ver.2
Home
|
Help
|
Advanced search
Previous release (v1)
2024-04-25 20:41:55, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_006539 1917 bp mRNA linear PRI 02-OCT-2023
DEFINITION Homo sapiens calcium voltage-gated channel auxiliary subunit gamma
3 (CACNG3), mRNA.
ACCESSION NM_006539
VERSION NM_006539.4
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 1917)
AUTHORS Shan E, Cao YN, Zhang Y, Chen W, Ren X, Zhu S, Xi X, Mu S, Ma M,
Zhi T and Li X.
TITLE Integrated profiling identifies CACNG3 as a prognostic biomarker
for patients with glioma
JOURNAL BMC Cancer 23 (1), 846 (2023)
PUBMED 37697240
REMARK GeneRIF: Integrated profiling identifies CACNG3 as a prognostic
biomarker for patients with glioma.
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 1917)
AUTHORS Spencer KL, Olson LM, Schnetz-Boutaud N, Gallins P, Wang G, Scott
WK, Agarwal A, Jakobsdottir J, Conley Y, Weeks DE, Gorin MB,
Pericak-Vance MA and Haines JL.
TITLE Dissection of chromosome 16p12 linkage peak suggests a possible
role for CACNG3 variants in age-related macular degeneration
susceptibility
JOURNAL Invest Ophthalmol Vis Sci 52 (3), 1748-1754 (2011)
PUBMED 21169531
REMARK GeneRIF: These results suggest that CACNG3 is the best candidate
for an age-related macular degeneration risk gene within the 16p12
linkage peak.
Publication Status: Online-Only
REFERENCE 3 (bases 1 to 1917)
AUTHORS Kato AS, Gill MB, Yu H, Nisenbaum ES and Bredt DS.
TITLE TARPs differentially decorate AMPA receptors to specify
neuropharmacology
JOURNAL Trends Neurosci 33 (5), 241-248 (2010)
PUBMED 20219255
REMARK Review article
REFERENCE 4 (bases 1 to 1917)
AUTHORS Sager C, Tapken D, Kott S and Hollmann M.
TITLE Functional modulation of AMPA receptors by transmembrane AMPA
receptor regulatory proteins
JOURNAL Neuroscience 158 (1), 45-54 (2009)
PUBMED 18304745
REMARK Review article
REFERENCE 5 (bases 1 to 1917)
AUTHORS Everett KV, Chioza B, Aicardi J, Aschauer H, Brouwer O, Callenbach
P, Covanis A, Dulac O, Eeg-Olofsson O, Feucht M, Friis M, Goutieres
F, Guerrini R, Heils A, Kjeldsen M, Lehesjoki AE, Makoff A, Nabbout
R, Olsson I, Sander T, Siren A, McKeigue P, Robinson R, Taske N,
Rees M and Gardiner M.
TITLE Linkage and association analysis of CACNG3 in childhood absence
epilepsy
JOURNAL Eur J Hum Genet 15 (4), 463-472 (2007)
PUBMED 17264864
REMARK GeneRIF: CACNG3 on chromosome 16p12-p13.1 may represent
susceptibility loci for CAE.
GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
Erratum:[Eur J Hum Genet. 2008 May;16(5):659-60]
REFERENCE 6 (bases 1 to 1917)
AUTHORS Chen RS, Deng TC, Garcia T, Sellers ZM and Best PM.
TITLE Calcium channel gamma subunits: a functionally diverse protein
family
JOURNAL Cell Biochem Biophys 47 (2), 178-186 (2007)
PUBMED 17652770
REMARK Review article
REFERENCE 7 (bases 1 to 1917)
AUTHORS Moss FJ, Dolphin AC and Clare JJ.
TITLE Human neuronal stargazin-like proteins, gamma2, gamma3 and gamma4;
an investigation of their specific localization in human brain and
their influence on CaV2.1 voltage-dependent calcium channels
expressed in Xenopus oocytes
JOURNAL BMC Neurosci 4, 23 (2003)
PUBMED 14505496
REMARK GeneRIF: examined distribution of the stargazin-like proteins
gamma2, gamma3, and gamma4 in human CNS: gamma2 is expressed in
cerebellum, cerebral cortex, hippocampus and thalamus, whereas
gamma3 abounds in cerebral cortex & amygdala and gamma4 in basal
ganglia
Publication Status: Online-Only
REFERENCE 8 (bases 1 to 1917)
AUTHORS Burgess DL, Gefrides LA, Foreman PJ and Noebels JL.
