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Previous release (v1)
2024-04-20 08:41:59, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001282454 2016 bp mRNA linear PRI 10-APR-2023
DEFINITION Homo sapiens sorting nexin 5 (SNX5), transcript variant 3, mRNA.
ACCESSION NM_001282454
VERSION NM_001282454.2
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 2016)
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 2016)
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 2016)
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 2016)
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 2016)
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 2016)
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 2016)
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 2016)
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 2016)
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 2016)
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 DA567854.1, BC062638.1 and
BC000100.3.
On Jun 2, 2019 this sequence version replaced NM_001282454.1.
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 (3) differs in the 5' structure,
lacks a portion of the 5' coding region, and initiates translation
at a downstream start codon, compared to variant 1. The encoded
isoform (b) has a shorter N-terminus, compared to 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 :: BC062638.1, SRR1803616.5041.1
[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
1-20 DA567854.1 198-217
21-1216 BC062638.1 3-1198
1217-2016 BC000100.3 1336-2135
FEATURES Location/Qualifiers
source 1..2016
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="20"
/map="20p11.23"
gene 1..2016
/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"
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..200
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 98..101
/gene="SNX5"
/replace="gaga"
/replace="gagaga"
/db_xref="dbSNP:1259091115"
variation 100
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035373852"
variation 101
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:776654591"
variation 105
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288689832"
variation 106..108
/gene="SNX5"
/replace="t"
/replace="tat"
/db_xref="dbSNP:2035373392"
variation 110..113
/gene="SNX5"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:2035373262"
variation 110
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1206332374"
variation 111
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1350964494"
variation 115
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:771005650"
variation 116
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:760825526"
variation 117
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:373912588"
variation 118
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600346707"
variation 121
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1283660391"
variation 122
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:768489364"
variation 124
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1026667819"
variation 126
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1349743268"
variation 127
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:114912822"
variation 128
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1382781142"
variation 131
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035372714"
variation 133
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:780017698"
variation 134
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:769806012"
variation 136
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1471065829"
variation 137
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:745830027"
variation 138
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035372471"
variation 139
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:995623696"
variation 143
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035372385"
variation 146
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:780781748"
variation 147
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:549069341"
variation 149
/gene="SNX5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1194704752"
variation 149
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244276135"
variation 152
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369770913"
variation 156
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035372087"
variation 156
/gene="SNX5"
/replace="g"
/replace="gg"
/db_xref="dbSNP:761822881"
variation 157
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:758771996"
variation 158
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1254857964"
variation 159
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1201444495"
variation 161
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035371937"
variation 162..167
/gene="SNX5"
/replace="ag"
/replace="agtgag"
/db_xref="dbSNP:1165317012"
variation 165..172
/gene="SNX5"
/replace="gagaga"
/replace="gagagaga"
/db_xref="dbSNP:752065385"
variation 167
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:376524578"
variation 168
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1263564623"
variation 169
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1217738961"
variation 171
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:765668419"
variation 173
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:61756173"
variation 178
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1005095808"
variation 179
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271924981"
variation 181
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:906768804"
variation 192
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:759972900"
variation 194
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1372329726"
variation 196
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:754353468"
variation 200
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454807382"
exon 201..311
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 202
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:769618774"
variation 203
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:767667071"
variation 204
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1182192347"
variation 206
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:761872888"
variation 208
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:774645859"
variation 210
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035337403"
variation 212
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2122386129"
variation 214
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:199902705"
variation 215
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:371471011"
variation 216
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201197486"
variation 221
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035337182"
variation 223
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1222326524"
variation 224
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:770945924"
variation 225
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:747066909"
variation 226
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:747003104"
variation 227..230
/gene="SNX5"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:2035336935"
variation 227
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:772532101"
variation 230
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035336894"
variation 231..234
/gene="SNX5"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1388349501"
variation 234
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:771628005"
variation 240
/gene="SNX5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1305548346"
variation 248
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1425820834"
variation 249
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035336664"
variation 250
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035336623"
variation 251
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:747739246"
variation 252
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1157675881"
variation 253
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1157685266"
variation 258..260
/gene="SNX5"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:770573662"
variation 260..265
/gene="SNX5"
/replace="tgtg"
/replace="tgtgtg"
/db_xref="dbSNP:2035336264"
variation 261
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1055378835"
variation 262
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1385171593"
variation 263
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1229077765"
variation 266
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398612701"
variation 269
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778601423"
variation 270
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1158931744"
variation 271
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:755301238"
variation 273
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1266496870"
variation 274
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201572215"
variation 279
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:780016243"
