6 (6), e202201852 (2023)
PUBMED 36977596
REMARK GeneRIF: The association of lipid transfer protein VPS13A with
endosomes is mediated by sorting nexin SNX5.
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 2099)
AUTHORS Li Z.
TITLE Overexpression of lncRNA HOXA-AS2 promotes the progression of oral
squamous cell carcinoma by mediating SNX5 expression
JOURNAL BMC Mol Cell Biol 23 (1), 59 (2022)
PUBMED 36528556
REMARK GeneRIF: Overexpression of lncRNA HOXA-AS2 promotes the progression
of oral squamous cell carcinoma by mediating SNX5 expression.
Publication Status: Online-Only
REFERENCE 3 (bases 1 to 2099)
AUTHORS Dong X, Yang Y, Zou Z, Zhao Y, Ci B, Zhong L, Bhave M, Wang L, Kuo
YC, Zang X, Zhong R, Aguilera ER, Richardson RB, Simonetti B,
Schoggins JW, Pfeiffer JK, Yu L, Zhang X, Xie Y, Schmid SL, Xiao G,
Gleeson PA, Ktistakis NT, Cullen PJ, Xavier RJ and Levine B.
TITLE Sorting nexin 5 mediates virus-induced autophagy and immunity
JOURNAL Nature 589 (7842), 456-461 (2021)
PUBMED 33328639
REMARK GeneRIF: Sorting nexin 5 mediates virus-induced autophagy and
immunity.
REFERENCE 4 (bases 1 to 2099)
AUTHORS Zhou Q, Huang T, Jiang Z, Ge C, Chen X, Zhang L, Zhao F, Zhu M,
Chen T, Cui Y, Li H, Yao M, Li J and Tian H.
TITLE Upregulation of SNX5 predicts poor prognosis and promotes
hepatocellular carcinoma progression by modulating the EGFR-ERK1/2
signaling pathway
JOURNAL Oncogene 39 (10), 2140-2155 (2020)
PUBMED 31819169
REMARK GeneRIF: Upregulation of SNX5 predicts poor prognosis and promotes
hepatocellular carcinoma progression by modulating the EGFR-ERK1/2
signaling pathway.
Erratum:[Oncogene. 2020 Oct;39(41):6511. PMID: 32895479]
REFERENCE 5 (bases 1 to 2099)
AUTHORS Li J, Chen T, Xie T, Yang YX, He TS and Xu LG.
TITLE SNX5 inhibits RLR-mediated antiviral signaling by targeting
RIG-I-VISA signalosome
JOURNAL Biochem Biophys Res Commun 522 (4), 889-896 (2020)
PUBMED 31806368
REMARK GeneRIF: SNX5 inhibits RLR-mediated antiviral signaling by
targeting RIG-I-VISA signalosome.
REFERENCE 6 (bases 1 to 2099)
AUTHORS Wassmer T, Attar N, Bujny MV, Oakley J, Traer CJ and Cullen PJ.
TITLE A loss-of-function screen reveals SNX5 and SNX6 as potential
components of the mammalian retromer
JOURNAL J Cell Sci 120 (Pt 1), 45-54 (2007)
PUBMED 17148574
REMARK GeneRIF: SNX5 and SNX6 may constitute functional equivalents of
Vps17p in mammalian retromer
REFERENCE 7 (bases 1 to 2099)
AUTHORS Merino-Trigo A, Kerr MC, Houghton F, Lindberg A, Mitchell C,
Teasdale RD and Gleeson PA.
TITLE Sorting nexin 5 is localized to a subdomain of the early endosomes
and is recruited to the plasma membrane following EGF stimulation
JOURNAL J Cell Sci 117 (Pt 26), 6413-6424 (2004)
PUBMED 15561769
REMARK GeneRIF: SNX5 is localized to a subdomain of the early endosomes
and is recruited to the cell membrane following EGF stimulation.
REFERENCE 8 (bases 1 to 2099)
AUTHORS Towler MC, Gleeson PA, Hoshino S, Rahkila P, Manalo V, Ohkoshi N,
Ordahl C, Parton RG and Brodsky FM.
TITLE Clathrin isoform CHC22, a component of neuromuscular and
myotendinous junctions, binds sorting nexin 5 and has increased
expression during myogenesis and muscle regeneration
JOURNAL Mol Biol Cell 15 (7), 3181-3195 (2004)
PUBMED 15133132
REFERENCE 9 (bases 1 to 2099)
AUTHORS Teasdale RD, Loci D, Houghton F, Karlsson L and Gleeson PA.
TITLE A large family of endosome-localized proteins related to sorting
nexin 1
JOURNAL Biochem J 358 (Pt 1), 7-16 (2001)
PUBMED 11485546
REFERENCE 10 (bases 1 to 2099)
AUTHORS Otsuki T, Kajigaya S, Ozawa K and Liu JM.
TITLE SNX5, a new member of the sorting nexin family, binds to the
Fanconi anemia complementation group A protein
JOURNAL Biochem Biophys Res Commun 265 (3), 630-635 (1999)
PUBMED 10600472
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AF121855.1 and BC000100.3.
On Jun 2, 2019 this sequence version replaced NM_152227.2.
Summary: This gene encodes a member of the sorting nexin family.
Members of this family contain a phox (PX) domain, which is a
phosphoinositide binding domain, and are involved in intracellular
trafficking. This protein functions in endosomal sorting, the
phosphoinositide-signaling pathway, and macropinocytosis. This gene
may play a role in the tumorigenesis of papillary thyroid
carcinoma. Alternative splicing results in multiple transcript
variants encoding different isoforms. [provided by RefSeq, Sep
2013].
Transcript Variant: This variant (1) differs in the 5' UTR,
compared to variant 2. Variants 1 and 2 encode the same protein
(isoform a).