TITLE A cluster of three novel Ca2+ channel gamma subunit genes on
chromosome 19q13.4: evolution and expression profile of the gamma
subunit gene family
JOURNAL Genomics 71 (3), 339-350 (2001)
PUBMED 11170751
REFERENCE 9 (bases 1 to 1917)
AUTHORS Burgess DL, Davis CF, Gefrides LA and Noebels JL.
TITLE Identification of three novel Ca(2+) channel gamma subunit genes
reveals molecular diversification by tandem and chromosome
duplication
JOURNAL Genome Res 9 (12), 1204-1213 (1999)
PUBMED 10613843
REFERENCE 10 (bases 1 to 1917)
AUTHORS Black JL 3rd and Lennon VA.
TITLE Identification and cloning of putative human neuronal voltage-gated
calcium channel gamma-2 and gamma-3 subunits: neurologic
implications
JOURNAL Mayo Clin Proc 74 (4), 357-361 (1999)
PUBMED 10221464
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AC004125.1.
On Aug 14, 2019 this sequence version replaced NM_006539.3.
Summary: The protein encoded by this gene is a type I transmembrane
AMPA receptor regulatory protein (TARP). TARPs regulate both
trafficking and channel gating of the AMPA receptors. This gene is
part of a functionally diverse eight-member protein subfamily of
the PMP-22/EMP/MP20 family. This gene is a susceptibility locus for
childhood absence epilepsy. [provided by RefSeq, Dec 2010].
Sequence Note: The RefSeq transcript and protein were derived from
genomic sequence to make the sequence consistent with the reference
genome assembly. The genomic coordinates used for the transcript
record were based on alignments.
##Evidence-Data-START##
Transcript exon combination :: AK095553.1, BC037899.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1968968, SAMEA2145743
[ECO:0000348]
##Evidence-Data-END##
##RefSeq-Attributes-START##
MANE Ensembl match :: ENST00000005284.4/ ENSP00000005284.4
RefSeq Select criteria :: based on single protein-coding transcript
##RefSeq-Attributes-END##
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-631 AC004125.1 11234-11864
632-715 AC004125.1 101633-101716
716-856 AC004125.1 109732-109872
857-1917 AC004125.1 116251-117311
FEATURES Location/Qualifiers
source 1..1917
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="16"
/map="16p12.1"
gene 1..1917
/gene="CACNG3"
/note="calcium voltage-gated channel auxiliary subunit
gamma 3"
/db_xref="GeneID:10368"
/db_xref="HGNC:HGNC:1407"
/db_xref="MIM:606403"
exon 1..631
/gene="CACNG3"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1898459909"
variation 2..8
/gene="CACNG3"
/replace="cac"
/replace="cactcac"
/db_xref="dbSNP:1348235491"
variation 3
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1307183796"
variation 4..6
/gene="CACNG3"
/replace="c"
/replace="ctc"
/db_xref="dbSNP:1898460039"
variation 4
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1898460012"
variation 5
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1055590789"
variation 6
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1410139833"
variation 8
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1372351835"
variation 10
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1898460152"
variation 12
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1383429149"
variation 15..18
/gene="CACNG3"
/replace="acct"
/replace="acctacct"
/db_xref="dbSNP:1332061773"
variation 15
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413801758"
variation 16
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295764275"
variation 17
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:750395139"
variation 23..25
/gene="CACNG3"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:534765159"
variation 33
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1471773726"
variation 34
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1411428792"
variation 37
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1183372834"
variation 43
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1898460605"
variation 45
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1484214214"
variation 47
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1224864205"
variation 48
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:116166933"
variation 50
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1278795059"
variation 61
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1898460769"
variation 65
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1224739881"
variation 66
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1326654840"
variation 67
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1287264724"
variation 68
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1898460850"
variation 75
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1228806885"
variation 77
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1898460898"
variation 78
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1021876391"
variation 79
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1898460956"
variation 82
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1596617069"
variation 88
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1898461017"
variation 90
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:995587941"
variation 91
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1898461092"
variation 96
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1898461129"
variation 98
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048017249"
variation 99
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:887040248"
variation 100
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1007735299"
variation 103
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1359669984"
variation 110
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:373928384"
variation 116
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1004054984"
variation 117
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1388211181"
variation 120
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2141341238"
variation 121
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:769681211"
variation 124
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1363567165"
variation 125
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1473678003"
variation 128..130
/gene="CACNG3"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:976304165"
variation 133
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1898461592"
variation 136
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:965224464"
variation 137
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1181635777"
variation 138
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1473413693"
variation 143
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1898461756"
variation 147
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1898461787"
variation 163
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1898461841"
variation 171
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1898461882"
variation 181
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1239665102"
variation 183
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:996629108"
variation 188
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1205038209"
variation 189
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1898462040"
variation 192
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1028374136"
variation 195..200
/gene="CACNG3"
/replace="cccccc"
/replace="cccccccc"
/db_xref="dbSNP:34370555"
variation 195
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1596617098"
variation 196
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1898462256"
variation 197
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:140890083"
variation 200
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1209014949"
variation 201..202
/gene="CACNG3"
/replace=""
/replace="t"
/db_xref="dbSNP:1898462556"
variation 201
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:149431324"
variation 203
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1420433178"
variation 204
