ver.2
Home
|
Help
|
Advanced search
Previous release (v1)
2024-04-26 09:12:46, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_014426 2341 bp mRNA linear PRI 10-APR-2023
DEFINITION Homo sapiens sorting nexin 5 (SNX5), transcript variant 2, mRNA.
ACCESSION NM_014426
VERSION NM_014426.4
KEYWORDS RefSeq; MANE Select.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 2341)
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 2341)
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 2341)
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 2341)
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 2341)
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 2341)
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 2341)
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 2341)
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 2341)
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 2341)
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 DB118420.1, BC093623.1 and
BC000100.3.
On Jun 2, 2019 this sequence version replaced NM_014426.3.
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 (2) represents the longest
transcript. 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 :: AK001793.1, AK129505.1 [ECO:0000332]
RNAseq introns :: mixed sample support SAMEA1965299,
SAMEA1966682 [ECO:0006172]
##Evidence-Data-END##
##RefSeq-Attributes-START##
MANE Ensembl match :: ENST00000377759.9/ ENSP00000366988.3
RefSeq Select criteria :: based on conservation, expression,
longest protein
##RefSeq-Attributes-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-74 DB118420.1 1-74
75-1639 BC093623.1 1-1565
1640-2341 BC000100.3 1434-2135
FEATURES Location/Qualifiers
source 1..2341
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="20"
/map="20p11.23"
gene 1..2341
/gene="SNX5"
/note="sorting nexin 5"
/db_xref="GeneID:27131"
/db_xref="HGNC:HGNC:14969"
/db_xref="MIM:605937"
exon 1..420
/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..100
/gene="SNX5"
/replace="ggtagg"
/replace="ggtaggtagg"
/db_xref="dbSNP:2035622079"
variation 95
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035622252"
misc_feature 97..99
/gene="SNX5"
/note="upstream in-frame stop codon"
variation 97
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035622194"
variation 100
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035622007"
variation 101..104
/gene="SNX5"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1303534478"
variation 103
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035621943"
variation 104
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1456140533"
variation 105
/gene="SNX5"
/replace=""
/replace="a"
/db_xref="dbSNP:1568602423"
variation 105
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122459034"
variation 110
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1405565310"
variation 111
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1039196335"
variation 112
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1370128268"
variation 116
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:943517724"
variation 118
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1366359411"
variation 121
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:909417820"
variation 122
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378602068"
variation 123
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035621195"
variation 127
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1282480442"
variation 128
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1180556177"
variation 132
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035620924"
variation 134
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035620834"
variation 136
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458410041"
variation 137
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:532832909"
variation 138
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:929294478"
variation 139
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1208446646"
variation 141
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:773254681"
variation 142
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1266388713"
variation 143
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:919295426"
variation 148
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1240122026"
variation 150
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035620067"
variation 151
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035619958"
variation 152
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035619861"
variation 153
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:992134825"
variation 154
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035619627"
variation 156
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:960757641"
variation 159
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306490953"
variation 160
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:771950195"
variation 161
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377198147"
variation 162..163
/gene="SNX5"
/replace=""
/replace="tg"
/db_xref="dbSNP:2122458101"
variation 162
/gene="SNX5"
/replace=""
/replace="t"
/db_xref="dbSNP:750516224"
variation 162
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1322386223"
variation 162
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:907466545"
variation 163
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1001632730"
variation 164
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1384715660"
variation 167
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1045928223"
variation 169
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1459102793"
variation 170
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:946084163"
variation 171
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035618737"
variation 172
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:748135408"
variation 174
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035618581"
variation 175
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:913222830"
variation 176
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035618449"
variation 177
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:565386318"
variation 178
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:926712809"
variation 181
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1160555867"
variation 183
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1440334630"
variation 184
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:760847499"
variation 185
/gene="SNX5"
/replace=""
/replace="t"
/db_xref="dbSNP:1320782041"
variation 186
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:768213203"
variation 187
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1435104516"
variation 189
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022631837"
variation 190
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268544345"
variation 192
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009509093"
variation 193
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213331584"
variation 194
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1487605628"
variation 195
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:956560094"
variation 196
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:748881680"
variation 197..200
/gene="SNX5"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1218164867"
variation 197
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035617540"
variation 199
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1266696698"
variation 202
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:546770209"
variation 203
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1161498526"
variation 204
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035617029"
variation 205
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1350850212"
variation 206
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035616867"
variation 208
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035616766"
variation 210
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1029303138"
variation 211
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:997868630"
variation 214..263
/gene="SNX5"
/replace="ggcggag"
/replace="ggcggagtccggaggcctcctgccgccgtcgggcagggaggccggcgg
ag"
/db_xref="dbSNP:1277353504"
variation 216
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2273451"
variation 217
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039478365"
variation 218
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035616268"
variation 220
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332436514"
variation 221
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035616075"
variation 223..265
/gene="SNX5"
/replace="cggaggcctcctgccgccgtcgggcagggaggccggcggaggc"
/replace="cggaggcctcctgccgccgtcgggcagggaggccggcggaggcctcct
gccgccgtcgggcagggaggccggcggaggc"
/db_xref="dbSNP:1176894243"
variation 223
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:561015558"
variation 224
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035615859"
variation 226
/gene="SNX5"
/replace=""
/replace="a"
/db_xref="dbSNP:1399115048"
variation 226
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122457024"
variation 227
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1600368458"
variation 228
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358563694"
variation 229..234
/gene="SNX5"
/replace="cct"
/replace="cctcct"
/db_xref="dbSNP:1344179737"
variation 229
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301398103"
variation 230
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1299888863"
variation 232
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:887990049"
variation 233
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1401647619"
variation 235
