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Previous release (v1)
2024-04-30 08:49:05, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_005518 2433 bp mRNA linear PRI 22-SEP-2023
DEFINITION Homo sapiens 3-hydroxy-3-methylglutaryl-CoA synthase 2 (HMGCS2),
transcript variant 1, mRNA; nuclear gene for mitochondrial product.
ACCESSION NM_005518
VERSION NM_005518.4
KEYWORDS RefSeq; MANE Select.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 2433)
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 2433)
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 2433)
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 2433)
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 2433)
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 2433)
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 2433)
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 2433)
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 2433)
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 2433)
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, BC044217.1,
BX104280.1 and AI215948.1.
On Aug 31, 2019 this sequence version replaced NM_005518.3.
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 (1) encodes the longer 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 :: BC044217.1, X83618.1 [ECO:0000332]
##Evidence-Data-END##
##RefSeq-Attributes-START##
gene product(s) localized to mito. :: reported by MitoCarta
MANE Ensembl match :: ENST00000369406.8/
ENSP00000358414.3
RefSeq Select criteria :: based on conservation,
expression, longest protein
##RefSeq-Attributes-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-469 BP420631.1 37-505
470-2056 BC044217.1 450-2036
2057-2413 BX104280.1 100-456
2414-2433 AI215948.1 18-37 c
FEATURES Location/Qualifiers
source 1..2433
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="1"
/map="1p12"
gene 1..2433
/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..165
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 2
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378718468"
variation 9
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557996242"
variation 17..46
/gene="HMGCS2"
/replace="ctgctgggtttctg"
/replace="ctgctgggtttctgaactgctgggtttctg"
/db_xref="dbSNP:1653329330"
variation 18
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375748805"
variation 19
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748496437"
variation 20
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:781631836"
variation 22
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1486911909"
variation 23
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1278829085"
variation 26
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:768747562"
misc_feature 29..31
/gene="HMGCS2"
/note="upstream in-frame stop codon"
variation 38
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1354847741"
variation 40
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1653329848"
variation 43
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327746517"
variation 45
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1262919647"
variation 51
/gene="HMGCS2"
/replace="ag"
/replace="c"
/db_xref="dbSNP:1571047245"
variation 51
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2289459"
variation 52
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1653328792"
variation 53
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335432862"
variation 57
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:952382288"
variation 59
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:780003924"
CDS 62..1588
/gene="HMGCS2"
/EC_number="2.3.3.10"
/note="isoform 1 precursor is encoded by transcript
variant 1; 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 1 precursor"
/protein_id="NP_005509.1"
/db_xref="CCDS:CCDS905.1"
/db_xref="GeneID:3158"
/db_xref="HGNC:HGNC:5008"
/db_xref="MIM:600234"
/translation="
MQRLLTPVKRILQLTRAVQETSLTPARLLPVAHQRFSTASAVPLAKTDTWPKDVGILALEVYFPAQYVDQTDLEKYNNVEAGKYTVGLGQTRMGFCSVQEDINSLCLTVVQRLMERIQLPWDSVGRLEVGTETIIDKSKAVKTVLMELFQDSGNTDIEGIDTTNACYGGTASLFNAANWMESSSWDGRYAMVVCGDIAVYPSGNARPTGGAGAVAMLIGPKAPLALERGLRGTHMENVYDFYKPNLASEYPIVDGKLSIQCYLRALDRCYTSYRKKIQNQWKQAGSDRPFTLDDLQYMIFHTPFCKMVQKSLARLMFNDFLSASSDTQTSLYKGLEAFGGLKLEDTYTNKDLDKALLKASQDMFDKKTKASLYLSTHNGNMYTSSLYGCLASLLSHHSAQELAGSRIGAFSYGSGLAASFFSFRVSQDAAPGSPLDKLVSSTSDLPKRLASRKCVSPEEFTEIMNQREQFYHKVNFSPPGDTNSLFPGTWYLERVDEQHRRKYARRPV"
transit_peptide 62..172
/gene="HMGCS2"
mat_peptide 173..1585
/gene="HMGCS2"
/product="hydroxymethylglutaryl-CoA synthase,
mitochondrial isoform 1"
misc_feature 209..1579
/gene="HMGCS2"
/note="3-hydroxy-3-methylglutaryl-CoA-synthase, eukaryotic
clade; Region: HMG-CoA-S_euk; TIGR01833"
/db_xref="CDD:273826"
misc_feature 308..310
/gene="HMGCS2"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0000250|UniProtKB:P54869; propagated from
UniProtKB/Swiss-Prot (P54868.1); acetylation site"
misc_feature 788..790
/gene="HMGCS2"
/note="N6-acetyllysine.
/evidence=ECO:0000250|UniProtKB:P54869; propagated from
UniProtKB/Swiss-Prot (P54868.1); acetylation site"
misc_feature 827..829
/gene="HMGCS2"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0000250|UniProtKB:P54869; propagated from
UniProtKB/Swiss-Prot (P54868.1); acetylation site"
misc_feature 977..979
/gene="HMGCS2"
/note="N6-acetyllysine.
/evidence=ECO:0000250|UniProtKB:P54869; propagated from
UniProtKB/Swiss-Prot (P54868.1); acetylation site"
misc_feature 989..991
/gene="HMGCS2"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0000250|UniProtKB:P54869; propagated from
UniProtKB/Swiss-Prot (P54868.1); acetylation site"
misc_feature 1085..1087
/gene="HMGCS2"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0000250|UniProtKB:P54869; propagated from
UniProtKB/Swiss-Prot (P54868.1); acetylation site"
misc_feature 1109..1111
/gene="HMGCS2"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0000250|UniProtKB:P54869; propagated from
UniProtKB/Swiss-Prot (P54868.1); acetylation site"
misc_feature 1121..1123
/gene="HMGCS2"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0000250|UniProtKB:P54869; propagated from
UniProtKB/Swiss-Prot (P54868.1); acetylation site"
misc_feature 1133..1135
/gene="HMGCS2"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0000250|UniProtKB:P54869; propagated from
UniProtKB/Swiss-Prot (P54868.1); acetylation site"
misc_feature 1358..1360
/gene="HMGCS2"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:24275569; propagated from
UniProtKB/Swiss-Prot (P54868.1); phosphorylation site"
misc_feature 1370..1372
/gene="HMGCS2"
/note="N6-acetyllysine.