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1898462646"
variation 210
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1596617106"
variation 211
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1898462721"
variation 218
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1898462756"
variation 222
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:913876107"
variation 226
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1898462851"
variation 229
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1898462889"
variation 230
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:762662582"
variation 234
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:909186417"
variation 235
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1567427191"
variation 236
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462315712"
variation 238
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1433030731"
variation 242
/gene="CACNG3"
/replace=""
/replace="c"
/db_xref="dbSNP:1898463178"
variation 244
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1898463220"
variation 245
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1321275670"
variation 247
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:554899263"
variation 251
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:928198502"
variation 266
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348652482"
variation 268
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:938194480"
variation 269
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1898463409"
variation 273
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406269144"
variation 274
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:990953303"
variation 277
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1187269602"
variation 285
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1898463533"
variation 287
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1449366303"
variation 288
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1898463586"
variation 290
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1898463611"
variation 291
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1246946691"
variation 295
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1188639422"
variation 296
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1898463705"
variation 304
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1898463742"
variation 307
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1898463768"
variation 308
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:2141341329"
variation 309
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1898463790"
variation 310
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1898463820"
variation 311
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:368009855"
variation 315..319
/gene="CACNG3"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1898463878"
variation 321
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:567328927"
variation 326
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:542929447"
variation 330
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1898464000"
variation 333
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1220586322"
variation 334
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:558770318"
variation 336
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:931052437"
variation 340
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1596617131"
variation 341
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1596617133"
variation 342
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:2141341348"
variation 344
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056338928"
variation 347
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1898464165"
variation 348
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:2141341351"
variation 350
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1898464182"
variation 355
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:892295887"
variation 360
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1898464264"
variation 361..364
/gene="CACNG3"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:945093162"
variation 361
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1596617140"
variation 362
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048546449"
variation 365
/gene="CACNG3"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1898464368"
variation 368
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298427625"
variation 370
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:757811826"
variation 371
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:773865647"
variation 372
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:765885399"
variation 374
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:368874081"
variation 376
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:754955162"
variation 378
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:371728578"
variation 380
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1432709473"
variation 381
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1307619737"
variation 382
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:755987658"
variation 383
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:778953751"
variation 386..391
/gene="CACNG3"
/replace="cc"
/replace="ccaacc"
/db_xref="dbSNP:1306534358"
variation 386
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1898464718"
variation 387
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:746132287"
variation 389
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:867380526"
variation 390
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1264868357"
variation 392
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2141341379"
variation 397
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1898464871"
variation 398
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:537810531"
variation 399
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:772222270"
variation 402
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775615485"
variation 408
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1898465058"
variation 409
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:901066179"
misc_feature 412..414
/gene="CACNG3"
/note="upstream in-frame stop codon"
variation 416
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1898465088"
variation 417
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:766905446"
CDS 421..1368
/gene="CACNG3"
/note="neuronal voltage-gated calcium channel gamma-3
subunit; voltage-gated calcium channel gamma subunit; TARP
gamma-3; transmembrane AMPAR regulatory protein gamma-3;
calcium channel, voltage-dependent, gamma subunit 3"
/codon_start=1
/product="voltage-dependent calcium channel gamma-3
subunit"
/protein_id="NP_006530.1"
/db_xref="CCDS:CCDS10620.1"
/db_xref="GeneID:10368"
/db_xref="HGNC:HGNC:1407"
/db_xref="MIM:606403"
/translation="
MRMCDRGIQMLITTVGAFAAFSLMTIAVGTDYWLYSRGVCRTKSTSDNETSRKNEEVMTHSGLWRTCCLEGAFRGVCKKIDHFPEDADYEQDTAEYLLRAVRASSVFPILSVTLLFFGGLCVAASEFHRSRHNVILSAGIFFVSAGLSNIIGIIVYISANAGDPGQRDSKKSYSYGWSFYFGAFSFIIAEIVGVVAVHIYIEKHQQLRAKSHSEFLKKSTFARLPPYRYRFRRRSSSRSTEPRSRDLSPISKGFHTIPSTDISMFTLSRDPSKITMGTLLNSDRDHAFLQFHNSTPKEFKESLHNNPANRRTTPV"
misc_feature 436..1008
/gene="CACNG3"
/note="PMP-22/EMP/MP20/Claudin family; Region:
PMP22_Claudin; cl21598"
/db_xref="CDD:451326"
misc_feature 442..504
/gene="CACNG3"
/note="propagated from UniProtKB/Swiss-Prot (O60359.1);
transmembrane region"
misc_feature 730..792
/gene="CACNG3"
/note="propagated from UniProtKB/Swiss-Prot (O60359.1);
transmembrane region"
misc_feature 823..885
/gene="CACNG3"
/note="propagated from UniProtKB/Swiss-Prot (O60359.1);
transmembrane region"
misc_feature 961..1023
/gene="CACNG3"
/note="propagated from UniProtKB/Swiss-Prot (O60359.1);
transmembrane region"
misc_feature 1162..1164
/gene="CACNG3"
/note="Phosphoserine.
