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Previous release (v1)
2025-07-16 02:35:09, GGRNA.v2 : RefSeq release 229 (Mar, 2025)
LOCUS NM_005125 1066 bp mRNA linear PRI 19-SEP-2024
DEFINITION Homo sapiens copper chaperone for superoxide dismutase (CCS), mRNA.
ACCESSION NM_005125 XM_938909
VERSION NM_005125.2
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 1066)
AUTHORS Yang,Y., Hao,X., Zhang,J., Gao,T., Huo,M., Liu,W., Hu,T., Ma,T.,
Yuan,B., Zhang,M., Teng,X., Yu,H., Huang,W. and Wang,Y.
TITLE The E3 ligase TRIM22 functions as a tumor suppressor in breast
cancer by targeting CCS for proteasomal degradation to inhibit
STAT3 signaling
JOURNAL Cancer Lett 600, 217157 (2024)
PUBMED 39127340
REMARK GeneRIF: The E3 ligase TRIM22 functions as a tumor suppressor in
breast cancer by targeting CCS for proteasomal degradation to
inhibit STAT3 signaling.
REFERENCE 2 (bases 1 to 1066)
AUTHORS Lu,Y., Chan,Y.T., Wu,J., Feng,Z., Yuan,H., Li,Q., Xing,T., Xu,L.,
Zhang,C., Tan,H.Y., Lee,T.K., Feng,Y. and Wang,N.
TITLE CRISPR/Cas9 screens unravel miR-3689a-3p regulating sorafenib
resistance in hepatocellular carcinoma via suppressing
CCS/SOD1-dependent mitochondrial oxidative stress
JOURNAL Drug Resist Updat 71, 101015 (2023)
PUBMED 37924725
REMARK GeneRIF: CRISPR/Cas9 screens unravel miR-3689a-3p regulating
sorafenib resistance in hepatocellular carcinoma via suppressing
CCS/SOD1-dependent mitochondrial oxidative stress.
REFERENCE 3 (bases 1 to 1066)
AUTHORS Morgenstern,M., Peikert,C.D., Lubbert,P., Suppanz,I., Klemm,C.,
Alka,O., Steiert,C., Naumenko,N., Schendzielorz,A., Melchionda,L.,
Muhlhauser,W.W.D., Knapp,B., Busch,J.D., Stiller,S.B.,
Dannenmaier,S., Lindau,C., Licheva,M., Eickhorst,C., Galbusera,R.,
Zerbes,R.M., Ryan,M.T., Kraft,C., Kozjak-Pavlovic,V., Drepper,F.,
Dennerlein,S., Oeljeklaus,S., Pfanner,N., Wiedemann,N. and
Warscheid,B.
TITLE Quantitative high-confidence human mitochondrial proteome and its
dynamics in cellular context
JOURNAL Cell Metab 33 (12), 2464-2483 (2021)
PUBMED 34800366
REFERENCE 4 (bases 1 to 1066)
AUTHORS Grasso,M., Bond,G.J., Kim,Y.J., Boyd,S., Matson Dzebo,M.,
Valenzuela,S., Tsang,T., Schibrowsky,N.A., Alwan,K.B.,
Blackburn,N.J., Burslem,G.M., Wittung-Stafshede,P., Winkler,D.D.,
Marmorstein,R. and Brady,D.C.
TITLE The copper chaperone CCS facilitates copper binding to MEK1/2 to
promote kinase activation
JOURNAL J Biol Chem 297 (6), 101314 (2021)
PUBMED 34715128
REMARK GeneRIF: The copper chaperone CCS facilitates copper binding to
MEK1/2 to promote kinase activation.
REFERENCE 5 (bases 1 to 1066)
AUTHORS Huttlin,E.L., Bruckner,R.J., Navarrete-Perea,J., Cannon,J.R.,
Baltier,K., Gebreab,F., Gygi,M.P., Thornock,A., Zarraga,G., Tam,S.,
Szpyt,J., Gassaway,B.M., Panov,A., Parzen,H., Fu,S., Golbazi,A.,
Maenpaa,E., Stricker,K., Guha Thakurta,S., Zhang,T., Rad,R.,
Pan,J., Nusinow,D.P., Paulo,J.A., Schweppe,D.K., Vaites,L.P.,
Harper,J.W. and Gygi,S.P.
