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Previous release (v1)
2024-04-19 12:35:10, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_003380 2154 bp mRNA linear PRI 04-JAN-2024
DEFINITION Homo sapiens vimentin (VIM), mRNA.
ACCESSION NM_003380
VERSION NM_003380.5
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 2154)
AUTHORS Hao P, Qu Q, Pang Z, Li L, Du S, Shang L, Jin C, Xu W, Ha Z, Jiang
Y, Chen J, Gao Z, Jin N, Wang J and Li C.
TITLE Interaction of species A rotavirus VP4 with the cellular proteins
vimentin and actin related protein 2 discovered by a proximity
interactome assay
JOURNAL J Virol 97 (12), e0137623 (2023)
PUBMED 37991368
REMARK GeneRIF: Interaction of species A rotavirus VP4 with the cellular
proteins vimentin and actin related protein 2 discovered by a
proximity interactome assay.
REFERENCE 2 (bases 1 to 2154)
AUTHORS Thalla DG and Lautenschlager F.
TITLE Extracellular vimentin: Battle between the devil and the angel
JOURNAL Curr Opin Cell Biol 85, 102265 (2023)
PUBMED 37866018
REMARK GeneRIF: Extracellular vimentin: Battle between the devil and the
angel.
Review article
REFERENCE 3 (bases 1 to 2154)
AUTHORS Hu WM, Li M, Ning JZ, Tang YQ, Song TB, Li LZ, Zou F, Cheng F and
Yu WM.
TITLE FAM171B stabilizes vimentin and enhances CCL2-mediated TAM
infiltration to promote bladder cancer progression
JOURNAL J Exp Clin Cancer Res 42 (1), 290 (2023)
PUBMED 37915048
REMARK GeneRIF: FAM171B stabilizes vimentin and enhances CCL2-mediated TAM
infiltration to promote bladder cancer progression.
Publication Status: Online-Only
REFERENCE 4 (bases 1 to 2154)
AUTHORS Zhang X, Chen X, Sun D, Song N, Li M, Zheng W, Yu Y, Ding G and
Jiang Y.
TITLE ENAH-202 promotes cancer progression in oral squamous cell
carcinoma by regulating ZNF502/VIM axis
JOURNAL Cancer Med 12 (22), 20892-20905 (2023)
PUBMED 37902191
REMARK GeneRIF: ENAH-202 promotes cancer progression in oral squamous cell
carcinoma by regulating ZNF502/VIM axis.
REFERENCE 5 (bases 1 to 2154)
AUTHORS Riegger J and Brenner RE.
TITLE Increase of cell surface vimentin is associated with vimentin
network disruption and subsequent stress-induced premature
senescence in human chondrocytes
JOURNAL Elife 12, e91453 (2023)
PUBMED 37855367
REMARK GeneRIF: Increase of cell surface vimentin is associated with
vimentin network disruption and subsequent stress-induced premature
senescence in human chondrocytes.
Publication Status: Online-Only
REFERENCE 6 (bases 1 to 2154)
AUTHORS Brunkener M and Georgatos SD.
TITLE Membrane-binding properties of filensin, a cytoskeletal protein of
the lens fiber cells
JOURNAL J Cell Sci 103 (Pt 3), 709-718 (1992)
PUBMED 1478967
REFERENCE 7 (bases 1 to 2154)
AUTHORS Norwitz ER, Fernandez-Shaw S, Barlow DH and Starkey PM.
TITLE Expression of intermediate filament in endometrial glands changes
with the onset of pregnancy and in endometriosis
JOURNAL Hum Reprod 6 (10), 1470-1473 (1991)
PUBMED 1722806
REFERENCE 8 (bases 1 to 2154)
AUTHORS Merdes A, Brunkener M, Horstmann H and Georgatos SD.
TITLE Filensin: a new vimentin-binding, polymerization-competent, and
membrane-associated protein of the lens fiber cell
JOURNAL J Cell Biol 115 (2), 397-410 (1991)
PUBMED 1918147
REFERENCE 9 (bases 1 to 2154)
AUTHORS Honore B, Madsen P, Basse B, Andersen A, Walbum E, Celis JE and
Leffers H.
TITLE Nucleotide sequence of cDNA covering the complete coding part of
the human vimentin gene
JOURNAL Nucleic Acids Res 18 (22), 6692 (1990)
PUBMED 2251132
REFERENCE 10 (bases 1 to 2154)
AUTHORS Gupta AK, Aubin JE and Waye MM.
TITLE Isolation of a human vimentin cDNA with a long 3'-noncoding region
from a human osteosarcoma cell line (MG-63)
JOURNAL Gene 86 (2), 303-304 (1990)
PUBMED 2323579
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DA980400.1, BQ050765.1 and
BC000163.2.
This sequence is a reference standard in the RefSeqGene project.
On Nov 23, 2018 this sequence version replaced NM_003380.4.
Summary: This gene encodes a type III intermediate filament
protein. Intermediate filaments, along with microtubules and actin
microfilaments, make up the cytoskeleton. The encoded protein is
responsible for maintaining cell shape and integrity of the
cytoplasm, and stabilizing cytoskeletal interactions. This protein
is involved in neuritogenesis and cholesterol transport and
functions as an organizer of a number of other critical proteins
involved in cell attachment, migration, and signaling. Bacterial
and viral pathogens have been shown to attach to this protein on
the host cell surface. Mutations in this gene are associated with
congenital cataracts in human patients. [provided by RefSeq, Aug
2017].