/evidence=ECO:0000250|UniProtKB:Q8VHX0; propagated from
UniProtKB/Swiss-Prot (O60359.1); phosphorylation site"
variation 421..424
/gene="CACNG3"
/replace="a"
/replace="atga"
/db_xref="dbSNP:750619795"
variation 426
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:2141341387"
variation 428
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1274847303"
variation 431
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1898465252"
variation 435
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1483851744"
variation 443
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1198163064"
variation 444
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:777123441"
variation 445
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1898465371"
variation 447
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:762103543"
variation 456
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:267604475"
variation 462
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1229743004"
variation 465
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:773492815"
variation 467
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:866765368"
variation 468
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1898465575"
variation 469
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1239763846"
variation 471
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1448024134"
variation 477
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762648569"
variation 478
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:751113122"
variation 480
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1431873407"
variation 498
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:996640577"
variation 504
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1028134002"
variation 507
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:754541329"
variation 510
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:767505349"
variation 513
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1567427282"
variation 520
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:752705408"
variation 522
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:755825355"
variation 523
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:777593685"
variation 530
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1898466061"
variation 536
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749083879"
variation 540
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1898466138"
variation 543
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1898466170"
variation 551
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:2141341427"
variation 553
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1434033989"
variation 554
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1298070750"
variation 557
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1371741316"
variation 558
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1898466304"
variation 560
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:147926451"
variation 561
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1464957594"
variation 565
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:868820485"
variation 573
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:758631203"
variation 576
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1230597836"
variation 579
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1596617244"
variation 582
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1898466559"
variation 589
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:566211427"
variation 592
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:866644527"
variation 598
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1898466654"
variation 600
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174731147"
variation 603
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1345072047"
variation 606
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1480562008"
variation 607
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:747021432"
variation 609
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:140223850"
variation 618
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:145675691"
variation 624
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:748626516"
exon 632..715
/gene="CACNG3"
/inference="alignment:Splign:2.1.0"
variation 633
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1388912149"
variation 641
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:375344869"
variation 645
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:140855664"
variation 646
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:150135113"
variation 651
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1319282167"
variation 652
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:111513623"
variation 654
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1219735535"
variation 660
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:765043632"
variation 661
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:750272065"
variation 663
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1225005945"
variation 664
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:755183039"
variation 665
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1482757532"
variation 669
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:781463498"
variation 672
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:752757837"
variation 679
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:756163536"
variation 681
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1164065959"
variation 687
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:368528326"
variation 688
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1426360236"
variation 700
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:749791046"
variation 701
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1369579426"
variation 702
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409857130"
variation 705
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:2141380040"
variation 708
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309317022"
variation 709
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771606027"
variation 711
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:779398247"
variation 715
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:200755015"
exon 716..856
/gene="CACNG3"
/inference="alignment:Splign:2.1.0"
variation 720
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1053482308"
variation 721
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1477040658"
variation 725
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187876902"
variation 726
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1185490798"
variation 727
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1596653663"
variation 730
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:775995807"
variation 731
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413362855"
variation 738
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:961765037"
variation 741
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176196941"
variation 744
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:892125561"
variation 745
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1281630768"
variation 755
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:747764888"
variation 758
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:769655076"
variation 759
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773149814"
variation 763
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1283447933"
variation 765
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1364878465"
variation 771
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:774241889"
variation 772
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1369935056"
variation 774
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:546224102"
variation 781
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1596653683"
variation 783
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:559474382"
variation 784
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:199880368"
variation 785
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:2141383796"
variation 786
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302084805"
variation 787
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1596653695"
variation 788
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:529886705"
variation 790
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002009149"
variation 794
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1900007912"
variation 799
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1596653700"
variation 802
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900007997"
variation 803
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1596653703"
variation 804
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:2141383806"
variation 805