TITLE Dual proteome-scale networks reveal cell-specific remodeling of the
human interactome
JOURNAL Cell 184 (11), 3022-3040 (2021)
PUBMED 33961781
REFERENCE 6 (bases 1 to 1066)
AUTHORS Lamb,A.L., Wernimont,A.K., Pufahl,R.A., O'Halloran,T.V. and
Rosenzweig,A.C.
TITLE Crystal structure of the second domain of the human copper
chaperone for superoxide dismutase
JOURNAL Biochemistry 39 (7), 1589-1595 (2000)
PUBMED 10677207
REFERENCE 7 (bases 1 to 1066)
AUTHORS Rae,T.D., Schmidt,P.J., Pufahl,R.A., Culotta,V.C. and
O'Halloran,T.V.
TITLE Undetectable intracellular free copper: the requirement of a copper
chaperone for superoxide dismutase
JOURNAL Science 284 (5415), 805-808 (1999)
PUBMED 10221913
REFERENCE 8 (bases 1 to 1066)
AUTHORS Rothstein,J.D., Dykes-Hoberg,M., Corson,L.B., Becker,M.,
Cleveland,D.W., Price,D.L., Culotta,V.C. and Wong,P.C.
TITLE The copper chaperone CCS is abundant in neurons and astrocytes in
human and rodent brain
JOURNAL J Neurochem 72 (1), 422-429 (1999)
PUBMED 9886096
REFERENCE 9 (bases 1 to 1066)
AUTHORS Casareno,R.L., Waggoner,D. and Gitlin,J.D.
TITLE The copper chaperone CCS directly interacts with copper/zinc
superoxide dismutase
JOURNAL J Biol Chem 273 (37), 23625-23628 (1998)
PUBMED 9726962
REFERENCE 10 (bases 1 to 1066)
AUTHORS Culotta,V.C., Klomp,L.W., Strain,J., Casareno,R.L., Krems,B. and
Gitlin,J.D.
TITLE The copper chaperone for superoxide dismutase
JOURNAL J Biol Chem 272 (38), 23469-23472 (1997)
PUBMED 9295278
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AP001157.4 and AF002210.1.
This sequence is a reference standard in the RefSeqGene project.
On Nov 22, 2018 this sequence version replaced NM_005125.1.
Summary: Copper chaperone for superoxide dismutase specifically
delivers Cu to copper/zinc superoxide dismutase and may activate
copper/zinc superoxide dismutase through direct insertion of the Cu
cofactor. [provided by RefSeq, Jul 2008].
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 :: SRR1163655.638477.1,
SRR1163655.337609.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1965299, SAMEA1966682
[ECO:0000348]
##Evidence-Data-END##
##RefSeq-Attributes-START##
MANE Ensembl match :: ENST00000533244.6/ ENSP00000436318.1
RefSeq Select criteria :: based on single protein-coding transcript
##RefSeq-Attributes-END##
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-34 AP001157.4 12289-12322
35-1066 AF002210.1 1-1032
FEATURES Location/Qualifiers
source 1..1066
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="11"
/map="11q13.2"
gene 1..1066
/gene="CCS"
/note="copper chaperone for superoxide dismutase"
/db_xref="GeneID:9973"
/db_xref="HGNC:HGNC:1613"
/db_xref="MIM:603864"
exon 1..116
/gene="CCS"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1858409449"
variation 3..32
/gene="CCS"
/replace="tccccgcgacgccgcgctggttggtgctcc"
/replace="tccccgcgacgccgcgctggttggtgctccccgcgacgccgcgctggt
tggtgctcc"
/db_xref="dbSNP:1858409543"
variation 3
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:1858409490"
variation 4
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:896047999"
variation 5
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:529841224"
variation 6
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:950332829"
variation 7
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858409769"
variation 9
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495328904"
variation 10
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1044682980"
variation 11
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495328917"
variation 12
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489745811"
variation 13
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:757854559"
variation 14
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858409989"
variation 15
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:376005966"
variation 17
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1333093133"
variation 18
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:112782649"
variation 20
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495328975"
variation 21
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:550245855"
variation 22
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1858410696"
variation 23
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:1858410750"
variation 24
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1317376720"
variation 25
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1293522486"
variation 26
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495329009"
variation 27
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495329012"
variation 28
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772007611"
variation 29
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495329030"
variation 30
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495329039"
variation 31
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:759603666"
variation 32
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:752579107"
variation 33
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1251401041"
variation 34
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:148810781"
variation 35
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2134976114"
variation 37..38
/gene="CCS"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1858411342"
variation 37
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:763826407"
variation 38
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751129288"
variation 39..45
/gene="CCS"
/replace="ggag"
/replace="ggaggag"
/db_xref="dbSNP:1858411491"
variation 39
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1858411436"
variation 40
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1477900898"
variation 41
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1169053556"
variation 43
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1019175597"
variation 45
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495329127"
variation 48
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:111984469"
variation 49
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1858411773"
variation 50
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:780512810"
variation 51
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1306834296"
variation 52
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:532915835"
variation 54
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1858412038"
variation 55
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:369185929"
variation 56
/gene="CCS"
/replace=""
/replace="c"
/db_xref="dbSNP:1193502346"
variation 56
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406335589"
variation 57
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:373408934"
variation 58
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1330371783"
variation 59
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495329169"
variation 60
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1028948765"
variation 61
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590826774"
variation 62
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1271907455"
variation 63
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495329202"
variation 64
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1339927313"
variation 66
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1226303520"
variation 67
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495329219"
variation 68..69
/gene="CCS"
/replace=""
/replace="tg"
/db_xref="dbSNP:2495329222"
variation 69
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495329225"
variation 70
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495329228"
variation 71
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:377577328"
variation 72
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858412682"
variation 75
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:75550902"
variation 76
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495329254"
variation 77
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495329258"
CDS 78..902
/gene="CCS"
/note="superoxide dismutase copper chaperone"
/codon_start=1
/product="copper chaperone for superoxide dismutase"
/protein_id="NP_005116.1"
/db_xref="CCDS:CCDS8146.1"
/db_xref="GeneID:9973"
/db_xref="HGNC:HGNC:1613"
/db_xref="MIM:603864"
/translation="
MASDSGNQGTLCTLEFAVQMTCQSCVDAVRKSLQGVAGVQDVEVHLEDQMVLVHTTLPSQEVQALLEGTGRQAVLKGMGSGQLQNLGAAVAILGGPGTVQGVVRFLQLTPERCLIEGTIDGLEPGLHGLHVHQYGDLTNNCNSCGNHFNPDGASHGGPQDSDRHRGDLGNVRADADGRAIFRMEDEQLKVWDVIGRSLIIDEGEDDLGRGGHPLSKITGNSGERLACGIIARSAGLFQNPKQICSCDGLTIWEERGRPIAGKGRKESAQPPAHL"
misc_feature 117..836
