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Previous release (v1)
2024-04-30 05:03:16, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001166107 2351 bp mRNA linear PRI 17-SEP-2023
DEFINITION Homo sapiens 3-hydroxy-3-methylglutaryl-CoA synthase 2 (HMGCS2),
transcript variant 2, mRNA; nuclear gene for mitochondrial product.
ACCESSION NM_001166107
VERSION NM_001166107.1
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 2351)
AUTHORS Mao H, Wang R, Shao F, Zhao M, Tian D, Xia H and Zhao Y.
TITLE HMGCS2 serves as a potential biomarker for inhibition of renal
clear cell carcinoma growth
JOURNAL Sci Rep 13 (1), 14629 (2023)
PUBMED 37670031
REMARK GeneRIF: HMGCS2 serves as a potential biomarker for inhibition of
renal clear cell carcinoma growth.
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 2351)
AUTHORS Bai M, Wu M, Jiang M, He J, Deng X, Xu S, Fan J, Miao M, Wang T, Li
Y, Yu X, Wang L, Zhang Y, Huang S, Yang L, Jia Z and Zhang A.
TITLE LONP1 targets HMGCS2 to protect mitochondrial function and
attenuate chronic kidney disease
JOURNAL EMBO Mol Med 15 (2), e16581 (2023)
PUBMED 36629048
REMARK GeneRIF: LONP1 targets HMGCS2 to protect mitochondrial function and
attenuate chronic kidney disease.
REFERENCE 3 (bases 1 to 2351)
AUTHORS Asif S, Kim RY, Fatica T, Sim J, Zhao X, Oh Y, Denoncourt A, Cheung
AC, Downey M, Mulvihill EE and Kim KH.
TITLE Hmgcs2-mediated ketogenesis modulates high-fat diet-induced
hepatosteatosis
JOURNAL Mol Metab 61, 101494 (2022)
PUBMED 35421611
REMARK GeneRIF: Hmgcs2-mediated ketogenesis modulates high-fat
diet-induced hepatosteatosis.
REFERENCE 4 (bases 1 to 2351)
AUTHORS Shizu R, Ezaki K, Sato T, Sugawara A, Hosaka T, Sasaki T and
Yoshinari K.
TITLE PXR Suppresses PPARalpha-Dependent HMGCS2 Gene Transcription by
Inhibiting the Interaction between PPARalpha and PGC1alpha
JOURNAL Cells 10 (12), 3550 (2021)
PUBMED 34944058
REMARK GeneRIF: PXR Suppresses PPARalpha-Dependent HMGCS2 Gene
Transcription by Inhibiting the Interaction between PPARalpha and
PGC1alpha.
Publication Status: Online-Only
REFERENCE 5 (bases 1 to 2351)
AUTHORS Han P, Wang Y, Luo W, Lu Y, Zhou X, Yang Y, Zheng Q, Li D, Wu S, Li
L, Zhang H, Zhao J, Zhang Z, Matskova L, Li P and Zhou X.
TITLE Epigenetic inactivation of hydroxymethylglutaryl CoA synthase
reduces ketogenesis and facilitates tumor cell motility in clear
cell renal carcinoma
JOURNAL Pathol Res Pract 227, 153622 (2021)
PUBMED 34624592
REMARK GeneRIF: Epigenetic inactivation of hydroxymethylglutaryl CoA
synthase reduces ketogenesis and facilitates tumor cell motility in
clear cell renal carcinoma.
REFERENCE 6 (bases 1 to 2351)
AUTHORS Bouchard L, Robert MF, Vinarov D, Stanley CA, Thompson GN, Morris
A, Leonard JV, Quant P, Hsu BY, Boneh A, Boukaftane Y, Ashmarina L,
Wang S, Miziorko H and Mitchell GA.
TITLE Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency:
clinical course and description of causal mutations in two patients
JOURNAL Pediatr Res 49 (3), 326-331 (2001)
PUBMED 11228257
REFERENCE 7 (bases 1 to 2351)
AUTHORS Boukaftane Y and Mitchell GA.
TITLE Cloning and characterization of the human mitochondrial
3-hydroxy-3-methylglutaryl CoA synthase gene
JOURNAL Gene 195 (2), 121-126 (1997)
PUBMED 9305755
REFERENCE 8 (bases 1 to 2351)
AUTHORS Mascaro C, Buesa C, Ortiz JA, Haro D and Hegardt FG.
TITLE Molecular cloning and tissue expression of human mitochondrial
3-hydroxy-3-methylglutaryl-CoA synthase
JOURNAL Arch Biochem Biophys 317 (2), 385-390 (1995)
PUBMED 7893153
REFERENCE 9 (bases 1 to 2351)
AUTHORS Boukaftane Y, Duncan A, Wang S, Labuda D, Robert MF, Sarrazin J,
Schappert K and Mitchell GA.
TITLE Human mitochondrial HMG CoA synthase: liver cDNA and partial
genomic cloning, chromosome mapping to 1p12-p13, and possible role
in vertebrate evolution
JOURNAL Genomics 23 (3), 552-559 (1994)
PUBMED 7851882
REFERENCE 10 (bases 1 to 2351)
AUTHORS Robinson,A.M. and Williamson,D.H.
TITLE Physiological roles of ketone bodies as substrates and signals in
mammalian tissues
JOURNAL Physiol Rev 60 (1), 143-187 (1980)
PUBMED 6986618
REMARK Review article
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from BP420631.1, AK303777.1,
BC044217.1, BX104280.1 and AI215948.1.
This sequence is a reference standard in the RefSeqGene project.
Summary: The protein encoded by this gene belongs to the HMG-CoA
synthase family. It is a mitochondrial enzyme that catalyzes the
first reaction of ketogenesis, a metabolic pathway that provides
lipid-derived energy for various organs during times of
carbohydrate deprivation, such as fasting. Mutations in this gene
are associated with HMG-CoA synthase deficiency. Alternatively
spliced transcript variants encoding different isoforms have been
found for this gene.[provided by RefSeq, Oct 2009].
Transcript Variant: This variant (2) is missing an in-frame coding
exon compared to variant 1. This results in a shorter isoform (2)
lacking an internal protein segment compared to isoform 1.