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: BC000100.3, SRR7346977.982725.1
[ECO:0000332]
RNAseq introns :: mixed sample support SAMEA1965299,
SAMEA1966682 [ECO:0006172]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-1493 AF121855.1 54-1546
1494-2099 BC000100.3 1530-2135
FEATURES Location/Qualifiers
source 1..2099
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="20"
/map="20p11.23"
gene 1..2099
/gene="SNX5"
/note="sorting nexin 5"
/db_xref="GeneID:27131"
/db_xref="HGNC:HGNC:14969"
/db_xref="MIM:605937"
exon 1..95
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:997158303"
variation 2
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1325249989"
variation 5
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1304032146"
variation 6
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:533901521"
variation 7
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:897598937"
misc_feature 8..10
/gene="SNX5"
/note="upstream in-frame stop codon"
variation 10
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:943571816"
variation 11
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2122460404"
variation 12
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:909482464"
variation 13
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:73901137"
variation 14
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1431887206"
variation 15
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1410470755"
variation 16
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035625475"
variation 17
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:776719574"
variation 21
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1371359219"
variation 22
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035625371"
variation 23..25
/gene="SNX5"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:2035625192"
variation 23
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035625319"
variation 24
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568602625"
variation 25
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:151018697"
variation 26
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:548223667"
variation 27
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:960516271"
variation 28
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056073130"
variation 29
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:569421658"
variation 31
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1600369372"
variation 32
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1480033971"
variation 33
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:928860076"
variation 34
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:536225849"
variation 35
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035624554"
variation 36
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422440213"
variation 37
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2122459989"
variation 39
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:903730066"
variation 41
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035624385"
variation 42
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122459931"
variation 43
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1184028474"
variation 44
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035624261"
variation 47
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:981426173"
variation 48
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:569537525"
variation 49
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1397920339"
variation 52
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:990631477"
variation 53
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1346500697"
variation 55
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1244192330"
variation 56
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035623709"
variation 57
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035623650"
variation 58
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035623599"
variation 59
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1300296452"
variation 60
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:957936699"
variation 63
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256004664"
variation 64
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035623432"
variation 66
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035623375"
variation 67
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:113330582"
variation 68..73
/gene="SNX5"
/replace="ggc"
/replace="ggcggc"
/db_xref="dbSNP:2035623064"
variation 69
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035623251"
variation 71
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1323392998"
variation 72
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1600369230"
variation 73..79
/gene="SNX5"
/replace="cctc"
/replace="cctcctc"
/db_xref="dbSNP:2122459441"
variation 74
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:892170732"
variation 75
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1051268320"
variation 76
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568602486"
variation 79
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:933755956"
variation 80
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035622751"
variation 85
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1448580673"
variation 86
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:899596805"
variation 87..90
/gene="SNX5"
/replace=""
/replace="ggag"
/db_xref="dbSNP:1168218136"
variation 88
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1162451236"
variation 90
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448717194"
variation 91
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:770839567"
variation 94
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1014712260"
variation 95
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035622252"
exon 96..178
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 96
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035608619"
variation 97
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035608513"
variation 98
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1005323010"
variation 101
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:770339125"
variation 102
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035608295"
variation 103
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035608192"
variation 104
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760521878"
variation 105
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1425252501"
variation 106
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:572996375"
variation 107
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:976023444"
variation 109
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:554659700"
variation 112
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035607586"
variation 113
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035607524"
variation 115
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1435495548"
variation 117
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035607412"
variation 118
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1317407357"
variation 121
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324516714"
variation 122
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600367635"
variation 124
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600367627"
variation 126
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:940615713"
variation 127
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600367600"
CDS 128..1342
/gene="SNX5"
/note="isoform a is encoded by transcript variant 1"
/codon_start=1
/product="sorting nexin-5 isoform a"
/protein_id="NP_689413.1"
/db_xref="CCDS:CCDS13130.1"
/db_xref="GeneID:27131"
/db_xref="HGNC:HGNC:14969"
/db_xref="MIM:605937"
/translation="
MAAVPELLQQQEEDRSKLRSVSVDLNVDPSLQIDIPDALSERDKVKFTVHTKTTLPTFQSPEFSVTRQHEDFVWLHDTLIETTDYAGLIIPPAPTKPDFDGPREKMQKLGEGEGSMTKEEFAKMKQELEAEYLAVFKKTVSSHEVFLQRLSSHPVLSKDRNFHVFLEYDQDLSVRRKNTKEMFGGFFKSVVKSADEVLFTGVKEVDDFFEQEKNFLINYYNRIKDSCVKADKMTRSHKNVADDYIHTAACLHSLALEEPTVIKKYLLKVAELFEKLRKVEGRVSSDEDLKLTELLRYYMLNIEAAKDLLYRRTKALIDYENSNKALDKARLKSKDVKLAEAHQQECCQKFEQLSESAKEELINFKRKRVAAFRKNLIEMSELEIKHARNNVSLLQSCIDLFKNN"
misc_feature 131..133
/gene="SNX5"
/note="N-acetylalanine.
/evidence=ECO:0007744|PubMed:19413330,
ECO:0007744|PubMed:22223895, ECO:0007744|PubMed:22814378;
propagated from UniProtKB/Swiss-Prot (Q9Y5X3.1);
acetylation site"
misc_feature 212..634
/gene="SNX5"
/note="The phosphoinositide binding Phox Homology domain
of Sorting Nexin 5; Region: PX_SNX5; cd07291"
/db_xref="CDD:132824"
misc_feature order(329..337,410..415,542..544)
/gene="SNX5"
/note="putative phosphoinositide binding site [chemical
binding]; other site"
/db_xref="CDD:132824"
misc_feature 632..910
/gene="SNX5"
/note="propagated from UniProtKB/Swiss-Prot (Q9Y5X3.1);
Region: Interaction with DOCK1.
/evidence=ECO:0000269|PubMed:18596235"
misc_feature 674..727
/gene="SNX5"
/note="propagated from UniProtKB/Swiss-Prot (Q9Y5X3.1);
Region: Membrane-binding amphipathic helix.
/evidence=ECO:0000303|PubMed:23085988"
misc_feature 680..1333
/gene="SNX5"
/note="The Bin/Amphiphysin/Rvs (BAR) domain of Sorting
Nexin 5; Region: BAR_SNX5; cd07663"
/db_xref="CDD:153347"
misc_feature 704..706
/gene="SNX5"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (Q9Y5X3.1); phosphorylation site"
misc_feature order(770..772,779..784,791..796,800..805,812..814,
821..826,833..835,854..859,863..868,875..877,884..889,
896..901,944..946,1211..1213,1220..1225,1229..1237,
1244..1246,1253..1258,1262..1270,1274..1279,1286..1291,
1295..1300,1307..1312,1316..1321)
/gene="SNX5"
/note="dimer interface [polypeptide binding]; other site"
/db_xref="CDD:153347"
misc_feature 950..952
/gene="SNX5"
/note="N6-acetyllysine.