/gene="CCS"
/note="copper, zinc superoxide dismutase; Region:
PLN02957"
/db_xref="CDD:215516"
misc_feature 339..779
/gene="CCS"
/note="propagated from UniProtKB/Swiss-Prot (O14618.1);
Region: Superoxide dismutase-like"
misc_feature 876..878
/gene="CCS"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:24275569; propagated from
UniProtKB/Swiss-Prot (O14618.1); phosphorylation site"
variation 78
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:978740750"
variation 79
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1225082492"
variation 80
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:866521646"
variation 81
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2134976193"
variation 82
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1265517169"
variation 85
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1451439150"
variation 87
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495329285"
variation 89
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495329293"
variation 90
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:2495329297"
variation 91
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:868824969"
variation 92..95
/gene="CCS"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:2495329318"
variation 92
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1244368874"
variation 94
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1448156238"
variation 97
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495329335"
variation 98..99
/gene="CCS"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1167431997"
variation 98
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495329336"
variation 100
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495329345"
variation 101
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1858413398"
variation 103
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1385243784"
variation 104
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:1425999785"
variation 105
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:199967551"
variation 106
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1389539698"
variation 108
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858413670"
variation 109
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:1858413736"
variation 110
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779228954"
variation 112
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1319985135"
variation 115
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:534912458"
variation 116
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:772323037"
exon 117..189
/gene="CCS"
/inference="alignment:Splign:2.1.0"
variation 118
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495330412"
variation 120
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:771093151"
variation 121
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:775571378"
variation 123
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495330423"
variation 124..125
/gene="CCS"
/replace=""
/replace="g"
/db_xref="dbSNP:772522566"
variation 125..126
/gene="CCS"
/replace=""
/replace="aactt"
/db_xref="dbSNP:773421206"
variation 125
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749120332"
variation 126
/gene="CCS"
/replace=""
/replace="g"
/db_xref="dbSNP:2495330451"
variation 126
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495330445"
variation 127
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495330455"
variation 128
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495330464"
variation 131
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1590827056"
variation 132
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495330474"
variation 134
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495330480"
variation 139
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495330485"
variation 140
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:959133362"
variation 143
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495330495"
variation 144
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1290499608"
variation 145..148
/gene="CCS"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:2495330501"
variation 145
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858422519"
variation 148
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1348825349"
variation 150..155
/gene="CCS"
/replace="tgtgtg"
/replace="tgtgtgtg"
/db_xref="dbSNP:2495330507"
variation 151
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:1228198720"
variation 152
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284262232"
variation 153
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495330524"
variation 155
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:768626429"
variation 156
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1319398432"
variation 157
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:774081476"
variation 158
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:543925670"
variation 159
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:767210418"
variation 160
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:113810834"
variation 161
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:563806954"
variation 162
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495330561"
variation 163
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495330567"
variation 165
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1430719934"
variation 166
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:760212307"
variation 167
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495330581"
variation 170
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495330587"
variation 172
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495330592"
variation 173
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:967951335"
variation 174
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495330609"
variation 176
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495330615"
variation 179
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:765810923"
variation 180
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:377031211"
variation 183
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495330629"
variation 184
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753372996"
variation 186
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:755501132"
variation 187
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1555064224"
variation 188
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:765740277"
variation 189
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1462599106"
exon 190..327
/gene="CCS"
/inference="alignment:Splign:2.1.0"
variation 191
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:919963984"
variation 194
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495341187"
variation 196
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:753207517"
variation 197
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495341199"
variation 198
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758837178"
variation 200
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2134981511"
variation 201
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495341210"
variation 203
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858528827"
variation 204
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:375013920"
variation 208
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590829557"
variation 210
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495341231"
variation 213
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:376196971"
variation 214
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495341237"
variation 215
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858529056"
variation 216
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1261036540"
variation 217
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:2495341254"
variation 219
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1391233822"
variation 220
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:751957472"
variation 222
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495341264"
variation 223
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186656903"
variation 224
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495341274"
variation 225
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:757621525"
variation 227
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495341288"
variation 233
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1448977810"
variation 236
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:572549240"