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1325822639"
variation 806
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:573392964"
variation 809
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900008153"
variation 810
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:758792364"
variation 814
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:780246762"
variation 816
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1217709737"
variation 818
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:747446701"
variation 819
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:147734423"
variation 820
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:780905732"
variation 821
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900008472"
variation 828
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1033444195"
variation 831
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:376566755"
variation 834
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430773509"
variation 838
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471345416"
variation 846
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1027866883"
variation 847
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1157555773"
variation 849
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900008771"
variation 850
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1410411220"
variation 852
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1388573108"
variation 854
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:769318826"
exon 857..1917
/gene="CACNG3"
/inference="alignment:Splign:2.1.0"
variation 857
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:868528231"
variation 858
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1299449747"
variation 870
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1403535923"
variation 873
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:946560806"
variation 875
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:776950399"
variation 888
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:762094078"
variation 900
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:770185514"
variation 901
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:140935639"
variation 903
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:371160374"
variation 904
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:766742794"
variation 907
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1164646213"
variation 909
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387243846"
variation 911
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900100317"
variation 912
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:531052899"
variation 913
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1168264667"
variation 915
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:950931829"
variation 919
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1488719446"
variation 920
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:150191653"
variation 927
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900100553"
variation 933
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:2141386828"
variation 934
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1411770090"
variation 939
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900100625"
variation 942
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1337356324"
variation 945
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900100712"
variation 953
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:867945636"
variation 954
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:767894450"
variation 957
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200040220"
variation 963
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201012526"
variation 972
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:988067948"
variation 978
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:865859398"
variation 979
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:753277538"
variation 982
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:779898573"
variation 984
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:867799411"
variation 987
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1362836342"
variation 988
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:2141386845"
variation 996
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:756804068"
variation 999
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:778665342"
variation 1000
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:2141386849"
variation 1002
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1340836313"
variation 1003
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:2141386854"
variation 1007
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:753398983"
variation 1008
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201337869"
variation 1009
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:771940327"
variation 1011
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:779968177"
variation 1017
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:746855116"
variation 1029
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:975194427"
variation 1030
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1448123792"
variation 1038
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900101464"
variation 1040
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1188135007"
variation 1043
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:770078893"
variation 1045
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1463552275"
variation 1046
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773586046"
variation 1049
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:771077901"
variation 1051
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277908363"
variation 1052
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:868272395"
variation 1053
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2141386889"
variation 1055
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:774336588"
variation 1056
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1340673025"
variation 1057
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1567227757"
variation 1059
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760067657"
variation 1070
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386142845"
variation 1074
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:2141386900"
variation 1078
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1348787142"
variation 1086
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:2141386904"
variation 1088
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775829243"
variation 1091
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:761031745"
variation 1092
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900101996"
variation 1093
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:763678715"
variation 1094
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1900102054"
variation 1095
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:753508977"
variation 1097
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1900102119"
variation 1098
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1324184575"
variation 1102
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1273746959"
variation 1104
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:2141386914"
variation 1108
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900102240"
variation 1109
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:756680276"
variation 1114
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1204864111"
variation 1115
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265586977"
variation 1116
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1900102388"
variation 1118
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:2141386925"
variation 1119
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463808401"
variation 1120
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:764770670"
variation 1121
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:749946987"
variation 1122
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1900102526"
variation 1123
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:758340002"
variation 1125
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:780204835"
variation 1130
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428678422"
variation 1132
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1900102685"
variation 1133
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:746746638"
variation 1134
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:920972250"
variation 1136
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409691606"
variation 1137
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1567227797"
variation 1138
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1189692879"
variation 1140