/evidence=ECO:0007744|PubMed:19608861; propagated from
UniProtKB/Swiss-Prot (Q9Y5X3.1); acetylation site"
variation 128
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1275437736"
variation 130
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:767372854"
variation 131
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035606824"
variation 132
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:994077057"
variation 133
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324361419"
variation 134
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223001375"
variation 135
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:536264072"
variation 136
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035606488"
variation 137
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035606417"
variation 140
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1429655738"
variation 142
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:377578366"
variation 148
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1600367509"
variation 149
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:907759445"
variation 150
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:898048064"
variation 151..160
/gene="SNX5"
/replace="gcagcagcag"
/replace="gcagcagcagcag"
/db_xref="dbSNP:951711191"
variation 152
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236181971"
variation 153
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035605857"
variation 154
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:774358404"
variation 155
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261428214"
variation 156
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1170529332"
variation 157
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:568802177"
variation 159..168
/gene="SNX5"
/replace="aggagga"
/replace="aggaggagga"
/db_xref="dbSNP:2035604591"
variation 159
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:146288789"
variation 160
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1270248894"
variation 163
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:748861582"
variation 165
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1196691857"
variation 166
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035604733"
variation 167
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035604669"
variation 169
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:979818375"
variation 171
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045114799"
variation 175
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:946791826"
exon 179..283
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 181..184
/gene="SNX5"
/replace="gaga"
/replace="gagaga"
/db_xref="dbSNP:1259091115"
variation 183
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035373852"
variation 184
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:776654591"
variation 188
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288689832"
variation 189..191
/gene="SNX5"
/replace="t"
/replace="tat"
/db_xref="dbSNP:2035373392"
variation 193..196
/gene="SNX5"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:2035373262"
variation 193
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1206332374"
variation 194
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1350964494"
variation 198
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:771005650"
variation 199
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:760825526"
variation 200
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:373912588"
variation 201
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600346707"
variation 204
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1283660391"
variation 205
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:768489364"
variation 207
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1026667819"
variation 209
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1349743268"
variation 210
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:114912822"
variation 211
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1382781142"
variation 214
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035372714"
variation 216
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:780017698"
variation 217
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:769806012"
variation 219
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1471065829"
variation 220
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:745830027"
variation 221
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035372471"
variation 222
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:995623696"
variation 226
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035372385"
variation 229
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:780781748"
variation 230
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:549069341"
variation 232
/gene="SNX5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1194704752"
variation 232
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244276135"
variation 235
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369770913"
variation 239
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035372087"
variation 239
/gene="SNX5"
/replace="g"
/replace="gg"
/db_xref="dbSNP:761822881"
variation 240
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:758771996"
variation 241
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1254857964"
variation 242
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1201444495"
variation 244
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035371937"
variation 245..250
/gene="SNX5"
/replace="ag"
/replace="agtgag"
/db_xref="dbSNP:1165317012"
variation 248..255
/gene="SNX5"
/replace="gagaga"
/replace="gagagaga"
/db_xref="dbSNP:752065385"
variation 250
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:376524578"
variation 251
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1263564623"
variation 252
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1217738961"
variation 254
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:765668419"
variation 256
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:61756173"
variation 261
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1005095808"
variation 262
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271924981"
variation 264
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:906768804"
variation 275
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:759972900"
variation 277
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1372329726"
variation 279
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:754353468"
variation 283
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454807382"
exon 284..394
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 285
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:769618774"
variation 286
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:767667071"
variation 287
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1182192347"
variation 289
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:761872888"
variation 291
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:774645859"
variation 293
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035337403"
variation 295
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2122386129"
variation 297
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:199902705"
variation 298
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:371471011"
variation 299
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201197486"
variation 304
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035337182"
variation 306
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1222326524"
variation 307
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:770945924"
variation 308
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:747066909"
variation 309
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:747003104"
variation 310..313
/gene="SNX5"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:2035336935"
variation 310
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:772532101"
variation 313
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035336894"
variation 314..317
/gene="SNX5"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1388349501"
variation 317
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:771628005"
variation 323
/gene="SNX5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1305548346"
variation 331
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1425820834"
variation 332
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035336664"
variation 333
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035336623"
variation 334
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:747739246"
variation 335
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1157675881"
variation 336
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1157685266"
variation 341..343
/gene="SNX5"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:770573662"
variation 343..348
/gene="SNX5"
/replace="tgtg"
/replace="tgtgtg"
/db_xref="dbSNP:2035336264"
variation 344
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1055378835"
variation 345
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1385171593"
variation 346
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1229077765"
variation 349
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398612701"
variation 352
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778601423"
variation 353
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1158931744"
variation 354
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:755301238"
variation 356
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1266496870"
variation 357
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201572215"
variation 362
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:780016243"
variation 363..367
/gene="SNX5"
/replace="tt"
/replace="ttatt"
/db_xref="dbSNP:746481295"
variation 363..364
/gene="SNX5"
/replace=""
/replace="tt"
/db_xref="dbSNP:1490484416"
variation 364
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:539421369"
variation 365
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:577883790"
variation 366
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:367713822"
variation 369
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:373578457"
variation 370..376
/gene="SNX5"
/replace="aaca"
/replace="aacaaca"
/db_xref="dbSNP:1457658492"
variation 372
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568593211"
variation 375
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:756537371"
variation 376
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259123995"
variation 379
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:750944242"
variation 381
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:141800072"
variation 387
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1004171492"
variation 389
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035335289"
variation 393..394
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:2035335195"
variation 393
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:757425738"
exon 395..516
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 395
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:913634871"
variation 399
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1451501722"
variation 402
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:6045116"
variation 404
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:778034613"
variation 405
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200913564"
variation 407
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035312236"
variation 408
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:6045115"
variation 411
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:765972467"
variation 412
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:148068583"
variation 416
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:750292296"
variation 418
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375257051"
variation 419