variation 280..284
/gene="SNX5"
/replace="tt"
/replace="ttatt"
/db_xref="dbSNP:746481295"
variation 280..281
/gene="SNX5"
/replace=""
/replace="tt"
/db_xref="dbSNP:1490484416"
variation 281
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:539421369"
variation 282
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:577883790"
variation 283
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:367713822"
variation 286
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:373578457"
variation 287..293
/gene="SNX5"
/replace="aaca"
/replace="aacaaca"
/db_xref="dbSNP:1457658492"
variation 289
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568593211"
variation 292
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:756537371"
variation 293
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259123995"
variation 296
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:750944242"
variation 298
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:141800072"
variation 304
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1004171492"
variation 306
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035335289"
variation 310..311
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:2035335195"
variation 310
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:757425738"
exon 312..433
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 312
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:913634871"
variation 316
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1451501722"
variation 319
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:6045116"
variation 321
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:778034613"
variation 322
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200913564"
variation 324
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035312236"
variation 325
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:6045115"
variation 328
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:765972467"
variation 329
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:148068583"
variation 333
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:750292296"
variation 335
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375257051"
variation 336
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:761676504"
variation 338
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2035311707"
variation 339
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035311622"
variation 341
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035311553"
variation 343
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330102667"
variation 346
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:773810235"
variation 349
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:541944674"
variation 351
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:751333774"
variation 352
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:762534744"
variation 355
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:775180856"
variation 356
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1449852546"
CDS 360..1259
/gene="SNX5"
/note="isoform b is encoded by transcript variant 3"
/codon_start=1
/product="sorting nexin-5 isoform b"
/protein_id="NP_001269383.1"
/db_xref="GeneID:27131"
/db_xref="HGNC:HGNC:14969"
/db_xref="MIM:605937"
/translation="
MQKLGEGEGSMTKEEFAKMKQELEAEYLAVFKKTVSSHEVFLQRLSSHPVLSKDRNFHVFLEYDQDLSVRRKNTKEMFGGFFKSVVKSADEVLFTGVKEVDDFFEQEKNFLINYYNRIKDSCVKADKMTRSHKNVADDYIHTAACLHSLALEEPTVIKKYLLKVAELFEKLRKVEGRVSSDEDLKLTELLRYYMLNIEAAKDLLYRRTKALIDYENSNKALDKARLKSKDVKLAEAHQQECCQKFEQLSESAKEELINFKRKRVAAFRKNLIEMSELEIKHARNNVSLLQSCIDLFKNN"
misc_feature <360..551
/gene="SNX5"
/note="The Phox Homology domain, a phosphoinositide
binding module; Region: PX_domain; cl02563"
/db_xref="CDD:445832"
misc_feature 597..1250
/gene="SNX5"
/note="The Bin/Amphiphysin/Rvs (BAR) domain of Sorting
Nexin 5; Region: BAR_SNX5; cd07663"
/db_xref="CDD:153347"
misc_feature order(687..689,696..701,708..713,717..722,729..731,
738..743,750..752,771..776,780..785,792..794,801..806,
813..818,861..863,1128..1130,1137..1142,1146..1154,
1161..1163,1170..1175,1179..1187,1191..1196,1203..1208,
1212..1217,1224..1229,1233..1238)
/gene="SNX5"
/note="dimer interface [polypeptide binding]; other site"
/db_xref="CDD:153347"
variation 365
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:770024480"
variation 378
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1249955302"
variation 380..393
/gene="SNX5"
/replace="tga"
/replace="tgaagggtctatga"
/db_xref="dbSNP:1877782574"
variation 384
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:143544203"
variation 385
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:936831855"
variation 386
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035310618"
variation 388
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1308559056"
variation 390
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295701590"
variation 397
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244533541"
variation 403
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2035310256"
variation 404
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:781435390"
variation 406
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380134146"
variation 409
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:771429766"
variation 414
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035310094"
variation 415
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:747525681"
variation 422
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:530067358"
variation 423
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259856845"
variation 426
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758612407"
variation 428
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035309850"
variation 430..431
/gene="SNX5"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2035309800"
variation 431
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1318554267"
variation 433
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:752967148"
exon 434..557
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 435
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1357902492"
variation 440..443
/gene="SNX5"
/replace="tc"
/replace="tctc"
/db_xref="dbSNP:764203671"
variation 443
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367569798"
variation 444
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1600341213"
variation 446
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:374271284"
variation 452
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1453349729"
variation 460
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:759144343"
variation 461..465
/gene="SNX5"
/replace="tgt"
/replace="tgtgt"
/db_xref="dbSNP:758896347"
variation 463
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:776990029"
variation 466..467
/gene="SNX5"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1480114725"
variation 466
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568591713"
variation 467
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:984501724"
variation 468
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:149308583"
variation 472
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:747509316"
variation 473
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1202750132"
variation 478..485
/gene="SNX5"
/replace="tctt"
/replace="tctttctt"
/db_xref="dbSNP:753236123"
variation 478
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039587252"
variation 479
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:778494613"
variation 481
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1259439663"
variation 482
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1313510303"
variation 483
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:138864959"
variation 485
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:114894362"
variation 486
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:911518496"
variation 488
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:748283767"
variation 489
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:775618449"
variation 490
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:755184448"
variation 491
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039586731"
variation 492..498
/gene="SNX5"
/replace="ctt"
/replace="ctttctt"
/db_xref="dbSNP:1282362052"
variation 492
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039586692"
variation 493
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:749474204"
variation 495
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:780981111"
variation 498..499
/gene="SNX5"
/replace=""
/replace="a"
/db_xref="dbSNP:1461724384"
variation 499..501
/gene="SNX5"
/replace=""
/replace="ctc"
/db_xref="dbSNP:1221647112"
variation 503
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1306556533"
variation 506
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1377691725"
variation 507
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:766537375"
variation 512
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1347271953"
variation 515
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:765535844"