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 :: BC066956.1, SRR14372080.1103016.1
[ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA2144120, SAMEA2148093
[ECO:0000348]
##Evidence-Data-END##
##RefSeq-Attributes-START##
MANE Ensembl match :: ENST00000544301.7/ ENSP00000446007.1
RefSeq Select criteria :: based on single protein-coding transcript
##RefSeq-Attributes-END##
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-18 DA980400.1 32-49
19-307 BQ050765.1 1-289
308-2154 BC000163.2 1-1847
FEATURES Location/Qualifiers
source 1..2154
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="10"
/map="10p13"
gene 1..2154
/gene="VIM"
/note="vimentin"
/db_xref="GeneID:7431"
/db_xref="HGNC:HGNC:12692"
/db_xref="MIM:193060"
exon 1..284
/gene="VIM"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1223721867"
variation 3
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775749306"
variation 7
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846712770"
variation 8
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:908246744"
variation 9
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:572292530"
variation 11..12
/gene="VIM"
/replace=""
/replace="aaaagccttt"
/db_xref="dbSNP:1227947811"
variation 11
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846712887"
variation 12
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1354773757"
variation 13
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1311528182"
variation 15
/gene="VIM"
/replace=""
/replace="t"
/db_xref="dbSNP:1237988428"
variation 15
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1248203642"
variation 18
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1376291953"
variation 20
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846713140"
variation 22
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1294561131"
variation 23
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:940913896"
variation 24
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1348483114"
variation 25
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1037985306"
variation 27
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1400893821"
variation 31
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1362124167"
variation 32
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846713390"
variation 33
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846713429"
variation 39
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1588730211"
variation 43
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1156485523"
variation 46
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1438502445"
variation 47
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1481546276"
variation 48
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:920740551"
variation 49
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1200338833"
variation 52
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428843880"
variation 57
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:932144102"
variation 62
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:150634167"
variation 65
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1216295707"
variation 67
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049137359"
variation 69
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:890509009"
variation 70
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772637318"
variation 72
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:888683375"
variation 78
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:2131678123"
variation 79
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846714119"
variation 82
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1001947317"
variation 83
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:2131678126"
variation 84
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1846714231"
variation 89
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:536007471"
variation 90
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1366161111"
variation 91
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1405918294"
variation 93
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1643293253"
variation 94
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:371486210"
variation 96
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846714445"
variation 97
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1342812399"
variation 99
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:903222283"
variation 100
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:2131678145"
variation 105
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:2131678149"
variation 111
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1000052726"
variation 112
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1418730821"
variation 113
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1032868502"
variation 114
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1014370330"
variation 118
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1412657565"
variation 119
/gene="VIM"
/replace=""
/replace="t"
/db_xref="dbSNP:1846714795"
variation 120
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:958886648"
variation 121
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1343216755"
variation 124
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846714965"
variation 126
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:763122823"
variation 130
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1219986383"
variation 131
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1024561754"
variation 137
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846715121"
variation 138
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846715167"
variation 139
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846715211"
variation 145
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846715250"
variation 146
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1191759564"
variation 149
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:971167990"
variation 151
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:190287996"
variation 152
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846715365"
variation 154
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846715405"
variation 155..156
/gene="VIM"
/replace=""
/replace="gg"
/db_xref="dbSNP:1256628899"
variation 155
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846715451"
variation 156
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846715529"
variation 158
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1338705775"
variation 159
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1755869128"
variation 160
/gene="VIM"
/replace="a"
/replace="aa"
/db_xref="dbSNP:201668694"
variation 160
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1278494509"
variation 163
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:908194238"
variation 164..169
/gene="VIM"
/replace="gtaagt"
/replace="gtaagtaagt"
/db_xref="dbSNP:1291780866"
variation 164
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846715842"
variation 166..167
/gene="VIM"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1342710687"
variation 168
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846716031"
variation 169
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1490468889"
variation 170
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:80339700"
variation 181
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846716243"
variation 182
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846716305"
variation 183
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846716370"
variation 185
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:115005130"
variation 186
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489915515"
variation 187
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:910930778"
variation 191..199
/gene="VIM"
/replace="gcgcgcg"
/replace="gcgcgcgcg"
/replace="gcgcgcgcgcg"
/db_xref="dbSNP:1237425386"
variation 192
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846716710"
variation 193
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1588730341"
variation 195
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:2131678227"
variation 196
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:537015100"
variation 197
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:932231626"
variation 198
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846716973"
variation 199
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1467171653"
variation 200
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846717056"
variation 202
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:745419154"
variation 206
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846717173"
variation 208
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1846717224"
variation 209
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:529428223"
variation 210
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1846717417"
variation 212
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846717464"
variation 214
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1477603770"
variation 216
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846717562"
variation 217
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1257068573"
variation 224
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1425731042"
variation 227
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846717685"
variation 229
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1163315350"
variation 230
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846717786"
variation 232
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846717834"
variation 233
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1363353369"
variation 234
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:912082460"
variation 235
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1236993750"
misc_feature 243..245
/gene="VIM"
/note="upstream in-frame stop codon"
variation 243
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1588730372"
variation 246
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846718029"
variation 248
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:547895152"
variation 249
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846718107"
variation 251
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846718146"
variation 253
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1041809363"
variation 254
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1320705789"
variation 255
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1048517924"
variation 257
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846718323"
variation 258
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846718375"
variation 259..261
/gene="VIM"
/replace="ctc"
/replace="ctctc"
/db_xref="dbSNP:910031805"
variation 265
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:937645221"
variation 266
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1056430328"
variation 268
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226269338"
variation 269
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:903295814"
variation 272
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:560417230"
variation 276
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846718868"
variation 278
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1588730396"
variation 280
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1041841777"
variation 280
/gene="VIM"
/replace="g"
/replace="gtg"
/replace="gtgag"
/db_xref="dbSNP:1588730404"
variation 281
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:903228052"
variation 282
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1285958440"
variation 283..284
/gene="VIM"
/replace=""
/replace="ag"
/db_xref="dbSNP:1588730414"
variation 283
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1846719297"
variation 284
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1000124528"
exon 285..994
/gene="VIM"
/inference="alignment:Splign:2.1.0"
variation 285
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:111294049"
variation 287
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:933795596"
variation 290
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846734852"
variation 291
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1046983690"
variation 293
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:886984871"
variation 298
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1846734995"
variation 299
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1826517504"
variation 302
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846735041"
variation 304
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846735081"
variation 307
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1259634473"
variation 310
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1266777155"
variation 314
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:192867529"
variation 315
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846735260"
variation 319..323
/gene="VIM"
/replace="aga"
/replace="agaga"
/db_xref="dbSNP:1358085542"
variation 319
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846735304"
variation 320
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1184010176"
variation 322
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1846735436"
variation 324
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846735489"
variation 325
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1846735522"
variation 327
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1242186290"
variation 329
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564372017"
variation 330
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:2131679100"
variation 331
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846735623"
variation 333
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1384309722"
variation 334
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1588731145"
variation 336
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1306231626"
variation 337
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1038477001"
variation 338
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1369476895"
variation 340
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846735893"
variation 344
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:894139166"
variation 350
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:574354033"
variation 351
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:915951014"
variation 353
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:11545555"
variation 356
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846736136"
variation 357
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1846736181"
variation 359
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1365033399"
variation 363
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:970174530"
variation 365
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1846736298"
variation 367
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846736420"
variation 369
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564372042"
variation 371
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:981807495"
variation 374
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1347149833"
variation 375
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:373139864"
variation 377
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1288308548"
variation 378
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1434066779"
variation 380
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:939907502"
variation 382
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1365067614"
variation 383
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:375938720"
variation 386
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768955645"
variation 388
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:559734613"
variation 389
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564372079"
variation 390
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:374772089"
variation 391..400
/gene="VIM"
/replace="cgccaccgcc"
/replace="cgccaccgccaccgcc"
/db_xref="dbSNP:1846737212"
variation 391..394
/gene="VIM"
/replace="cgcc"
/replace="cgccgcc"
/db_xref="dbSNP:780490354"
variation 395
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564372087"
variation 398
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1300093636"
variation 399
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:931113731"
variation 400
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748278063"
variation 401
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:773418308"
variation 402..409
/gene="VIM"
/replace="ccgcccag"
/replace="ccgcccagcccatcgccaccctccgcccag"
/db_xref="dbSNP:1846737499"
variation 403
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:760750553"
variation 404
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:766395068"
variation 405
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:200253669"
variation 407
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:764964401"
variation 410
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:3758410"
variation 411
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1478357437"
variation 412
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190892630"
variation 414
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1588731250"
variation 415
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846737986"
variation 416
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:758065868"
variation 417
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:2131679216"
variation 418
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473802054"
variation 419
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:2131679219"
variation 420
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:564342704"
variation 421
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:902216410"
variation 424
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1403305145"
variation 429
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:751048382"
variation 430
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1326037440"
CDS 432..1832
/gene="VIM"
/note="epididymis secretory sperm binding protein"
/codon_start=1
/product="vimentin"
/protein_id="NP_003371.2"
/db_xref="CCDS:CCDS7120.1"
/db_xref="GeneID:7431"
/db_xref="HGNC:HGNC:12692"
/db_xref="MIM:193060"
/translation="
MSTRSVSSSSYRRMFGGPGTASRPSSSRSYVTTSTRTYSLGSALRPSTSRSLYASSPGGVYATRSSAVRLRSSVPGVRLLQDSVDFSLADAINTEFKNTRTNEKVELQELNDRFANYIDKVRFLEQQNKILLAELEQLKGQGKSRLGDLYEEEMRELRRQVDQLTNDKARVEVERDNLAEDIMRLREKLQEEMLQREEAENTLQSFRQDVDNASLARLDLERKVESLQEEIAFLKKLHEEEIQELQAQIQEQHVQIDVDVSKPDLTAALRDVRQQYESVAAKNLQEAEEWYKSKFADLSEAANRNNDALRQAKQESTEYRRQVQSLTCEVDALKGTNESLERQMREMEENFAVEAANYQDTIGRLQDEIQNMKEEMARHLREYQDLLNVKMALDIEIATYRKLLEGEESRISLPLPNFSSLNLRETNLDSLPLVDTHSKRTLLIKTVETRDGQVINETSQHHDDLE"
misc_feature 432..527
/gene="VIM"
/note="propagated from UniProtKB/Swiss-Prot (P08670.4);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 435..716
/gene="VIM"
/note="propagated from UniProtKB/Swiss-Prot (P08670.4);
Region: Head"
misc_feature 435..437
/gene="VIM"
/note="N-acetylserine. /evidence=ECO:0000269|Ref.13;
propagated from UniProtKB/Swiss-Prot (P08670.4);
acetylation site"
misc_feature 444..446
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0000269|PubMed:14762106,
ECO:0007744|PubMed:18669648; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 450..452
/gene="VIM"
/note="O-linked (GlcNAc) serine, alternate.