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:761676504"
variation 421
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2035311707"
variation 422
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035311622"
variation 424
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035311553"
variation 426
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330102667"
variation 429
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:773810235"
variation 432
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:541944674"
variation 434
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:751333774"
variation 435
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:762534744"
variation 438
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:775180856"
variation 439
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1449852546"
variation 448
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:770024480"
variation 461
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1249955302"
variation 463..476
/gene="SNX5"
/replace="tga"
/replace="tgaagggtctatga"
/db_xref="dbSNP:1877782574"
variation 467
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:143544203"
variation 468
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:936831855"
variation 469
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035310618"
variation 471
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1308559056"
variation 473
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295701590"
variation 480
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244533541"
variation 486
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2035310256"
variation 487
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:781435390"
variation 489
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380134146"
variation 492
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:771429766"
variation 497
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035310094"
variation 498
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:747525681"
variation 505
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:530067358"
variation 506
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259856845"
variation 509
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758612407"
variation 511
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035309850"
variation 513..514
/gene="SNX5"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2035309800"
variation 514
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1318554267"
variation 516
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:752967148"
exon 517..640
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 518
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1357902492"
variation 523..526
/gene="SNX5"
/replace="tc"
/replace="tctc"
/db_xref="dbSNP:764203671"
variation 526
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367569798"
variation 527
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1600341213"
variation 529
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:374271284"
variation 535
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1453349729"
variation 543
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:759144343"
variation 544..548
/gene="SNX5"
/replace="tgt"
/replace="tgtgt"
/db_xref="dbSNP:758896347"
variation 546
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:776990029"
variation 549..550
/gene="SNX5"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1480114725"
variation 549
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568591713"
variation 550
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:984501724"
variation 551
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:149308583"
variation 555
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:747509316"
variation 556
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1202750132"
variation 561..568
/gene="SNX5"
/replace="tctt"
/replace="tctttctt"
/db_xref="dbSNP:753236123"
variation 561
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039587252"
variation 562
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:778494613"
variation 564
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1259439663"
variation 565
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1313510303"
variation 566
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:138864959"
variation 568
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:114894362"
variation 569
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:911518496"
variation 571
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:748283767"
variation 572
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:775618449"
variation 573
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:755184448"
variation 574
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039586731"
variation 575..581
/gene="SNX5"
/replace="ctt"
/replace="ctttctt"
/db_xref="dbSNP:1282362052"
variation 575
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039586692"
variation 576
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:749474204"
variation 578
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:780981111"
variation 581..582
/gene="SNX5"
/replace=""
/replace="a"
/db_xref="dbSNP:1461724384"
variation 582..584
/gene="SNX5"
/replace=""
/replace="ctc"
/db_xref="dbSNP:1221647112"
variation 586
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1306556533"
variation 589
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1377691725"
variation 590
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:766537375"
variation 595
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1347271953"
variation 598
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:765535844"
variation 600
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1381652637"
variation 602
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1377629220"
variation 605
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:562671037"
variation 606
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:145056868"
variation 607
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:764069035"
variation 615
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:752213767"
variation 627
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1174664787"
variation 630
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:141177501"
variation 635
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122373807"
variation 636
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430521006"
variation 639
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1193090244"
exon 641..736
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 641
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1449714069"
variation 645
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242072592"
variation 646
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:764792798"
variation 650
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:754515928"
variation 652
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:971873857"
variation 653
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:753501671"
variation 654
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:373259467"
variation 656
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039568968"
variation 660
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568590918"
variation 662
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:369531337"
variation 664
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:760421737"
variation 666..669
/gene="SNX5"
/replace="a"
/replace="aaga"
/db_xref="dbSNP:776457970"
variation 668..670
/gene="SNX5"
/replace=""
/replace="gag"
/db_xref="dbSNP:1568590890"
variation 670
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2273448"
variation 671
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:773669633"
variation 673
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:767996285"
variation 677
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:762321613"
variation 678
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1016189430"
variation 681
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1382114770"
variation 689
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:774777225"
variation 690
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039568075"
variation 691
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768775709"
variation 693..697
/gene="SNX5"
/replace="gtg"
/replace="gtgtg"
/db_xref="dbSNP:2039567932"
variation 694
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1350116173"
variation 695..700
/gene="SNX5"
/replace="gtg"
/replace="gtggtg"
/db_xref="dbSNP:766077215"
variation 697
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:999459680"
variation 701..704
/gene="SNX5"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:760378599"
variation 711
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039567737"
variation 717
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1408735967"
variation 722
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:749367679"
variation 724
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169945560"
variation 727
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1189203678"
variation 728
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:775569763"
variation 730
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1429912003"
variation 731
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1600339525"
variation 733
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1384065540"
exon 737..842
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 739
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:771873224"
variation 740
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438067837"
variation 744
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1349939628"
variation 746
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:536752229"
variation 747
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:747946291"
variation 748..753
/gene="SNX5"
/replace="ctt"
/replace="cttctt"
/db_xref="dbSNP:1568590288"
variation 748
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:778786704"
variation 751
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1398560975"
variation 754
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:768434696"
variation 757
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:895155684"
variation 760
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:145652755"
variation 762
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:755741863"
variation 763
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1427034923"
variation 764
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:750094863"
variation 769
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039548692"
variation 775
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:140595658"
variation 776
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488882701"
variation 777
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:895276778"
variation 778
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:781031324"
variation 780..781
/gene="SNX5"
/replace="ac"
/replace="acac"
/db_xref="dbSNP:2039548499"
variation 783
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:757620155"
variation 786
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:369193496"
variation 787
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:764524638"
variation 788
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039548338"
variation 789
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:763312847"
variation 793
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2122364312"
variation 794
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1285811074"
variation 795
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:753263158"
variation 796
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1600338049"
variation 807
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1003613074"
variation 814
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:765299262"
variation 817
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:759656136"