variation 517
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1381652637"
variation 519
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1377629220"
variation 522
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:562671037"
variation 523
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:145056868"
variation 524
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:764069035"
variation 532
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:752213767"
variation 544
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1174664787"
variation 547
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:141177501"
variation 552
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122373807"
variation 553
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430521006"
variation 556
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1193090244"
exon 558..653
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 558
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1449714069"
variation 562
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242072592"
variation 563
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:764792798"
variation 567
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:754515928"
variation 569
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:971873857"
variation 570
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:753501671"
variation 571
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:373259467"
variation 573
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039568968"
variation 577
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568590918"
variation 579
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:369531337"
variation 581
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:760421737"
variation 583..586
/gene="SNX5"
/replace="a"
/replace="aaga"
/db_xref="dbSNP:776457970"
variation 585..587
/gene="SNX5"
/replace=""
/replace="gag"
/db_xref="dbSNP:1568590890"
variation 587
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2273448"
variation 588
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:773669633"
variation 590
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:767996285"
variation 594
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:762321613"
variation 595
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1016189430"
variation 598
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1382114770"
variation 606
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:774777225"
variation 607
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039568075"
variation 608
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768775709"
variation 610..614
/gene="SNX5"
/replace="gtg"
/replace="gtgtg"
/db_xref="dbSNP:2039567932"
variation 611
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1350116173"
variation 612..617
/gene="SNX5"
/replace="gtg"
/replace="gtggtg"
/db_xref="dbSNP:766077215"
variation 614
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:999459680"
variation 618..621
/gene="SNX5"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:760378599"
variation 628
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039567737"
variation 634
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1408735967"
variation 639
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:749367679"
variation 641
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169945560"
variation 644
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1189203678"
variation 645
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:775569763"
variation 647
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1429912003"
variation 648
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1600339525"
variation 650
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1384065540"
exon 654..759
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 656
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:771873224"
variation 657
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438067837"
variation 661
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1349939628"
variation 663
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:536752229"
variation 664
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:747946291"
variation 665..670
/gene="SNX5"
/replace="ctt"
/replace="cttctt"
/db_xref="dbSNP:1568590288"
variation 665
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:778786704"
variation 668
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1398560975"
variation 671
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:768434696"
variation 674
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:895155684"
variation 677
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:145652755"
variation 679
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:755741863"
variation 680
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1427034923"
variation 681
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:750094863"
variation 686
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039548692"
variation 692
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:140595658"
variation 693
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488882701"
variation 694
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:895276778"
variation 695
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:781031324"
variation 697..698
/gene="SNX5"
/replace="ac"
/replace="acac"
/db_xref="dbSNP:2039548499"
variation 700
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:757620155"
variation 703
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:369193496"
variation 704
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:764524638"
variation 705
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039548338"
variation 706
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:763312847"
variation 710
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2122364312"
variation 711
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1285811074"
variation 712
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:753263158"
variation 713
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1600338049"
variation 724
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1003613074"
variation 731
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:765299262"
variation 734
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:759656136"
variation 741
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:776814309"
variation 743
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039547996"
variation 744..745
/gene="SNX5"
/replace=""
/replace="tacag"
/db_xref="dbSNP:2039547954"
variation 745
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760983459"
variation 746
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:773948183"
variation 747
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039547826"
variation 748
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403617338"
variation 749
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1178206917"
variation 751
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:768508088"
variation 754
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039547669"
variation 756..760
/gene="SNX5"
/replace="aaa"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:774286425"
variation 756
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1201341354"
exon 760..835
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 760
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775544916"
variation 761
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:769804400"
variation 762
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775946902"
variation 766
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122363667"
variation 767
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:539455748"
variation 768
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:746639789"
variation 769
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:777524319"
variation 770
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:758742720"
variation 772
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274696039"
variation 773
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:919703922"
variation 775
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:146672356"
variation 776
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:779284935"
variation 777
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:963553925"
variation 779..785
/gene="SNX5"
/replace="cc"
/replace="ccacacc"
/db_xref="dbSNP:2039545565"
variation 780
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568590075"
variation 782
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:755407618"
variation 785
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:372550237"
variation 786
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756281625"
variation 788
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039545307"
variation 791
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122363494"
variation 793
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:750577873"
variation 794