/evidence=ECO:0000250|UniProtKB:P54869; propagated from
UniProtKB/Swiss-Prot (P54868.1); acetylation site"
misc_feature 1379..1381
/gene="HMGCS2"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:24275569; propagated from
UniProtKB/Swiss-Prot (P54868.1); phosphorylation site"
misc_feature 1400..1402
/gene="HMGCS2"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0000250|UniProtKB:P54869; propagated from
UniProtKB/Swiss-Prot (P54868.1); acetylation site"
misc_feature 1427..1429
/gene="HMGCS2"
/note="Phosphoserine.
/evidence=ECO:0000250|UniProtKB:P54869; propagated from
UniProtKB/Swiss-Prot (P54868.1); phosphorylation site"
misc_feature 1478..1480
/gene="HMGCS2"
/note="N6-acetyllysine, alternate.
/evidence=ECO:0000250|UniProtKB:P54869; propagated from
UniProtKB/Swiss-Prot (P54868.1); acetylation site"
misc_feature 1490..1492
/gene="HMGCS2"
/note="Phosphoserine.
/evidence=ECO:0000250|UniProtKB:P22791; propagated from
UniProtKB/Swiss-Prot (P54868.1); phosphorylation site"
variation 62
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1653328335"
variation 63
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758462859"
variation 67
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1353408775"
variation 68
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750380692"
variation 69
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:72695184"
variation 73
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1653327172"
variation 78
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189194662"
variation 80
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:757083410"
variation 82
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:368678169"
variation 83
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101283706"
variation 84
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1452551580"
variation 87
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144004292"
variation 88
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:757188613"
variation 89
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:373202578"
variation 90
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:766960590"
variation 91
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256262455"
variation 92
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1653326072"
variation 96
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:939049952"
variation 99..100
/gene="HMGCS2"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2101283660"
variation 100
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:759067886"
variation 104
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1286736541"
variation 105
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1008466802"
variation 108
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773898985"
variation 111..114
/gene="HMGCS2"
/replace="cggt"
/replace="cggtcggt"
/db_xref="dbSNP:1557996143"
variation 111
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:587712415"
variation 112
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:762327005"
variation 115
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1557996139"
variation 117
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101283600"
variation 119
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1332746126"
variation 124
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:777148971"
variation 126..128
/gene="HMGCS2"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1653324348"
variation 130
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:769000173"
variation 132
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369221781"
variation 133
/gene="HMGCS2"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2101283564"
variation 133
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:780272061"
variation 134
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:144744634"
variation 136
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:745916413"
variation 137
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:893820165"
variation 138
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1653322892"
variation 139
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:763901461"
variation 140
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376238143"
variation 141
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:757169217"
variation 144
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653322600"
variation 145
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1170811310"
variation 149
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:202069145"
variation 151
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653322264"
variation 152
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244351356"
variation 153
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1233603916"
variation 155
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:755897068"
variation 156
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:199651321"
variation 157
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:767168451"
variation 159
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:759183803"
variation 164
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653321576"
variation 165
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751101083"
exon 166..620
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 166
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1231210408"
variation 169
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:775905632"
variation 172
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200675569"
variation 173
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:77241754"
variation 174
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282393883"
variation 176
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208729772"
variation 177..180
/gene="HMGCS2"
/replace=""
/replace="cctc"
/db_xref="dbSNP:1475398406"
variation 178
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653158226"
variation 180
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1346871356"
variation 183..189
/gene="HMGCS2"
/replace="c"
/replace="ctgtccc"
/db_xref="dbSNP:1278392688"
variation 185
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:375279621"
variation 187
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:774514655"
variation 189
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:771019602"
variation 192
/gene="HMGCS2"
/replace=""
/replace="t"
/db_xref="dbSNP:1331676978"
variation 192
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:749336738"
variation 196
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200816212"
variation 197
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653157137"
variation 201
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1653157007"
variation 203
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:199670317"
variation 207
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:756404916"
variation 208
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1571042872"
variation 210
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:866803752"
variation 211
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653156489"
variation 212
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1653156396"
variation 214
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653156303"
variation 217
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:772149969"
variation 220
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201239391"
variation 221
/gene="HMGCS2"
/replace=""
/replace="g"
/db_xref="dbSNP:1160328101"
variation 221
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:28937320"
variation 223
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:911961081"
variation 229
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051817360"
variation 230
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402619037"
variation 232..233
/gene="HMGCS2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2101274491"
variation 232
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571042818"
variation 235
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138739620"
variation 236
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:181428774"
variation 237
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1653154898"
variation 242..243
/gene="HMGCS2"
/replace=""
/replace="ccaatatggccctggaggccaa"
/db_xref="dbSNP:1553241079"
variation 242
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:746685363"
variation 243
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:779833095"
variation 243
/gene="HMGCS2"
/replace="t"
/replace="tggccctggaggccaat"
/db_xref="dbSNP:747388657"
variation 247
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1199311850"
variation 250
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:758019802"
variation 252
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1185689932"
variation 253
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1571042770"
variation 255
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1485324823"
variation 256
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042762"
variation 257
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1653153732"
variation 259
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:749941890"
variation 266
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1217700912"
variation 268
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:142709072"
variation 269
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1653153296"
variation 270
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469630685"
variation 271
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:756658111"
variation 272
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571042738"
variation 274
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:145514933"
variation 277
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1571042729"
variation 278
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042719"
variation 281
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587688416"
variation 283
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:759842428"
variation 284
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1571042703"
variation 285
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:774598305"
variation 286
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:774411362"
variation 288
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413432644"
variation 289
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042674"
variation 293
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:766584879"
variation 296
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:763001714"
variation 298
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433333813"
variation 301
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571042651"
variation 302
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:151187711"
variation 304
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:761845625"
variation 306
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653149765"
variation 307
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1479205954"
variation 309
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462212320"
variation 310
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1420068119"
variation 312
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1162910493"
variation 313
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042624"
variation 314
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:776664327"
variation 315..316
/gene="HMGCS2"
/replace=""
/replace="g"
/db_xref="dbSNP:1571042612"
variation 316
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:768623326"
variation 318
/gene="HMGCS2"
/replace=""
/replace="t"
/db_xref="dbSNP:1571042603"
variation 318
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1187974723"
variation 319
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1484767754"
variation 321
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:768463219"
variation 322
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:779916834"
variation 323
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469561308"
variation 324
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1270679177"
variation 325
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2101273969"
variation 327
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:114033510"
variation 330
/gene="HMGCS2"
/replace=""
/replace="a"
/db_xref="dbSNP:1557994116"
variation 331..332
/gene="HMGCS2"
/replace=""
/replace="c"
/db_xref="dbSNP:1571042548"
variation 331
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:41302817"
variation 333