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:372501690"
variation 236
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1288458231"
variation 237
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:756464600"
variation 238
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:975990654"
variation 240
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1600368358"
variation 242
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035614537"
variation 243
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:746282041"
variation 244
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781638399"
variation 246
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035614134"
variation 247
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322035609"
variation 248..252
/gene="SNX5"
/replace=""
/replace="aggga"
/db_xref="dbSNP:1265784752"
variation 248
/gene="SNX5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:754898957"
variation 249..272
/gene="SNX5"
/replace="g"
/replace="gggaggccggcggaggcggggccg"
/db_xref="dbSNP:1309217374"
variation 249
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:542612877"
variation 251
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1477005697"
variation 253
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1389916257"
variation 254..260
/gene="SNX5"
/replace="g"
/replace="gccggcg"
/db_xref="dbSNP:2122456531"
variation 255
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:929547430"
variation 256
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302616550"
variation 257
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1195111186"
variation 258
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035613476"
variation 259
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:968686651"
variation 261
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:558615988"
variation 262
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2035613228"
variation 264
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568602094"
variation 266
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056354927"
variation 268
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1163379021"
variation 269
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1198193940"
variation 270
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1364199877"
variation 271
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2273450"
variation 273
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:112283591"
variation 277
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:544225493"
variation 279
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190812703"
variation 280
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:758612326"
variation 281
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1244905880"
variation 282
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035612073"
variation 283
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:926702737"
variation 287
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:374905911"
variation 290
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205779327"
variation 292
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272274106"
variation 293
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:968268850"
variation 294
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:763375417"
variation 296..313
/gene="SNX5"
/replace="ggcggcggc"
/replace="ggcggcggcggc"
/replace="ggcggcggcggcggc"
/replace="ggcggcggcggcggcggc"
/replace="ggcggcggcggcggcggcggc"
/replace="ggcggcggcggcggcggcggcggc"
/replace="ggcggcggcggcggcggcggcggcggc"
/db_xref="dbSNP:rs767551520"
variation 297..298
/gene="SNX5"
/replace="gc"
/replace="gccgc"
/db_xref="dbSNP:1239393332"
variation 297
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035611490"
variation 299
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035611343"
variation 301
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:915107938"
variation 302
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473262120"
variation 304
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1338220553"
variation 305
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:988391914"
variation 306
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451799199"
variation 307
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169772817"
variation 308..348
/gene="SNX5"
/replace="ggcggcccagcttcttctttcctcgcacagccaggcggccc"
/replace="ggcggcccagcttcttctttcctcgcacagccaggcggcccagcttct
tctttcctcgcacagccaggcggccc"
/db_xref="dbSNP:1453777820"
variation 310
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035610804"
variation 311
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035610702"
variation 314
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035610429"
variation 315
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:189097719"
variation 317
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1484207805"
variation 318..326
/gene="SNX5"
/replace="cttctt"
/replace="cttcttctt"
/db_xref="dbSNP:536243297"
variation 318
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1029587579"
variation 319
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367074751"
variation 320
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:997815936"
variation 321
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:540394350"
variation 322
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035609577"
variation 323
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2122455803"
variation 324
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1337406431"
variation 327
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035609216"
variation 328
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600367826"
variation 329
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1018033167"
variation 331
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1339542674"
variation 332
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1276141616"
variation 335
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1466486704"
variation 337
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1332296330"
variation 338
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035608619"
variation 339
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035608513"
variation 340
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1005323010"
variation 343
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:770339125"
variation 344
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035608295"
variation 345
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035608192"
variation 346
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760521878"
variation 347
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1425252501"
variation 348
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:572996375"
variation 349
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:976023444"
variation 351
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:554659700"
variation 354
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035607586"
variation 355
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035607524"
variation 357
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1435495548"
variation 359
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035607412"
variation 360
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1317407357"
variation 363
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324516714"
variation 364
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600367635"
variation 366
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600367627"
variation 368
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:940615713"
variation 369
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600367600"
CDS 370..1584
/gene="SNX5"
/note="isoform a is encoded by transcript variant 2"
/codon_start=1
/product="sorting nexin-5 isoform a"
/protein_id="NP_055241.1"
/db_xref="CCDS:CCDS13130.1"
/db_xref="GeneID:27131"
/db_xref="HGNC:HGNC:14969"
/db_xref="MIM:605937"
/translation="
MAAVPELLQQQEEDRSKLRSVSVDLNVDPSLQIDIPDALSERDKVKFTVHTKTTLPTFQSPEFSVTRQHEDFVWLHDTLIETTDYAGLIIPPAPTKPDFDGPREKMQKLGEGEGSMTKEEFAKMKQELEAEYLAVFKKTVSSHEVFLQRLSSHPVLSKDRNFHVFLEYDQDLSVRRKNTKEMFGGFFKSVVKSADEVLFTGVKEVDDFFEQEKNFLINYYNRIKDSCVKADKMTRSHKNVADDYIHTAACLHSLALEEPTVIKKYLLKVAELFEKLRKVEGRVSSDEDLKLTELLRYYMLNIEAAKDLLYRRTKALIDYENSNKALDKARLKSKDVKLAEAHQQECCQKFEQLSESAKEELINFKRKRVAAFRKNLIEMSELEIKHARNNVSLLQSCIDLFKNN"
misc_feature 373..375
/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 454..876
/gene="SNX5"
/note="The phosphoinositide binding Phox Homology domain
of Sorting Nexin 5; Region: PX_SNX5; cd07291"
/db_xref="CDD:132824"
misc_feature order(571..579,652..657,784..786)
/gene="SNX5"
/note="putative phosphoinositide binding site [chemical
binding]; other site"
/db_xref="CDD:132824"
misc_feature 874..1152
/gene="SNX5"
/note="propagated from UniProtKB/Swiss-Prot (Q9Y5X3.1);
Region: Interaction with DOCK1.
/evidence=ECO:0000269|PubMed:18596235"
misc_feature 916..969
/gene="SNX5"
/note="propagated from UniProtKB/Swiss-Prot (Q9Y5X3.1);
Region: Membrane-binding amphipathic helix.
/evidence=ECO:0000303|PubMed:23085988"
misc_feature 922..1575
/gene="SNX5"
/note="The Bin/Amphiphysin/Rvs (BAR) domain of Sorting
Nexin 5; Region: BAR_SNX5; cd07663"
/db_xref="CDD:153347"
misc_feature 946..948
/gene="SNX5"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (Q9Y5X3.1); phosphorylation site"
misc_feature order(1012..1014,1021..1026,1033..1038,1042..1047,
1054..1056,1063..1068,1075..1077,1096..1101,1105..1110,
1117..1119,1126..1131,1138..1143,1186..1188,1453..1455,
1462..1467,1471..1479,1486..1488,1495..1500,1504..1512,
1516..1521,1528..1533,1537..1542,1549..1554,1558..1563)
/gene="SNX5"
/note="dimer interface [polypeptide binding]; other site"
/db_xref="CDD:153347"
misc_feature 1192..1194
/gene="SNX5"
/note="N6-acetyllysine.