/evidence=ECO:0000269|PubMed:20068230; propagated from
UniProtKB/Swiss-Prot (P08670.4); glycosylation site"
misc_feature 450..452
/gene="VIM"
/note="Phosphoserine, by PKA and PKC, alternate.
/evidence=ECO:0000269|PubMed:14762106; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 453..455
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0000269|PubMed:14762106; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 456..458
/gene="VIM"
/note="Phosphoserine, by PKC.
/evidence=ECO:0000269|PubMed:14762106; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 459..461
/gene="VIM"
/note="Phosphoserine, by PKC.
/evidence=ECO:0000269|PubMed:14762106; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 471..734
/gene="VIM"
/note="Intermediate filament head (DNA binding) region;
Region: Filament_head; pfam04732"
/db_xref="CDD:428095"
misc_feature 489..491
/gene="VIM"
/note="Phosphothreonine.
/evidence=ECO:0007744|PubMed:20068231,
ECO:0007744|PubMed:24275569; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 504..506
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:18669648,
ECO:0007744|PubMed:23186163, ECO:0007744|PubMed:24275569;
propagated from UniProtKB/Swiss-Prot (P08670.4);
phosphorylation site"
misc_feature 507..509
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 528..530
/gene="VIM"
/note="O-linked (GlcNAc) threonine.
/evidence=ECO:0000269|PubMed:20068230; propagated from
UniProtKB/Swiss-Prot (P08670.4); glycosylation site"
misc_feature 531..533
/gene="VIM"
/note="O-linked (GlcNAc) serine, alternate.
/evidence=ECO:0000269|PubMed:20068230; propagated from
UniProtKB/Swiss-Prot (P08670.4); glycosylation site"
misc_feature 531..533
/gene="VIM"
/note="Phosphoserine, by PKC, alternate.
/evidence=ECO:0007744|PubMed:18669648; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 546..548
/gene="VIM"
/note="Phosphoserine, by CaMK2, PKA, PKC and ROCK2.
/evidence=ECO:0000269|PubMed:14762106,
ECO:0007744|PubMed:18669648, ECO:0007744|PubMed:23186163,
ECO:0007744|PubMed:24275569; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 555..557
/gene="VIM"
/note="Phosphoserine, by PKC.
/evidence=ECO:0000269|PubMed:14762106,
ECO:0007744|PubMed:18669648, ECO:0007744|PubMed:20068231,
ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 570..572
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:20068231,
ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 576..578
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 582..584
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:18669648,
ECO:0007744|PubMed:19690332, ECO:0007744|PubMed:20068231,
ECO:0007744|PubMed:21406692, ECO:0007744|PubMed:23186163;
propagated from UniProtKB/Swiss-Prot (P08670.4);
phosphorylation site"
misc_feature 588..590
/gene="VIM"
/note="Phosphotyrosine.
/evidence=ECO:0000250|UniProtKB:P20152; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 594..596
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0000250|UniProtKB:P31000; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 597..599
/gene="VIM"
/note="Phosphoserine, by CDK5 and CDK1.
/evidence=ECO:0000269|PubMed:21465480, ECO:0000269|Ref.14,
ECO:0007744|PubMed:16964243, ECO:0007744|PubMed:18669648,
ECO:0007744|PubMed:19690332, ECO:0007744|PubMed:20068231,
ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 612..614
/gene="VIM"
/note="Phosphotyrosine.
/evidence=ECO:0007744|PubMed:18669648,
ECO:0007744|PubMed:19690332, ECO:0007744|PubMed:23186163;
propagated from UniProtKB/Swiss-Prot (P08670.4);
phosphorylation site"
misc_feature 627..629
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 645..647
/gene="VIM"
/note="Phosphoserine, by AURKB and ROCK2.
/evidence=ECO:0000269|PubMed:12458200,
ECO:0000269|PubMed:14762106, ECO:0007744|PubMed:18669648;
propagated from UniProtKB/Swiss-Prot (P08670.4);
phosphorylation site"
misc_feature 648..650
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0000269|PubMed:14762106,
ECO:0007744|PubMed:18669648, ECO:0007744|PubMed:20068231,
ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 678..680
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:18669648,
ECO:0007744|PubMed:20068231, ECO:0007744|PubMed:24275569;
propagated from UniProtKB/Swiss-Prot (P08670.4);
phosphorylation site"
misc_feature 690..692
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:24275569; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 717..824
/gene="VIM"
/note="propagated from UniProtKB/Swiss-Prot (P08670.4);
Region: Coil 1A"
misc_feature 735..1661
/gene="VIM"
/note="Intermediate filament protein; Region: Filament;
pfam00038"
/db_xref="CDD:425436"
misc_feature 780..782
/gene="VIM"
/note="Phosphotyrosine.