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:192667852"
variation 1141
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:771108279"
variation 1143
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:774476683"
variation 1150
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1900103104"
variation 1151
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:867196696"
variation 1154
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:746004181"
variation 1161
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:2049947949"
variation 1164
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772502664"
variation 1165
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:760977685"
variation 1170
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:148951012"
variation 1176
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285699316"
variation 1178
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1224456416"
variation 1179
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:369770246"
variation 1185
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:761500512"
variation 1188
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1261662568"
variation 1191
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:144805488"
variation 1198
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1596655633"
variation 1199..1201
/gene="CACNG3"
/replace="ctg"
/replace="ctgctg"
/db_xref="dbSNP:1900103578"
variation 1200
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1184663295"
variation 1208
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1320428854"
variation 1209
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:749942057"
variation 1218
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900103729"
variation 1219
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268507884"
variation 1220
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1490519733"
variation 1221
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:535955331"
variation 1222
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1201725642"
variation 1224
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1027898569"
variation 1225
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:757999426"
variation 1226
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:766372843"
variation 1228
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1159817893"
variation 1229
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1365323329"
variation 1237
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900104167"
variation 1238
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900104209"
variation 1239
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:751583718"
variation 1242
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1475402829"
variation 1243
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274887564"
variation 1246
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:887982558"
variation 1247
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:2141387009"
variation 1250
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1417412443"
variation 1251
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:755010085"
variation 1252
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1365835395"
variation 1253
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1900104551"
variation 1254
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:2141387023"
variation 1257
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:781113189"
variation 1258
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1305652725"
variation 1260
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:747952124"
variation 1262
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900104687"
variation 1263
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900104727"
variation 1264
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1391312147"
variation 1266
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:757499213"
variation 1267
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:779008969"
variation 1269
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900104945"
variation 1270
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:555623613"
variation 1271
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1291260230"
variation 1278
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:754621466"
variation 1279
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900105202"
variation 1280
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1224741138"
variation 1281
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1249697064"
variation 1282
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1900105356"
variation 1284
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174281245"
variation 1286
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:906360580"
variation 1287
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201697296"
variation 1289
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:780499242"
variation 1291
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1414072446"
variation 1293
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900105698"
variation 1297
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1177685887"
variation 1298
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:747483476"
variation 1302
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2141387046"
variation 1306
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:937809173"
variation 1308
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1421786069"
variation 1314
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1192925451"
variation 1317
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:769196310"
variation 1324
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777036867"
variation 1326
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1426146208"
variation 1327
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1166396730"
variation 1328
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1567227891"
variation 1329
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1353381063"
variation 1331
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462094142"
variation 1340
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762148926"
variation 1341
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:12928078"
variation 1342
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:765960030"
variation 1347
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:751166724"
variation 1350
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:899225129"
variation 1351
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1248441351"
variation 1352
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1272807643"
variation 1354
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:759533995"
variation 1355
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:767420584"
variation 1358
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2141387091"
variation 1359
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:971445303"
variation 1360
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482242077"
variation 1362
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:201263434"
variation 1363
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1047741779"
variation 1365
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:779145467"
variation 1366
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:183390886"
variation 1370..1386
/gene="CACNG3"
/replace="ctgacctctg"
/replace="ctgacctctgacctctg"
/replace="ctgacctctgacctctgacctctg"
/db_xref="dbSNP:751696916"
variation 1371
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:956009086"
variation 1374
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:750673689"
variation 1375
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1900107450"
variation 1378
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1567227932"
variation 1383
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:758658928"
variation 1385
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1356730695"
variation 1387..1390
/gene="CACNG3"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1900107631"
variation 1387
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:111975365"
variation 1388..1389
/gene="CACNG3"
/replace=""
/replace="tt"
/db_xref="dbSNP:1900107658"
variation 1392
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:368106492"
variation 1393
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:781552218"
variation 1394..1396
/gene="CACNG3"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1567227943"
variation 1396
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1019578291"
variation 1398
/gene="CACNG3"
/replace=""
/replace="g"
/db_xref="dbSNP:1447400952"
variation 1399
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:748499141"
variation 1401
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:770088454"
variation 1402