/evidence=ECO:0007744|PubMed:19608861; propagated from
UniProtKB/Swiss-Prot (Q9Y5X3.1); acetylation site"
variation 370
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1275437736"
variation 372
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:767372854"
variation 373
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035606824"
variation 374
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:994077057"
variation 375
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324361419"
variation 376
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223001375"
variation 377
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:536264072"
variation 378
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035606488"
variation 379
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035606417"
variation 382
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1429655738"
variation 384
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:377578366"
variation 390
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1600367509"
variation 391
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:907759445"
variation 392
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:898048064"
variation 393..402
/gene="SNX5"
/replace="gcagcagcag"
/replace="gcagcagcagcag"
/db_xref="dbSNP:951711191"
variation 394
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236181971"
variation 395
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035605857"
variation 396
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:774358404"
variation 397
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261428214"
variation 398
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1170529332"
variation 399
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:568802177"
variation 401..410
/gene="SNX5"
/replace="aggagga"
/replace="aggaggagga"
/db_xref="dbSNP:2035604591"
variation 401
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:146288789"
variation 402
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1270248894"
variation 405
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:748861582"
variation 407
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1196691857"
variation 408
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035604733"
variation 409
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035604669"
variation 411
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:979818375"
variation 413
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045114799"
variation 417
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:946791826"
exon 421..525
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 423..426
/gene="SNX5"
/replace="gaga"
/replace="gagaga"
/db_xref="dbSNP:1259091115"
variation 425
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035373852"
variation 426
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:776654591"
variation 430
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288689832"
variation 431..433
/gene="SNX5"
/replace="t"
/replace="tat"
/db_xref="dbSNP:2035373392"
variation 435..438
/gene="SNX5"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:2035373262"
variation 435
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1206332374"
variation 436
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1350964494"
variation 440
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:771005650"
variation 441
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:760825526"
variation 442
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:373912588"
variation 443
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600346707"
variation 446
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1283660391"
variation 447
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:768489364"
variation 449
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1026667819"
variation 451
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1349743268"
variation 452
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:114912822"
variation 453
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1382781142"
variation 456
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035372714"
variation 458
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:780017698"
variation 459
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:769806012"
variation 461
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1471065829"
variation 462
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:745830027"
variation 463
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035372471"
variation 464
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:995623696"
variation 468
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035372385"
variation 471
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:780781748"
variation 472
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:549069341"
variation 474
/gene="SNX5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1194704752"
variation 474
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244276135"
variation 477
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369770913"
variation 481
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035372087"
variation 481
/gene="SNX5"
/replace="g"
/replace="gg"
/db_xref="dbSNP:761822881"
variation 482
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:758771996"
variation 483
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1254857964"
variation 484
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1201444495"
variation 486
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035371937"
variation 487..492
/gene="SNX5"
/replace="ag"
/replace="agtgag"
/db_xref="dbSNP:1165317012"
variation 490..497
/gene="SNX5"
/replace="gagaga"
/replace="gagagaga"
/db_xref="dbSNP:752065385"
variation 492
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:376524578"
variation 493
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1263564623"
variation 494
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1217738961"
variation 496
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:765668419"
variation 498
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:61756173"
variation 503
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1005095808"
variation 504
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271924981"
variation 506
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:906768804"
variation 517
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:759972900"
variation 519
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1372329726"
variation 521
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:754353468"
variation 525
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454807382"
exon 526..636
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 527
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:769618774"
variation 528
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:767667071"
variation 529
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1182192347"
variation 531
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:761872888"
variation 533
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:774645859"
variation 535
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035337403"
variation 537
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2122386129"
variation 539
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:199902705"
variation 540
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:371471011"
variation 541
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201197486"
variation 546
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2035337182"
variation 548
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1222326524"
variation 549
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:770945924"
variation 550
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:747066909"
variation 551
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:747003104"
variation 552..555
/gene="SNX5"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:2035336935"
variation 552
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:772532101"
variation 555
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035336894"
variation 556..559
/gene="SNX5"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1388349501"
variation 559
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:771628005"
variation 565
/gene="SNX5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1305548346"
variation 573
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1425820834"
variation 574
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035336664"
variation 575
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035336623"
variation 576
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:747739246"
variation 577
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1157675881"
variation 578
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1157685266"
variation 583..585
/gene="SNX5"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:770573662"
variation 585..590
/gene="SNX5"
/replace="tgtg"
/replace="tgtgtg"
/db_xref="dbSNP:2035336264"
variation 586
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1055378835"
variation 587
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1385171593"
variation 588
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1229077765"
variation 591
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398612701"
variation 594
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778601423"
variation 595
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1158931744"
variation 596
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:755301238"
variation 598
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1266496870"
variation 599
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201572215"
variation 604
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:780016243"
variation 605..609
/gene="SNX5"
/replace="tt"
/replace="ttatt"
/db_xref="dbSNP:746481295"
variation 605..606
/gene="SNX5"
/replace=""
/replace="tt"
/db_xref="dbSNP:1490484416"
variation 606
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:539421369"
variation 607
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:577883790"
variation 608
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:367713822"
variation 611
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:373578457"
variation 612..618
/gene="SNX5"
/replace="aaca"
/replace="aacaaca"
/db_xref="dbSNP:1457658492"
variation 614
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568593211"
variation 617
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:756537371"
variation 618
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259123995"
variation 621
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:750944242"
variation 623
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:141800072"
variation 629
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1004171492"
variation 631
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035335289"
variation 635..636
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:2035335195"
variation 635
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:757425738"
exon 637..758
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 637
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:913634871"
variation 641
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1451501722"
variation 644
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:6045116"
variation 646
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:778034613"
variation 647
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200913564"
variation 649
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035312236"
variation 650
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:6045115"
variation 653
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:765972467"
variation 654
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:148068583"
variation 658
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:750292296"
variation 660
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375257051"
variation 661
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:761676504"