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411549449"
variation 797
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1371274389"
variation 799
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:767828190"
variation 800
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422988314"
variation 803
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1689155065"
variation 804
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568589996"
variation 807
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:762147468"
variation 812
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201917236"
variation 813
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:199879416"
variation 815
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:752501049"
variation 818
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:765139003"
variation 819
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1024912169"
variation 821
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:142401289"
variation 823
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:933765716"
variation 824
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039544539"
variation 826
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1012239568"
variation 827
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:776699156"
variation 829
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:770319083"
variation 830
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1251939558"
variation 831
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:760284212"
variation 832
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:959376180"
variation 835
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1383204344"
exon 836..875
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 836
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:201254238"
variation 837
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174952563"
variation 840
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:936890145"
variation 842
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:768979593"
variation 843
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:925334521"
variation 849
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256410289"
variation 851
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039528172"
variation 854
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:975500012"
variation 860
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:148084267"
variation 863
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1184666064"
variation 865
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039528023"
variation 866
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:770297045"
variation 870
/gene="SNX5"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1274165829"
variation 870
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427557303"
variation 872
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:909732542"
variation 875
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039527821"
exon 876..962
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 876
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147786677"
variation 879..880
/gene="SNX5"
/replace=""
/replace="gt"
/db_xref="dbSNP:2039526517"
variation 879
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:768497425"
variation 882..883
/gene="SNX5"
/replace=""
/replace="gaa"
/db_xref="dbSNP:2039526443"
variation 882
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1449657202"
variation 884
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:762545436"
variation 885
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201856245"
variation 886
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039526288"
variation 887
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:531468330"
variation 888
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:746381456"
variation 889
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:777316494"
variation 891
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039526080"
variation 895
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039526046"
variation 896
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:746787153"
variation 897
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039525953"
variation 899..901
/gene="SNX5"
/replace="a"
/replace="aga"
/db_xref="dbSNP:2039525874"
variation 899
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1319616399"
variation 901
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1034021590"
variation 905
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1455594809"
variation 909
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039525736"
variation 911
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:115502408"
variation 913..917
/gene="SNX5"
/replace="a"
/replace="agcta"
/db_xref="dbSNP:2039525606"
variation 915
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:11542902"
variation 920..923
/gene="SNX5"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:2039525564"
variation 927
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200592783"
variation 930
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:758576026"
variation 931
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1190962856"
variation 933
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:749326525"
variation 935
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1555786324"
variation 937
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1450715208"
variation 938
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341433087"
variation 939
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:779888972"
variation 940
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010214897"
variation 941
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370183961"
variation 943
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:892756287"
variation 944
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750333452"
variation 945
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:767494545"
variation 946
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:751031852"
variation 947
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039524511"
variation 948
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:377697187"
variation 953
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:545649463"
variation 956
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1399442648"
variation 957
/gene="SNX5"
/replace=""
/replace="g"
/db_xref="dbSNP:1161092921"
variation 959
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:377587399"
variation 960
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473690617"
variation 962
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:6075268"
exon 963..1122
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 966
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1366343069"
variation 967
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272535976"
variation 968
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1257117073"
variation 970
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:777331458"
variation 971
/gene="SNX5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2039505429"
variation 971
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:943128366"
variation 972
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1331254032"
variation 975
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:757885596"
variation 978
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376255348"
variation 979
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:764745399"
variation 982
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1238028570"
variation 983
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:373050708"
variation 987
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:754185526"
variation 989
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:756212310"
variation 990
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:931574098"
variation 991
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1415935246"
variation 992
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:766859506"
variation 994
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:761246039"
variation 995
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600334226"
variation 997
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1568588503"
variation 1000
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:773664052"
variation 1001
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568588496"
variation 1004
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:772163613"
variation 1009..1016
/gene="SNX5"
/replace="caaa"
/replace="caaacaaa"
/db_xref="dbSNP:1269135366"
variation 1009
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1466559123"
variation 1010..1012
/gene="SNX5"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1296634228"
variation 1017
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:918799378"
variation 1018
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203604800"
variation 1019
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:974448932"