/evidence=ECO:0007744|PubMed:15592455; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 789..791
/gene="VIM"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0007744|PubMed:19608861; propagated from
UniProtKB/Swiss-Prot (P08670.4); acetylation site"
misc_feature 816..818
/gene="VIM"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0000250|UniProtKB:P20152; propagated from
UniProtKB/Swiss-Prot (P08670.4); acetylation site"
misc_feature 825..890
/gene="VIM"
/note="propagated from UniProtKB/Swiss-Prot (P08670.4);
Region: Linker 1"
misc_feature 846..848
/gene="VIM"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0007744|PubMed:19608861; propagated from
UniProtKB/Swiss-Prot (P08670.4); acetylation site"
misc_feature 861..863
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:18669648,
ECO:0007744|PubMed:20068231, ECO:0007744|PubMed:21406692;
propagated from UniProtKB/Swiss-Prot (P08670.4);
phosphorylation site"
misc_feature 891..1166
/gene="VIM"
/note="propagated from UniProtKB/Swiss-Prot (P08670.4);
Region: Coil 1B"
misc_feature 933..935
/gene="VIM"
/note="N6-acetyllysine.
/evidence=ECO:0000250|UniProtKB:P20152; propagated from
UniProtKB/Swiss-Prot (P08670.4); acetylation site"
misc_feature 993..995
/gene="VIM"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0000250|UniProtKB:P20152; propagated from
UniProtKB/Swiss-Prot (P08670.4); acetylation site"
misc_feature 1071..1073
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:17081983,
ECO:0007744|PubMed:20068231, ECO:0007744|PubMed:23186163,
ECO:0007744|PubMed:24275569; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 1098..1100
/gene="VIM"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0000250|UniProtKB:P20152; propagated from
UniProtKB/Swiss-Prot (P08670.4); acetylation site"
misc_feature 1107..1109
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:20068231,
ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 1134..1136
/gene="VIM"
/note="N6-acetyllysine.
/evidence=ECO:0000250|UniProtKB:P20152; propagated from
UniProtKB/Swiss-Prot (P08670.4); acetylation site"
misc_feature 1167..1235
/gene="VIM"
/note="propagated from UniProtKB/Swiss-Prot (P08670.4);
Region: Linker 12"
misc_feature 1236..1652
/gene="VIM"
/note="propagated from UniProtKB/Swiss-Prot (P08670.4);
Region: Coil 2"
misc_feature 1311..1313
/gene="VIM"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0000250|UniProtKB:P20152; propagated from
UniProtKB/Swiss-Prot (P08670.4); acetylation site"
misc_feature 1326..1328
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:20068231,
ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 1404..1406
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0000250|UniProtKB:P20152; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 1407..1418
/gene="VIM"
/note="propagated from UniProtKB/Swiss-Prot (P08670.4);
Region: [IL]-x-C-x-x-[DE] motif.
/evidence=ECO:0000305|PubMed:25417112"
misc_feature 1482..1484
/gene="VIM"
/note="Stutter; propagated from UniProtKB/Swiss-Prot
(P08670.4); other site"
misc_feature 1548..1550
/gene="VIM"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0007744|PubMed:19608861; propagated from
UniProtKB/Swiss-Prot (P08670.4); acetylation site"
misc_feature 1653..1829
/gene="VIM"
/note="propagated from UniProtKB/Swiss-Prot (P08670.4);
Region: Tail"
misc_feature 1656..1658
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:18669648; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 1665..1667
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:17081983,
ECO:0007744|PubMed:17924679, ECO:0007744|PubMed:18669648,
ECO:0007744|PubMed:18691976, ECO:0007744|PubMed:20068231;
propagated from UniProtKB/Swiss-Prot (P08670.4);
phosphorylation site"
misc_feature 1686..1688
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:20068231,
ECO:0007744|PubMed:23186163, ECO:0007744|PubMed:24275569;
propagated from UniProtKB/Swiss-Prot (P08670.4);
phosphorylation site"
misc_feature 1689..1691
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0000269|PubMed:14762106,
ECO:0007744|PubMed:20068231, ECO:0007744|PubMed:23186163;
propagated from UniProtKB/Swiss-Prot (P08670.4);
phosphorylation site"
misc_feature 1707..1709
/gene="VIM"
/note="Phosphothreonine.
/evidence=ECO:0007744|PubMed:20068231,
ECO:0007744|PubMed:24275569; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 1719..1721
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0000269|PubMed:14762106,
ECO:0007744|PubMed:20068231, ECO:0007744|PubMed:23186163,
ECO:0007744|PubMed:24275569; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 1737..1739
/gene="VIM"
/note="Phosphothreonine.
/evidence=ECO:0007744|PubMed:20068231,
ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 1743..1745
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 1764..1766
/gene="VIM"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0007744|PubMed:19608861; propagated from
UniProtKB/Swiss-Prot (P08670.4); acetylation site"
misc_feature 1767..1769
/gene="VIM"
/note="Phosphothreonine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 1803..1805
/gene="VIM"
/note="Phosphothreonine.
/evidence=ECO:0000269|PubMed:14762106; propagated from
UniProtKB/Swiss-Prot (P08670.4); phosphorylation site"
misc_feature 1806..1808
/gene="VIM"
/note="Phosphoserine.
/evidence=ECO:0000269|PubMed:14762106,
ECO:0007744|PubMed:18669648, ECO:0007744|PubMed:20068231,
ECO:0007744|PubMed:21406692, ECO:0007744|PubMed:23186163;
propagated from UniProtKB/Swiss-Prot (P08670.4);
phosphorylation site"
variation 434
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846738598"
variation 435
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:756656437"
variation 437
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:780501367"
variation 439
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846738793"
variation 441
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1436554874"
variation 445..446
/gene="VIM"
/replace="c"
/replace="cc"
/db_xref="dbSNP:864309690"
variation 446
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:377255736"
variation 447
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:755242950"
variation 448
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1230052576"
variation 451
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:2131679250"
variation 453
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1288770216"
variation 454
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779204525"
variation 456..462
/gene="VIM"
/replace="tcct"
/replace="tcctcct"
/db_xref="dbSNP:749805536"
variation 457
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846739243"
variation 461
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:748381490"
variation 463
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1452327776"
variation 465
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1220895620"
variation 466
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1245254535"
variation 467
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1484172325"
variation 469
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846739569"
variation 470
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1031859925"
variation 472
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278642875"
variation 475
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1846739712"
variation 476
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772407997"
variation 477
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773471865"
variation 480
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:747053288"
variation 484
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:11545549"
variation 485..487
/gene="VIM"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1846739997"
variation 485
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415150705"
variation 486
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:771023210"
variation 488
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1322281451"
variation 491
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1363106467"
variation 493
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:776383614"
variation 494
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:765009320"
variation 497
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1202092452"
variation 498
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:910563895"
variation 499
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:527439944"
variation 500
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1349662848"
variation 501
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846740484"
variation 503
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1174783297"
variation 506
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:957631225"
variation 508
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846740611"
variation 509
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1439751541"
variation 510
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775343323"
variation 511
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1356941925"
variation 513
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1194887764"
variation 515
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1259578413"
variation 520
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846740908"
variation 522
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:762644216"
variation 527
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1260508481"
variation 528
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:763707422"
variation 529
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1344328729"
variation 530
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:531385322"
variation 531
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1725985429"
variation 532
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846741218"
variation 533
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846741261"
variation 534
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:756711607"
variation 537
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:766889315"
variation 538
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:754236131"
variation 539
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846741476"
variation 545
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1238606775"
variation 547
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846741575"
variation 552
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:755500924"
variation 554
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:779199559"
variation 557
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1382854843"
variation 558
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:748519640"
variation 559
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:758730926"
variation 560
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1846741857"
variation 562
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318337726"
variation 565
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:778098458"
variation 566
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:771076339"
variation 569
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1279005584"
variation 570..573
/gene="VIM"
/replace=""
/replace="agca"
/db_xref="dbSNP:1554775788"
variation 571
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1335964173"
variation 573
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:201189169"
variation 574
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:745851443"
variation 576
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:769749512"
variation 577
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1312761190"
variation 578..579
/gene="VIM"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1229957937"
variation 578
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1367516245"
variation 580
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:11545553"
variation 582
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846742850"
variation 583
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:775190116"
variation 584
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274240494"
variation 585
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1588731496"
variation 590
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846743131"
variation 591
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1294995968"
variation 592
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1337671316"
variation 595
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762699034"
variation 596
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1408873660"
variation 597
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:768322635"
variation 598
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:773938980"
variation 599
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:761320242"
variation 600
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:767007282"
variation 601
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:749931833"
variation 602
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:760007125"
variation 603
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1215537817"
variation 604
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1564372278"
variation 605
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:2131679423"
variation 609..612
/gene="VIM"
/replace="gtgt"
/replace="gtgtgtgt"
/db_xref="dbSNP:1169271871"
variation 609
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1253533842"
variation 611
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1388964411"
variation 613
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:765742006"
variation 617
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846744300"
variation 620
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846744345"
variation 622
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1474263020"