variation 663
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2035311707"
variation 664
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035311622"
variation 666
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2035311553"
variation 668
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330102667"
variation 671
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:773810235"
variation 674
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:541944674"
variation 676
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:751333774"
variation 677
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:762534744"
variation 680
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:775180856"
variation 681
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1449852546"
variation 690
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:770024480"
variation 703
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1249955302"
variation 705..718
/gene="SNX5"
/replace="tga"
/replace="tgaagggtctatga"
/db_xref="dbSNP:1877782574"
variation 709
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:143544203"
variation 710
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:936831855"
variation 711
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2035310618"
variation 713
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1308559056"
variation 715
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295701590"
variation 722
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244533541"
variation 728
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2035310256"
variation 729
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:781435390"
variation 731
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380134146"
variation 734
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:771429766"
variation 739
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035310094"
variation 740
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:747525681"
variation 747
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:530067358"
variation 748
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259856845"
variation 751
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758612407"
variation 753
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2035309850"
variation 755..756
/gene="SNX5"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2035309800"
variation 756
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1318554267"
variation 758
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:752967148"
exon 759..882
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 760
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1357902492"
variation 765..768
/gene="SNX5"
/replace="tc"
/replace="tctc"
/db_xref="dbSNP:764203671"
variation 768
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367569798"
variation 769
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1600341213"
variation 771
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:374271284"
variation 777
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1453349729"
variation 785
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:759144343"
variation 786..790
/gene="SNX5"
/replace="tgt"
/replace="tgtgt"
/db_xref="dbSNP:758896347"
variation 788
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:776990029"
variation 791..792
/gene="SNX5"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1480114725"
variation 791
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568591713"
variation 792
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:984501724"
variation 793
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:149308583"
variation 797
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:747509316"
variation 798
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1202750132"
variation 803..810
/gene="SNX5"
/replace="tctt"
/replace="tctttctt"
/db_xref="dbSNP:753236123"
variation 803
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039587252"
variation 804
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:778494613"
variation 806
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1259439663"
variation 807
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1313510303"
variation 808
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:138864959"
variation 810
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:114894362"
variation 811
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:911518496"
variation 813
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:748283767"
variation 814
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:775618449"
variation 815
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:755184448"
variation 816
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039586731"
variation 817..823
/gene="SNX5"
/replace="ctt"
/replace="ctttctt"
/db_xref="dbSNP:1282362052"
variation 817
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039586692"
variation 818
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:749474204"
variation 820
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:780981111"
variation 823..824
/gene="SNX5"
/replace=""
/replace="a"
/db_xref="dbSNP:1461724384"
variation 824..826
/gene="SNX5"
/replace=""
/replace="ctc"
/db_xref="dbSNP:1221647112"
variation 828
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1306556533"
variation 831
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1377691725"
variation 832
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:766537375"
variation 837
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1347271953"
variation 840
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:765535844"
variation 842
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1381652637"
variation 844
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1377629220"
variation 847
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:562671037"
variation 848
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:145056868"
variation 849
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:764069035"
variation 857
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:752213767"
variation 869
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1174664787"
variation 872
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:141177501"
variation 877
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122373807"
variation 878
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430521006"
variation 881
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1193090244"
exon 883..978
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 883
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1449714069"
variation 887
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242072592"
variation 888
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:764792798"
variation 892
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:754515928"
variation 894
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:971873857"
variation 895
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:753501671"
variation 896
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:373259467"
variation 898
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039568968"
variation 902
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568590918"
variation 904
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:369531337"
variation 906
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:760421737"
variation 908..911
/gene="SNX5"
/replace="a"
/replace="aaga"
/db_xref="dbSNP:776457970"
variation 910..912
/gene="SNX5"
/replace=""
/replace="gag"
/db_xref="dbSNP:1568590890"
variation 912
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2273448"
variation 913
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:773669633"
variation 915
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:767996285"
variation 919
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:762321613"
variation 920
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1016189430"
variation 923
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1382114770"
variation 931
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:774777225"
variation 932
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039568075"
variation 933
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768775709"
variation 935..939
/gene="SNX5"
/replace="gtg"
/replace="gtgtg"
/db_xref="dbSNP:2039567932"
variation 936
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1350116173"
variation 937..942
/gene="SNX5"
/replace="gtg"
/replace="gtggtg"
/db_xref="dbSNP:766077215"
variation 939
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:999459680"
variation 943..946
/gene="SNX5"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:760378599"
variation 953
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039567737"
variation 959
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1408735967"
variation 964
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:749367679"
variation 966
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169945560"
variation 969
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1189203678"
variation 970
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:775569763"
variation 972
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1429912003"
variation 973
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1600339525"
variation 975
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1384065540"
exon 979..1084
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 981
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:771873224"
variation 982
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438067837"
variation 986
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1349939628"
variation 988
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:536752229"
variation 989
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:747946291"
variation 990..995
/gene="SNX5"
/replace="ctt"
/replace="cttctt"
/db_xref="dbSNP:1568590288"
variation 990
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:778786704"
variation 993
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1398560975"
variation 996
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:768434696"
variation 999
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:895155684"
variation 1002
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:145652755"
variation 1004
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:755741863"
variation 1005
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1427034923"
variation 1006
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:750094863"
variation 1011
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039548692"
variation 1017
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:140595658"
variation 1018
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488882701"
variation 1019
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:895276778"
variation 1020
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:781031324"
variation 1022..1023
/gene="SNX5"
/replace="ac"
/replace="acac"
/db_xref="dbSNP:2039548499"
variation 1025
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:757620155"
variation 1028
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:369193496"
variation 1029
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:764524638"
variation 1030
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039548338"
variation 1031
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:763312847"
variation 1035
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2122364312"
variation 1036
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1285811074"
variation 1037
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:753263158"
variation 1038
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1600338049"
variation 1049
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1003613074"
variation 1056
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:765299262"
variation 1059
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:759656136"
variation 1066
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:776814309"
variation 1068