variation 239
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858529598"
variation 240
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495341306"
variation 241
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:931376573"
variation 244
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:756170953"
variation 245
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:778751146"
variation 248
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:771870101"
variation 250
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495341335"
variation 252
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:777609216"
variation 254
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858529924"
variation 256
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:1858530088"
variation 257..258
/gene="CCS"
/replace="g"
/replace="gg"
/db_xref="dbSNP:766499383"
variation 257
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:1565060472"
variation 259
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:1480989311"
variation 260
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746772329"
variation 261
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495341372"
variation 266
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:974123207"
variation 269
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495341381"
variation 270
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:770615243"
variation 271
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495341392"
variation 272
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495341397"
variation 273
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:148223729"
variation 275
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495341410"
variation 276
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1251428681"
variation 279..280
/gene="CCS"
/replace="g"
/replace="gg"
/db_xref="dbSNP:773282636"
variation 280
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495341422"
variation 282
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:541530482"
variation 283
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1331010335"
variation 284
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1206554592"
variation 285
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:61731812"
variation 286
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775873249"
variation 287
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495341515"
variation 288
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:763610047"
variation 289
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:150675115"
variation 290
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2134981615"
variation 291
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495341539"
variation 292
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:752012956"
variation 295
/gene="CCS"
/replace=""
/replace="c"
/db_xref="dbSNP:2495341554"
variation 295
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200810443"
variation 296
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:750621987"
variation 298
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495341567"
variation 299
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858531380"
variation 300
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590829614"
variation 302
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:377031880"
variation 303..304
/gene="CCS"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2495341577"
variation 304
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495341582"
variation 305..307
/gene="CCS"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:2495341588"
variation 308
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495341594"
variation 309
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756157198"
variation 311
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:780127005"
variation 314
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:370094773"
variation 317
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:565700050"
variation 318
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:140920411"
variation 321
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:532214069"
variation 323
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495341635"
variation 325
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021695433"
variation 326
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495341644"
variation 327
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:777662396"
exon 328..505
/gene="CCS"
/inference="alignment:Splign:2.1.0"
variation 329
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1369482120"
variation 331
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495342261"
variation 333
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:2495342262"
variation 335..339
/gene="CCS"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1858535627"
variation 336
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1273050957"
variation 338
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:144968320"
variation 340
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1386105144"
variation 343
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:2495342289"
variation 344
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495342295"
variation 345
/gene="CCS"
/replace=""
/replace="g"
/db_xref="dbSNP:2495342300"
variation 345
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1858535861"
variation 347
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1158303822"
variation 348
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495342308"
variation 349
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:2495342313"
variation 350
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495342315"
variation 355
/gene="CCS"
/replace=""
/replace="t"
/db_xref="dbSNP:776919671"
variation 355
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495342321"
variation 356..362
/gene="CCS"
/replace="ggggg"
/replace="gggggg"
/replace="ggggggg"
/replace="gggggggg"
/db_xref="dbSNP:759691599"
variation 356
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:61731811"
variation 357
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495342349"
variation 360
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495342352"
variation 361
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:185900251"
variation 362
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:745643257"
variation 363
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:755832884"
variation 364
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:2495342371"
variation 366
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1201410621"
variation 367
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:779831247"
variation 368
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858536796"
variation 370
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858536855"
variation 371
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:140142704"
variation 372
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:149989199"
variation 374
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495342414"
variation 375
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858537074"
variation 377
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1858537106"
variation 379
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:552779599"
variation 380
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748612840"
variation 381
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:182830642"
variation 382
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858537349"
variation 384
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201630725"
variation 385
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:773695641"
variation 387
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:371247817"
variation 388
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:375835478"
variation 389
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271419732"
variation 392
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1435644135"
variation 393
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495342505"
variation 394
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495342508"
variation 395
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858537842"
variation 396
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495342520"
variation 397
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:2495342526"
variation 399
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:932871572"
variation 401
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1327491339"