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 :: AK303777.1 [ECO:0000332]
##Evidence-Data-END##
##RefSeq-Attributes-START##
gene product(s) localized to mito. :: reported by MitoCarta
##RefSeq-Attributes-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-496 BP420631.1 10-505
497-1572 AK303777.1 470-1545
1573-1957 BC044217.1 1652-2036
1958-2314 BX104280.1 100-456
2315-2351 AI215948.1 1-37 c
FEATURES Location/Qualifiers
source 1..2351
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="1"
/map="1p12"
gene 1..2351
/gene="HMGCS2"
/note="3-hydroxy-3-methylglutaryl-CoA synthase 2"
/db_xref="GeneID:3158"
/db_xref="HGNC:HGNC:5008"
/db_xref="MIM:600234"
exon 1..192
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 2
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1413093676"
variation 8
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1377517627"
variation 12
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:145228152"
variation 13
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:587596327"
variation 14
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653331001"
variation 16
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1450484694"
variation 17
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1653330887"
variation 20
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1453141244"
variation 21
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:587720678"
variation 29
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378718468"
variation 36
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557996242"
variation 44..73
/gene="HMGCS2"
/replace="ctgctgggtttctg"
/replace="ctgctgggtttctgaactgctgggtttctg"
/db_xref="dbSNP:1653329330"
variation 45
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375748805"
variation 46
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748496437"
variation 47
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:781631836"
variation 49
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1486911909"
variation 50
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1278829085"
variation 53
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:768747562"
misc_feature 56..58
/gene="HMGCS2"
/note="upstream in-frame stop codon"
variation 65
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1354847741"
variation 67
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1653329848"
variation 70
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327746517"
variation 72
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1262919647"
variation 78
/gene="HMGCS2"
/replace="ag"
/replace="c"
/db_xref="dbSNP:1571047245"
variation 78
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2289459"
variation 79
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1653328792"
variation 80
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335432862"
variation 84
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:952382288"
variation 86
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:780003924"
CDS 89..1489
/gene="HMGCS2"
/EC_number="2.3.3.10"
/note="isoform 2 precursor is encoded by transcript
variant 2; 3-hydroxy-3-methylglutaryl-Coenzyme A synthase
2 (mitochondrial); hydroxymethylglutaryl-CoA synthase,
mitochondrial; testicular tissue protein Li 88; HMG-CoA
synthase; 3-hydroxy-3-methylglutaryl-CoA synthase 2
(mitochondrial)"
/codon_start=1
/product="hydroxymethylglutaryl-CoA synthase,
mitochondrial isoform 2 precursor"
/protein_id="NP_001159579.1"
/db_xref="CCDS:CCDS53353.1"
/db_xref="GeneID:3158"
/db_xref="HGNC:HGNC:5008"
/db_xref="MIM:600234"
/translation="
MQRLLTPVKRILQLTRAVQETSLTPARLLPVAHQRFSTASAVPLAKTDTWPKDVGILALEVYFPAQYVDQTDLEKYNNVEAGKYTVGLGQTRMGFCSVQEDINSLCLTVVQRLMERIQLPWDSVGRLEVGTETIIDKSKAVKTVLMELFQDSGNTDIEGIDTTNACYGGTASLFNAANWMESSSWDGLRGTHMENVYDFYKPNLASEYPIVDGKLSIQCYLRALDRCYTSYRKKIQNQWKQAGSDRPFTLDDLQYMIFHTPFCKMVQKSLARLMFNDFLSASSDTQTSLYKGLEAFGGLKLEDTYTNKDLDKALLKASQDMFDKKTKASLYLSTHNGNMYTSSLYGCLASLLSHHSAQELAGSRIGAFSYGSGLAASFFSFRVSQDAAPGSPLDKLVSSTSDLPKRLASRKCVSPEEFTEIMNQREQFYHKVNFSPPGDTNSLFPGTWYLERVDEQHRRKYARRPV"
transit_peptide 89..199
/gene="HMGCS2"
mat_peptide 200..1486
/gene="HMGCS2"
/product="hydroxymethylglutaryl-CoA synthase,
mitochondrial isoform 2"
misc_feature 236..1480
/gene="HMGCS2"
/note="3-hydroxy-3-methylglutaryl-CoA-synthase, eukaryotic
clade; Region: HMG-CoA-S_euk; TIGR01833"
/db_xref="CDD:273826"
variation 89
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1653328335"
variation 90
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758462859"
variation 94
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1353408775"
variation 95
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750380692"
variation 96
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:72695184"
variation 100
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1653327172"
variation 105
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189194662"
variation 107
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:757083410"
variation 109
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:368678169"
variation 110
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101283706"
variation 111
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1452551580"
variation 114
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144004292"
variation 115
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:757188613"
variation 116
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:373202578"
variation 117
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:766960590"
variation 118
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256262455"
variation 119
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1653326072"
variation 123
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:939049952"
variation 126..127
/gene="HMGCS2"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2101283660"
variation 127
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:759067886"
variation 131
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1286736541"
variation 132
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1008466802"
variation 135
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773898985"
variation 138..141
/gene="HMGCS2"
/replace="cggt"
/replace="cggtcggt"
/db_xref="dbSNP:1557996143"
variation 138
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:587712415"
variation 139
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:762327005"
variation 142
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1557996139"
variation 144
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101283600"
variation 146
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1332746126"
variation 151
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:777148971"
variation 153..155
/gene="HMGCS2"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1653324348"
variation 157
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:769000173"
variation 159
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369221781"
variation 160
/gene="HMGCS2"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2101283564"
variation 160
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:780272061"
variation 161
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:144744634"
variation 163
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:745916413"
variation 164
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:893820165"
variation 165
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1653322892"
variation 166
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:763901461"
variation 167
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376238143"
variation 168
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:757169217"
variation 171
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653322600"
variation 172
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1170811310"
variation 176
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:202069145"
variation 178
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653322264"
variation 179
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244351356"
variation 180
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1233603916"
variation 182
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:755897068"
variation 183
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:199651321"
variation 184
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:767168451"
variation 186
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:759183803"
variation 191
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653321576"
variation 192
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751101083"
exon 193..647
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 193
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1231210408"
variation 196
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:775905632"
variation 199
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200675569"
variation 200
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:77241754"
variation 201
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282393883"
variation 203
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208729772"
variation 204..207
/gene="HMGCS2"
/replace=""
/replace="cctc"
/db_xref="dbSNP:1475398406"
variation 205
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653158226"
variation 207
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1346871356"
variation 210..216
/gene="HMGCS2"
/replace="c"
/replace="ctgtccc"
/db_xref="dbSNP:1278392688"
variation 212
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:375279621"
variation 214
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:774514655"
variation 216
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:771019602"
variation 219
/gene="HMGCS2"
/replace=""
/replace="t"
/db_xref="dbSNP:1331676978"
variation 219
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:749336738"
variation 223
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200816212"
variation 224
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653157137"
variation 228
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1653157007"
variation 230
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:199670317"
variation 234
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:756404916"
variation 235
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1571042872"
variation 237
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:866803752"
variation 238
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653156489"
variation 239
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1653156396"
variation 241
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653156303"
variation 244
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:772149969"
variation 247
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201239391"
variation 248
/gene="HMGCS2"
/replace=""
/replace="g"
/db_xref="dbSNP:1160328101"
variation 248
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:28937320"
variation 250
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:911961081"
variation 256
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051817360"
variation 257
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402619037"
variation 259..260
/gene="HMGCS2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2101274491"
variation 259
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571042818"
variation 262
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138739620"
variation 263
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:181428774"
variation 264
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1653154898"
variation 269..270
/gene="HMGCS2"
/replace=""
/replace="ccaatatggccctggaggccaa"
/db_xref="dbSNP:1553241079"
variation 269
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:746685363"
variation 270
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:779833095"
variation 270
/gene="HMGCS2"
/replace="t"
/replace="tggccctggaggccaat"
/db_xref="dbSNP:747388657"
variation 274
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1199311850"
variation 277
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:758019802"
variation 279
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1185689932"
variation 280
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1571042770"
variation 282
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1485324823"
variation 283