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:587697520"
variation 335
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771955824"
variation 336
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144921290"
variation 337
/gene="HMGCS2"
/replace=""
/replace="t"
/db_xref="dbSNP:1571042532"
variation 340
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557994090"
variation 342
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101273865"
variation 346
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1653147167"
variation 349
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303628202"
variation 350
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571042520"
variation 351
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1024035971"
variation 352
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1571042505"
variation 353
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1653146548"
variation 354
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042499"
variation 357
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:781647908"
variation 358
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:147746231"
variation 359
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332784240"
variation 363
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:751909473"
variation 364
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201187096"
variation 366
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:766672926"
variation 367
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:955697615"
variation 368
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101273736"
variation 372
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:763241833"
variation 373
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1571042452"
variation 374
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1653144748"
variation 377
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:750575658"
variation 379
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1426710599"
variation 384
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:765384188"
variation 385
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372251981"
variation 386
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:776751915"
variation 389
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250760247"
variation 391
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571042415"
variation 394
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653144051"
variation 395
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:768707273"
variation 396
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:145633208"
variation 397
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1260008829"
variation 400
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1252609545"
variation 402
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1653142058"
variation 406
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397104251"
variation 407
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200607527"
variation 408
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:147906427"
variation 409
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146073837"
variation 410
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1453735975"
variation 411
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571042378"
variation 412
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:928663340"
variation 413
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1571042362"
variation 414
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1235493293"
variation 418
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1246669403"
variation 419
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:758033248"
variation 421
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1571042342"
variation 424
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:770521945"
variation 425
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368014391"
variation 427
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138170167"
variation 428
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1300010645"
variation 429
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:755489615"
variation 430
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:780926888"
variation 433
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:751997256"
variation 436
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1173958102"
variation 437
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1436348108"
variation 439
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1393101212"
variation 440
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:780431922"
variation 442
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587616028"
variation 445
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1251993883"
variation 448
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:750709310"
variation 450
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375313694"
variation 454
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:587741129"
variation 457
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:753951770"
variation 460
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1553241043"
variation 463
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1212314291"
variation 465
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1350489274"
variation 468
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101273359"
variation 470
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653138229"
variation 473
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:764209022"
variation 476
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1232767876"
variation 478
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571042244"
variation 481
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370900322"
variation 483
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406920400"
variation 487
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1321279061"
variation 489
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:760689678"
variation 490
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571042209"
variation 491
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:775528207"
variation 492
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:767366737"
variation 496
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:759228303"
variation 497
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1313393068"
variation 503
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:890302302"
variation 504
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1557993914"
variation 505
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1557993907"
variation 506
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:774091075"
variation 512
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1172810724"
variation 517
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1653136294"
variation 519
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:770478547"
variation 520
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:748883811"
variation 522
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1338594261"
variation 523
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042145"
variation 529
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042139"
variation 530
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051823691"
variation 531
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:916186024"
variation 532
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042115"
variation 533
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:756896188"
variation 537
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:866366934"
variation 538
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1026894407"
variation 539
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:993282740"
variation 540
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:748155656"
variation 543
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653134824"
variation 546
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:780406594"
variation 549
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1486964047"
variation 550
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653134557"
variation 552
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1289541397"
variation 553
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042077"
variation 556
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1255800042"
variation 557
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1653134202"
variation 559
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042062"
variation 561
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:137852640"
variation 562
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:758839673"
variation 563
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:746217014"
variation 565
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571042028"
variation 567
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1237226874"
variation 568
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653133530"
variation 570
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:779249605"
variation 571
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1653133264"
variation 572
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653133134"
variation 573
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653132966"
variation 576
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:867469566"
variation 578
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:757431290"
variation 579
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653132655"
variation 580
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:879133941"
variation 581
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:137852636"
variation 585
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653132393"
variation 586
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274983621"
variation 588
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:764299408"
variation 589
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1653132160"
variation 590
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1333199361"
variation 591
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1401213260"
variation 592
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653131909"
variation 593
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1382579134"
variation 594
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1386957244"
variation 595
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752729912"
variation 597
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1456425510"
variation 598
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1653131406"
variation 601
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1161245291"
variation 603
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1384449317"
variation 604
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1417914069"
variation 607
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:587662618"
variation 610
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1653130925"
variation 611
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:759434636"
variation 612
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1653130753"
variation 616
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1653130666"
variation 617
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:774032165"
variation 618
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:778262961"
variation 619
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2101272788"
variation 620
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1420066501"
exon 621..746
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 622
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:764867139"
variation 623
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1227400362"
variation 624
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:761373362"
variation 627
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1305154516"
variation 630
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1427843883"
variation 631
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201735169"
variation 632
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1329968704"
variation 633
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:760862396"
variation 636
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652985111"
variation 637
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1410967304"
variation 640
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:759988740"
variation 643
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652984669"