variation 824
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:776814309"
variation 826
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039547996"
variation 827..828
/gene="SNX5"
/replace=""
/replace="tacag"
/db_xref="dbSNP:2039547954"
variation 828
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760983459"
variation 829
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:773948183"
variation 830
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039547826"
variation 831
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403617338"
variation 832
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1178206917"
variation 834
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:768508088"
variation 837
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039547669"
variation 839..843
/gene="SNX5"
/replace="aaa"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:774286425"
variation 839
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1201341354"
exon 843..918
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 843
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775544916"
variation 844
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:769804400"
variation 845
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775946902"
variation 849
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122363667"
variation 850
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:539455748"
variation 851
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:746639789"
variation 852
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:777524319"
variation 853
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:758742720"
variation 855
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274696039"
variation 856
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:919703922"
variation 858
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:146672356"
variation 859
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:779284935"
variation 860
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:963553925"
variation 862..868
/gene="SNX5"
/replace="cc"
/replace="ccacacc"
/db_xref="dbSNP:2039545565"
variation 863
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568590075"
variation 865
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:755407618"
variation 868
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:372550237"
variation 869
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756281625"
variation 871
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039545307"
variation 874
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122363494"
variation 876
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:750577873"
variation 877
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411549449"
variation 880
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1371274389"
variation 882
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:767828190"
variation 883
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422988314"
variation 886
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1689155065"
variation 887
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568589996"
variation 890
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:762147468"
variation 895
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201917236"
variation 896
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:199879416"
variation 898
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:752501049"
variation 901
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:765139003"
variation 902
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1024912169"
variation 904
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:142401289"
variation 906
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:933765716"
variation 907
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039544539"
variation 909
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1012239568"
variation 910
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:776699156"
variation 912
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:770319083"
variation 913
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1251939558"
variation 914
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:760284212"
variation 915
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:959376180"
variation 918
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1383204344"
exon 919..958
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 919
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:201254238"
variation 920
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174952563"
variation 923
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:936890145"
variation 925
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:768979593"
variation 926
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:925334521"
variation 932
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256410289"
variation 934
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039528172"
variation 937
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:975500012"
variation 943
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:148084267"
variation 946
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1184666064"
variation 948
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039528023"
variation 949
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:770297045"
variation 953
/gene="SNX5"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1274165829"
variation 953
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427557303"
variation 955
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:909732542"
variation 958
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039527821"
exon 959..1045
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 959
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147786677"
variation 962..963
/gene="SNX5"
/replace=""
/replace="gt"
/db_xref="dbSNP:2039526517"
variation 962
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:768497425"
variation 965..966
/gene="SNX5"
/replace=""
/replace="gaa"
/db_xref="dbSNP:2039526443"
variation 965
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1449657202"
variation 967
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:762545436"
variation 968
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201856245"
variation 969
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039526288"
variation 970
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:531468330"
variation 971
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:746381456"
variation 972
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:777316494"
variation 974
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039526080"
variation 978
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039526046"
variation 979
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:746787153"
variation 980
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039525953"
variation 982..984
/gene="SNX5"
/replace="a"
/replace="aga"
/db_xref="dbSNP:2039525874"
variation 982
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1319616399"
variation 984
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1034021590"
variation 988
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1455594809"
variation 992
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039525736"
variation 994
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:115502408"
variation 996..1000
/gene="SNX5"
/replace="a"
/replace="agcta"
/db_xref="dbSNP:2039525606"
variation 998
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:11542902"
variation 1003..1006
/gene="SNX5"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:2039525564"
variation 1010
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200592783"
variation 1013
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:758576026"
variation 1014
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1190962856"
variation 1016
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:749326525"
variation 1018
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1555786324"
variation 1020
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1450715208"
variation 1021
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341433087"
variation 1022
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:779888972"
variation 1023
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010214897"
variation 1024
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370183961"
variation 1026
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:892756287"
variation 1027
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750333452"
variation 1028
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:767494545"
variation 1029
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:751031852"
variation 1030
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039524511"
variation 1031
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:377697187"
variation 1036
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:545649463"
variation 1039
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1399442648"
variation 1040
/gene="SNX5"
/replace=""
/replace="g"
/db_xref="dbSNP:1161092921"
variation 1042
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:377587399"
variation 1043
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473690617"
variation 1045
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:6075268"
exon 1046..1205
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 1049
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1366343069"
variation 1050
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272535976"
variation 1051
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1257117073"
variation 1053
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:777331458"
variation 1054
/gene="SNX5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2039505429"
variation 1054
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:943128366"
variation 1055
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1331254032"
variation 1058
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:757885596"
variation 1061
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376255348"
variation 1062
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:764745399"
variation 1065
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1238028570"
variation 1066
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:373050708"
variation 1070
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:754185526"
variation 1072
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:756212310"
variation 1073
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:931574098"
variation 1074
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1415935246"
variation 1075
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:766859506"
variation 1077
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:761246039"
variation 1078
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600334226"
variation 1080
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1568588503"
variation 1083
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:773664052"
variation 1084
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568588496"
variation 1087
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:772163613"
variation 1092..1099
/gene="SNX5"
/replace="caaa"
/replace="caaacaaa"
/db_xref="dbSNP:1269135366"
variation 1092
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1466559123"
variation 1093..1095
/gene="SNX5"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1296634228"
variation 1100
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:918799378"
variation 1101
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203604800"
variation 1102
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:974448932"
variation 1103
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:369908673"
variation 1105
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1600334150"
variation 1107
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:912034125"