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042762"
variation 284
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1653153732"
variation 286
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:749941890"
variation 293
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1217700912"
variation 295
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:142709072"
variation 296
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1653153296"
variation 297
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469630685"
variation 298
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:756658111"
variation 299
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571042738"
variation 301
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:145514933"
variation 304
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1571042729"
variation 305
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042719"
variation 308
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587688416"
variation 310
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:759842428"
variation 311
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1571042703"
variation 312
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:774598305"
variation 313
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:774411362"
variation 315
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413432644"
variation 316
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042674"
variation 320
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:766584879"
variation 323
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:763001714"
variation 325
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433333813"
variation 328
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571042651"
variation 329
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:151187711"
variation 331
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:761845625"
variation 333
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653149765"
variation 334
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1479205954"
variation 336
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462212320"
variation 337
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1420068119"
variation 339
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1162910493"
variation 340
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042624"
variation 341
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:776664327"
variation 342..343
/gene="HMGCS2"
/replace=""
/replace="g"
/db_xref="dbSNP:1571042612"
variation 343
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:768623326"
variation 345
/gene="HMGCS2"
/replace=""
/replace="t"
/db_xref="dbSNP:1571042603"
variation 345
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1187974723"
variation 346
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1484767754"
variation 348
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:768463219"
variation 349
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:779916834"
variation 350
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469561308"
variation 351
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1270679177"
variation 352
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2101273969"
variation 354
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:114033510"
variation 357
/gene="HMGCS2"
/replace=""
/replace="a"
/db_xref="dbSNP:1557994116"
variation 358..359
/gene="HMGCS2"
/replace=""
/replace="c"
/db_xref="dbSNP:1571042548"
variation 358
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:41302817"
variation 360
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:587697520"
variation 362
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771955824"
variation 363
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144921290"
variation 364
/gene="HMGCS2"
/replace=""
/replace="t"
/db_xref="dbSNP:1571042532"
variation 367
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557994090"
variation 369
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101273865"
variation 373
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1653147167"
variation 376
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303628202"
variation 377
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571042520"
variation 378
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1024035971"
variation 379
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1571042505"
variation 380
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1653146548"
variation 381
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042499"
variation 384
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:781647908"
variation 385
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:147746231"
variation 386
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332784240"
variation 390
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:751909473"
variation 391
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201187096"
variation 393
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:766672926"
variation 394
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:955697615"
variation 395
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101273736"
variation 399
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:763241833"
variation 400
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1571042452"
variation 401
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1653144748"
variation 404
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:750575658"
variation 406
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1426710599"
variation 411
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:765384188"
variation 412
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372251981"
variation 413
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:776751915"
variation 416
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250760247"
variation 418
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571042415"
variation 421
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653144051"
variation 422
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:768707273"
variation 423
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:145633208"
variation 424
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1260008829"
variation 427
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1252609545"
variation 429
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1653142058"
variation 433
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397104251"
variation 434
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200607527"
variation 435
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:147906427"
variation 436
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146073837"
variation 437
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1453735975"
variation 438
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571042378"
variation 439
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:928663340"
variation 440
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1571042362"
variation 441
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1235493293"
variation 445
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1246669403"
variation 446
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:758033248"
variation 448
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1571042342"
variation 451
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:770521945"
variation 452
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368014391"
variation 454
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138170167"
variation 455
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1300010645"
variation 456
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:755489615"
variation 457
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:780926888"
variation 460
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:751997256"
variation 463
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1173958102"
variation 464
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1436348108"
variation 466
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1393101212"
variation 467
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:780431922"
variation 469
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587616028"
variation 472
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1251993883"
variation 475
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:750709310"
variation 477
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375313694"
variation 481
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:587741129"
variation 484
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:753951770"
variation 487
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1553241043"
variation 490
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1212314291"
variation 492
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1350489274"
variation 495
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101273359"
variation 497
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653138229"
variation 500
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:764209022"
variation 503
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1232767876"
variation 505
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571042244"
variation 508
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370900322"
variation 510
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406920400"
variation 514
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1321279061"
variation 516
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:760689678"
variation 517
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571042209"
variation 518
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:775528207"
variation 519
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:767366737"
variation 523
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:759228303"
variation 524
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1313393068"
variation 530
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:890302302"
variation 531
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1557993914"
variation 532
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1557993907"
variation 533
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:774091075"
variation 539
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1172810724"
variation 544
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1653136294"
variation 546
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:770478547"
variation 547
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:748883811"
variation 549
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1338594261"
variation 550
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042145"
variation 556
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042139"
variation 557
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051823691"
variation 558
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:916186024"
variation 559
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042115"
variation 560
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:756896188"
variation 564
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:866366934"
variation 565
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1026894407"
variation 566
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:993282740"
variation 567
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:748155656"
variation 570
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653134824"
variation 573
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:780406594"
variation 576
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1486964047"
variation 577
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653134557"
variation 579
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1289541397"
variation 580
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042077"
variation 583
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1255800042"
variation 584
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1653134202"
variation 586
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042062"
variation 588
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:137852640"
variation 589
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:758839673"