variation 403..406
/gene="CCS"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:36016381"
variation 403
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043318773"
variation 406
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495342565"
variation 407
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495342572"
variation 409
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:893430352"
variation 411
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:776789603"
variation 412
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:759613252"
variation 414
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423666174"
variation 415
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1858538910"
variation 416
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858538954"
variation 418..422
/gene="CCS"
/replace="tc"
/replace="tcatc"
/db_xref="dbSNP:1858539004"
variation 419
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858539049"
variation 420
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:765242047"
variation 422
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:946018387"
variation 423
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:202148109"
variation 425
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495342637"
variation 426
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212014528"
variation 427
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:535153686"
variation 430
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495342653"
variation 433
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495342659"
variation 437
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:145161523"
variation 438
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:750283280"
variation 440
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:755818904"
variation 441
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1447182412"
variation 442
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192682564"
variation 443
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495342695"
variation 444
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187346032"
variation 446
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:186651111"
variation 447
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:573428621"
variation 448
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:748883006"
variation 451
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:754553140"
variation 455
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858540084"
variation 456..473
/gene="CCS"
/replace="cat"
/replace="catggactccacgtccat"
/db_xref="dbSNP:2495342741"
variation 457
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1457561971"
variation 458
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495342755"
variation 460
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495342763"
variation 464
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495342769"
variation 467
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:574904327"
variation 468
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:368191906"
variation 471
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:907258856"
variation 472
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1305192085"
variation 473
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495342800"
variation 475
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1733081233"
variation 476
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:772680331"
variation 477
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495342812"
variation 479
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:773541450"
variation 480..483
/gene="CCS"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:2495342830"
variation 480
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:747428310"
variation 481
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1858540619"
variation 483
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1247340250"
variation 485
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:201708896"
variation 486
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1565060776"
variation 487
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:759811702"
variation 490
/gene="CCS"
/replace=""
/replace="c"
/db_xref="dbSNP:2495342883"
variation 490
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495342874"
variation 491
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:200506331"
variation 492
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1209720592"
variation 494
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1858541039"
variation 495
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:2495342898"
variation 497
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:765438439"
variation 498
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:199717297"
variation 499
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1463899910"
variation 500
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:775586150"
variation 502
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1256162047"
variation 503
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495342928"
variation 504
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495342932"
variation 505
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858541379"
exon 506..566
/gene="CCS"
/inference="alignment:Splign:2.1.0"
variation 508
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858554933"
variation 509
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:778343149"
variation 510
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1237426833"
variation 511
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1291577431"
variation 512
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495344814"
variation 513
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:2495344817"
variation 514
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858556171"
variation 515
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2134982666"
variation 516
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:747412790"
variation 522
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495344834"
variation 524
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:771414162"
variation 525
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495344844"
variation 526
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1457266419"
variation 528
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495344853"
variation 529
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:781602860"
variation 530
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:901108390"
variation 531
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1472132891"
variation 532
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495344870"
variation 533
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495344873"
variation 534
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495344877"
variation 535
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273026506"
variation 536
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858556570"
variation 540
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:367757609"
variation 541
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1379269105"
variation 542
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495344893"
variation 543..547
/gene="CCS"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:2495344898"
variation 544
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495344904"
variation 545
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:746198055"
variation 546
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:934899550"
variation 547
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1441790843"
variation 548..552
/gene="CCS"
/replace="ccc"
/replace="cccc"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:1375089490"
variation 548
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1410596348"
variation 549
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:989474920"
variation 550
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495344933"
variation 551
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:149172285"
variation 552
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495344940"
variation 553
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:775527758"
variation 554
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495344948"
variation 556
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1391159087"
variation 558
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:1273929029"
variation 559