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773670781"
variation 1403
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1900108005"
variation 1405
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:371528746"
variation 1408..1412
/gene="CACNG3"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1567227954"
variation 1409
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1215175969"
variation 1410
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:770765848"
variation 1411
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1310581603"
variation 1412
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773994251"
variation 1413
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900108230"
variation 1414
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:759124153"
variation 1416
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1462448444"
variation 1421
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1159811342"
variation 1424
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1442046761"
variation 1428
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1900108323"
variation 1431
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1900108354"
variation 1432
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1900108381"
variation 1440
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1900108406"
variation 1444
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1254516594"
variation 1449
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900108459"
variation 1450
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1028040545"
variation 1451
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1483778283"
variation 1453
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1900108553"
variation 1455
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1237764953"
variation 1463
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:576740603"
variation 1467
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900108651"
variation 1475
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900108674"
variation 1479..1492
/gene="CACNG3"
/replace="aatg"
/replace="aatgaaaccaaatg"
/db_xref="dbSNP:1900108698"
variation 1480
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1350931056"
variation 1483
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1381140644"
variation 1491
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1240823891"
variation 1495
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318578980"
variation 1499
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:928985762"
variation 1503
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900108835"
variation 1507
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1227590165"
variation 1512
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1379616575"
variation 1516
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1304848603"
variation 1520
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1398357016"
variation 1522
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1003003393"
variation 1526
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360018699"
variation 1532
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900109051"
variation 1537
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1031853771"
variation 1538
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:957771807"
variation 1539
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1900109150"
variation 1542
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1596655817"
variation 1543
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1900109203"
variation 1546
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1900109219"
variation 1547..1548
/gene="CACNG3"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1367294034"
variation 1547
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1049781286"
variation 1548
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1900109371"
variation 1557..1560
/gene="CACNG3"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1157088001"
variation 1557
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1596655820"
variation 1562
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416385316"
variation 1565
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1900109493"
variation 1567
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:545662251"
variation 1568
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1900109580"
variation 1569
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1487079626"
variation 1570
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1396993096"
variation 1571
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261836993"
variation 1572
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:989132395"
variation 1573..1574
/gene="CACNG3"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:61695823"
variation 1575..1576
/gene="CACNG3"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:397955591"
variation 1577
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:913569599"
variation 1578
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900109903"
variation 1582
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1044562012"
variation 1585
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1294860612"
variation 1588
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1900110005"
variation 1589
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:751893103"
variation 1590
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:907349631"
variation 1592
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1340054884"
variation 1598
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900110157"
variation 1600
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1279064223"
variation 1601
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402002781"
variation 1602
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1596655842"
variation 1603
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900110238"
variation 1609..1611
/gene="CACNG3"
/replace="tgt"
/replace="tgtgt"
/db_xref="dbSNP:1900110295"
variation 1609
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1388635424"
variation 1610
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002990151"
variation 1617
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2141387228"
variation 1618
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1448343228"
variation 1623
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900110382"
variation 1624
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900110405"
variation 1630
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1031754641"
variation 1632
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1168893909"
variation 1635
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:967066159"
variation 1640
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900110550"
variation 1645
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900110569"
variation 1648
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1900110595"
variation 1650
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900110637"
variation 1653
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:374427047"
variation 1655
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011539526"
variation 1659
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900110734"
variation 1662
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1022643094"
variation 1663
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1429817100"
variation 1666
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:553122217"
variation 1667
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1264624348"
variation 1668
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1209188252"
variation 1682
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488729844"
variation 1686
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274828736"
variation 1688
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1257424817"
variation 1689
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1335833664"
variation 1690
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1900111032"
variation 1692
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345428130"
variation 1695
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900111091"
variation 1696
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900111117"
variation 1698
/gene="CACNG3"
/replace=""
/replace="a"
/db_xref="dbSNP:753035318"
variation 1698
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:986388423"
variation 1699..1704
/gene="CACNG3"
/replace="gggggg"
/replace="ggggggg"
/db_xref="dbSNP:1900111203"
variation 1700
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1253993685"
variation 1701
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900111234"
variation 1703
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:28671632"
variation 1704
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:975843066"
variation 1705
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900111400"