variation 590
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:746217014"
variation 592
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042028"
variation 594
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1237226874"
variation 595
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653133530"
variation 597
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:779249605"
variation 598
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1653133264"
variation 599
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653133134"
variation 600
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653132966"
variation 603
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:867469566"
variation 605
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:757431290"
variation 606
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653132655"
variation 607
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:879133941"
variation 608
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:137852636"
variation 612
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653132393"
variation 613
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274983621"
variation 615
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:764299408"
variation 616
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1653132160"
variation 617
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1333199361"
variation 618
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1401213260"
variation 619
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653131909"
variation 620
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1382579134"
variation 621
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1386957244"
variation 622
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752729912"
variation 624
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1456425510"
variation 625
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653131406"
variation 628
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1161245291"
variation 630
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1384449317"
variation 631
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1417914069"
variation 634
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:587662618"
variation 637
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653130925"
variation 638
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:759434636"
variation 639
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1653130753"
variation 643
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1653130666"
variation 644
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:774032165"
variation 645
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:778262961"
variation 646
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2101272788"
variation 647
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1420066501"
exon 648..812
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 648
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:752239721"
variation 650..651
/gene="HMGCS2"
/replace=""
/replace="acaaaaga"
/db_xref="dbSNP:1652956572"
variation 651
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1485342949"
variation 657
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1002548815"
variation 663
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101262615"
variation 664
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:767069915"
variation 666
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:773806829"
variation 667
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101262597"
variation 673
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:367770104"
variation 675
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652955948"
variation 676
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419921025"
variation 678..689
/gene="HMGCS2"
/replace="a"
/replace="atgacttctaca"
/db_xref="dbSNP:1193946325"
variation 679
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652955748"
variation 681
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762211049"
variation 686
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652955496"
variation 687
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375071247"
variation 688
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:145838142"
variation 689
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1247037912"
variation 692
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652954795"
variation 694
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1469399815"
variation 697
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652954559"
variation 701
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652954445"
variation 703
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652954332"
variation 705
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:768912442"
variation 706
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1219952938"
variation 708
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1333189037"
variation 709
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:909075571"
variation 712
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652953647"
variation 713
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652953530"
variation 716
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:767113695"
variation 717
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1274079819"
variation 718
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:761483416"
variation 720
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1249021511"
variation 721
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:775549228"
variation 722
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1047602183"
variation 724
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652952471"
variation 727
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:745824260"
variation 728
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:778797644"
variation 730
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:757041759"
variation 731
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:749102995"
variation 732..734
/gene="HMGCS2"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1553240525"
variation 733
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571037509"
variation 734
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:777348530"
variation 736
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571037496"
variation 739
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355056794"
variation 741
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652951110"
variation 742..748
/gene="HMGCS2"
/replace=""
/replace="gtgctac"
/db_xref="dbSNP:1571037483"
variation 742
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1172184574"
variation 744
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652950860"
variation 747
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1466691522"
variation 748
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427576637"
variation 749..750
/gene="HMGCS2"
/replace="t"
/replace="tt"
/db_xref="dbSNP:2101262353"
variation 749
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652950477"
variation 751
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652950310"
variation 751
/gene="HMGCS2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1557991791"
variation 752
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:773945291"
variation 753
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372095379"
variation 756
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:767157843"
variation 757
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652949915"
variation 758
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571037457"
variation 759
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:918691885"
variation 764
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652949602"
variation 765
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371306326"
variation 767
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190133412"
variation 767
/gene="HMGCS2"
/replace="t"
/replace="tt"
/db_xref="dbSNP:757352789"
variation 769
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:866934006"
variation 772
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:751009381"
variation 773
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571037428"
variation 775
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:765772883"
variation 776
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571037413"
variation 778
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1571037408"
variation 782
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:587677809"
variation 783
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:370058829"
variation 784
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571037388"
variation 785..791
/gene="HMGCS2"
/replace="aaaaaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:1557991740"
variation 785
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652948216"
variation 787
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652948128"
variation 789
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:764302250"
variation 790
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652947931"
variation 791
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:760913527"
variation 792
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:775637086"
variation 795
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:898393396"
variation 796
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:772186726"
variation 798
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375716442"
variation 800
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1299801129"
variation 801
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652947252"
variation 803
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407962244"
variation 805
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652947097"
variation 808
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:202211261"
variation 809
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370438695"
exon 813..978
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 813
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201182715"
variation 815
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1246961486"
variation 819
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1338450583"
variation 820
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1992376"
variation 821
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587671242"
variation 824
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:142637231"
variation 825
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:183046298"
variation 827
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:751683757"
variation 828
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:146296049"
variation 829
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652877239"
variation 833
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:148892048"
variation 836
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:769844821"
variation 838
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652876948"
variation 841
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761787433"
variation 842
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144103604"
variation 843
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1186326463"
variation 844..846
/gene="HMGCS2"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:753878217"
variation 848
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652876404"
variation 849..852
/gene="HMGCS2"
/replace="agta"
/replace="agtagta"
/db_xref="dbSNP:764306891"
variation 849
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:865947488"
variation 851
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:768535206"
variation 853
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048438"
variation 854
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:376554104"
variation 856
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:138086607"
variation 857
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1273931880"
variation 859..860
/gene="HMGCS2"
/replace=""
/replace="gaaa"
/db_xref="dbSNP:1417242901"
variation 862
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1211527690"
variation 865
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:763775014"