variation 623
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:34171769"
variation 625
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402661582"
variation 628
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846744571"
variation 630
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:369470034"
variation 631
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1445952624"
variation 633
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:778153530"
variation 635
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:11545547"
variation 636
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1435968814"
variation 637
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:928603903"
variation 638
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846745109"
variation 639..667
/gene="VIM"
/replace="ct"
/replace="ctgcggagcagcgtgcccggggtgcggct"
/db_xref="dbSNP:755419803"
variation 642
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1235698818"
variation 643
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:777756098"
variation 644
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344818407"
variation 646
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1202137863"
variation 650
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846745504"
variation 651
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1270633135"
variation 654
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:757539736"
variation 655
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402686254"
variation 656
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564372335"
variation 657
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:972743635"
variation 658
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:781179445"
variation 659
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:111616371"
variation 660
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:184701100"
variation 661
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:11545548"
variation 662
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846746236"
variation 663
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:865981174"
variation 664
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1325594598"
variation 665
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1480009625"
variation 668
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846746638"
variation 669
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1173957268"
variation 670
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1846746781"
variation 671
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1564372376"
variation 672
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:867740022"
variation 675
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1413835853"
variation 680
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:779995083"
variation 681
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1050023359"
variation 683
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1382898134"
variation 684
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:749097460"
variation 686
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1385094399"
variation 687
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324531976"
variation 689
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846747549"
variation 692
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846747639"
variation 693
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1330720517"
variation 694
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1221861802"
variation 697
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1290632621"
variation 698
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846747931"
variation 701
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1330170107"
variation 702
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1228337366"
variation 709
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1259476721"
variation 710
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1484647461"
variation 711
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1452623960"
variation 713
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:144539901"
variation 714
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:868327359"
variation 715
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1267669767"
variation 716
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1038272949"
variation 717
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:774132663"
variation 723
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:529112487"
variation 724
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1253712799"
variation 728
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1472762224"
variation 743
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1158368392"
variation 747
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1361987967"
variation 748
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1459555504"
variation 750
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:867113544"
variation 752
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163932067"
variation 753
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1390058731"
variation 754
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403341247"
variation 758
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:761507856"
variation 765
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:546992824"
variation 767
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:534064028"
variation 768
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1305547785"
variation 770
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324002909"
variation 771
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1246101455"
variation 776
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1265543287"
variation 779
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:943771920"
variation 780
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:772634201"
variation 786
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846749913"
variation 796
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846749958"
variation 801
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1219813951"
variation 803
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1253507122"
variation 804
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846750403"
variation 806
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1425939424"
variation 808
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:565243670"
variation 809
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846750563"
variation 810
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1483298145"
variation 811
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:760190137"
variation 812
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1248095048"
variation 814
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846750746"
variation 815
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:147857896"
variation 818
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:2131679622"
variation 820
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:902288870"
variation 821
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:113013980"
variation 823
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1053391219"
variation 825
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1216233618"
variation 827
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:11545554"
variation 830
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:565335496"
variation 833
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1045526760"
variation 834
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:532905834"
variation 844
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1437046531"
variation 845
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461837697"
variation 854
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:2131679660"
variation 855
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1296829264"
variation 860
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846751655"
variation 862
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:757461918"
variation 864
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:781436766"
variation 865
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:2131679674"
variation 869
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1042003"
variation 872
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1312562294"
variation 873
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:750493891"
variation 875
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243129674"
variation 876
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1245849739"
variation 878
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846752109"
variation 881
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846752150"
variation 882
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:121917775"
variation 884
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1281806487"
variation 885
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:141319821"
variation 889
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:999034093"
variation 890
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846752401"
variation 892
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323790047"
variation 893
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:779864520"
variation 894
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:749293841"
variation 895
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:778724394"
variation 896
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201028257"
variation 897
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:747904058"
variation 899
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846752790"
variation 900
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1406458665"
variation 902
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846752887"
variation 903
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1457202484"
variation 904
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442903146"
variation 905
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846753033"
variation 907
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:771651752"
variation 908
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390810752"
variation 912
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:772870142"
variation 913
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:746513281"
variation 914
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1361269617"
variation 917
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:2131679745"
variation 920
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201551781"
variation 921
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:377524590"
variation 923
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1588731958"
variation 924
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:569704234"
variation 929
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:774888281"
variation 930
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:267602430"
variation 931
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:762190767"
variation 935
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1588731974"
variation 937
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:767649276"
variation 939
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1361960709"
variation 940
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1846753969"
variation 941
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1588731993"
variation 944
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:750589084"
variation 945
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:11545550"
variation 948
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:756282194"
variation 949
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:766499205"
variation 953
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:746924511"
variation 954
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1313812412"
variation 955
/gene="VIM"
/replace=""
/replace="g"
/db_xref="dbSNP:779272287"
variation 956
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753896793"
variation 961
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262487660"
variation 962
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1459941371"
variation 963
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846754654"
variation 966
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1200409133"
variation 968
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:754952038"
variation 969
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:866834871"
variation 971
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:778785495"
variation 973
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:149942621"
variation 974
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427520431"
variation 975
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1434157425"
variation 976
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1035750972"
variation 977
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:961464401"
variation 978
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:972689698"
variation 979
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1427593011"
variation 980
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846755659"
variation 981
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1459289381"
variation 982
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1321743889"
variation 983
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284367198"
variation 984
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:201325757"
variation 985
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:11545551"
variation 988