variation 644
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:774872599"
variation 647
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:149314406"
variation 649
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441882920"
variation 650
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101263939"
variation 654
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:749637124"
variation 655
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1195712336"
variation 656
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:150140061"
variation 658
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1057521346"
variation 659
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1246163712"
variation 661
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1182648503"
variation 662
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1439432172"
variation 663
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652983127"
variation 666..670
/gene="HMGCS2"
/replace="gt"
/replace="gtggt"
/db_xref="dbSNP:759006818"
variation 667
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1270791990"
variation 669
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:587631357"
variation 672
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652982553"
variation 673
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652982450"
variation 677
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748337518"
variation 678
/gene="HMGCS2"
/replace=""
/replace="g"
/db_xref="dbSNP:1343879814"
variation 678
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1064797117"
variation 681
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652981816"
variation 682
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:886045207"
variation 685
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:781161689"
variation 686
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386014089"
variation 689..692
/gene="HMGCS2"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:746333616"
variation 692
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:755037311"
variation 693..694
/gene="HMGCS2"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1451885079"
variation 694
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:370124069"
variation 695
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:137852638"
variation 697
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652980488"
variation 704
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:779939076"
variation 705
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146945061"
variation 710
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1412936947"
variation 711
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652979947"
variation 712
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:145699892"
variation 714
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369834382"
variation 716
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:79038451"
variation 717
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:761456576"
variation 718
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1167346246"
variation 719
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1249772723"
variation 721
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:929760980"
variation 722
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652978822"
variation 723
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1485974535"
variation 725
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652978532"
variation 726
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259292158"
variation 728
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376815328"
variation 731
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1394267813"
variation 733
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1311179686"
variation 734
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1284518599"
variation 736
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2101263677"
variation 737
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1225178556"
variation 740
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1347897263"
variation 743
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:763531478"
variation 744
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760210450"
exon 747..911
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 747
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:752239721"
variation 749..750
/gene="HMGCS2"
/replace=""
/replace="acaaaaga"
/db_xref="dbSNP:1652956572"
variation 750
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1485342949"
variation 756
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1002548815"
variation 762
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101262615"
variation 763
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:767069915"
variation 765
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:773806829"
variation 766
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101262597"
variation 772
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:367770104"
variation 774
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652955948"
variation 775
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419921025"
variation 777..788
/gene="HMGCS2"
/replace="a"
/replace="atgacttctaca"
/db_xref="dbSNP:1193946325"
variation 778
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652955748"
variation 780
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762211049"
variation 785
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652955496"
variation 786
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375071247"
variation 787
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:145838142"
variation 788
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1247037912"
variation 791
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652954795"
variation 793
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1469399815"
variation 796
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652954559"
variation 800
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652954445"
variation 802
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652954332"
variation 804
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:768912442"
variation 805
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1219952938"
variation 807
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1333189037"
variation 808
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:909075571"
variation 811
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652953647"
variation 812
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652953530"
variation 815
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:767113695"
variation 816
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1274079819"
variation 817
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:761483416"
variation 819
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1249021511"
variation 820
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:775549228"
variation 821
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1047602183"
variation 823
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652952471"
variation 826
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:745824260"
variation 827
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:778797644"
variation 829
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:757041759"
variation 830
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:749102995"
variation 831..833
/gene="HMGCS2"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1553240525"
variation 832
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571037509"
variation 833
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:777348530"
variation 835
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571037496"
variation 838
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355056794"
variation 840
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652951110"
variation 841..847
/gene="HMGCS2"
/replace=""
/replace="gtgctac"
/db_xref="dbSNP:1571037483"
variation 841
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1172184574"
variation 843
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652950860"
variation 846
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1466691522"
variation 847
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427576637"
variation 848..849
/gene="HMGCS2"
/replace="t"
/replace="tt"
/db_xref="dbSNP:2101262353"
variation 848
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652950477"
variation 850
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652950310"
variation 850
/gene="HMGCS2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1557991791"
variation 851
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:773945291"
variation 852
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372095379"
variation 855
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:767157843"
variation 856
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652949915"
variation 857
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571037457"
variation 858
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:918691885"
variation 863
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652949602"
variation 864
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371306326"
variation 866
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190133412"
variation 866
/gene="HMGCS2"
/replace="t"
/replace="tt"
/db_xref="dbSNP:757352789"
variation 868
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:866934006"
variation 871
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:751009381"
variation 872
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571037428"
variation 874
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:765772883"
variation 875
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571037413"
variation 877
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1571037408"
variation 881
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:587677809"
variation 882
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:370058829"
variation 883
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571037388"
variation 884..890
/gene="HMGCS2"
/replace="aaaaaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:1557991740"
variation 884
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652948216"
variation 886
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652948128"
variation 888
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:764302250"
variation 889
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652947931"
variation 890
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:760913527"
variation 891
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:775637086"
variation 894
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:898393396"
variation 895
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:772186726"
variation 897
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375716442"
variation 899
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1299801129"
variation 900
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652947252"
variation 902
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407962244"
variation 904
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652947097"
variation 907
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:202211261"
variation 908
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370438695"
exon 912..1077
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 912
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201182715"
variation 914
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1246961486"
variation 918
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1338450583"
variation 919
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1992376"
variation 920
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587671242"
variation 923
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:142637231"
variation 924
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:183046298"
variation 926
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:751683757"
variation 927
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:146296049"
variation 928
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652877239"
variation 932
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:148892048"
variation 935
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:769844821"
variation 937
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652876948"
variation 940
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761787433"
variation 941