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:763126852"
variation 560
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:371482988"
variation 562
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495344967"
variation 563
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858557533"
variation 564
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:142340643"
variation 565
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:146737817"
variation 566
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495344977"
exon 567..644
/gene="CCS"
/inference="alignment:Splign:2.1.0"
variation 568
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:755199781"
variation 569
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779176053"
variation 570
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:140345138"
variation 571
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:772209003"
variation 572
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:200121959"
variation 573
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:745854670"
variation 574..577
/gene="CCS"
/replace="ga"
/replace="gaga"
/db_xref="dbSNP:2495354273"
variation 576
/gene="CCS"
/replace=""
/replace="g"
/db_xref="dbSNP:2495354280"
variation 578..579
/gene="CCS"
/replace=""
/replace="cc"
/db_xref="dbSNP:2495354287"
variation 579..580
/gene="CCS"
/replace=""
/replace="ct"
/db_xref="dbSNP:1189669219"
variation 579
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1168513397"
variation 581
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1238152007"
variation 582
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495354302"
variation 585
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:951105505"
variation 586
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:769765686"
variation 587
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1177548511"
variation 588
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775188180"
variation 589
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:986521418"
variation 590
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858637347"
variation 591
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375633567"
variation 592
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773748375"
variation 593
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:773953643"
variation 594
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:145400974"
variation 596
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:766956703"
variation 597
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495354371"
variation 598
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858637751"
variation 601
/gene="CCS"
/replace=""
/replace="c"
/db_xref="dbSNP:1219899061"
variation 601
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495354374"
variation 602
/gene="CCS"
/replace=""
/replace="t"
/db_xref="dbSNP:2495354382"
variation 604
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:2495354384"
variation 605
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:372097218"
variation 606
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:146522916"
variation 607
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495354396"
variation 608
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:1858638031"
variation 609
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:140863701"
variation 610
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:150097654"
variation 611
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:755325271"
variation 612
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:367642079"
variation 613
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858638331"
variation 614
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590832456"
variation 615
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858638433"
variation 616
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495354432"
variation 617
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495354438"
variation 619
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:2495354443"
variation 621
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:1305672429"
variation 622
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858638538"
variation 624
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590832465"
variation 625
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1232835580"
variation 628
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1478603087"
variation 630
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495354521"
variation 631
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:1193419706"
variation 633
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495354535"
variation 634..639
/gene="CCS"
/replace="agcagc"
/replace="agcagcagc"
/db_xref="dbSNP:2495354548"
variation 634
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:375174622"
variation 635
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495354550"
variation 636
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:2495354555"
variation 644
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:200644962"
exon 645..748
/gene="CCS"
/inference="alignment:Splign:2.1.0"
variation 645
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1473015445"
variation 647
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1453301076"
variation 649..651
/gene="CCS"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:2495354828"
variation 651
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760212703"
variation 652
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1391644547"
variation 654
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495354849"
variation 656
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495354857"
variation 659
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:766821533"
variation 660
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:754333716"
variation 663
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:201766493"
variation 664
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:373460235"
variation 665
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323859066"
variation 666
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:779434367"
variation 667
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:765752116"
variation 668
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495354902"
variation 670
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495354911"
variation 671
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298352017"
variation 672..677
/gene="CCS"
/replace="att"
/replace="attatt"
/db_xref="dbSNP:2495354929"
variation 673
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495354936"
variation 676
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1279347900"
variation 677
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:753104213"
variation 678
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495354953"
variation 681
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:761126838"
variation 682
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:758732809"
variation 683
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1590832578"
variation 684
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495354978"
variation 685
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778116806"
variation 686..691
/gene="CCS"
/replace="aga"
/replace="agaaga"
/db_xref="dbSNP:2495354999"
variation 686
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:536515042"
variation 687
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:751710858"
variation 689
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:201296030"
variation 690
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1271851594"
variation 692
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1858642000"
variation 693
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495355030"
variation 694
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:2495355033"
variation 698
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1468382994"
variation 700
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1565063023"
variation 701
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:779860835"
variation 702
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1565063055"
variation 703..706
/gene="CCS"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:753056942"
variation 703
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1858642313"
variation 704
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1249423611"
variation 706
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495355090"
variation 708