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1588732106"
variation 990
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:777297315"
variation 992
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846756153"
variation 994
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1343201036"
exon 995..1055
/gene="VIM"
/inference="alignment:Splign:2.1.0"
variation 995
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1351847897"
variation 1000..1007
/gene="VIM"
/replace="aggag"
/replace="aggaggag"
/db_xref="dbSNP:1281686142"
variation 1001
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:888498183"
variation 1002
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:373295180"
variation 1006
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1334832994"
variation 1008
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1007423361"
variation 1009
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1005304137"
variation 1010
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:767474660"
variation 1012
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1228442247"
variation 1014
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1303380482"
variation 1017
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1269811567"
variation 1019
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846773970"
variation 1020
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846774011"
variation 1023
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1406182336"
variation 1026
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1363228886"
variation 1029
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1037734535"
variation 1030
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:145760831"
variation 1031
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:755867026"
variation 1032
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1461281372"
variation 1033
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:765911800"
variation 1036
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:866251474"
variation 1038
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1386842396"
variation 1040
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:148956484"
variation 1043
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:143636314"
variation 1045
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846774646"
variation 1046
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:778351047"
variation 1052
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846774740"
variation 1054
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1085307141"
exon 1056..1151
/gene="VIM"
/inference="alignment:Splign:2.1.0"
variation 1056
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448514100"
variation 1061
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:61761616"
variation 1062
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1455890040"
variation 1063
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846832573"
variation 1064
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:773230033"
variation 1065
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:760525619"
variation 1066
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:116800063"
variation 1069
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:776474793"
variation 1070
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:775483110"
variation 1071
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1846832944"
variation 1073
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:759162591"
variation 1074
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846833082"
variation 1077
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:138235394"
variation 1080
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:752236825"
variation 1081
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:762391438"
variation 1084
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846833414"
variation 1086
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1349809735"
variation 1091
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:768016203"
variation 1094
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1310277495"
variation 1095
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1304135302"
variation 1096
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:750994048"
variation 1101
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846833850"
variation 1103
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1236184497"
variation 1104
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:897144372"
variation 1108
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1301514675"
variation 1112
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1305482290"
variation 1114
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:756629184"
variation 1116
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846834198"
variation 1117
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846834256"
variation 1118
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:780328725"
variation 1121
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:754196814"
variation 1123
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1358309285"
variation 1124
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846834549"
variation 1131
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846834613"
variation 1137
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846834685"
variation 1141
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:755181628"
variation 1142
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1252856204"
variation 1145
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:141244457"
variation 1146
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:748255267"
variation 1148
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1248288717"
variation 1149
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1399047851"
variation 1150
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:550798765"
exon 1152..1313
/gene="VIM"
/inference="alignment:Splign:2.1.0"
variation 1156
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846836697"
variation 1159
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:992484456"
variation 1163
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:775250376"
variation 1166
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846836840"
variation 1172
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1404795916"
variation 1173
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846836921"
variation 1176
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1445166789"
variation 1179
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1290316532"
variation 1180
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:145152785"
variation 1181
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1381266556"
variation 1183
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846837154"
variation 1184
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1314004123"
variation 1185
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846837247"
variation 1186
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:776147609"
variation 1187
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846837288"
variation 1188
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846837334"
variation 1189
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:773762488"
variation 1190
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:761334638"
variation 1192
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:2131682481"
variation 1193
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:777132960"
variation 1196
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403926080"
variation 1197
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:139037306"
variation 1199
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:377349430"
variation 1200
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:753092108"
variation 1202
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846837767"
variation 1203
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:758735029"
variation 1205
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:141519986"
variation 1208
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:764331554"
variation 1209
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:985623715"
variation 1210
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846838234"
variation 1212
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1257540470"
variation 1213
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1480960201"
variation 1215
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846838324"
variation 1216
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846838371"
variation 1217
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846838408"
variation 1227
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:113576905"
variation 1228
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:150878383"
variation 1229
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:137961338"
variation 1231
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402903305"
variation 1237
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:781127817"
variation 1238
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:745874397"
variation 1239
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846838829"
variation 1240
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1452626097"
variation 1244
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:4903"
variation 1245
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:199515026"
variation 1247
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1588734853"
variation 1248
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1175193193"
variation 1249
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:371176373"
variation 1250
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1588734865"
variation 1254
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846839280"
variation 1256
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:773992008"
variation 1258
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:2131682546"
variation 1260
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:747619298"
variation 1261
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232637574"
variation 1262
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1225351627"
variation 1264
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1048526047"
variation 1266
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1356703491"
variation 1267
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285046692"
variation 1269
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:147133187"
variation 1273
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:772585290"
variation 1283
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:760172409"
variation 1285
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846839913"
variation 1286
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:765809278"
variation 1289
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846840068"
variation 1292
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1199175580"
variation 1293
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:776031097"
variation 1295
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1588734910"
variation 1296
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471445445"
variation 1302
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:763360647"
variation 1304
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201299921"
variation 1307
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1588734921"
variation 1309
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:764236805"
variation 1310
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:11254467"
exon 1314..1439
/gene="VIM"
/inference="alignment:Splign:2.1.0"
variation 1315
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:747735685"
variation 1317
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:578255169"
variation 1318
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:2131683098"
variation 1329
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:2131683101"
variation 1330
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:144238562"
variation 1331
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1327165886"
variation 1332
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:754861364"
variation 1334
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1235352018"
variation 1335
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:778821394"
variation 1338
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:2131683110"
variation 1339
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752407631"
variation 1341
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:758102529"
variation 1342
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:552165238"
variation 1343
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:965528949"
variation 1345
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:2131683119"
variation 1346
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846857641"
variation 1348
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:746534016"
variation 1349
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1588735438"
variation 1351
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393644707"
variation 1352
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:770500248"
variation 1353
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:11545546"
variation 1356
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1328451159"
variation 1360
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:780835078"
variation 1361
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846858093"
variation 1363