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144103604"
variation 942
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1186326463"
variation 943..945
/gene="HMGCS2"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:753878217"
variation 947
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652876404"
variation 948..951
/gene="HMGCS2"
/replace="agta"
/replace="agtagta"
/db_xref="dbSNP:764306891"
variation 948
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:865947488"
variation 950
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:768535206"
variation 952
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048438"
variation 953
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:376554104"
variation 955
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:138086607"
variation 956
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1273931880"
variation 958..959
/gene="HMGCS2"
/replace=""
/replace="gaaa"
/db_xref="dbSNP:1417242901"
variation 961
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1211527690"
variation 964
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:763775014"
variation 966
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652875135"
variation 968
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1359922140"
variation 969
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:778400323"
variation 970
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652874836"
variation 974
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571035721"
variation 977
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:756625778"
variation 978
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:748587465"
variation 982
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1431740041"
variation 990
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367180826"
variation 997
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1331997383"
variation 1000
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339633294"
variation 1001
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:781567781"
variation 1002
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:755313968"
variation 1003
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652873712"
variation 1007
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:587664208"
variation 1008
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1045222753"
variation 1013
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1407518921"
variation 1014
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:766507770"
variation 1017
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652873146"
variation 1018
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:894730177"
variation 1022
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1163255653"
variation 1024
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:758565101"
variation 1026
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:750485856"
variation 1028
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371906223"
variation 1036
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368471603"
variation 1041
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:930829392"
variation 1045
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652872377"
variation 1047
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652872291"
variation 1048
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253654665"
variation 1050
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:919408055"
variation 1051
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2101258162"
variation 1052..1053
/gene="HMGCS2"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1652871929"
variation 1052
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:776664576"
variation 1057
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652871835"
variation 1061
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:764027082"
variation 1063
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1266588243"
variation 1075
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:141213676"
variation 1076
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775277893"
variation 1077
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:74889853"
exon 1078..1248
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 1078
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:777182302"
variation 1080
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101254831"
variation 1081
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265709999"
variation 1087
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652810178"
variation 1090
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:769058291"
variation 1091
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2101254797"
variation 1098
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1181436986"
variation 1099
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:747485297"
variation 1100
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652809713"
variation 1102
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652809624"
variation 1104
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:966875458"
variation 1105
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:780316550"
variation 1107
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1025175254"
variation 1109
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571033686"
variation 1113
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1426493337"
variation 1114
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772437190"
variation 1115
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:746145498"
variation 1118
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:779242610"
variation 1119
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652808686"
variation 1124
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652808604"
variation 1126
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1364211191"
variation 1130
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:757475645"
variation 1135
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652808173"
variation 1139
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1286992834"
variation 1140
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353365984"
variation 1141
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:753951704"
variation 1142
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380312324"
variation 1143
/gene="HMGCS2"
/replace=""
/replace="a"
/db_xref="dbSNP:1652807640"
variation 1143
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1286357569"
variation 1144
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:991904954"
variation 1146
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652807341"
variation 1147
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777939704"
variation 1150
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:762443891"
variation 1151
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652807016"
variation 1153
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752639075"
variation 1154
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:767236647"
variation 1155
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:759352736"
variation 1156
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:587690380"
variation 1159
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652806464"
variation 1163
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1557989960"
variation 1164
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652806263"
variation 1169
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652806163"
variation 1171
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:774953281"
variation 1172
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:766003583"
variation 1173
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:762536796"
variation 1174
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:772715543"
variation 1175
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652805571"
variation 1179
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652805414"
variation 1180
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:769310958"
variation 1181
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1327737396"
variation 1185
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:151328418"
variation 1186
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:776046708"
variation 1188
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:772359110"
variation 1189
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:764568941"
variation 1190..1193
/gene="HMGCS2"
/replace="ca"
/replace="caca"
/db_xref="dbSNP:756272484"
variation 1191
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652804611"
variation 1193
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:746227549"
variation 1194
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263957408"
variation 1200
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:779332852"
variation 1201
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1266985661"
variation 1202
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1215654921"
variation 1203
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771289268"
variation 1206
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652803762"
variation 1211
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1292399691"
variation 1214
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:4716"
variation 1215..1217
/gene="HMGCS2"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1571033506"
variation 1217
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1378975136"
variation 1218
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:777744720"
variation 1219
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652803184"
variation 1222
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:756169207"
variation 1223
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:752626288"
variation 1224
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:781186067"
variation 1226
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1437031967"
variation 1228
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:754826235"
variation 1229
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:751371132"
variation 1230
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1404540409"
variation 1232
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1166279238"
variation 1236
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:766097440"
variation 1237
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652802208"
variation 1238
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652802125"
variation 1242..1244
/gene="HMGCS2"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1423575599"
variation 1246
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:267597953"
variation 1247
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:762627608"
variation 1248
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144329134"
exon 1249..1355
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 1249
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:763443637"
variation 1254
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:12117456"
variation 1257
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1356884646"
variation 1258
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1034584179"
variation 1260
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1305902474"
variation 1261
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101249833"
variation 1262
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1454719802"
variation 1267
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:760149713"
variation 1268
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652725108"
variation 1270
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:774949209"
variation 1272
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1557988855"
variation 1277
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1282825298"
variation 1278
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:139620933"
variation 1279
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413334730"
variation 1281
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:766898190"
variation 1283
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471802697"
variation 1286
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652724277"
variation 1287
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2101249765"
variation 1288
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2101249759"
variation 1291
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:763378721"
variation 1293