variation 867
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652875135"
variation 869
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1359922140"
variation 870
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:778400323"
variation 871
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652874836"
variation 875
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571035721"
variation 878
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:756625778"
variation 879
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:748587465"
variation 883
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1431740041"
variation 891
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367180826"
variation 898
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1331997383"
variation 901
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339633294"
variation 902
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:781567781"
variation 903
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:755313968"
variation 904
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652873712"
variation 908
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:587664208"
variation 909
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1045222753"
variation 914
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1407518921"
variation 915
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:766507770"
variation 918
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652873146"
variation 919
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:894730177"
variation 923
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1163255653"
variation 925
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:758565101"
variation 927
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:750485856"
variation 929
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371906223"
variation 937
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368471603"
variation 942
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:930829392"
variation 946
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652872377"
variation 948
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652872291"
variation 949
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253654665"
variation 951
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:919408055"
variation 952
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2101258162"
variation 953..954
/gene="HMGCS2"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1652871929"
variation 953
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:776664576"
variation 958
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652871835"
variation 962
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:764027082"
variation 964
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1266588243"
variation 976
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:141213676"
variation 977
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775277893"
variation 978
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:74889853"
exon 979..1149
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 979
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:777182302"
variation 981
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101254831"
variation 982
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265709999"
variation 988
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652810178"
variation 991
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:769058291"
variation 992
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2101254797"
variation 999
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1181436986"
variation 1000
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:747485297"
variation 1001
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652809713"
variation 1003
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652809624"
variation 1005
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:966875458"
variation 1006
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:780316550"
variation 1008
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1025175254"
variation 1010
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571033686"
variation 1014
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1426493337"
variation 1015
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772437190"
variation 1016
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:746145498"
variation 1019
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:779242610"
variation 1020
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652808686"
variation 1025
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652808604"
variation 1027
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1364211191"
variation 1031
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:757475645"
variation 1036
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652808173"
variation 1040
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1286992834"
variation 1041
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353365984"
variation 1042
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:753951704"
variation 1043
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380312324"
variation 1044
/gene="HMGCS2"
/replace=""
/replace="a"
/db_xref="dbSNP:1652807640"
variation 1044
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1286357569"
variation 1045
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:991904954"
variation 1047
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652807341"
variation 1048
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777939704"
variation 1051
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:762443891"
variation 1052
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652807016"
variation 1054
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752639075"
variation 1055
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:767236647"
variation 1056
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:759352736"
variation 1057
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:587690380"
variation 1060
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652806464"
variation 1064
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1557989960"
variation 1065
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652806263"
variation 1070
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652806163"
variation 1072
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:774953281"
variation 1073
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:766003583"
variation 1074
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:762536796"
variation 1075
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:772715543"
variation 1076
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652805571"
variation 1080
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652805414"
variation 1081
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:769310958"
variation 1082
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1327737396"
variation 1086
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:151328418"
variation 1087
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:776046708"
variation 1089
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:772359110"
variation 1090
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:764568941"
variation 1091..1094
/gene="HMGCS2"
/replace="ca"
/replace="caca"
/db_xref="dbSNP:756272484"
variation 1092
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652804611"
variation 1094
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:746227549"
variation 1095
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263957408"
variation 1101
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:779332852"
variation 1102
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1266985661"
variation 1103
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1215654921"
variation 1104
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771289268"
variation 1107
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652803762"
variation 1112
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1292399691"
variation 1115
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:4716"
variation 1116..1118
/gene="HMGCS2"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1571033506"
variation 1118
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1378975136"
variation 1119
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:777744720"
variation 1120
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652803184"
variation 1123
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:756169207"
variation 1124
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:752626288"
variation 1125
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:781186067"
variation 1127
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1437031967"
variation 1129
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:754826235"
variation 1130
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:751371132"
variation 1131
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1404540409"
variation 1133
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1166279238"
variation 1137
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:766097440"
variation 1138
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652802208"
variation 1139
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652802125"
variation 1143..1145
/gene="HMGCS2"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1423575599"
variation 1147
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:267597953"
variation 1148
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:762627608"
variation 1149
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144329134"
exon 1150..1256
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 1150
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:763443637"
variation 1155
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:12117456"
variation 1158
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1356884646"
variation 1159
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1034584179"
variation 1161
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1305902474"
variation 1162
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101249833"
variation 1163
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1454719802"
variation 1168
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:760149713"
variation 1169
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652725108"
variation 1171
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:774949209"
variation 1173
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1557988855"
variation 1178
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1282825298"
variation 1179
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:139620933"
variation 1180
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413334730"
variation 1182
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:766898190"
variation 1184
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471802697"
variation 1187
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652724277"
variation 1188
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2101249765"
variation 1189
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2101249759"
variation 1192
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:763378721"
variation 1194
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557988835"
variation 1196
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652724028"
variation 1197
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652723944"
variation 1198
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:773364048"
variation 1203
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1224665560"
variation 1207
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571031412"
variation 1214
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652723582"
variation 1216
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101249712"
variation 1218
/gene="HMGCS2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1287002055"
variation 1222
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:15609"
variation 1224..1232
/gene="HMGCS2"
/replace="tttc"
/replace="tttcatttc"
/db_xref="dbSNP:772305902"
variation 1224