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039547996"
variation 1069..1070
/gene="SNX5"
/replace=""
/replace="tacag"
/db_xref="dbSNP:2039547954"
variation 1070
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760983459"
variation 1071
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:773948183"
variation 1072
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039547826"
variation 1073
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403617338"
variation 1074
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1178206917"
variation 1076
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:768508088"
variation 1079
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039547669"
variation 1081..1085
/gene="SNX5"
/replace="aaa"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:774286425"
variation 1081
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1201341354"
exon 1085..1160
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 1085
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775544916"
variation 1086
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:769804400"
variation 1087
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775946902"
variation 1091
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122363667"
variation 1092
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:539455748"
variation 1093
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:746639789"
variation 1094
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:777524319"
variation 1095
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:758742720"
variation 1097
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274696039"
variation 1098
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:919703922"
variation 1100
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:146672356"
variation 1101
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:779284935"
variation 1102
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:963553925"
variation 1104..1110
/gene="SNX5"
/replace="cc"
/replace="ccacacc"
/db_xref="dbSNP:2039545565"
variation 1105
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568590075"
variation 1107
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:755407618"
variation 1110
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:372550237"
variation 1111
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756281625"
variation 1113
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039545307"
variation 1116
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122363494"
variation 1118
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:750577873"
variation 1119
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411549449"
variation 1122
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1371274389"
variation 1124
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:767828190"
variation 1125
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422988314"
variation 1128
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1689155065"
variation 1129
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568589996"
variation 1132
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:762147468"
variation 1137
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201917236"
variation 1138
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:199879416"
variation 1140
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:752501049"
variation 1143
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:765139003"
variation 1144
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1024912169"
variation 1146
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:142401289"
variation 1148
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:933765716"
variation 1149
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039544539"
variation 1151
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1012239568"
variation 1152
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:776699156"
variation 1154
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:770319083"
variation 1155
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1251939558"
variation 1156
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:760284212"
variation 1157
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:959376180"
variation 1160
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1383204344"
exon 1161..1200
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 1161
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:201254238"
variation 1162
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174952563"
variation 1165
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:936890145"
variation 1167
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:768979593"
variation 1168
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:925334521"
variation 1174
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256410289"
variation 1176
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039528172"
variation 1179
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:975500012"
variation 1185
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:148084267"
variation 1188
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1184666064"
variation 1190
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039528023"
variation 1191
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:770297045"
variation 1195
/gene="SNX5"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1274165829"
variation 1195
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427557303"
variation 1197
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:909732542"
variation 1200
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039527821"
exon 1201..1287
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 1201
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147786677"
variation 1204..1205
/gene="SNX5"
/replace=""
/replace="gt"
/db_xref="dbSNP:2039526517"
variation 1204
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:768497425"
variation 1207..1208
/gene="SNX5"
/replace=""
/replace="gaa"
/db_xref="dbSNP:2039526443"
variation 1207
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1449657202"
variation 1209
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:762545436"
variation 1210
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201856245"
variation 1211
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039526288"
variation 1212
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:531468330"
variation 1213
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:746381456"
variation 1214
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:777316494"
variation 1216
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039526080"
variation 1220
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039526046"
variation 1221
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:746787153"
variation 1222
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039525953"
variation 1224..1226
/gene="SNX5"
/replace="a"
/replace="aga"
/db_xref="dbSNP:2039525874"
variation 1224
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1319616399"
variation 1226
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1034021590"
variation 1230
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1455594809"
variation 1234
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039525736"
variation 1236
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:115502408"
variation 1238..1242
/gene="SNX5"
/replace="a"
/replace="agcta"
/db_xref="dbSNP:2039525606"
variation 1240
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:11542902"
variation 1245..1248
/gene="SNX5"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:2039525564"
variation 1252
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200592783"
variation 1255
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:758576026"
variation 1256
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1190962856"
variation 1258
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:749326525"
variation 1260
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1555786324"
variation 1262
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1450715208"
variation 1263
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341433087"
variation 1264
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:779888972"
variation 1265
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010214897"
variation 1266
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370183961"
variation 1268
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:892756287"
variation 1269
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750333452"
variation 1270
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:767494545"
variation 1271
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:751031852"
variation 1272
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039524511"
variation 1273
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:377697187"
variation 1278
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:545649463"
variation 1281
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1399442648"
variation 1282
/gene="SNX5"
/replace=""
/replace="g"
/db_xref="dbSNP:1161092921"
variation 1284
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:377587399"
variation 1285
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473690617"
variation 1287
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:6075268"
exon 1288..1447
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 1291
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1366343069"
variation 1292
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272535976"
variation 1293
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1257117073"
variation 1295
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:777331458"
variation 1296
/gene="SNX5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2039505429"
variation 1296
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:943128366"
variation 1297
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1331254032"
variation 1300
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:757885596"
variation 1303
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376255348"
variation 1304
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:764745399"
variation 1307
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1238028570"
variation 1308
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:373050708"
variation 1312
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:754185526"
variation 1314
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:756212310"
variation 1315
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:931574098"
variation 1316
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1415935246"
variation 1317
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:766859506"
variation 1319
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:761246039"
variation 1320
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600334226"
variation 1322
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1568588503"
variation 1325
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:773664052"
variation 1326
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568588496"
variation 1329
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:772163613"
variation 1334..1341
/gene="SNX5"
/replace="caaa"
/replace="caaacaaa"
/db_xref="dbSNP:1269135366"
variation 1334
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1466559123"
variation 1335..1337
/gene="SNX5"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1296634228"
variation 1342
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:918799378"
variation 1343
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203604800"
variation 1344
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:974448932"
variation 1345
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:369908673"
variation 1347
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1600334150"
variation 1349
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:912034125"
variation 1350
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:761850586"