variation 1108
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:761850586"
variation 1109
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:774514947"
variation 1112
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:984136576"
variation 1115
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:768722799"
variation 1116
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:950977818"
variation 1117
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:749517967"
variation 1123
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367124276"
variation 1124
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:371601931"
variation 1126
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1447206103"
variation 1132
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:61762680"
variation 1133
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:116425682"
variation 1137
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369543726"
variation 1138
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039503350"
variation 1144
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1389596422"
variation 1149
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777619898"
variation 1152
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:575775461"
variation 1154
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1279236186"
variation 1156
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039503004"
variation 1158
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:994789511"
variation 1166
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1207947801"
variation 1168
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039502799"
variation 1171
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:557200574"
variation 1174
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:149888152"
variation 1180
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039502601"
variation 1183
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748179170"
variation 1184
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:539118133"
variation 1188
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:766842736"
variation 1189
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:761164423"
variation 1190
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:139196479"
variation 1193
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:767866368"
variation 1195
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174920602"
variation 1196
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1014269336"
variation 1202
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1389101703"
exon 1206..1291
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 1211
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:752166913"
variation 1214
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:899691950"
variation 1218
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039441536"
variation 1223
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:150810533"
variation 1224
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:376369085"
variation 1228
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1456539681"
variation 1230
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352015839"
variation 1232
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:926801905"
variation 1233
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213057977"
variation 1234
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:775569544"
variation 1235
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039441181"
variation 1238
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:765401451"
variation 1239
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:759807895"
variation 1244..1251
/gene="SNX5"
/replace="agaa"
/replace="agaaagaa"
/db_xref="dbSNP:1246970013"
variation 1244
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:963224770"
variation 1249
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:772822159"
variation 1256
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250585416"
variation 1257
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:771957175"
variation 1259
/gene="SNX5"
/replace=""
/replace="g"
/db_xref="dbSNP:754299876"
variation 1264
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1207692038"
variation 1269
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039440535"
variation 1272
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039440464"
variation 1274
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:368439202"
variation 1284
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039440370"
variation 1286
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039440327"
variation 1288
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:774466954"
variation 1290
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:919586287"
exon 1292..2099
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 1293
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039429974"
variation 1294
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122332348"
variation 1296
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:758844519"
variation 1297
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:565150872"
variation 1298..1300
/gene="SNX5"
/replace=""
/replace="gtc"
/db_xref="dbSNP:1568586000"
variation 1300
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:9322"
variation 1302
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1255467063"
variation 1304
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1198629369"
variation 1309
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039429650"
variation 1310
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1484305155"
variation 1312
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:746546895"
variation 1315
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1281066272"
variation 1316
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:755121199"
variation 1322
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1340221518"
variation 1324
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424987446"
variation 1326
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039429384"
variation 1327
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039429355"
variation 1328
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1300279115"
variation 1330
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753981963"
variation 1333
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:766577881"
variation 1334
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:760842315"
variation 1339
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1398257211"
variation 1344
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039429117"
variation 1345
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751335974"
variation 1347
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:763998462"
variation 1348
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302341672"
variation 1355
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1326522762"
variation 1356
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:762972531"
variation 1358..1359
/gene="SNX5"
/replace=""
/replace="aa"
/db_xref="dbSNP:1170088020"
variation 1359
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200970421"
variation 1363..1367
/gene="SNX5"
/replace="aa"
/replace="aagaa"
/db_xref="dbSNP:766948155"
variation 1363
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:769156235"
variation 1365
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:759037260"
variation 1371
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:776036588"
variation 1373
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:371955197"
variation 1376..1384
/gene="SNX5"
/replace="gaaag"
/replace="gaaagaaag"
/db_xref="dbSNP:761318673"
variation 1376
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1204447961"
variation 1379
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039428434"
variation 1380
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1336500426"
variation 1384
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1482105412"
variation 1385
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284080595"
variation 1386
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1196584700"
variation 1391
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:746676277"
variation 1393
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:554810351"
variation 1394
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:536739314"
variation 1395
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:995359763"
variation 1396
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409996009"
variation 1397
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:779861998"
variation 1399
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039427824"
variation 1401
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039427772"
variation 1402
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039427733"
variation 1403
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1291535815"
variation 1406
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1487772249"
variation 1409
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:575555700"
variation 1410
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039427548"
variation 1413
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039427506"
variation 1416
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:371827386"
variation 1417
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:557278713"
variation 1420
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039427367"
variation 1425
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:538165341"
variation 1427
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039427314"
variation 1428
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:905507675"
variation 1432
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:142219759"
variation 1439
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122331718"
variation 1440
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:148718726"
variation 1442
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039427193"
variation 1447
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:534007104"
variation 1452
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039427134"
variation 1453
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122331673"
variation 1454
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1298737959"
variation 1455
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:757178008"
variation 1457..1464
/gene="SNX5"
/replace="aata"
/replace="aataaata"
/db_xref="dbSNP:531340560"
variation 1459
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039427052"
variation 1461..1464
/gene="SNX5"
/replace="aata"
/replace="c"
/db_xref="dbSNP:1555785657"
variation 1465
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:146534301"
variation 1466
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039426924"
variation 1468
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039426901"
variation 1475
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039426879"
variation 1476
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370623964"
variation 1479
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:750091723"
variation 1481
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039426788"
variation 1482
/gene="SNX5"
/replace=""
/replace="c"
/db_xref="dbSNP:2039426754"
variation 1483
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:144308630"
variation 1485
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039426682"
variation 1491
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039426645"
variation 1497
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:943007940"
variation 1501
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1314785774"
variation 1502
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:764131449"
variation 1503
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1039309322"
variation 1504
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230082990"
variation 1511..1517
/gene="SNX5"