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652723339"
variation 1225
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2101249690"
variation 1226
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1201210514"
variation 1230
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652723182"
variation 1232
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:137852637"
variation 1233
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748252959"
variation 1234
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:186771480"
variation 1237
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652722253"
variation 1238
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:768676776"
variation 1239
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:747000856"
variation 1240
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1269917499"
variation 1241
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:779938993"
variation 1244
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1334904424"
variation 1245
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652721671"
variation 1249
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:755119914"
variation 1251
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:141769037"
variation 1253
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:971540603"
variation 1255
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1472370665"
exon 1257..1382
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 1257
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1446564405"
variation 1258
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:770584941"
variation 1259
/gene="HMGCS2"
/replace="t"
/replace="tat"
/db_xref="dbSNP:1553239855"
variation 1260
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652701530"
variation 1262..1265
/gene="HMGCS2"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1652700979"
variation 1262
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:749020250"
variation 1263
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1487366289"
variation 1268
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652700847"
variation 1270
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652700728"
variation 1271
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652700590"
variation 1273
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:111284724"
variation 1273
/gene="HMGCS2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1652700451"
variation 1274
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:587623606"
variation 1277
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:752268224"
variation 1278
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652699823"
variation 1279
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:780781898"
variation 1282
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226057083"
variation 1284
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:758974137"
variation 1285
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:78280338"
variation 1286
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1256038787"
variation 1287
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765680777"
variation 1290
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210167963"
variation 1293
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1571030681"
variation 1294
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324745132"
variation 1295
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:754122611"
variation 1296
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1018386936"
variation 1304
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:61729865"
variation 1305..1313
/gene="HMGCS2"
/replace="gcct"
/replace="gcctagcct"
/db_xref="dbSNP:2101248147"
variation 1305
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:760833472"
variation 1306
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303432261"
variation 1307
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:775555477"
variation 1310
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:772007817"
variation 1311
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1166429808"
variation 1312
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:759542743"
variation 1316
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:587727388"
variation 1317
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:770800317"
variation 1321..1328
/gene="HMGCS2"
/replace="gtgtgt"
/replace="gtgtgtgt"
/db_xref="dbSNP:1267844674"
variation 1324
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652696758"
variation 1325
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:749033432"
variation 1327
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:143463960"
variation 1330
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:769574264"
variation 1333
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:747762161"
variation 1334..1339
/gene="HMGCS2"
/replace="gag"
/replace="gaggag"
/db_xref="dbSNP:746197576"
variation 1334
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:780869942"
variation 1336
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652696152"
variation 1339
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:754421987"
variation 1351
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276125317"
variation 1354
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344814686"
variation 1355..1356
/gene="HMGCS2"
/replace="a"
/replace="aa"
/db_xref="dbSNP:779321975"
variation 1358
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:587606870"
variation 1359
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:779280964"
variation 1360
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410813519"
variation 1363
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:757694113"
variation 1364
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1327062942"
variation 1367
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:754218759"
variation 1371
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:764380176"
variation 1372
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652694966"
variation 1377
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:756362495"
variation 1378
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:760737262"
variation 1380
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1251813781"
variation 1381
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:142776952"
variation 1382
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1428518237"
exon 1383..1494
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 1383
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1223577754"
variation 1384
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652635564"
variation 1387
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:751604096"
variation 1393
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:766442654"
variation 1397
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1286156922"
variation 1398
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:954149886"
variation 1401
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652635062"
variation 1404
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1557987604"
variation 1405
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1274987443"
variation 1407
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1382059473"
variation 1408
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473777473"
variation 1411
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652634630"
variation 1413
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:763005476"
variation 1414..1421
/gene="HMGCS2"
/replace="cc"
/replace="ccttttcc"
/db_xref="dbSNP:1652634252"
variation 1414
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652634445"
variation 1415
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652634353"
variation 1421
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652634170"
variation 1423
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416274127"
variation 1424
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652633973"
variation 1425
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1203892179"
variation 1429
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:773260075"
variation 1431
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:765161813"
variation 1432
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652633599"
variation 1435..1436
/gene="HMGCS2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1158368570"
variation 1436
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652633419"
variation 1441
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:761693466"
variation 1442
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:776399237"
variation 1443
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587593961"
variation 1445
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:746610244"
variation 1447
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:774897830"
variation 1448
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652632697"
variation 1450
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189946297"
variation 1451
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:771524777"
variation 1452
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1486025242"
variation 1454
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:927944310"
variation 1455
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:749846010"
variation 1456
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557987526"
variation 1458
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:778223568"
variation 1460
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:756539895"
variation 1461
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:137852639"
variation 1463
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:781563101"
variation 1464
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:372079931"
variation 1471
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:755185680"
variation 1473..1475
/gene="HMGCS2"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1258406005"
variation 1473
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:751754816"
variation 1475
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780044819"
variation 1476
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:758519315"
variation 1477
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1437142528"
variation 1478
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374568676"
variation 1479
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587717007"
variation 1480
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:761781401"
variation 1481
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753575448"
variation 1483
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:587677028"
variation 1484
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:76773981"
variation 1487
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:775189501"
variation 1491
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186406205"
variation 1492
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652629664"
exon 1495..2340
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 1501
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:182407677"
variation 1508
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652544019"
variation 1512
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652543930"
variation 1514
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:959339642"
variation 1518
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:747007842"
variation 1520
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2101240446"
variation 1526
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313731544"
variation 1527
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:776201032"
variation 1528
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:921601572"
variation 1530
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652543392"
variation 1533
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652543313"
variation 1534
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1283923655"
variation 1537
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1351829384"
variation 1541
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1417770076"
variation 1547
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:770591879"
variation 1549
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1284502124"