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557988835"
variation 1295
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652724028"
variation 1296
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652723944"
variation 1297
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:773364048"
variation 1302
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1224665560"
variation 1306
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571031412"
variation 1313
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652723582"
variation 1315
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2101249712"
variation 1317
/gene="HMGCS2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1287002055"
variation 1321
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:15609"
variation 1323..1331
/gene="HMGCS2"
/replace="tttc"
/replace="tttcatttc"
/db_xref="dbSNP:772305902"
variation 1323
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652723339"
variation 1324
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2101249690"
variation 1325
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1201210514"
variation 1329
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652723182"
variation 1331
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:137852637"
variation 1332
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748252959"
variation 1333
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:186771480"
variation 1336
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652722253"
variation 1337
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:768676776"
variation 1338
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:747000856"
variation 1339
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1269917499"
variation 1340
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:779938993"
variation 1343
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1334904424"
variation 1344
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652721671"
variation 1348
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:755119914"
variation 1350
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:141769037"
variation 1352
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:971540603"
variation 1354
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1472370665"
exon 1356..1481
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 1356
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1446564405"
variation 1357
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:770584941"
variation 1358
/gene="HMGCS2"
/replace="t"
/replace="tat"
/db_xref="dbSNP:1553239855"
variation 1359
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652701530"
variation 1361..1364
/gene="HMGCS2"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1652700979"
variation 1361
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:749020250"
variation 1362
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1487366289"
variation 1367
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652700847"
variation 1369
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652700728"
variation 1370
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652700590"
variation 1372
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:111284724"
variation 1372
/gene="HMGCS2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1652700451"
variation 1373
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:587623606"
variation 1376
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:752268224"
variation 1377
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652699823"
variation 1378
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:780781898"
variation 1381
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226057083"
variation 1383
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:758974137"
variation 1384
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:78280338"
variation 1385
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1256038787"
variation 1386
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765680777"
variation 1389
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210167963"
variation 1392
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1571030681"
variation 1393
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324745132"
variation 1394
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:754122611"
variation 1395
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1018386936"
variation 1403
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:61729865"
variation 1404..1412
/gene="HMGCS2"
/replace="gcct"
/replace="gcctagcct"
/db_xref="dbSNP:2101248147"
variation 1404
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:760833472"
variation 1405
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303432261"
variation 1406
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:775555477"
variation 1409
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:772007817"
variation 1410
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1166429808"
variation 1411
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:759542743"
variation 1415
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:587727388"
variation 1416
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:770800317"
variation 1420..1427
/gene="HMGCS2"
/replace="gtgtgt"
/replace="gtgtgtgt"
/db_xref="dbSNP:1267844674"
variation 1423
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652696758"
variation 1424
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:749033432"
variation 1426
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:143463960"
variation 1429
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:769574264"
variation 1432
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:747762161"
variation 1433..1438
/gene="HMGCS2"
/replace="gag"
/replace="gaggag"
/db_xref="dbSNP:746197576"
variation 1433
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:780869942"
variation 1435
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652696152"
variation 1438
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:754421987"
variation 1450
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276125317"
variation 1453
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344814686"
variation 1454..1455
/gene="HMGCS2"
/replace="a"
/replace="aa"
/db_xref="dbSNP:779321975"
variation 1457
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:587606870"
variation 1458
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:779280964"
variation 1459
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410813519"
variation 1462
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:757694113"
variation 1463
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1327062942"
variation 1466
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:754218759"
variation 1470
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:764380176"
variation 1471
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652694966"
variation 1476
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:756362495"
variation 1477
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:760737262"
variation 1479
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1251813781"
variation 1480
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:142776952"
variation 1481
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1428518237"
exon 1482..1593
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 1482
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1223577754"
variation 1483
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652635564"
variation 1486
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:751604096"
variation 1492
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:766442654"
variation 1496
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1286156922"
variation 1497
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:954149886"
variation 1500
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652635062"
variation 1503
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1557987604"
variation 1504
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1274987443"
variation 1506
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1382059473"
variation 1507
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473777473"
variation 1510
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652634630"
variation 1512
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:763005476"
variation 1513..1520
/gene="HMGCS2"
/replace="cc"
/replace="ccttttcc"
/db_xref="dbSNP:1652634252"
variation 1513
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652634445"
variation 1514
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652634353"
variation 1520
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652634170"
variation 1522
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416274127"
variation 1523
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652633973"
variation 1524
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1203892179"
variation 1528
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:773260075"
variation 1530
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:765161813"
variation 1531
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652633599"
variation 1534..1535
/gene="HMGCS2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1158368570"
variation 1535
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652633419"
variation 1540
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:761693466"
variation 1541
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:776399237"
variation 1542
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587593961"
variation 1544
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:746610244"
variation 1546
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:774897830"
variation 1547
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652632697"
variation 1549
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189946297"
variation 1550
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:771524777"
variation 1551
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1486025242"
variation 1553
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:927944310"
variation 1554
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:749846010"
variation 1555
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557987526"
variation 1557
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:778223568"
variation 1559
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:756539895"
variation 1560
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:137852639"
variation 1562
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:781563101"
variation 1563
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:372079931"
variation 1570
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:755185680"
variation 1572..1574
/gene="HMGCS2"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1258406005"
variation 1572
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:751754816"
variation 1574
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780044819"
variation 1575
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:758519315"
variation 1576
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1437142528"
variation 1577
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374568676"
variation 1578
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587717007"
variation 1579
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:761781401"
variation 1580
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753575448"
variation 1582
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:587677028"
variation 1583
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:76773981"
variation 1586
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:775189501"
variation 1590
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186406205"
variation 1591
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652629664"
exon 1594..2433
/gene="HMGCS2"
/inference="alignment:Splign:2.1.0"
variation 1600
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:182407677"
variation 1607
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652544019"
variation 1611
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652543930"
variation 1613
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:959339642"
variation 1617
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:747007842"
variation 1619
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2101240446"
variation 1625
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313731544"
variation 1626
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:776201032"