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:749857760"
variation 1369
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316382347"
variation 1374
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:769012996"
variation 1379
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1588735451"
variation 1380
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846858307"
variation 1381
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1588735455"
variation 1382
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1588735457"
variation 1384
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1264296526"
variation 1390
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:371431143"
variation 1392
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:762030566"
variation 1401
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1171701809"
variation 1402
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:779403092"
variation 1403
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:772347590"
variation 1405
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773352810"
variation 1411
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1374235575"
variation 1412
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1193383296"
variation 1414
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:760880333"
variation 1418
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:147429387"
variation 1423
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1588735491"
variation 1425
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:200772352"
variation 1428
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:753894774"
variation 1435
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:924667179"
variation 1439
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:111932484"
exon 1440..1660
/gene="VIM"
/inference="alignment:Splign:2.1.0"
variation 1440
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:369763215"
variation 1441
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:778153870"
variation 1447
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846865347"
variation 1449
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1456684069"
variation 1452
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:747338188"
variation 1455
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:771168882"
variation 1456
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:376802470"
variation 1460
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:745965859"
variation 1463
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:769833820"
variation 1464
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775627643"
variation 1465
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:116370722"
variation 1472..1473
/gene="VIM"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2131683474"
variation 1472
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1049424533"
variation 1476
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:2131683483"
variation 1477
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1846865757"
variation 1478
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:764080683"
variation 1480
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846865871"
variation 1482
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:200740172"
variation 1486
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:866598895"
variation 1487
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:531588660"
variation 1488
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:767278443"
variation 1489
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846866107"
variation 1492
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:766141377"
variation 1495
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:750107979"
variation 1497
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:2131683527"
variation 1499
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846866264"
variation 1502
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:2131683536"
variation 1505
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2131683537"
variation 1506
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1197860827"
variation 1507
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1261710176"
variation 1511
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:139818786"
variation 1512
/gene="VIM"
/replace=""
/replace="a"
/db_xref="dbSNP:2131683553"
variation 1512
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:765859276"
variation 1516
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:114322672"
variation 1517
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1297590942"
variation 1518
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846866642"
variation 1519
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:778207118"
variation 1520
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1311257498"
variation 1521
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751935909"
variation 1522
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:371054027"
variation 1523
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:116696668"
variation 1531
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846866919"
variation 1533
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:2131683589"
variation 1535
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:781618375"
variation 1536..1537
/gene="VIM"
/replace=""
/replace="aagatgtctggtgttat"
/db_xref="dbSNP:2131683592"
variation 1538
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1588735928"
variation 1541
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465571388"
variation 1542
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:2131683597"
variation 1546
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:746135750"
variation 1549
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:770025384"
variation 1550
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:780026360"
variation 1553
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:749331181"
variation 1554
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:768727457"
variation 1556
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1588735943"
variation 1557
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846867547"
variation 1558
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846867609"
variation 1559
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:2131683616"
variation 1563
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:201530534"
variation 1564..1565
/gene="VIM"
/replace=""
/replace="gt"
/db_xref="dbSNP:759564522"
variation 1564
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:761834421"
variation 1565
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:773034702"
variation 1567
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:760289106"
variation 1568
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846868059"
variation 1569
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1358822322"
variation 1570
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1218008674"
variation 1571
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256043076"
variation 1572
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:749084801"
variation 1573
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:35157876"
variation 1574
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:758992086"
variation 1577
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1482400000"
variation 1578
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1188442437"
variation 1580
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:764590816"
variation 1581
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1267792443"
variation 1586
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:374050623"
variation 1587
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:752126893"
variation 1591
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1588736025"
variation 1593
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846869078"
variation 1594
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846869140"
variation 1598
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1846869205"
variation 1602
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1432057333"
variation 1608
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846869327"
variation 1612
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1258626020"
variation 1614
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846869455"
variation 1615
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1470562734"
variation 1616
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1176198427"
variation 1621
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1357615634"
variation 1631
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:757749881"
variation 1649
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1023005847"
variation 1652
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:150986868"
variation 1653
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564374858"
variation 1655
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846870001"
variation 1656
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846870066"
variation 1658
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:750758121"
exon 1661..1704
/gene="VIM"
/inference="alignment:Splign:2.1.0"
variation 1661
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:373859810"
variation 1666
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:750766626"
variation 1674
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:756434736"
variation 1677
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1564374995"
variation 1678
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:11545541"
variation 1680
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1276819494"
variation 1688
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:11545556"
variation 1690
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1490612095"
variation 1693
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1038093456"
variation 1694
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:766644642"
variation 1696
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:754167157"
variation 1697
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:140482660"
variation 1698
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:760767925"
exon 1705..1790
/gene="VIM"
/inference="alignment:Splign:2.1.0"
variation 1713
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846888892"
variation 1719
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:955350530"
variation 1722
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:982699474"
variation 1724
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:150003485"
variation 1725
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846889041"
variation 1728
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:768266467"
variation 1731
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:146586974"
variation 1733
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1405354231"
variation 1737
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1467601802"
variation 1738..1744
/gene="VIM"
/replace="cccactc"
/replace="cccactcccactc"
/db_xref="dbSNP:1171511721"
variation 1739
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:761281774"
variation 1743
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1442649286"
variation 1746
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1371902872"
variation 1747
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:372394023"
variation 1751
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1588736694"
variation 1754
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846889570"
variation 1756
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:777161019"
variation 1757
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:759925135"
variation 1758
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424831707"
variation 1760
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:371063888"
variation 1762
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:765564921"
variation 1763
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:753033876"
variation 1768
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:763073277"
variation 1769
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:764285210"
variation 1778
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:751564309"
variation 1784
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1460602699"
variation 1786
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:757220075"
variation 1788
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1414174359"
exon 1791..2154
/gene="VIM"
/inference="alignment:Splign:2.1.0"
variation 1791
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1214438836"
variation 1793
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1355411378"
variation 1796
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:756019006"
variation 1797
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:779935723"
variation 1798
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1846907214"
variation 1799
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:753533838"
variation 1800
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:376668602"
variation 1801
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:754678758"
variation 1802
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:778375034"
variation 1803
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:747701399"
variation 1804
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:771777895"
variation 1805..1806
/gene="VIM"
/replace="tt"
/replace="tttt"
/db_xref="dbSNP:1846907790"
variation 1808
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278582700"
variation 1811
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846907904"