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:749192348"
variation 713
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:1192088102"
variation 714
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368654282"
variation 715
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:768467295"
variation 716
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2134987024"
variation 719
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858642761"
variation 722
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495355125"
variation 723
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:1858642816"
variation 724
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1162473097"
variation 726
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1858642915"
variation 727
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495355142"
variation 728
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:1858642966"
variation 730
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495355151"
variation 731
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:1417100062"
variation 734
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:377383808"
variation 736
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:1457644812"
variation 737
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:778748665"
variation 738
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:1387294260"
variation 739
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:747910396"
variation 740
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1185600202"
variation 741
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:576527998"
variation 743
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495355181"
variation 744
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495355185"
variation 746
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:772807257"
exon 749..1066
/gene="CCS"
/inference="alignment:Splign:2.1.0"
variation 749
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:763414106"
variation 753
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495355578"
variation 754
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1430828366"
variation 755
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495355590"
variation 756
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:996714499"
variation 758
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1394977685"
variation 760
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:138370847"
variation 762
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1021893681"
variation 763
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:968590662"
variation 766
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858647089"
variation 768
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495355610"
variation 769
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:977341120"
variation 770
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1372587590"
variation 771
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:774566620"
variation 772
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302260691"
variation 775
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858647371"
variation 776
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:767604410"
variation 777..782
/gene="CCS"
/replace="gctggc"
/replace="gctggctggc"
/db_xref="dbSNP:2495355646"
variation 777
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:10061"
variation 778
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:750568458"
variation 781
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495355659"
variation 783
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756139724"
variation 784..787
/gene="CCS"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:2495355687"
variation 784
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:1858647588"
variation 785..797
/gene="CCS"
/replace="tttccagaacccc"
/replace="tttccagaacccctttccagaacccc"
/db_xref="dbSNP:2495355699"
variation 785
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210411614"
variation 789
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:765194748"
variation 791
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:923937645"
variation 792
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858647839"
variation 793
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:752568011"
variation 794
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858647968"
variation 795
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:992639743"
variation 796
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1858648075"
variation 799
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1047957280"
variation 801
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:908148014"
variation 805
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:944659445"
variation 806
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1040413982"
variation 808
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495355754"
variation 809
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:758314066"
variation 810
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858648421"
variation 812..813
/gene="CCS"
/replace="t"
/replace="tt"
/db_xref="dbSNP:2495355769"
variation 812
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495355766"
variation 813
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:561125812"
variation 815
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:201606373"
variation 816
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:149284164"
variation 818
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:756979792"
variation 819
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2134987307"
variation 820
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:920101011"
variation 822
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495355800"
variation 824
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858648845"
variation 825
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:2495355811"
variation 826
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495355814"
variation 829
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858648894"
variation 830
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1127141"
variation 831
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495355828"
variation 833
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495355831"
variation 835
/gene="CCS"
/replace=""
/replace="a"
/db_xref="dbSNP:2495355833"
variation 836
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495355837"
variation 837..839
/gene="CCS"
/replace="g"
/replace="gag"
/db_xref="dbSNP:2495355846"
variation 837
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1324559395"
variation 840
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745413014"
variation 841
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:769362989"
variation 845
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495355867"
variation 846
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1292967871"
variation 847
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:373751466"
variation 848
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1245199841"
variation 851
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1275000196"
variation 852
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:143494418"
variation 854
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:886764512"
variation 855
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:769281643"
variation 860
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:137970813"
variation 863
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495355897"
variation 865
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:143215772"
variation 867
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:767806191"
variation 868
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:147502080"
variation 872
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1166028704"
variation 875..876
/gene="CCS"
/replace="gt"
/replace="gtgt"
/db_xref="dbSNP:2495355922"
variation 877
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495355927"
variation 879
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760753625"
variation 880
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:554910347"
variation 881
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1127145"
variation 882
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1388793900"
variation 885..889
/gene="CCS"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:748697782"
variation 885
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:867758567"
variation 886