variation 1020
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:369908673"
variation 1022
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1600334150"
variation 1024
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:912034125"
variation 1025
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:761850586"
variation 1026
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:774514947"
variation 1029
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:984136576"
variation 1032
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:768722799"
variation 1033
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:950977818"
variation 1034
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:749517967"
variation 1040
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367124276"
variation 1041
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:371601931"
variation 1043
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1447206103"
variation 1049
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:61762680"
variation 1050
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:116425682"
variation 1054
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369543726"
variation 1055
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039503350"
variation 1061
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1389596422"
variation 1066
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777619898"
variation 1069
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:575775461"
variation 1071
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1279236186"
variation 1073
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039503004"
variation 1075
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:994789511"
variation 1083
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1207947801"
variation 1085
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039502799"
variation 1088
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:557200574"
variation 1091
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:149888152"
variation 1097
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039502601"
variation 1100
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748179170"
variation 1101
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:539118133"
variation 1105
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:766842736"
variation 1106
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:761164423"
variation 1107
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:139196479"
variation 1110
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:767866368"
variation 1112
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174920602"
variation 1113
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1014269336"
variation 1119
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1389101703"
exon 1123..1208
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 1128
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:752166913"
variation 1131
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:899691950"
variation 1135
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039441536"
variation 1140
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:150810533"
variation 1141
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:376369085"
variation 1145
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1456539681"
variation 1147
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352015839"
variation 1149
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:926801905"
variation 1150
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213057977"
variation 1151
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:775569544"
variation 1152
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039441181"
variation 1155
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:765401451"
variation 1156
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:759807895"
variation 1161..1168
/gene="SNX5"
/replace="agaa"
/replace="agaaagaa"
/db_xref="dbSNP:1246970013"
variation 1161
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:963224770"
variation 1166
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:772822159"
variation 1173
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250585416"
variation 1174
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:771957175"
variation 1176
/gene="SNX5"
/replace=""
/replace="g"
/db_xref="dbSNP:754299876"
variation 1181
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1207692038"
variation 1186
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039440535"
variation 1189
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039440464"
variation 1191
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:368439202"
variation 1201
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039440370"
variation 1203
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039440327"
variation 1205
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:774466954"
variation 1207
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:919586287"
exon 1209..2016
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 1210
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039429974"
variation 1211
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122332348"
variation 1213
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:758844519"
variation 1214
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:565150872"
variation 1215..1217
/gene="SNX5"
/replace=""
/replace="gtc"
/db_xref="dbSNP:1568586000"
variation 1217
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:9322"
variation 1219
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1255467063"
variation 1221
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1198629369"
variation 1226
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039429650"
variation 1227
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1484305155"
variation 1229
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:746546895"
variation 1232
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1281066272"
variation 1233
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:755121199"
variation 1239
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1340221518"
variation 1241
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424987446"
variation 1243
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039429384"
variation 1244
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039429355"
variation 1245
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1300279115"
variation 1247
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753981963"
variation 1250
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:766577881"
variation 1251
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:760842315"
variation 1256
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1398257211"
variation 1261
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039429117"
variation 1262
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751335974"
variation 1264
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:763998462"
variation 1265
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302341672"
variation 1272
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1326522762"
variation 1273
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:762972531"
variation 1275..1276
/gene="SNX5"
/replace=""
/replace="aa"
/db_xref="dbSNP:1170088020"
variation 1276
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200970421"
variation 1280..1284
/gene="SNX5"
/replace="aa"
/replace="aagaa"
/db_xref="dbSNP:766948155"
variation 1280
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:769156235"
variation 1282
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:759037260"
variation 1288
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:776036588"
variation 1290
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:371955197"
variation 1293..1301
/gene="SNX5"
/replace="gaaag"
/replace="gaaagaaag"
/db_xref="dbSNP:761318673"
variation 1293
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1204447961"
variation 1296
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039428434"
variation 1297
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1336500426"
variation 1301
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1482105412"
variation 1302
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284080595"
variation 1303
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1196584700"
variation 1308
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:746676277"
variation 1310
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:554810351"
variation 1311
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:536739314"
variation 1312
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:995359763"
variation 1313
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409996009"
variation 1314
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:779861998"
variation 1316
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039427824"
variation 1318
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039427772"