variation 1351
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:774514947"
variation 1354
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:984136576"
variation 1357
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:768722799"
variation 1358
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:950977818"
variation 1359
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:749517967"
variation 1365
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367124276"
variation 1366
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:371601931"
variation 1368
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1447206103"
variation 1374
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:61762680"
variation 1375
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:116425682"
variation 1379
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369543726"
variation 1380
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039503350"
variation 1386
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1389596422"
variation 1391
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777619898"
variation 1394
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:575775461"
variation 1396
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1279236186"
variation 1398
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039503004"
variation 1400
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:994789511"
variation 1408
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1207947801"
variation 1410
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039502799"
variation 1413
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:557200574"
variation 1416
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:149888152"
variation 1422
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039502601"
variation 1425
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748179170"
variation 1426
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:539118133"
variation 1430
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:766842736"
variation 1431
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:761164423"
variation 1432
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:139196479"
variation 1435
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:767866368"
variation 1437
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174920602"
variation 1438
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1014269336"
variation 1444
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1389101703"
exon 1448..1533
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 1453
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:752166913"
variation 1456
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:899691950"
variation 1460
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039441536"
variation 1465
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:150810533"
variation 1466
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:376369085"
variation 1470
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1456539681"
variation 1472
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352015839"
variation 1474
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:926801905"
variation 1475
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213057977"
variation 1476
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:775569544"
variation 1477
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039441181"
variation 1480
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:765401451"
variation 1481
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:759807895"
variation 1486..1493
/gene="SNX5"
/replace="agaa"
/replace="agaaagaa"
/db_xref="dbSNP:1246970013"
variation 1486
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:963224770"
variation 1491
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:772822159"
variation 1498
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250585416"
variation 1499
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:771957175"
variation 1501
/gene="SNX5"
/replace=""
/replace="g"
/db_xref="dbSNP:754299876"
variation 1506
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1207692038"
variation 1511
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039440535"
variation 1514
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039440464"
variation 1516
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:368439202"
variation 1526
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039440370"
variation 1528
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039440327"
variation 1530
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:774466954"
variation 1532
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:919586287"
exon 1534..2341
/gene="SNX5"
/inference="alignment:Splign:2.1.0"
variation 1535
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039429974"
variation 1536
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122332348"
variation 1538
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:758844519"
variation 1539
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:565150872"
variation 1540..1542
/gene="SNX5"
/replace=""
/replace="gtc"
/db_xref="dbSNP:1568586000"
variation 1542
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:9322"
variation 1544
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1255467063"
variation 1546
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1198629369"
variation 1551
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039429650"
variation 1552
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1484305155"
variation 1554
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:746546895"
variation 1557
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1281066272"
variation 1558
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:755121199"
variation 1564
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1340221518"
variation 1566
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424987446"
variation 1568
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039429384"
variation 1569
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039429355"
variation 1570
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1300279115"
variation 1572
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753981963"
variation 1575
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:766577881"
variation 1576
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:760842315"
variation 1581
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1398257211"
variation 1586
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039429117"
variation 1587
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751335974"
variation 1589
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:763998462"
variation 1590
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302341672"
variation 1597
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1326522762"
variation 1598
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:762972531"
variation 1600..1601
/gene="SNX5"
/replace=""
/replace="aa"
/db_xref="dbSNP:1170088020"
variation 1601
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200970421"
variation 1605..1609
/gene="SNX5"
/replace="aa"
/replace="aagaa"
/db_xref="dbSNP:766948155"
variation 1605
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:769156235"
variation 1607
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:759037260"
variation 1613
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:776036588"
variation 1615
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:371955197"
variation 1618..1626
/gene="SNX5"
/replace="gaaag"
/replace="gaaagaaag"
/db_xref="dbSNP:761318673"
variation 1618
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1204447961"
variation 1621
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039428434"
variation 1622
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1336500426"
variation 1626
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1482105412"
variation 1627
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284080595"
variation 1628
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1196584700"
variation 1633
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:746676277"
variation 1635
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:554810351"
variation 1636
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:536739314"
variation 1637
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:995359763"
variation 1638
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409996009"
variation 1639
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:779861998"
variation 1641
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039427824"
variation 1643
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039427772"
variation 1644
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039427733"
variation 1645
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1291535815"
variation 1648
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1487772249"
variation 1651
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:575555700"
variation 1652
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039427548"
variation 1655
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039427506"
variation 1658
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:371827386"
variation 1659
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:557278713"
variation 1662
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039427367"
variation 1667
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:538165341"
variation 1669
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039427314"
variation 1670
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:905507675"
variation 1674
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:142219759"
variation 1681
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122331718"
variation 1682
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:148718726"
variation 1684
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039427193"
variation 1689
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:534007104"
variation 1694
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039427134"
variation 1695
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122331673"
variation 1696
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1298737959"
variation 1697
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:757178008"
variation 1699..1706
/gene="SNX5"
/replace="aata"
/replace="aataaata"
/db_xref="dbSNP:531340560"
variation 1701
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039427052"
variation 1703..1706
/gene="SNX5"
/replace="aata"
/replace="c"
/db_xref="dbSNP:1555785657"
variation 1707
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:146534301"
variation 1708
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039426924"
variation 1710
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039426901"
variation 1717
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039426879"
variation 1718
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370623964"
variation 1721
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:750091723"
variation 1723
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039426788"
variation 1724
/gene="SNX5"
/replace=""
/replace="c"
/db_xref="dbSNP:2039426754"
variation 1725
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:144308630"
variation 1727
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039426682"
variation 1733
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039426645"
variation 1739
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:943007940"
variation 1743
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1314785774"
variation 1744
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:764131449"
variation 1745
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1039309322"
variation 1746
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230082990"
variation 1753..1759
/gene="SNX5"
/replace="tatt"
/replace="tattatt"
/db_xref="dbSNP:1252333910"
variation 1755
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039426476"
variation 1758