variation 1550
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:148106058"
variation 1551
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1487056819"
variation 1559
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1215176488"
variation 1561
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256456049"
variation 1565
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:746537667"
variation 1567
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143718202"
variation 1568
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652542226"
variation 1570
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652542147"
variation 1571
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2101240346"
variation 1572
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1184930959"
variation 1574
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652541997"
variation 1578
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652541919"
variation 1581
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1236721331"
variation 1582..1586
/gene="HMGCS2"
/replace=""
/replace="ctggt"
/db_xref="dbSNP:1440069329"
variation 1588
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652541655"
variation 1589
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:962842435"
variation 1590..1591
/gene="HMGCS2"
/replace=""
/replace="atgaatttttaa"
/db_xref="dbSNP:1160442408"
variation 1590
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652541498"
variation 1591
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652541312"
variation 1601
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:148963389"
variation 1602
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:587762730"
variation 1603
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1248273681"
variation 1605
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571026960"
variation 1606
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174297384"
variation 1615
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016341601"
variation 1620
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652539784"
variation 1623
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1404648332"
variation 1628
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:965967252"
variation 1634
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1333723178"
variation 1636
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1336794842"
variation 1644
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:587686291"
variation 1649
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:771526508"
variation 1652
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1307712218"
variation 1654
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138575225"
variation 1655
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:886491306"
variation 1667
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1027479499"
variation 1670
/gene="HMGCS2"
/replace=""
/replace="c"
/db_xref="dbSNP:1652538297"
variation 1670
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652538189"
variation 1673
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1274559603"
variation 1682
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1245391247"
variation 1690
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030291437"
variation 1691
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:755165196"
variation 1693..1717
/gene="HMGCS2"
/replace="ggg"
/replace="gggcttatggtgctatggactaggg"
/db_xref="dbSNP:1180207146"
variation 1701
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2101240205"
variation 1703
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652537495"
variation 1705
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1198439043"
variation 1706
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277460396"
variation 1708
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652537134"
variation 1710
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652537016"
variation 1711
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:895243002"
variation 1712
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652536782"
variation 1713
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652536126"
variation 1715
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652536007"
variation 1717
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571026871"
variation 1718
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:997897520"
variation 1722..1729
/gene="HMGCS2"
/replace=""
/replace="tttgtgaa"
/db_xref="dbSNP:200828254"
variation 1727..1732
/gene="HMGCS2"
/replace="gaaaga"
/replace="gaaagaaaga"
/db_xref="dbSNP:1652534892"
variation 1727
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:753304242"
variation 1730
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652535108"
variation 1731
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652534992"
variation 1732
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652534823"
variation 1733
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199462871"
variation 1734
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:902731885"
variation 1739
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1464609687"
variation 1742
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652534535"
variation 1746
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1172276496"
variation 1748
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652534347"
variation 1751
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652534265"
variation 1753
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749814204"
variation 1759
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1011205317"
variation 1760
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1376596454"
variation 1766
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:893973335"
variation 1767
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1049951208"
variation 1768..1772
/gene="HMGCS2"
/replace="a"
/replace="aatca"
/db_xref="dbSNP:2101240050"
variation 1773
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652533637"
variation 1775
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652533528"
variation 1783
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039677206"
variation 1786
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1230361877"
variation 1788
/gene="HMGCS2"
/replace=""
/replace="g"
/db_xref="dbSNP:1652533221"
variation 1793
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652533119"
variation 1802
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652533003"
variation 1806
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273887760"
variation 1809
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:936894312"
variation 1816
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2101240001"
variation 1821
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:56828380"
variation 1822
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:770214388"
variation 1825
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652532598"
variation 1828
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1299161228"
variation 1829
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1040012812"
variation 1831
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1269363162"
variation 1832..1833
/gene="HMGCS2"
/replace=""
/replace="tggtggatggagcggtgttt"
/db_xref="dbSNP:1652532192"
variation 1832
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:587723389"
variation 1833
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652532110"
variation 1835
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571026733"
variation 1837
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:144826622"
variation 1838
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:587641803"
variation 1840
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376608094"
variation 1842
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557986311"
variation 1843
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1478950779"
variation 1851..1862
/gene="HMGCS2"
/replace="ttatta"
/replace="ttattatta"
/replace="ttattattatta"
/db_xref="dbSNP:140599791"
variation 1852..1854
/gene="HMGCS2"
/replace="t"
/replace="tat"
/db_xref="dbSNP:1438745411"
variation 1857
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1571026700"
variation 1859
/gene="HMGCS2"
/replace=""
/replace="a"
/db_xref="dbSNP:1652530883"
variation 1860
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:991849328"
variation 1861
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:983323260"
variation 1862
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1571026672"
variation 1869
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557986293"
variation 1875
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:770080416"
variation 1879
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652530272"
variation 1880
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652530175"
variation 1883
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652530051"
variation 1886
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652529916"
variation 1887
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652529811"
variation 1889
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1294233713"
variation 1898
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1458722285"
variation 1909
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652529572"
variation 1915
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571026636"
variation 1920
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295814905"
variation 1922
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1461912455"
variation 1923
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571026616"
variation 1924
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652529162"
variation 1927
/gene="HMGCS2"
/replace=""
/replace="a"
/db_xref="dbSNP:1652529107"
variation 1928
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:920407273"
variation 1929
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1357602330"
variation 1930
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:937658755"
variation 1933
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1384601125"
regulatory 1935..1940
/regulatory_class="polyA_signal_sequence"
/gene="HMGCS2"
/note="hexamer: ATTAAA"
variation 1937
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:990630239"
variation 1938
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652528706"
variation 1939
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1299933733"
variation 1940
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652528559"
variation 1942..1948
/gene="HMGCS2"
/replace="agaga"
/replace="agagaga"
/db_xref="dbSNP:1450484328"
variation 1945
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1172913511"
variation 1946
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1340572398"
variation 1947
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652528320"
variation 1948
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1571026561"
variation 1954
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652528084"
variation 1955
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571026553"
polyA_site 1957
/gene="HMGCS2"
/note="major polyA site"
variation 1959
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:746232231"
variation 1965
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652527841"
variation 1967
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:926582357"
variation 1968
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:141106649"
variation 1970
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1192597071"
variation 1973
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035521301"
variation 1980
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1487435009"
variation 1981
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:587625788"
variation 1983
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1209140121"
variation 1985
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652527196"
variation 1986
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652527115"
variation 1987
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652527046"
variation 1992
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1003508550"
variation 1993
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652526864"
variation 1996
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1489307748"