variation 1319
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039427733"
variation 1320
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1291535815"
variation 1323
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1487772249"
variation 1326
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:575555700"
variation 1327
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039427548"
variation 1330
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039427506"
variation 1333
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:371827386"
variation 1334
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:557278713"
variation 1337
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039427367"
variation 1342
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:538165341"
variation 1344
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039427314"
variation 1345
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:905507675"
variation 1349
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:142219759"
variation 1356
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122331718"
variation 1357
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:148718726"
variation 1359
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039427193"
variation 1364
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:534007104"
variation 1369
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039427134"
variation 1370
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122331673"
variation 1371
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1298737959"
variation 1372
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:757178008"
variation 1374..1381
/gene="SNX5"
/replace="aata"
/replace="aataaata"
/db_xref="dbSNP:531340560"
variation 1376
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039427052"
variation 1378..1381
/gene="SNX5"
/replace="aata"
/replace="c"
/db_xref="dbSNP:1555785657"
variation 1382
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:146534301"
variation 1383
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039426924"
variation 1385
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039426901"
variation 1392
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039426879"
variation 1393
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370623964"
variation 1396
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:750091723"
variation 1398
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039426788"
variation 1399
/gene="SNX5"
/replace=""
/replace="c"
/db_xref="dbSNP:2039426754"
variation 1400
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:144308630"
variation 1402
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039426682"
variation 1408
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039426645"
variation 1414
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:943007940"
variation 1418
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1314785774"
variation 1419
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:764131449"
variation 1420
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1039309322"
variation 1421
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230082990"
variation 1428..1434
/gene="SNX5"
/replace="tatt"
/replace="tattatt"
/db_xref="dbSNP:1252333910"
variation 1430
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039426476"
variation 1433
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2069934060"
variation 1435
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:911216203"
variation 1436
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:984054405"
variation 1437
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568585836"
variation 1441
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039426278"
variation 1448
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196155183"
variation 1449
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1244496719"
variation 1450
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1461466609"
variation 1454
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1182671331"
variation 1456
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039426025"
variation 1457
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1770941695"
variation 1463
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039425968"
variation 1465
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1411342318"
variation 1470
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335159343"
variation 1480
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:944947469"
variation 1481
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:952719088"
variation 1484
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1460427547"
variation 1485
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:918646258"
variation 1487
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039425614"
variation 1490
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039425564"
variation 1492
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039425518"
variation 1493..1497
/gene="SNX5"
/replace=""
/replace="ccaaa"
/db_xref="dbSNP:2039425475"
variation 1497
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039425435"
variation 1501
/gene="SNX5"
/replace=""
/replace="t"
/db_xref="dbSNP:2039425397"
variation 1502
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039425344"
variation 1507
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039425286"
variation 1508
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039425241"
variation 1509..1511
/gene="SNX5"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2039425186"
variation 1509
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1285744903"
variation 1511
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242410101"
variation 1512
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:759475864"
variation 1518
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:529746738"
variation 1519
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:960127663"
variation 1520
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039424988"
variation 1521
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1437344760"
variation 1524
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039424879"
variation 1528..1532
/gene="SNX5"
/replace="ta"
/replace="tacta"
/db_xref="dbSNP:1296767244"
variation 1529
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039424830"
variation 1531
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1384234188"
variation 1533
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:368804838"
variation 1534
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1035551965"
variation 1536
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1307402154"
variation 1537..1538
/gene="SNX5"
/replace=""
/replace="ag"
/db_xref="dbSNP:2039424567"
variation 1538
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:182707782"
variation 1541
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:751680899"
variation 1542
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039424466"
variation 1544
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1913350496"
variation 1546
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1386575721"
variation 1548
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600327497"
variation 1549
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:983421324"
variation 1551
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1486662985"
variation 1552..1553
/gene="SNX5"
/replace=""
/replace="a"
/db_xref="dbSNP:776534036"
variation 1557
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600327467"
variation 1559..1561
/gene="SNX5"
/replace="t"
/replace="tct"
/db_xref="dbSNP:1186842922"
variation 1559
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039424252"
variation 1561
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122331039"
variation 1562
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1260840524"
variation 1564
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1476796471"
variation 1567
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:970032481"
variation 1575
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039424123"
variation 1576
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021559030"
variation 1578..1582
/gene="SNX5"
/replace="catca"
/replace="catcatca"
/db_xref="dbSNP:2039424055"
variation 1578
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011223706"
variation 1581
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429918767"
variation 1583
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039424028"
variation 1591
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039423998"
variation 1595..1597
/gene="SNX5"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:771890587"
variation 1597
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:950686219"
variation 1604
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039423890"
variation 1607
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:973872949"
variation 1609
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039423826"
variation 1612