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2069934060"
variation 1760
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:911216203"
variation 1761
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:984054405"
variation 1762
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568585836"
variation 1766
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039426278"
variation 1773
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196155183"
variation 1774
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1244496719"
variation 1775
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1461466609"
variation 1779
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1182671331"
variation 1781
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039426025"
variation 1782
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1770941695"
variation 1788
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039425968"
variation 1790
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1411342318"
variation 1795
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335159343"
variation 1805
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:944947469"
variation 1806
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:952719088"
variation 1809
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1460427547"
variation 1810
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:918646258"
variation 1812
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039425614"
variation 1815
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039425564"
variation 1817
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039425518"
variation 1818..1822
/gene="SNX5"
/replace=""
/replace="ccaaa"
/db_xref="dbSNP:2039425475"
variation 1822
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039425435"
variation 1826
/gene="SNX5"
/replace=""
/replace="t"
/db_xref="dbSNP:2039425397"
variation 1827
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039425344"
variation 1832
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039425286"
variation 1833
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039425241"
variation 1834..1836
/gene="SNX5"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2039425186"
variation 1834
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1285744903"
variation 1836
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242410101"
variation 1837
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:759475864"
variation 1843
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:529746738"
variation 1844
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:960127663"
variation 1845
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039424988"
variation 1846
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1437344760"
variation 1849
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039424879"
variation 1853..1857
/gene="SNX5"
/replace="ta"
/replace="tacta"
/db_xref="dbSNP:1296767244"
variation 1854
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039424830"
variation 1856
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1384234188"
variation 1858
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:368804838"
variation 1859
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1035551965"
variation 1861
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1307402154"
variation 1862..1863
/gene="SNX5"
/replace=""
/replace="ag"
/db_xref="dbSNP:2039424567"
variation 1863
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:182707782"
variation 1866
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:751680899"
variation 1867
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039424466"
variation 1869
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1913350496"
variation 1871
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1386575721"
variation 1873
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600327497"
variation 1874
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:983421324"
variation 1876
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1486662985"
variation 1877..1878
/gene="SNX5"
/replace=""
/replace="a"
/db_xref="dbSNP:776534036"
variation 1882
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600327467"
variation 1884..1886
/gene="SNX5"
/replace="t"
/replace="tct"
/db_xref="dbSNP:1186842922"
variation 1884
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039424252"
variation 1886
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122331039"
variation 1887
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1260840524"
variation 1889
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1476796471"
variation 1892
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:970032481"
variation 1900
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039424123"
variation 1901
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021559030"
variation 1903..1907
/gene="SNX5"
/replace="catca"
/replace="catcatca"
/db_xref="dbSNP:2039424055"
variation 1903
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011223706"
variation 1906
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429918767"
variation 1908
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039424028"
variation 1916
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039423998"
variation 1920..1922
/gene="SNX5"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:771890587"
variation 1922
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:950686219"
variation 1929
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039423890"
variation 1932
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:973872949"
variation 1934
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039423826"
variation 1937
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1357593625"
variation 1940
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039423778"
variation 1942..1944
/gene="SNX5"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1361783193"
variation 1942
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:962598977"
variation 1944
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1289784530"
variation 1951
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:568781721"
variation 1953
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1023875289"
variation 1956
/gene="SNX5"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2039423475"
variation 1957
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039423424"
variation 1958
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1320096935"
variation 1960
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122330854"
variation 1961
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122330842"
variation 1962
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039423310"
variation 1963
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039423261"
variation 1969
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039423200"
variation 1974
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462169346"
variation 1978..1979
/gene="SNX5"
/replace=""
/replace="caa"
/db_xref="dbSNP:2039423109"
variation 1983
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:550125314"
variation 1984
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:766470468"
variation 1985
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039422960"
variation 1992
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318332187"
variation 1993
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:997299785"
variation 1994
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039422838"
variation 2001
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161813233"
variation 2002
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039422768"
variation 2012
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:6111748"
variation 2013
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:901337465"
variation 2015..2018
/gene="SNX5"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1568585710"
variation 2016
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568585715"
variation 2019
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600327342"
variation 2026
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:531965047"
variation 2029
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201317282"
variation 2036
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039422524"
variation 2037
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600327319"
variation 2038
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039422450"
variation 2040
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1269463295"
variation 2042
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374117869"
variation 2045
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191079596"
variation 2046
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1465827275"
variation 2049
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039422233"
variation 2052
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:763200506"
variation 2054
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423200244"
variation 2059
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402663646"
variation 2060..2061
/gene="SNX5"
/replace=""
/replace="a"
/db_xref="dbSNP:1207644577"
variation 2060
/gene="SNX5"
/replace="c"
/replace="catgc"
/db_xref="dbSNP:2039422137"
variation 2062
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1160185665"
variation 2063
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1451805234"
variation 2064..2073
/gene="SNX5"
/replace="t"
/replace="tgtttgtact"
/db_xref="dbSNP:1436462084"
variation 2066..2068
/gene="SNX5"
/replace=""
/replace="ttt"
/db_xref="dbSNP:1291657231"
variation 2066
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1305376611"
variation 2067
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1366687155"
variation 2070..2074
/gene="SNX5"
/replace="ta"
/replace="tacta"
/db_xref="dbSNP:1355445876"
variation 2070
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039421939"
variation 2072
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039421917"
variation 2073
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1272543487"
variation 2074
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:565263963"
variation 2075
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039421778"
variation 2077
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:1223863367"
variation 2081..2085
/gene="SNX5"
/replace="ca"
/replace="cagca"
/db_xref="dbSNP:1351090703"
variation 2082
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1305760918"
variation 2085
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039421649"
variation 2086
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039421627"
variation 2088
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039421590"
variation 2093
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039421558"
variation 2097..2107
/gene="SNX5"
/replace="tttat"
/replace="tttatctttat"
/db_xref="dbSNP:1224374493"
variation 2097..2099
/gene="SNX5"
/replace="ttt"
/replace="tttttagccactttcgtagtctattttgtgtcaactggagttt"
/db_xref="dbSNP:2039421520"
variation 2101
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:773353395"
variation 2103..2105
/gene="SNX5"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:2039421426"
variation 2105..2110
/gene="SNX5"
/replace="tata"
/replace="tatata"
/db_xref="dbSNP:1490156627"
variation 2105
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039421385"
variation 2106
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039421341"
variation 2108
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:540519922"
variation 2110
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:911437716"
variation 2111
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1219363041"
variation 2112
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039421064"
variation 2113
/gene="SNX5"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1245043780"
variation 2114..2116
/gene="SNX5"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:999197260"
variation 2114
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039420972"
variation 2115
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039420930"