variation 1627
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:921601572"
variation 1629
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652543392"
variation 1632
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652543313"
variation 1633
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1283923655"
variation 1636
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1351829384"
variation 1640
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1417770076"
variation 1646
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:770591879"
variation 1648
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1284502124"
variation 1649
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:148106058"
variation 1650
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1487056819"
variation 1658
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1215176488"
variation 1660
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256456049"
variation 1664
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:746537667"
variation 1666
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143718202"
variation 1667
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652542226"
variation 1669
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652542147"
variation 1670
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2101240346"
variation 1671
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1184930959"
variation 1673
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652541997"
variation 1677
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652541919"
variation 1680
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1236721331"
variation 1681..1685
/gene="HMGCS2"
/replace=""
/replace="ctggt"
/db_xref="dbSNP:1440069329"
variation 1687
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652541655"
variation 1688
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:962842435"
variation 1689..1690
/gene="HMGCS2"
/replace=""
/replace="atgaatttttaa"
/db_xref="dbSNP:1160442408"
variation 1689
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652541498"
variation 1690
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652541312"
variation 1700
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:148963389"
variation 1701
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:587762730"
variation 1702
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1248273681"
variation 1704
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571026960"
variation 1705
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174297384"
variation 1714
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016341601"
variation 1719
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652539784"
variation 1722
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1404648332"
variation 1727
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:965967252"
variation 1733
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1333723178"
variation 1735
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1336794842"
variation 1743
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:587686291"
variation 1748
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:771526508"
variation 1751
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1307712218"
variation 1753
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138575225"
variation 1754
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:886491306"
variation 1766
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1027479499"
variation 1769
/gene="HMGCS2"
/replace=""
/replace="c"
/db_xref="dbSNP:1652538297"
variation 1769
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652538189"
variation 1772
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1274559603"
variation 1781
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1245391247"
variation 1789
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030291437"
variation 1790
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:755165196"
variation 1792..1816
/gene="HMGCS2"
/replace="ggg"
/replace="gggcttatggtgctatggactaggg"
/db_xref="dbSNP:1180207146"
variation 1800
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2101240205"
variation 1802
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652537495"
variation 1804
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1198439043"
variation 1805
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277460396"
variation 1807
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652537134"
variation 1809
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652537016"
variation 1810
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:895243002"
variation 1811
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652536782"
variation 1812
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652536126"
variation 1814
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652536007"
variation 1816
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571026871"
variation 1817
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:997897520"
variation 1821..1828
/gene="HMGCS2"
/replace=""
/replace="tttgtgaa"
/db_xref="dbSNP:200828254"
variation 1826..1831
/gene="HMGCS2"
/replace="gaaaga"
/replace="gaaagaaaga"
/db_xref="dbSNP:1652534892"
variation 1826
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:753304242"
variation 1829
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652535108"
variation 1830
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652534992"
variation 1831
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652534823"
variation 1832
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199462871"
variation 1833
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:902731885"
variation 1838
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1464609687"
variation 1841
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652534535"
variation 1845
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1172276496"
variation 1847
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652534347"
variation 1850
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652534265"
variation 1852
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749814204"
variation 1858
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1011205317"
variation 1859
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1376596454"
variation 1865
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:893973335"
variation 1866
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1049951208"
variation 1867..1871
/gene="HMGCS2"
/replace="a"
/replace="aatca"
/db_xref="dbSNP:2101240050"
variation 1872
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652533637"
variation 1874
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652533528"
variation 1882
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039677206"
variation 1885
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1230361877"
variation 1887
/gene="HMGCS2"
/replace=""
/replace="g"
/db_xref="dbSNP:1652533221"
variation 1892
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652533119"
variation 1901
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652533003"
variation 1905
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273887760"
variation 1908
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:936894312"
variation 1915
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2101240001"
variation 1920
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:56828380"
variation 1921
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:770214388"
variation 1924
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652532598"
variation 1927
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1299161228"
variation 1928
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1040012812"
variation 1930
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1269363162"
variation 1931..1932
/gene="HMGCS2"
/replace=""
/replace="tggtggatggagcggtgttt"
/db_xref="dbSNP:1652532192"
variation 1931
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:587723389"
variation 1932
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652532110"
variation 1934
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571026733"
variation 1936
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:144826622"
variation 1937
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:587641803"
variation 1939
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376608094"
variation 1941
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557986311"
variation 1942
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1478950779"
variation 1950..1961
/gene="HMGCS2"
/replace="ttatta"
/replace="ttattatta"
/replace="ttattattatta"
/db_xref="dbSNP:140599791"
variation 1951..1953
/gene="HMGCS2"
/replace="t"
/replace="tat"
/db_xref="dbSNP:1438745411"
variation 1956
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1571026700"
variation 1958
/gene="HMGCS2"
/replace=""
/replace="a"
/db_xref="dbSNP:1652530883"
variation 1959
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:991849328"
variation 1960
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:983323260"
variation 1961
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1571026672"
variation 1968
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557986293"
variation 1974
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:770080416"
variation 1978
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652530272"
variation 1979
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652530175"
variation 1982
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652530051"
variation 1985
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652529916"
variation 1986
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652529811"
variation 1988
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1294233713"
variation 1997
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1458722285"
variation 2008
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652529572"
variation 2014
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571026636"
variation 2019
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295814905"
variation 2021
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1461912455"
variation 2022
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571026616"
variation 2023
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652529162"
variation 2026
/gene="HMGCS2"
/replace=""
/replace="a"
/db_xref="dbSNP:1652529107"
variation 2027
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:920407273"
variation 2028
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1357602330"
variation 2029
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:937658755"
variation 2032
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1384601125"
regulatory 2034..2039
/regulatory_class="polyA_signal_sequence"
/gene="HMGCS2"
/note="hexamer: ATTAAA"
variation 2036
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:990630239"
variation 2037
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652528706"
variation 2038
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1299933733"
variation 2039
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652528559"
variation 2041..2047
/gene="HMGCS2"
/replace="agaga"
/replace="agagaga"
/db_xref="dbSNP:1450484328"
variation 2044
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1172913511"
variation 2045
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1340572398"
variation 2046
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652528320"
variation 2047
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1571026561"
variation 2053
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652528084"
variation 2054
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1571026553"
polyA_site 2056
/gene="HMGCS2"
/note="major polyA site"
variation 2058
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:746232231"
variation 2064
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652527841"
variation 2066
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:926582357"
variation 2067
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:141106649"
variation 2069
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1192597071"
variation 2072
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035521301"
variation 2079
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1487435009"
variation 2080
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:587625788"
variation 2082
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1209140121"
variation 2084
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652527196"