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1357593625"
variation 1615
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039423778"
variation 1617..1619
/gene="SNX5"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1361783193"
variation 1617
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:962598977"
variation 1619
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1289784530"
variation 1626
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:568781721"
variation 1628
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1023875289"
variation 1631
/gene="SNX5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2039423475"
variation 1632
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039423424"
variation 1633
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1320096935"
variation 1635
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122330854"
variation 1636
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122330842"
variation 1637
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039423310"
variation 1638
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039423261"
variation 1644
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039423200"
variation 1649
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462169346"
variation 1653..1654
/gene="SNX5"
/replace=""
/replace="caa"
/db_xref="dbSNP:2039423109"
variation 1658
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:550125314"
variation 1659
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:766470468"
variation 1660
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039422960"
variation 1667
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318332187"
variation 1668
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:997299785"
variation 1669
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039422838"
variation 1676
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161813233"
variation 1677
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039422768"
variation 1687
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:6111748"
variation 1688
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:901337465"
variation 1690..1693
/gene="SNX5"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1568585710"
variation 1691
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568585715"
variation 1694
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600327342"
variation 1701
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:531965047"
variation 1704
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201317282"
variation 1711
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039422524"
variation 1712
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600327319"
variation 1713
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039422450"
variation 1715
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1269463295"
variation 1717
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374117869"
variation 1720
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191079596"
variation 1721
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1465827275"
variation 1724
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039422233"
variation 1727
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:763200506"
variation 1729
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423200244"
variation 1734
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402663646"
variation 1735..1736
/gene="SNX5"
/replace=""
/replace="a"
/db_xref="dbSNP:1207644577"
variation 1735
/gene="SNX5"
/replace="c"
/replace="catgc"
/db_xref="dbSNP:2039422137"
variation 1737
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1160185665"
variation 1738
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1451805234"
variation 1739..1748
/gene="SNX5"
/replace="t"
/replace="tgtttgtact"
/db_xref="dbSNP:1436462084"
variation 1741..1743
/gene="SNX5"
/replace=""
/replace="ttt"
/db_xref="dbSNP:1291657231"
variation 1741
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1305376611"
variation 1742
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1366687155"
variation 1745..1749
/gene="SNX5"
/replace="ta"
/replace="tacta"
/db_xref="dbSNP:1355445876"
variation 1745
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039421939"
variation 1747
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039421917"
variation 1748
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1272543487"
variation 1749
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:565263963"
variation 1750
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039421778"
variation 1752
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1223863367"
variation 1756..1760
/gene="SNX5"
/replace="ca"
/replace="cagca"
/db_xref="dbSNP:1351090703"
variation 1757
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1305760918"
variation 1760
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039421649"
variation 1761
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039421627"
variation 1763
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039421590"
variation 1768
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039421558"
variation 1772..1782
/gene="SNX5"
/replace="tttat"
/replace="tttatctttat"
/db_xref="dbSNP:1224374493"
variation 1772..1774
/gene="SNX5"
/replace="ttt"
/replace="tttttagccactttcgtagtctattttgtgtcaactggagttt"
/db_xref="dbSNP:2039421520"
variation 1776
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:773353395"
variation 1778..1780
/gene="SNX5"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:2039421426"
variation 1780..1785
/gene="SNX5"
/replace="tata"
/replace="tatata"
/db_xref="dbSNP:1490156627"
variation 1780
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039421385"
variation 1781
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039421341"
variation 1783
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:540519922"
variation 1785
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:911437716"
variation 1786
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1219363041"
variation 1787
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039421064"
variation 1788
/gene="SNX5"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1245043780"
variation 1789..1791
/gene="SNX5"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:999197260"
variation 1789
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039420972"
variation 1790
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039420930"
variation 1793
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411271978"
variation 1795..1800
/gene="SNX5"
/replace="cct"
/replace="cctcct"
/db_xref="dbSNP:2039420648"
variation 1795
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600327191"
variation 1796
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039420757"
variation 1797
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039420715"
variation 1800..1806
/gene="SNX5"
/replace="tttttt"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:138735602"
variation 1800
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039420609"
variation 1804
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039420569"
variation 1806
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:902149576"
variation 1810
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1048642229"
variation 1811
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1011052781"
variation 1813
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1366628745"
variation 1814..1818
/gene="SNX5"
/replace="ata"
/replace="atata"
/db_xref="dbSNP:1491406291"
variation 1814
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:931283455"
variation 1815
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:528717075"
variation 1817..1818
/gene="SNX5"
/replace=""
/replace="ttctctcccctc"
/db_xref="dbSNP:768591111"
variation 1817
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322080720"
variation 1819
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568585613"
variation 1820
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:973208165"
variation 1823
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039419952"
variation 1826..1837
/gene="SNX5"
/replace=""
/replace="gaggggagagaa"
/db_xref="dbSNP:760678044"
variation 1826
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039419902"
variation 1828
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:191911856"
variation 1836..1838
/gene="SNX5"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:2039419757"
variation 1837
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:928448940"
variation 1839
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1405085636"
variation 1841
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600327102"
variation 1842
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1315465166"
variation 1844
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039419577"
variation 1848
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039419528"
variation 1852
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397693482"
variation 1858
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:775573928"