variation 2118
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411271978"
variation 2120..2125
/gene="SNX5"
/replace="cct"
/replace="cctcct"
/db_xref="dbSNP:2039420648"
variation 2120
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600327191"
variation 2121
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039420757"
variation 2122
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039420715"
variation 2125..2131
/gene="SNX5"
/replace="tttttt"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:138735602"
variation 2125
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039420609"
variation 2129
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039420569"
variation 2131
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:902149576"
variation 2135
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1048642229"
variation 2136
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1011052781"
variation 2138
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1366628745"
variation 2139..2143
/gene="SNX5"
/replace="ata"
/replace="atata"
/db_xref="dbSNP:1491406291"
variation 2139
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:931283455"
variation 2140
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:528717075"
variation 2142..2143
/gene="SNX5"
/replace=""
/replace="ttctctcccctc"
/db_xref="dbSNP:768591111"
variation 2142
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322080720"
variation 2144
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568585613"
variation 2145
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:973208165"
variation 2148
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039419952"
variation 2151..2162
/gene="SNX5"
/replace=""
/replace="gaggggagagaa"
/db_xref="dbSNP:760678044"
variation 2151
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039419902"
variation 2153
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:191911856"
variation 2161..2163
/gene="SNX5"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:2039419757"
variation 2162
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:928448940"
variation 2164
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1405085636"
variation 2166
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600327102"
variation 2167
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1315465166"
variation 2169
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039419577"
variation 2173
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039419528"
variation 2177
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397693482"
variation 2183
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:775573928"
variation 2185
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1170956708"
variation 2186
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:979925972"
variation 2187..2192
/gene="SNX5"
/replace="aa"
/replace="aaataa"
/db_xref="dbSNP:1205253178"
variation 2187..2189
/gene="SNX5"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:772097411"
variation 2189
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039419259"
variation 2190
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:969881688"
variation 2193
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039419155"
variation 2194..2198
/gene="SNX5"
/replace="gt"
/replace="gtggt"
/db_xref="dbSNP:2039419015"
variation 2194
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1021524020"
variation 2195
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:990095105"
variation 2196
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1237703974"
variation 2205
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039418979"
variation 2207
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1456588817"
variation 2207
/gene="SNX5"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1185735736"
variation 2212..2220
/gene="SNX5"
/replace=""
/replace="tggccagat"
/db_xref="dbSNP:1472634660"
variation 2212
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039418892"
variation 2215
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039418864"
variation 2218
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386106437"
variation 2219
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122329733"
variation 2221
/gene="SNX5"
/replace="a"
/replace="c"
/db_xref="dbSNP:762228171"
variation 2222
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:944856516"
variation 2225
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390163069"
variation 2227
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169305519"
variation 2229
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397581153"
variation 2231
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:188249622"
variation 2232
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:997668549"
variation 2233
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1445489293"
variation 2238
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:920578915"
variation 2239
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122329629"
variation 2240
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1217983153"
variation 2241
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:139589175"
variation 2243..2250
/gene="SNX5"
/replace="ccc"
/replace="cccctccc"
/db_xref="dbSNP:1568585534"
variation 2243
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1017776897"
variation 2246
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:14885"
variation 2255..2256
/gene="SNX5"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2039418257"
variation 2257
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205648775"
variation 2258
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1007037066"
variation 2259
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:970538638"
variation 2262..2267
/gene="SNX5"
/replace="gggggg"
/replace="ggggggg"
/db_xref="dbSNP:1185835233"
variation 2263
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039418056"
variation 2264
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039418013"
variation 2265
/gene="SNX5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039417962"
variation 2267
/gene="SNX5"
/replace="c"
/replace="g"
/db_xref="dbSNP:1442080376"
variation 2268
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600326934"
variation 2269
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1244233456"
variation 2274
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:575781578"
variation 2275
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:889962847"
variation 2276
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1422126945"
variation 2280
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039417529"
variation 2283..2294
/gene="SNX5"
/replace="g"
/replace="gtatgtctttgg"
/db_xref="dbSNP:2039417189"
variation 2283
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1470633345"
variation 2285
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039417446"
variation 2286
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600326907"
variation 2289
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039417349"
variation 2290..2292
/gene="SNX5"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:2039417306"
variation 2291
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:777068179"
variation 2292
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:931587892"
variation 2295
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1207142763"
variation 2299
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039417090"
variation 2300
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039417049"
variation 2302..2308
/gene="SNX5"
/replace="tttttt"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:966388240"
variation 2302
/gene="SNX5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1320012387"
variation 2304
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:897159440"
variation 2305..2310
/gene="SNX5"
/replace="t"
/replace="ttttat"
/db_xref="dbSNP:111911412"
variation 2306
/gene="SNX5"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039416890"
variation 2308..2311
/gene="SNX5"
/replace="ta"
/replace="tata"
/db_xref="dbSNP:2122329334"
variation 2308
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:1399312343"
variation 2309
/gene="SNX5"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039416725"
variation 2311..2313
/gene="SNX5"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1219857253"
variation 2312
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039416669"
variation 2316..2323
/gene="SNX5"
/replace="ata"
/replace="atataata"
/db_xref="dbSNP:2039416498"
variation 2316
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010696503"
variation 2318..2324
/gene="SNX5"
/replace="ataa"
/replace="ataataa"
/db_xref="dbSNP:2039416474"
variation 2318
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037067912"
variation 2319
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:545454309"
variation 2320..2329
/gene="SNX5"
/replace="aataa"
/replace="aataaaataa"
/db_xref="dbSNP:779222776"
variation 2325..2330
/gene="SNX5"
/replace="aat"
/replace="aataat"
/db_xref="dbSNP:1600326840"
regulatory 2325..2330
/regulatory_class="polyA_signal_sequence"
/gene="SNX5"
/note="hexamer: AATAAT"
variation 2327
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273259844"
variation 2330
/gene="SNX5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193402301"
variation 2331
/gene="SNX5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:182670803"
variation 2332
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:558940088"
variation 2334
/gene="SNX5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568585465"
variation 2338
/gene="SNX5"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039416184"
polyA_site 2341
/gene="SNX5"
/note="major polyA site"
ORIGIN
ctttctctagacgcgtcttgctgggagagtgtccgttgcttcccgtccgtgtcgcggccctgcggttggcggcctcctcgtggagcggagcaagggtaggccccacgtggcgtctttgcccggctccaagatggacggcagcggggactgggaggctgctctgggggagcacgtggcgccctgctcgcctgctcccggggcagctgggatggtggcggagtccggaggcctcctgccgccgtcgggcagggaggccggcggaggcggggccgtggccgcccccgagaggcgcccaggcggcggcggcggcggcccagcttcttctttcctcgcacagccaggcggcccctgctcgagtcccgcgtcgccatggccgcggttcccgagttgctgcagcagcaggaggaggaccgcagcaagctgagatctgtatctgtggacctgaatgttgatccctcgcttcagattgacatacctgatgcgctcagtgagagagacaaagtcaaatttacagtgcacacaaagaccacactgcccacgtttcagagcccagagttttctgttacaaggcaacatgaagactttgtgtggctacatgacactcttattgaaacaacagactatgctgggcttattattccacctgctcctacgaagcccgactttgatggtcctcgagagaagatgcagaaactgggagaaggtgaagggtctatgaccaaagaagaatttgccaagatgaaacaagaactggaagctgagtatctcgctgtgtttaagaagactgtgtcctcccatgaagtctttcttcagcggctttcttctcaccctgttctcagtaaagatcgcaactttcatgttttcctggaatatgatcaggatctaagtgttaggcggaaaaatactaaagagatgtttggtggcttcttcaaaagtgtggtgaaaagtgctgatgaagtcctttttactggagttaaggaggtagatgacttctttgagcaagagaagaacttccttattaactattacaataggatcaaagattcttgtgtgaaagctgacaaaatgaccagatctcataaaaatgttgccgatgactatatccacaccgcagcctgcttacatagcctggctttagaagagcccacagtcatcaaaaagtacctattgaaggttgctgagctatttgaaaaactaaggaaagtagagggtcgagtttcatcagatgaagatttgaagctaacagagctcctccgatactacatgctcaacattgaagctgctaaggatctcttatacagacgcaccaaagccctcattgactatgagaactcaaacaaagctctggataaggcccggttaaagagcaaagacgtcaagttggctgaggcacaccagcaggagtgctgccagaaatttgaacaactttccgaatctgcaaaagaagaactgataaatttcaaacggaagagagtggcagcatttagaaagaatctaattgaaatgtctgaactggaaataaaacatgccaggaacaatgtctcccttttgcagagctgtattgacttgttcaagaataactgatatgccttcactcagaagaaaagaaatgaatgtgaaagaaagccaagcatcacttgcacttaaatcattaccacggaagatatattagcttcaactttagtttaaaattatgtgaataaatattttgatttctacaaatcttaacatttaaccatgttggtttaaaaatattattgcttgctacttggacataactaatttttccttgtgcatttaatacctctgggcagaatccaaatactgggttctcccgtagttcgtctttagttactaagaaagggtgtaggacacattagccttctggaaacaagtagaagccatcacctggcccatgtccctacaaacccatgattgtcagggaggtgccagttacagcaggtgattcagctacttgaggtcggtaacagaccttccattcctcactgaaggtggggtttgtgtttttgttttgccctgttactccactggtagtcatctggtgtttgtactataacaacagcaagaaaatctcatttatctttatatactctttgcacctcctttttttagtcgagatataaatatttgaggggagagaaatatctacaggtatatatggaaacaaataatgtggtctgctttataagatggccagatctacattaggaaaagtataagccccctccctaatggccgctggggggtgagggcggtgtgttgtatgtctttgggtgtttgtttttttataaagcatataataaaataatcgtgctactaa
//
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]