/replace="tatt"
/replace="tattatt"
/db_xref="dbSNP:1252333910"
variation 1513
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039426476"
variation 1516
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2069934060"
variation 1518
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:911216203"
variation 1519
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:984054405"
variation 1520
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568585836"
variation 1524
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039426278"
variation 1531
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196155183"
variation 1532
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1244496719"
variation 1533
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1461466609"
variation 1537
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1182671331"
variation 1539
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039426025"
variation 1540
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1770941695"
variation 1546
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039425968"
variation 1548
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1411342318"
variation 1553
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335159343"
variation 1563
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:944947469"
variation 1564
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:952719088"
variation 1567
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1460427547"
variation 1568
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:918646258"
variation 1570
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039425614"
variation 1573
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039425564"
variation 1575
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039425518"
variation 1576..1580
/gene="SNX5"
/replace=""
/replace="ccaaa"
/db_xref="dbSNP:2039425475"
variation 1580
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039425435"
variation 1584
/gene="SNX5"
/replace=""
/replace="t"
/db_xref="dbSNP:2039425397"
variation 1585
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039425344"
variation 1590
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039425286"
variation 1591
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039425241"
variation 1592..1594
/gene="SNX5"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2039425186"
variation 1592
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1285744903"
variation 1594
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242410101"
variation 1595
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:759475864"
variation 1601
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:529746738"
variation 1602
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:960127663"
variation 1603
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039424988"
variation 1604
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1437344760"
variation 1607
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039424879"
variation 1611..1615
/gene="SNX5"
/replace="ta"
/replace="tacta"
/db_xref="dbSNP:1296767244"
variation 1612
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039424830"
variation 1614
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1384234188"
variation 1616
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:368804838"
variation 1617
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1035551965"
variation 1619
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1307402154"
variation 1620..1621
/gene="SNX5"
/replace=""
/replace="ag"
/db_xref="dbSNP:2039424567"
variation 1621
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:182707782"
variation 1624
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:751680899"
variation 1625
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039424466"
variation 1627
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1913350496"
variation 1629
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1386575721"
variation 1631
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600327497"
variation 1632
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:983421324"
variation 1634
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1486662985"
variation 1635..1636
/gene="SNX5"
/replace=""
/replace="a"
/db_xref="dbSNP:776534036"
variation 1640
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600327467"
variation 1642..1644
/gene="SNX5"
/replace="t"
/replace="tct"
/db_xref="dbSNP:1186842922"
variation 1642
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039424252"
variation 1644
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122331039"
variation 1645
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1260840524"
variation 1647
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1476796471"
variation 1650
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:970032481"
variation 1658
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039424123"
variation 1659
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021559030"
variation 1661..1665
/gene="SNX5"
/replace="catca"
/replace="catcatca"
/db_xref="dbSNP:2039424055"
variation 1661
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011223706"
variation 1664
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429918767"
variation 1666
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039424028"
variation 1674
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039423998"
variation 1678..1680
/gene="SNX5"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:771890587"
variation 1680
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:950686219"
variation 1687
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039423890"
variation 1690
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:973872949"
variation 1692
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039423826"
variation 1695
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1357593625"
variation 1698
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039423778"
variation 1700..1702
/gene="SNX5"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1361783193"
variation 1700
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:962598977"
variation 1702
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1289784530"
variation 1709
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:568781721"
variation 1711
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1023875289"
variation 1714
/gene="SNX5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2039423475"
variation 1715
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039423424"
variation 1716
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1320096935"
variation 1718
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122330854"
variation 1719
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122330842"
variation 1720
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039423310"
variation 1721
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039423261"
variation 1727
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039423200"
variation 1732
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462169346"
variation 1736..1737
/gene="SNX5"
/replace=""
/replace="caa"
/db_xref="dbSNP:2039423109"
variation 1741
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:550125314"
variation 1742
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:766470468"
variation 1743
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039422960"
variation 1750
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318332187"
variation 1751
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:997299785"
variation 1752
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039422838"
variation 1759
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161813233"
variation 1760
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039422768"
variation 1770
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:6111748"
variation 1771
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:901337465"
variation 1773..1776
/gene="SNX5"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1568585710"
variation 1774
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568585715"
variation 1777
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600327342"
variation 1784
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:531965047"
variation 1787
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201317282"
variation 1794
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039422524"
variation 1795
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600327319"
variation 1796
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039422450"
variation 1798
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1269463295"
variation 1800
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374117869"
variation 1803
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191079596"
variation 1804
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1465827275"
variation 1807
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039422233"
variation 1810
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:763200506"
variation 1812
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423200244"
variation 1817
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402663646"
variation 1818..1819
/gene="SNX5"
/replace=""
/replace="a"
/db_xref="dbSNP:1207644577"
variation 1818
/gene="SNX5"
/replace="c"
/replace="catgc"
/db_xref="dbSNP:2039422137"
variation 1820
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1160185665"
variation 1821
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1451805234"
variation 1822..1831
/gene="SNX5"
/replace="t"
/replace="tgtttgtact"
/db_xref="dbSNP:1436462084"
variation 1824..1826
/gene="SNX5"
/replace=""
/replace="ttt"
/db_xref="dbSNP:1291657231"
variation 1824
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1305376611"
variation 1825
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1366687155"
variation 1828..1832
/gene="SNX5"
/replace="ta"
/replace="tacta"
/db_xref="dbSNP:1355445876"
variation 1828
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039421939"
variation 1830
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039421917"
variation 1831
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1272543487"
variation 1832
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:565263963"
variation 1833
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039421778"
variation 1835
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1223863367"
variation 1839..1843
/gene="SNX5"
/replace="ca"
/replace="cagca"
/db_xref="dbSNP:1351090703"
variation 1840
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1305760918"
variation 1843
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039421649"
variation 1844
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039421627"
variation 1846
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039421590"
variation 1851
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039421558"
variation 1855..1865
/gene="SNX5"
/replace="tttat"
/replace="tttatctttat"
/db_xref="dbSNP:1224374493"
variation 1855..1857
/gene="SNX5"
/replace="ttt"
/replace="tttttagccactttcgtagtctattttgtgtcaactggagttt"
/db_xref="dbSNP:2039421520"
variation 1859
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:773353395"
variation 1861..1863
/gene="SNX5"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:2039421426"
variation 1863..1868
/gene="SNX5"
/replace="tata"
/replace="tatata"
/db_xref="dbSNP:1490156627"
variation 1863
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039421385"
variation 1864
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039421341"
variation 1866
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:540519922"
variation 1868
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:911437716"
variation 1869
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1219363041"
variation 1870
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039421064"
variation 1871
/gene="SNX5"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1245043780"