variation 1860
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1170956708"
variation 1861
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:979925972"
variation 1862..1867
/gene="SNX5"
/replace="aa"
/replace="aaataa"
/db_xref="dbSNP:1205253178"
variation 1862..1864
/gene="SNX5"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:772097411"
variation 1864
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039419259"
variation 1865
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:969881688"
variation 1868
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039419155"
variation 1869..1873
/gene="SNX5"
/replace="gt"
/replace="gtggt"
/db_xref="dbSNP:2039419015"
variation 1869
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1021524020"
variation 1870
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:990095105"
variation 1871
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1237703974"
variation 1880
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039418979"
variation 1882
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1456588817"
variation 1882
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1185735736"
variation 1887..1895
/gene="SNX5"
/replace=""
/replace="tggccagat"
/db_xref="dbSNP:1472634660"
variation 1887
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039418892"
variation 1890
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039418864"
variation 1893
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386106437"
variation 1894
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122329733"
variation 1896
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:762228171"
variation 1897
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:944856516"
variation 1900
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390163069"
variation 1902
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169305519"
variation 1904
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397581153"
variation 1906
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:188249622"
variation 1907
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:997668549"
variation 1908
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1445489293"
variation 1913
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:920578915"
variation 1914
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122329629"
variation 1915
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1217983153"
variation 1916
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:139589175"
variation 1918..1925
/gene="SNX5"
/replace="ccc"
/replace="cccctccc"
/db_xref="dbSNP:1568585534"
variation 1918
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1017776897"
variation 1921
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:14885"
variation 1930..1931
/gene="SNX5"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2039418257"
variation 1932
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205648775"
variation 1933
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1007037066"
variation 1934
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:970538638"
variation 1937..1942
/gene="SNX5"
/replace="gggggg"
/replace="ggggggg"
/db_xref="dbSNP:1185835233"
variation 1938
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039418056"
variation 1939
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039418013"
variation 1940
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039417962"
variation 1942
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1442080376"
variation 1943
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600326934"
variation 1944
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1244233456"
variation 1949
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:575781578"
variation 1950
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:889962847"
variation 1951
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1422126945"
variation 1955
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039417529"
variation 1958..1969
/gene="SNX5"
/replace="g"
/replace="gtatgtctttgg"
/db_xref="dbSNP:2039417189"
variation 1958
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1470633345"
variation 1960
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039417446"
variation 1961
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600326907"
variation 1964
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039417349"
variation 1965..1967
/gene="SNX5"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:2039417306"
variation 1966
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:777068179"
variation 1967
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:931587892"
variation 1970
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1207142763"
variation 1974
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039417090"
variation 1975
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039417049"
variation 1977..1983
/gene="SNX5"
/replace="tttttt"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:966388240"
variation 1977
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1320012387"
variation 1979
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:897159440"
variation 1980..1985
/gene="SNX5"
/replace="t"
/replace="ttttat"
/db_xref="dbSNP:111911412"
variation 1981
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039416890"
variation 1983..1986
/gene="SNX5"
/replace="ta"
/replace="tata"
/db_xref="dbSNP:2122329334"
variation 1983
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1399312343"
variation 1984
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039416725"
variation 1986..1988
/gene="SNX5"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1219857253"
variation 1987
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039416669"
variation 1991..1998
/gene="SNX5"
/replace="ata"
/replace="atataata"
/db_xref="dbSNP:2039416498"
variation 1991
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010696503"
variation 1993..1999
/gene="SNX5"
/replace="ataa"
/replace="ataataa"
/db_xref="dbSNP:2039416474"
variation 1993
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037067912"
variation 1994
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:545454309"
variation 1995..2004
/gene="SNX5"
/replace="aataa"
/replace="aataaaataa"
/db_xref="dbSNP:779222776"
variation 2000..2005
/gene="SNX5"
/replace="aat"
/replace="aataat"
/db_xref="dbSNP:1600326840"
regulatory 2000..2005
/regulatory_class="polyA_signal_sequence"
/gene="SNX5"
/note="hexamer: AATAAT"
variation 2002
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273259844"
variation 2005
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193402301"
variation 2006
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:182670803"
variation 2007
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:558940088"
variation 2009
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568585465"
variation 2013
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039416184"
polyA_site 2016
/gene="SNX5"
/note="major polyA site"
ORIGIN
ctttctctagacgcgtcttgctgggagagtgtccgttgcttcccgtccgtgtcgcggccctgcggttggcggcctcctcgtggagcggagcaaggctgagatctgtatctgtggacctgaatgttgatccctcgcttcagattgacatacctgatgcgctcagtgagagagacaaagtcaaatttacagtgcacacaaagaccacactgcccacgtttcagagcccagagttttctgttacaaggcaacatgaagactttgtgtggctacatgacactcttattgaaacaacagactatgctgggcttattattccacctgctcctacgaagcccgactttgatggtcctcgagagaagatgcagaaactgggagaaggtgaagggtctatgaccaaagaagaatttgccaagatgaaacaagaactggaagctgagtatctcgctgtgtttaagaagactgtgtcctcccatgaagtctttcttcagcggctttcttctcaccctgttctcagtaaagatcgcaactttcatgttttcctggaatatgatcaggatctaagtgttaggcggaaaaatactaaagagatgtttggtggcttcttcaaaagtgtggtgaaaagtgctgatgaagtcctttttactggagttaaggaggtagatgacttctttgagcaagagaagaacttccttattaactattacaataggatcaaagattcttgtgtgaaagctgacaaaatgaccagatctcataaaaatgttgccgatgactatatccacaccgcagcctgcttacatagcctggctttagaagagcccacagtcatcaaaaagtacctattgaaggttgctgagctatttgaaaaactaaggaaagtagagggtcgagtttcatcagatgaagatttgaagctaacagagctcctccgatactacatgctcaacattgaagctgctaaggatctcttatacagacgcaccaaagccctcattgactatgagaactcaaacaaagctctggataaggcccggttaaagagcaaagacgtcaagttggctgaggcacaccagcaggagtgctgccagaaatttgaacaactttccgaatctgcaaaagaagaactgataaatttcaaacggaagagagtggcagcatttagaaagaatctaattgaaatgtctgaactggaaataaaacatgccaggaacaatgtctcccttttgcagagctgtattgacttgttcaagaataactgatatgccttcactcagaagaaaagaaatgaatgtgaaagaaagccaagcatcacttgcacttaaatcattaccacggaagatatattagcttcaactttagtttaaaattatgtgaataaatattttgatttctacaaatcttaacatttaaccatgttggtttaaaaatattattgcttgctacttggacataactaatttttccttgtgcatttaatacctctgggcagaatccaaatactgggttctcccgtagttcgtctttagttactaagaaagggtgtaggacacattagccttctggaaacaagtagaagccatcacctggcccatgtccctacaaacccatgattgtcagggaggtgccagttacagcaggtgattcagctacttgaggtcggtaacagaccttccattcctcactgaaggtggggtttgtgtttttgttttgccctgttactccactggtagtcatctggtgtttgtactataacaacagcaagaaaatctcatttatctttatatactctttgcacctcctttttttagtcgagatataaatatttgaggggagagaaatatctacaggtatatatggaaacaaataatgtggtctgctttataagatggccagatctacattaggaaaagtataagccccctccctaatggccgctggggggtgagggcggtgtgttgtatgtctttgggtgtttgtttttttataaagcatataataaaataatcgtgctactaa
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
[Full Text]