variation 1997
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:962552022"
variation 2004
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652526585"
variation 2005
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652526472"
variation 2007
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1191847928"
variation 2012
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652526269"
variation 2016
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:781321001"
variation 2017
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2101239615"
variation 2023
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652526053"
variation 2032
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1254329985"
variation 2036
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1423109904"
variation 2037
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652525732"
variation 2039
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652525677"
variation 2040
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:908390016"
variation 2041
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652525544"
variation 2048
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424762085"
variation 2051
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571026483"
variation 2053
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571026476"
variation 2054
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587721879"
variation 2057
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652525088"
variation 2059
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652525007"
variation 2061
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652524937"
variation 2062
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2101239557"
variation 2065
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1209976880"
variation 2066..2075
/gene="HMGCS2"
/replace="tgtccccttg"
/replace="tgtccccttgtccccttg"
/db_xref="dbSNP:1652524480"
variation 2066
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:374153483"
variation 2070
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1249554243"
variation 2073
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652524556"
variation 2075
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1367261193"
variation 2078
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652524322"
variation 2079
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652524239"
variation 2083
/gene="HMGCS2"
/replace=""
/replace="a"
/db_xref="dbSNP:1652524162"
variation 2086
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1457886082"
variation 2090
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146520328"
variation 2094
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:950821538"
variation 2097
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:894085982"
variation 2098
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652523774"
variation 2099
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571026448"
variation 2104..2105
/gene="HMGCS2"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2101239474"
variation 2105
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295980523"
variation 2117
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:868114000"
variation 2122
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1557986174"
variation 2125
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2101239449"
variation 2131..2153
/gene="HMGCS2"
/replace="aagaacggtagaacacagcttcc"
/replace="aagaacggtagaacacagcttccaccaaagaacggtagaacacagctt
cc"
/db_xref="dbSNP:1652522864"
variation 2131
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360760869"
variation 2136
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030360366"
variation 2137
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:997437985"
variation 2139
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1319664147"
variation 2141
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652523104"
variation 2144
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1232326301"
variation 2147
/gene="HMGCS2"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1652522925"
variation 2154
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:757470646"
variation 2159
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:900216785"
variation 2163
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652522621"
variation 2166
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:3894543"
variation 2168
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355962162"
variation 2169
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571026395"
variation 2170
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652522337"
variation 2171
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652522262"
variation 2180
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1373543854"
variation 2183
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652522116"
variation 2186
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652522050"
variation 2187
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652521989"
variation 2188..2194
/gene="HMGCS2"
/replace="aga"
/replace="agacaga"
/db_xref="dbSNP:1262779364"
variation 2189
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:191519973"
variation 2192..2197
/gene="HMGCS2"
/replace="ag"
/replace="agagag"
/db_xref="dbSNP:1483674460"
variation 2192
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1214458570"
variation 2194
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652521673"
variation 2199
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587742820"
variation 2202..2204
/gene="HMGCS2"
/replace="a"
/replace="aga"
/db_xref="dbSNP:1302051309"
variation 2208
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1254562212"
variation 2209
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652521148"
variation 2210
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423594330"
variation 2211
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1159849025"
variation 2212
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652520676"
variation 2215
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652520615"
variation 2216
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1390905324"
variation 2218
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1371725596"
variation 2223
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587661345"
variation 2225
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344066942"
variation 2229
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652520203"
variation 2232..2239
/gene="HMGCS2"
/replace="atcttctt"
/replace="atcttcttatcttctt"
/db_xref="dbSNP:1376772547"
variation 2233
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1681433017"
variation 2235
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1448349780"
variation 2240
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1304215870"
variation 2247..2248
/gene="HMGCS2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1451570804"
variation 2252
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1001534919"
variation 2253
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:587601584"
variation 2254
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587722758"
variation 2256
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009711595"
variation 2261
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285463688"
variation 2262
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652519414"
variation 2267
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652519338"
variation 2271
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1312815124"
variation 2274
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212594496"
variation 2277
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:896263189"
variation 2279
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056596081"
variation 2280
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:937730116"
variation 2281
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:41313276"
variation 2282
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652518749"
variation 2286
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1240610116"
variation 2292
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652518608"
variation 2296
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1438437573"
variation 2301
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1178530898"
variation 2302
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1406688635"
variation 2304
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2101239098"
variation 2308
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587609056"
variation 2311
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:116264779"
variation 2313
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652518037"
regulatory 2317..2322
/regulatory_class="polyA_signal_sequence"
/gene="HMGCS2"
/note="hexamer: AATAAA"
variation 2317
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2101239069"
variation 2318
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:941284777"
variation 2320..2326
/gene="HMGCS2"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:1652517637"
variation 2320
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:76803215"
variation 2323
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:758484729"
variation 2324..2335
/gene="HMGCS2"
/replace="aaataaat"
/replace="aaataaataaat"
/db_xref="dbSNP:779871668"
variation 2325
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:982608638"
variation 2329
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331730560"
variation 2332
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1418038381"
variation 2333
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1444527376"
polyA_site 2334
/gene="HMGCS2"
variation 2335..2338
/gene="HMGCS2"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1248269743"
variation 2337
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:959472145"
ORIGIN
ataaagtcctgccgggcaccactgggcatctctttcaaggtttctgctgggtttctgaactgctgggtttctgcttgctcctctggagatgcagcgtctgttgactccagtgaagcgcattctgcaactgacaagagcggtgcaggaaacctccctcacacctgctcgcctgctcccagtagcccaccaaaggttttctacagcctctgctgtccccctggccaaaacagatacttggccaaaggacgtgggcatcctggccctggaggtctacttcccagcccaatatgtggaccaaactgacctggagaagtataacaatgtggaagcaggaaagtatacagtgggcttgggccagacccgtatgggcttctgctcagtccaagaggacatcaactccctgtgcctgacggtggtgcaacggctgatggagcgcatacagctcccatgggactctgtgggcaggctggaagtaggcactgagaccatcattgacaagtccaaagctgtcaaaacagtgctcatggaactcttccaggattcaggcaatactgatattgagggcatagataccaccaatgcctgctacggtggtactgcctccctcttcaatgctgccaactggatggagtccagttcctgggatgggctgaggggaacccatatggagaatgtgtatgacttctacaaaccaaatttggcctcggagtacccaatagtggatgggaagctttccatccagtgctacttgcgggccttggatcgatgttacacatcataccgtaaaaaaatccagaatcagtggaagcaagctggcagcgatcgacccttcacccttgacgatttacagtacatgatctttcatacacccttttgcaagatggtccagaagtctctggctcgcctgatgttcaatgacttcctgtcagccagcagtgacacacaaaccagcttatataaggggctggaggctttcggggggctaaagctggaagacacctacaccaacaaggacctggataaagcacttctaaaggcctctcaggacatgttcgacaagaaaaccaaggcttccctttacctctccactcacaatgggaacatgtacacctcatccctgtacgggtgcctggcctcgcttctgtcccaccactctgcccaagaactggctggctccaggattggtgccttctcttatggctctggtttagcagcaagtttcttttcatttcgagtatcccaggatgctgctccaggctctcccctggacaagttggtgtccagcacatcagacctgccaaaacgcctagcctcccgaaagtgtgtgtctcctgaggagttcacagaaataatgaaccaaagagagcaattctaccataaggtgaatttctccccacctggtgacacaaacagccttttcccaggtacttggtacctggagcgagtggacgagcagcatcgccgaaagtatgcccggcgtcccgtctaaaggtgttctgcagatccatggaaagcttcctgggaaacgtatgctagcagagcttctccccgtgaatcatatttttaagatcccactcttagctggtaaatgaatttgaatcgacatagtagccccataagcatcagccctgtagagtgaggagccatctctagcgggcccttcattcctctccatgctgcaatcactgtcctgggcttatggtgctatggactaggggtcctttgtgaaagagcaagatggagcaatggagagaagacctcttcctgaatcactggactccagaaatgtgcatgcagatcagctgttgccttcaagatccagataaactttcctgtcatgtgttagaactttattattattaatattgttaaacttctgtgctgttcctgtgaatctccaaattttgtaccttgttctaagctaatatatagcaattaaaaagagagaaagaggaaatgattcctgcgtttcttggaacccagaatacaaacccagcctaacatgcagcaagcctgctagaccttgtgggtcagagggctgggtccttgcctcacaggctgcctctgtccccttgcaattccattctatttctgccacatgccaagtgctatgacaggtacaaggcaaataagaacggtagaacacagcttcccccagcccacttccctgttctaaagacaccacatagacagagagcagcagacaggggccagcaggagctgtagttcagatcttcttggtcattccttgccgctgttatttgaacaaataaacacagcgcaaaggttaacaagtttttgccttctatagccaaaaataaaaaaataaataaattttgaaaaaaaaaaaa
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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