variation 1872..1874
/gene="SNX5"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:999197260"
variation 1872
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039420972"
variation 1873
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039420930"
variation 1876
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411271978"
variation 1878..1883
/gene="SNX5"
/replace="cct"
/replace="cctcct"
/db_xref="dbSNP:2039420648"
variation 1878
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600327191"
variation 1879
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039420757"
variation 1880
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039420715"
variation 1883..1889
/gene="SNX5"
/replace="tttttt"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:138735602"
variation 1883
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039420609"
variation 1887
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039420569"
variation 1889
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:902149576"
variation 1893
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1048642229"
variation 1894
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1011052781"
variation 1896
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1366628745"
variation 1897..1901
/gene="SNX5"
/replace="ata"
/replace="atata"
/db_xref="dbSNP:1491406291"
variation 1897
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:931283455"
variation 1898
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:528717075"
variation 1900..1901
/gene="SNX5"
/replace=""
/replace="ttctctcccctc"
/db_xref="dbSNP:768591111"
variation 1900
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322080720"
variation 1902
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568585613"
variation 1903
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:973208165"
variation 1906
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039419952"
variation 1909..1920
/gene="SNX5"
/replace=""
/replace="gaggggagagaa"
/db_xref="dbSNP:760678044"
variation 1909
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039419902"
variation 1911
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:191911856"
variation 1919..1921
/gene="SNX5"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:2039419757"
variation 1920
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:928448940"
variation 1922
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1405085636"
variation 1924
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600327102"
variation 1925
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1315465166"
variation 1927
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039419577"
variation 1931
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039419528"
variation 1935
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397693482"
variation 1941
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:775573928"
variation 1943
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1170956708"
variation 1944
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:979925972"
variation 1945..1950
/gene="SNX5"
/replace="aa"
/replace="aaataa"
/db_xref="dbSNP:1205253178"
variation 1945..1947
/gene="SNX5"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:772097411"
variation 1947
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039419259"
variation 1948
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:969881688"
variation 1951
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039419155"
variation 1952..1956
/gene="SNX5"
/replace="gt"
/replace="gtggt"
/db_xref="dbSNP:2039419015"
variation 1952
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1021524020"
variation 1953
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:990095105"
variation 1954
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1237703974"
variation 1963
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039418979"
variation 1965
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1456588817"
variation 1965
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1185735736"
variation 1970..1978
/gene="SNX5"
/replace=""
/replace="tggccagat"
/db_xref="dbSNP:1472634660"
variation 1970
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039418892"
variation 1973
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039418864"
variation 1976
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386106437"
variation 1977
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122329733"
variation 1979
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:762228171"
variation 1980
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:944856516"
variation 1983
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390163069"
variation 1985
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169305519"
variation 1987
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397581153"
variation 1989
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:188249622"
variation 1990
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:997668549"
variation 1991
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1445489293"
variation 1996
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:920578915"
variation 1997
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122329629"
variation 1998
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1217983153"
variation 1999
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:139589175"
variation 2001..2008
/gene="SNX5"
/replace="ccc"
/replace="cccctccc"
/db_xref="dbSNP:1568585534"
variation 2001
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1017776897"
variation 2004
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:14885"
variation 2013..2014
/gene="SNX5"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2039418257"
variation 2015
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205648775"
variation 2016
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1007037066"
variation 2017
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:970538638"
variation 2020..2025
/gene="SNX5"
/replace="gggggg"
/replace="ggggggg"
/db_xref="dbSNP:1185835233"
variation 2021
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039418056"
variation 2022
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039418013"
variation 2023
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039417962"
variation 2025
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1442080376"
variation 2026
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600326934"
variation 2027
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1244233456"
variation 2032
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:575781578"
variation 2033
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:889962847"
variation 2034
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1422126945"
variation 2038
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039417529"
variation 2041..2052
/gene="SNX5"
/replace="g"
/replace="gtatgtctttgg"
/db_xref="dbSNP:2039417189"
variation 2041
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1470633345"
variation 2043
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039417446"
variation 2044
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600326907"
variation 2047
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039417349"
variation 2048..2050
/gene="SNX5"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:2039417306"
variation 2049
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:777068179"
variation 2050
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:931587892"
variation 2053
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1207142763"
variation 2057
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039417090"
variation 2058
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039417049"
variation 2060..2066
/gene="SNX5"
/replace="tttttt"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:966388240"
variation 2060
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1320012387"
variation 2062
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:897159440"
variation 2063..2068
/gene="SNX5"
/replace="t"
/replace="ttttat"
/db_xref="dbSNP:111911412"
variation 2064
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039416890"
variation 2066..2069
/gene="SNX5"
/replace="ta"
/replace="tata"
/db_xref="dbSNP:2122329334"
variation 2066
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1399312343"
variation 2067
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039416725"
variation 2069..2071
/gene="SNX5"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1219857253"
variation 2070
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039416669"
variation 2074..2081
/gene="SNX5"
/replace="ata"
/replace="atataata"
/db_xref="dbSNP:2039416498"
variation 2074
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010696503"
variation 2076..2082
/gene="SNX5"
/replace="ataa"
/replace="ataataa"
/db_xref="dbSNP:2039416474"
variation 2076
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037067912"
variation 2077
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:545454309"
variation 2078..2087
/gene="SNX5"
/replace="aataa"
/replace="aataaaataa"
/db_xref="dbSNP:779222776"
variation 2083..2088
/gene="SNX5"
/replace="aat"
/replace="aataat"
/db_xref="dbSNP:1600326840"
regulatory 2083..2088
/regulatory_class="polyA_signal_sequence"
/gene="SNX5"
/note="hexamer: AATAAT"
variation 2085
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273259844"
variation 2088
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193402301"
variation 2089
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:182670803"
variation 2090
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:558940088"
variation 2092
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568585465"
variation 2096
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039416184"
polyA_site 2099
/gene="SNX5"
/note="major polyA site"
ORIGIN
ctttctctagacgcgtcttgctgggagagtgtccgttgcttcccgtccgtgtcgcggccctgcggttggcggcctcctcgtggagcggagcaaggccaggcggcccctgctcgagtcccgcgtcgccatggccgcggttcccgagttgctgcagcagcaggaggaggaccgcagcaagctgagatctgtatctgtggacctgaatgttgatccctcgcttcagattgacatacctgatgcgctcagtgagagagacaaagtcaaatttacagtgcacacaaagaccacactgcccacgtttcagagcccagagttttctgttacaaggcaacatgaagactttgtgtggctacatgacactcttattgaaacaacagactatgctgggcttattattccacctgctcctacgaagcccgactttgatggtcctcgagagaagatgcagaaactgggagaaggtgaagggtctatgaccaaagaagaatttgccaagatgaaacaagaactggaagctgagtatctcgctgtgtttaagaagactgtgtcctcccatgaagtctttcttcagcggctttcttctcaccctgttctcagtaaagatcgcaactttcatgttttcctggaatatgatcaggatctaagtgttaggcggaaaaatactaaagagatgtttggtggcttcttcaaaagtgtggtgaaaagtgctgatgaagtcctttttactggagttaaggaggtagatgacttctttgagcaagagaagaacttccttattaactattacaataggatcaaagattcttgtgtgaaagctgacaaaatgaccagatctcataaaaatgttgccgatgactatatccacaccgcagcctgcttacatagcctggctttagaagagcccacagtcatcaaaaagtacctattgaaggttgctgagctatttgaaaaactaaggaaagtagagggtcgagtttcatcagatgaagatttgaagctaacagagctcctccgatactacatgctcaacattgaagctgctaaggatctcttatacagacgcaccaaagccctcattgactatgagaactcaaacaaagctctggataaggcccggttaaagagcaaagacgtcaagttggctgaggcacaccagcaggagtgctgccagaaatttgaacaactttccgaatctgcaaaagaagaactgataaatttcaaacggaagagagtggcagcatttagaaagaatctaattgaaatgtctgaactggaaataaaacatgccaggaacaatgtctcccttttgcagagctgtattgacttgttcaagaataactgatatgccttcactcagaagaaaagaaatgaatgtgaaagaaagccaagcatcacttgcacttaaatcattaccacggaagatatattagcttcaactttagtttaaaattatgtgaataaatattttgatttctacaaatcttaacatttaaccatgttggtttaaaaatattattgcttgctacttggacataactaatttttccttgtgcatttaatacctctgggcagaatccaaatactgggttctcccgtagttcgtctttagttactaagaaagggtgtaggacacattagccttctggaaacaagtagaagccatcacctggcccatgtccctacaaacccatgattgtcagggaggtgccagttacagcaggtgattcagctacttgaggtcggtaacagaccttccattcctcactgaaggtggggtttgtgtttttgttttgccctgttactccactggtagtcatctggtgtttgtactataacaacagcaagaaaatctcatttatctttatatactctttgcacctcctttttttagtcgagatataaatatttgaggggagagaaatatctacaggtatatatggaaacaaataatgtggtctgctttataagatggccagatctacattaggaaaagtataagccccctccctaatggccgctggggggtgagggcggtgtgttgtatgtctttgggtgtttgtttttttataaagcatataataaaataatcgtgctactaa
//
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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