variation 1813
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:777412987"
variation 1815
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1158260463"
variation 1816
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:11545543"
variation 1817
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:368414175"
variation 1818
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:372258946"
variation 1819
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:775956508"
variation 1820
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:376851316"
variation 1821
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:763181437"
variation 1823
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781197884"
variation 1831
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:369406521"
variation 1836
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:774501100"
variation 1839
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406867842"
variation 1842
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:2131685060"
variation 1843
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846908862"
variation 1844
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:144519674"
variation 1845
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1308031858"
variation 1846..1847
/gene="VIM"
/replace=""
/replace="tggtgcaa"
/db_xref="dbSNP:1588737310"
variation 1846
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846909058"
variation 1851
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1468678816"
variation 1852
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:767629215"
variation 1853
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846909313"
variation 1855..1862
/gene="VIM"
/replace=""
/replace="caatatat"
/db_xref="dbSNP:1588737327"
variation 1856
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846909404"
variation 1857
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:571601510"
variation 1860
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1265772352"
variation 1861
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846909585"
variation 1862
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846909635"
variation 1868
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846909680"
variation 1873
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1429245264"
variation 1875
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760635500"
variation 1876..1881
/gene="VIM"
/replace="aaaaaa"
/replace="aaaaaaa"
/db_xref="dbSNP:2131685085"
variation 1876
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1588737344"
variation 1878
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:750627825"
variation 1879
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:766176270"
variation 1880
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846910086"
variation 1882
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:753683416"
variation 1884
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846910231"
variation 1886
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1846910298"
variation 1887
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:12667"
variation 1892
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1039681305"
variation 1899
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1419968335"
variation 1902
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:557450449"
variation 1903
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1244394114"
variation 1910
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461941920"
variation 1912
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846910743"
variation 1916
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:922507761"
variation 1920..1921
/gene="VIM"
/replace=""
/replace="a"
/db_xref="dbSNP:1588737376"
variation 1922
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846910848"
variation 1925
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846910875"
variation 1926
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846910916"
variation 1927
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846910962"
variation 1934
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1460796559"
variation 1938
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:933953860"
variation 1939
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:112279926"
variation 1940
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:2131685111"
variation 1941
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:1846911101"
variation 1942
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1588737391"
variation 1949
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846911169"
variation 1955
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:879850578"
variation 1959
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002791003"
variation 1961
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:9235"
variation 1962
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1588737403"
variation 1965
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010758891"
variation 1968
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:186277663"
variation 1969
/gene="VIM"
/replace=""
/replace="t"
/db_xref="dbSNP:1588737412"
variation 1970
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1338746898"
variation 1971
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:555098108"
variation 1972
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1588737417"
variation 1973
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1588737421"
variation 1974
/gene="VIM"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:9059"
variation 1975
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846911679"
variation 1978
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:189996263"
variation 1979
/gene="VIM"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:9486"
variation 1983
/gene="VIM"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1001870717"
variation 1984
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1034728296"
variation 1986
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1846911927"
variation 1989
/gene="VIM"
/replace=""
/replace="t"
/db_xref="dbSNP:1588737443"
variation 1990
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353081201"
variation 1992
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1588737451"
variation 1993
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1009945979"
variation 1994
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:9485"
variation 1995
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1170218553"
variation 2000
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1846912156"
variation 2001
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1021308922"
variation 2002
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:541300349"
variation 2005
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846912291"
variation 2007
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:975346755"
variation 2010..2012
/gene="VIM"
/replace="gtt"
/replace="gttgtt"
/db_xref="dbSNP:1846912369"
variation 2014
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1357419304"
variation 2015
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1443547684"
variation 2017
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846912467"
variation 2018
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:896040910"
variation 2019
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:542155813"
variation 2021
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1014530164"
variation 2022
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1479628564"
variation 2023
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:559111736"
variation 2027
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:9484"
variation 2033
/gene="VIM"
/replace=""
/replace="a"
/db_xref="dbSNP:1588737483"
variation 2033
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846912728"
variation 2036..2037
/gene="VIM"
/replace=""
/replace="g"
/db_xref="dbSNP:1588737492"
variation 2036
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026333067"
variation 2037
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:951519538"
variation 2038
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1360432697"
variation 2040
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:984260754"
variation 2042
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:987730587"
variation 2044
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1016934463"
variation 2049
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:577584527"
variation 2050
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:940631919"
variation 2053
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846913243"
variation 2055
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1307839140"
variation 2058
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1846913316"
variation 2060
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:11545542"
variation 2061..2064
/gene="VIM"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1588737522"
variation 2061
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393598482"
variation 2064..2065
/gene="VIM"
/replace=""
/replace="ag"
/db_xref="dbSNP:1588737524"
variation 2065
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846913462"
variation 2066
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846913494"
variation 2069..2072
/gene="VIM"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1588737527"
variation 2071
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:544641752"
variation 2075
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846913588"
variation 2077
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:975371925"
variation 2079
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:3249"
variation 2086
/gene="VIM"
/replace="a"
/replace="t"
/db_xref="dbSNP:1846913651"
variation 2089
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:920648723"
variation 2090
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:934005023"
variation 2091..2100
/gene="VIM"
/replace="ttttttttt"
/replace="tttttttttt"
/replace="ttttttttttt"
/db_xref="dbSNP:948147691"
variation 2100
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:988047951"
variation 2101
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:913818319"
variation 2102
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1588737550"
variation 2104
/gene="VIM"
/replace="c"
/replace="g"
/db_xref="dbSNP:1588737558"
variation 2106
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:530574581"
variation 2110
/gene="VIM"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:543289845"
variation 2115
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:777452849"
variation 2116
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1415508816"
variation 2119
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1846914179"
variation 2124
/gene="VIM"
/replace="g"
/replace="t"
/db_xref="dbSNP:1049341"
variation 2131..2132
/gene="VIM"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1199863936"
regulatory 2134..2139
/regulatory_class="polyA_signal_sequence"
/gene="VIM"
/note="hexamer: AATAAA"
variation 2135
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1158887580"
variation 2145
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:1588737586"
variation 2151
/gene="VIM"
/replace="a"
/replace="g"
/db_xref="dbSNP:937770720"
variation 2152
/gene="VIM"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400391286"
polyA_site 2154
/gene="VIM"
/note="major polyA site"
variation 2154
/gene="VIM"
/replace="a"
/replace="c"
/db_xref="dbSNP:3179873"
ORIGIN
gggaggcccacgtatggcgcctctccaaaggctgcagaagtttcttgctaacaaaaagtccgcacattcgagcaaagacaggctttagcgagttattaaaaacttaggggcgctcttgtcccccacagggcccgaccgcacacagcaaggcgatggcccagctgtaagttggtagcactgagaactagcagcgcgcgcggagcccgctgagacttgaatcaatctggtctaacggtttcccctaaaccgctaggagccctcaatcggcgggacagcagggcgcgtcctctgccactctcgctccgaggtccccgcgccagagacgcagccgcgctcccaccacccacacccaccgcgccctcgttcgcctcttctccgggagccagtccgcgccaccgccgccgcccaggccatcgccaccctccgcagccatgtccaccaggtccgtgtcctcgtcctcctaccgcaggatgttcggcggcccgggcaccgcgagccggccgagctccagccggagctacgtgactacgtccacccgcacctacagcctgggcagcgcgctgcgccccagcaccagccgcagcctctacgcctcgtccccgggcggcgtgtatgccacgcgctcctctgccgtgcgcctgcggagcagcgtgcccggggtgcggctcctgcaggactcggtggacttctcgctggccgacgccatcaacaccgagttcaagaacacccgcaccaacgagaaggtggagctgcaggagctgaatgaccgcttcgccaactacatcgacaaggtgcgcttcctggagcagcagaataagatcctgctggccgagctcgagcagctcaagggccaaggcaagtcgcgcctgggggacctctacgaggaggagatgcgggagctgcgccggcaggtggaccagctaaccaacgacaaagcccgcgtcgaggtggagcgcgacaacctggccgaggacatcatgcgcctccgggagaaattgcaggaggagatgcttcagagagaggaagccgaaaacaccctgcaatctttcagacaggatgttgacaatgcgtctctggcacgtcttgaccttgaacgcaaagtggaatctttgcaagaagagattgcctttttgaagaaactccacgaagaggaaatccaggagctgcaggctcagattcaggaacagcatgtccaaatcgatgtggatgtttccaagcctgacctcacggctgccctgcgtgacgtacgtcagcaatatgaaagtgtggctgccaagaacctgcaggaggcagaagaatggtacaaatccaagtttgctgacctctctgaggctgccaaccggaacaatgacgccctgcgccaggcaaagcaggagtccactgagtaccggagacaggtgcagtccctcacctgtgaagtggatgcccttaaaggaaccaatgagtccctggaacgccagatgcgtgaaatggaagagaactttgccgttgaagctgctaactaccaagacactattggccgcctgcaggatgagattcagaatatgaaggaggaaatggctcgtcaccttcgtgaataccaagacctgctcaatgttaagatggcccttgacattgagattgccacctacaggaagctgctggaaggcgaggagagcaggatttctctgcctcttccaaacttttcctccctgaacctgagggaaactaatctggattcactccctctggttgatacccactcaaaaaggacacttctgattaagacggttgaaactagagatggacaggttatcaacgaaacttctcagcatcacgatgaccttgaataaaaattgcacacactcagtgcagcaatatattaccagcaagaataaaaaagaaatccatatcttaaagaaacagctttcaagtgcctttctgcagtttttcaggagcgcaagatagatttggaataggaataagctctagttcttaacaaccgacactcctacaagatttagaaaaaagtttacaacataatctagtttacagaaaaatcttgtgctagaatactttttaaaaggtattttgaataccattaaaactgcttttttttttccagcaagtatccaaccaacttggttctgcttcaataaatctttggaaaaactc
//
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]