variation 2085
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652527115"
variation 2086
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652527046"
variation 2091
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1003508550"
variation 2092
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652526864"
variation 2095
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1489307748"
variation 2096
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:962552022"
variation 2103
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652526585"
variation 2104
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652526472"
variation 2106
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1191847928"
variation 2111
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652526269"
variation 2115
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:781321001"
variation 2116
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2101239615"
variation 2122
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652526053"
variation 2131
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1254329985"
variation 2135
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1423109904"
variation 2136
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652525732"
variation 2138
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652525677"
variation 2139
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:908390016"
variation 2140
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652525544"
variation 2147
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424762085"
variation 2150
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571026483"
variation 2152
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571026476"
variation 2153
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587721879"
variation 2156
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652525088"
variation 2158
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652525007"
variation 2160
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652524937"
variation 2161
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2101239557"
variation 2164
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1209976880"
variation 2165..2174
/gene="HMGCS2"
/replace="tgtccccttg"
/replace="tgtccccttgtccccttg"
/db_xref="dbSNP:1652524480"
variation 2165
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:374153483"
variation 2169
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1249554243"
variation 2172
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652524556"
variation 2174
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1367261193"
variation 2177
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652524322"
variation 2178
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652524239"
variation 2182
/gene="HMGCS2"
/replace=""
/replace="a"
/db_xref="dbSNP:1652524162"
variation 2185
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1457886082"
variation 2189
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146520328"
variation 2193
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:950821538"
variation 2196
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:894085982"
variation 2197
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652523774"
variation 2198
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1571026448"
variation 2203..2204
/gene="HMGCS2"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2101239474"
variation 2204
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295980523"
variation 2216
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:868114000"
variation 2221
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1557986174"
variation 2224
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2101239449"
variation 2230..2252
/gene="HMGCS2"
/replace="aagaacggtagaacacagcttcc"
/replace="aagaacggtagaacacagcttccaccaaagaacggtagaacacagctt
cc"
/db_xref="dbSNP:1652522864"
variation 2230
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360760869"
variation 2235
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030360366"
variation 2236
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:997437985"
variation 2238
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1319664147"
variation 2240
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652523104"
variation 2243
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1232326301"
variation 2246
/gene="HMGCS2"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1652522925"
variation 2253
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:757470646"
variation 2258
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:900216785"
variation 2262
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652522621"
variation 2265
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:3894543"
variation 2267
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355962162"
variation 2268
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1571026395"
variation 2269
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652522337"
variation 2270
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652522262"
variation 2279
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1373543854"
variation 2282
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652522116"
variation 2285
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652522050"
variation 2286
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652521989"
variation 2287..2293
/gene="HMGCS2"
/replace="aga"
/replace="agacaga"
/db_xref="dbSNP:1262779364"
variation 2288
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:191519973"
variation 2291..2296
/gene="HMGCS2"
/replace="ag"
/replace="agagag"
/db_xref="dbSNP:1483674460"
variation 2291
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1214458570"
variation 2293
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652521673"
variation 2298
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587742820"
variation 2301..2303
/gene="HMGCS2"
/replace="a"
/replace="aga"
/db_xref="dbSNP:1302051309"
variation 2307
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1254562212"
variation 2308
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652521148"
variation 2309
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423594330"
variation 2310
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1159849025"
variation 2311
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652520676"
variation 2314
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652520615"
variation 2315
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1390905324"
variation 2317
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1371725596"
variation 2322
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587661345"
variation 2324
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344066942"
variation 2328
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652520203"
variation 2331..2338
/gene="HMGCS2"
/replace="atcttctt"
/replace="atcttcttatcttctt"
/db_xref="dbSNP:1376772547"
variation 2332
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1681433017"
variation 2334
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1448349780"
variation 2339
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1304215870"
variation 2346..2347
/gene="HMGCS2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1451570804"
variation 2351
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1001534919"
variation 2352
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:587601584"
variation 2353
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587722758"
variation 2355
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009711595"
variation 2360
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285463688"
variation 2361
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652519414"
variation 2366
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652519338"
variation 2370
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1312815124"
variation 2373
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212594496"
variation 2376
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:896263189"
variation 2378
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056596081"
variation 2379
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:937730116"
variation 2380
/gene="HMGCS2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:41313276"
variation 2381
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652518749"
variation 2385
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1240610116"
variation 2391
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652518608"
variation 2395
/gene="HMGCS2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1438437573"
variation 2400
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1178530898"
variation 2401
/gene="HMGCS2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1406688635"
variation 2403
/gene="HMGCS2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2101239098"
variation 2407
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:587609056"
variation 2410
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:116264779"
variation 2412
/gene="HMGCS2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652518037"
regulatory 2416..2421
/regulatory_class="polyA_signal_sequence"
/gene="HMGCS2"
/note="hexamer: AATAAA"
variation 2416
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2101239069"
variation 2417
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:941284777"
variation 2419..2425
/gene="HMGCS2"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:1652517637"
variation 2419
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:76803215"
variation 2422
/gene="HMGCS2"
/replace="a"
/replace="t"
/db_xref="dbSNP:758484729"
variation 2424
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:982608638"
variation 2428
/gene="HMGCS2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331730560"
variation 2431
/gene="HMGCS2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1418038381"
variation 2432
/gene="HMGCS2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1444527376"
polyA_site 2433
/gene="HMGCS2"
ORIGIN
atctctttcaaggtttctgctgggtttctgaactgctgggtttctgcttgctcctctggagatgcagcgtctgttgactccagtgaagcgcattctgcaactgacaagagcggtgcaggaaacctccctcacacctgctcgcctgctcccagtagcccaccaaaggttttctacagcctctgctgtccccctggccaaaacagatacttggccaaaggacgtgggcatcctggccctggaggtctacttcccagcccaatatgtggaccaaactgacctggagaagtataacaatgtggaagcaggaaagtatacagtgggcttgggccagacccgtatgggcttctgctcagtccaagaggacatcaactccctgtgcctgacggtggtgcaacggctgatggagcgcatacagctcccatgggactctgtgggcaggctggaagtaggcactgagaccatcattgacaagtccaaagctgtcaaaacagtgctcatggaactcttccaggattcaggcaatactgatattgagggcatagataccaccaatgcctgctacggtggtactgcctccctcttcaatgctgccaactggatggagtccagttcctgggatggtcgttatgccatggtggtctgtggagacattgccgtctatcccagtggtaatgctcgtcccacaggtggggccggagctgtggctatgctgattgggcccaaggcccctctggccctggagcgagggctgaggggaacccatatggagaatgtgtatgacttctacaaaccaaatttggcctcggagtacccaatagtggatgggaagctttccatccagtgctacttgcgggccttggatcgatgttacacatcataccgtaaaaaaatccagaatcagtggaagcaagctggcagcgatcgacccttcacccttgacgatttacagtacatgatctttcatacacccttttgcaagatggtccagaagtctctggctcgcctgatgttcaatgacttcctgtcagccagcagtgacacacaaaccagcttatataaggggctggaggctttcggggggctaaagctggaagacacctacaccaacaaggacctggataaagcacttctaaaggcctctcaggacatgttcgacaagaaaaccaaggcttccctttacctctccactcacaatgggaacatgtacacctcatccctgtacgggtgcctggcctcgcttctgtcccaccactctgcccaagaactggctggctccaggattggtgccttctcttatggctctggtttagcagcaagtttcttttcatttcgagtatcccaggatgctgctccaggctctcccctggacaagttggtgtccagcacatcagacctgccaaaacgcctagcctcccgaaagtgtgtgtctcctgaggagttcacagaaataatgaaccaaagagagcaattctaccataaggtgaatttctccccacctggtgacacaaacagccttttcccaggtacttggtacctggagcgagtggacgagcagcatcgccgaaagtatgcccggcgtcccgtctaaaggtgttctgcagatccatggaaagcttcctgggaaacgtatgctagcagagcttctccccgtgaatcatatttttaagatcccactcttagctggtaaatgaatttgaatcgacatagtagccccataagcatcagccctgtagagtgaggagccatctctagcgggcccttcattcctctccatgctgcaatcactgtcctgggcttatggtgctatggactaggggtcctttgtgaaagagcaagatggagcaatggagagaagacctcttcctgaatcactggactccagaaatgtgcatgcagatcagctgttgccttcaagatccagataaactttcctgtcatgtgttagaactttattattattaatattgttaaacttctgtgctgttcctgtgaatctccaaattttgtaccttgttctaagctaatatatagcaattaaaaagagagaaagaggaaatgattcctgcgtttcttggaacccagaatacaaacccagcctaacatgcagcaagcctgctagaccttgtgggtcagagggctgggtccttgcctcacaggctgcctctgtccccttgcaattccattctatttctgccacatgccaagtgctatgacaggtacaaggcaaataagaacggtagaacacagcttcccccagcccacttccctgttctaaagacaccacatagacagagagcagcagacaggggccagcaggagctgtagttcagatcttcttggtcattccttgccgctgttatttgaacaaataaacacagcgcaaaggttaacaagtttttgccttctatagccaaaaataaaaaaataaataaa
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
[Full Text]