variation 1708
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:918967301"
variation 1710
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:747640437"
variation 1711
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:572464415"
variation 1712
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:2141387270"
variation 1713
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:757796494"
variation 1715..1727
/gene="CACNG3"
/replace="ctccatcaggcgc"
/replace="ctccatcaggcgctccatcaggcgc"
/db_xref="dbSNP:1900111498"
variation 1716
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1900111537"
variation 1719
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:574546623"
variation 1720
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1463152735"
variation 1724
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1238803434"
variation 1725
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:541800330"
variation 1726
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:137859960"
variation 1727
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772576542"
variation 1728
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:558375077"
variation 1729
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2141387293"
variation 1733
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176673057"
variation 1734
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900111816"
variation 1736..1749
/gene="CACNG3"
/replace="ttgtc"
/replace="ttgtccccattgtc"
/db_xref="dbSNP:1900111850"
variation 1739
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1457195167"
variation 1740
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1044658167"
variation 1741
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:920699611"
variation 1743
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1197811919"
variation 1745
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900111977"
variation 1748
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900112003"
variation 1749
/gene="CACNG3"
/replace="c"
/replace="cc"
/db_xref="dbSNP:755123705"
variation 1754
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:930711506"
variation 1756
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900112072"
variation 1757
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1343051858"
variation 1758
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2141387304"
variation 1761
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1900112128"
variation 1768
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900112154"
variation 1779
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1255500305"
variation 1781
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1379636110"
variation 1782
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:750539338"
variation 1784
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1596655919"
variation 1785
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1596655921"
variation 1787
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1900112321"
variation 1788
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1466844298"
variation 1791
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307766018"
variation 1793
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900112404"
variation 1799
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:550909998"
variation 1802
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1003041183"
variation 1804
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:778249741"
variation 1805
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1900112534"
variation 1806
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900112564"
variation 1807
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1172423997"
variation 1809
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900112629"
variation 1810
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043774"
variation 1811
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1053197640"
variation 1816
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1596655942"
variation 1817
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1900112742"
variation 1819
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:891845484"
variation 1821
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1012006224"
variation 1824..1828
/gene="CACNG3"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:1171635980"
variation 1826
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:142339736"
variation 1839
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900112878"
variation 1840
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1466141128"
variation 1848
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396343841"
variation 1849
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1009271740"
variation 1851
/gene="CACNG3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1467590540"
variation 1854
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1156804352"
variation 1855
/gene="CACNG3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1900112994"
variation 1856
/gene="CACNG3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900113030"
variation 1858
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1021604057"
variation 1859
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:186790670"
variation 1860
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:533673027"
variation 1866
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:996386853"
variation 1871
/gene="CACNG3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1900113157"
variation 1874
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:547275500"
variation 1879
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1596655959"
variation 1880
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2141387350"
variation 1887
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201218582"
variation 1888..1889
/gene="CACNG3"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1900113292"
regulatory 1890..1895
/regulatory_class="polyA_signal_sequence"
/gene="CACNG3"
/note="hexamer: ATTAAA"
variation 1895
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1900113316"
variation 1898
/gene="CACNG3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1900113343"
variation 1902
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1486722844"
variation 1903
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1900113400"
variation 1907..1911
/gene="CACNG3"
/replace="gt"
/replace="gtcgt"
/db_xref="dbSNP:1283910347"
variation 1908
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302916178"
variation 1909
/gene="CACNG3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:957824158"
variation 1910
/gene="CACNG3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1745772984"
variation 1914
/gene="CACNG3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1281771032"
variation 1915
/gene="CACNG3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243157869"
polyA_site 1917
/gene="CACNG3"
/note="major polyA site"
ORIGIN
acactcacacagagacctctctgggtttctttgccttgagtctcccggggctgtgagaagccaggcgcatctcaaaccgagctggcagctccaggctccggagccatgccctgcacggaccctcgtctttaccacgctcctgaggaatgaaaggaacccagggaccctcagaaggcagcagtgatgcggaccaaccccccggagcctgcacccttccgagggccataggcgacccagggaactggagagagctccagaaaggaaatcccagctttcccaaagtccctgtggatgctgacaaaaggagacctgaatttttggaagagcctgtactaggttacccggctgcagagtgattttcccctccggcactgactctccccctccaacccccagccgtccagagtaccatgaagaattatgaggatgtgtgacagaggtatccagatgttgatcaccactgtaggagcctttgccgcttttagtttaatgaccattgcagtgggcacggactactggttatattccagaggtgtgtgcaggactaaatctacaagtgataatgaaaccagcaggaagaatgaagaagtaatgacccattcggggctgtggaggacctgctgcctagaaggggctttccgaggcgtgtgcaagaaaatcgatcacttccctgaagatgctgactacgaacaggacacagccgaatatctcctgcgagctgtgagggcctccagtgtcttccccatcctcagtgtcacgctgctgttcttcggcgggctctgcgtggcagccagtgagttccaccgcagcagacacaacgtcattctcagcgcgggcatcttttttgtctctgcagggttaagcaacatcattggcatcatagtttatatatcagccaacgccggagaccccgggcagcgtgactccaaaaaaagttactcctatggttggtccttttatttcggagccttctctttcatcatcgcagaaattgtaggagtggttgccgtgcacatctatattgaaaaacatcagcagttacgagccaaatcccactcggagttcctgaagaaatctacttttgcccgcctcccaccctacaggtatcgattccggaggcggtcaagttctcgctccaccgagcccagatcccgagacctgtcccccatcagcaaaggcttccacaccatcccttccactgacatctcgatgttcaccctctcccgggacccctcaaagatcaccatggggaccctcctcaactccgaccgggaccacgcttttctacagttccacaattccacacccaaagagttcaaagagtcactgcataataatccggccaacaggcgcaccacgcccgtctgaactgacctctgacctctgccccacgcccagcacagccttgggggaagtgtacagagatgtctctgaggttgcatggcatggtccttgtgatggtattactttttacaaagaatgaaaccaaatggactcagccctctcccacattttcccctcaccctccaagtcctaacccctccatcctctctaacttttcaagccaatcccttaatgtcattcctctctctgtgtatctgtgccagatgttttcctttcttccttctttactggaaggacctccacattcttccctccttggaagaggactttactaaaagtcacaggtggtggccaggggggatttccgaatctccatcaggcgcgctcatagttgtccccattgtctacccacacaaatcctcaggaaaccaaccaccgcccaggtggccctgagggaggcattcacctttatgtgttagaaaaacatgaccagaaatcaaagatgtcagagccccgaagcagctaatgtaataagcactcatgttattaaaggttttgccttgtcgtaaccaa
//
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]