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021421444"
variation 887
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1286789446"
variation 888
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:201533764"
variation 889
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1396407088"
variation 890
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1294831181"
variation 893
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858651081"
variation 894
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:1332411066"
variation 896
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495355987"
variation 897
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:2495355989"
variation 899
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1232666141"
variation 900
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495355997"
variation 904
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:2495355998"
variation 907
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495356001"
variation 908
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495356008"
variation 909..910
/gene="CCS"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1858651388"
variation 909
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:763913397"
variation 910
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1858651438"
variation 912
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:551837298"
variation 914
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495356017"
variation 915
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858651538"
variation 918
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:201822594"
variation 919
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495356023"
variation 921
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:780901578"
variation 922
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745458704"
variation 924
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495356034"
variation 925
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250013956"
variation 926
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:2495356038"
variation 927
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:968581206"
variation 933
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:755815575"
variation 934
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495356052"
variation 935
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858651834"
variation 936
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495356059"
variation 937
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:971734484"
variation 938
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495356067"
variation 940
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:779777761"
variation 941
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282895165"
variation 942
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:773363948"
variation 944
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858652069"
variation 945
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495356086"
variation 946
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495356089"
variation 947
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495356094"
variation 951
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495356099"
variation 953
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590832939"
variation 954
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495356109"
variation 955
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1352433334"
variation 957
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495356122"
variation 958
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495356126"
variation 960
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:956673986"
variation 962..966
/gene="CCS"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:2495356137"
variation 962
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1308695596"
variation 963
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1303447066"
variation 964
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495356144"
variation 965
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495356147"
variation 966
/gene="CCS"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1395680359"
variation 967
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495356156"
variation 969
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:747225308"
variation 970
/gene="CCS"
/replace=""
/replace="g"
/db_xref="dbSNP:2495356163"
variation 972..973
/gene="CCS"
/replace=""
/replace="a"
/db_xref="dbSNP:2495356175"
variation 972
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858652413"
variation 975
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495356180"
variation 976
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:2495356182"
variation 977..979
/gene="CCS"
/replace="tt"
/replace="ttt"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1467405865"
variation 977
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495356186"
variation 978
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495356193"
variation 979
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1033983953"
variation 980
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1367186809"
variation 981
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858652655"
variation 984
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495356206"
variation 985
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1175302988"
variation 986
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858652750"
variation 990
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1479223261"
variation 991
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:2495356219"
variation 992
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495356227"
variation 995
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495356228"
variation 996
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495356234"
variation 997
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495356239"
variation 1000
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495356244"
variation 1001
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495356247"
variation 1002
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:2495356250"
variation 1005
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590832969"
variation 1007
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495356262"
variation 1008
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858652882"
variation 1009
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:2495356269"
variation 1010..1012
/gene="CCS"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1858652927"
variation 1011
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1413594531"
variation 1013
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1858653038"
variation 1014
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:1858653086"
variation 1015
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858653135"
variation 1018
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495356283"
variation 1019
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:958398936"
variation 1021
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:1419068765"
variation 1022
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1389505234"
variation 1023
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495356293"
variation 1029
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495356296"
variation 1031
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2134987485"
variation 1032
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495356302"
variation 1033
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327974797"
variation 1034
/gene="CCS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2495356310"
variation 1035
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2495356312"
variation 1036
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1336230801"
variation 1037
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1858653419"
regulatory 1041..1046
/regulatory_class="polyA_signal_sequence"
/gene="CCS"
/note="hexamer: AATGAA"
variation 1041
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2495356316"
variation 1042
/gene="CCS"
/replace="a"
/replace="t"
/db_xref="dbSNP:2495356321"
variation 1043
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:973789740"
variation 1045..1047
/gene="CCS"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:2495356328"
variation 1045
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:558948617"
variation 1046
/gene="CCS"
/replace="a"
/replace="c"
/db_xref="dbSNP:2495356335"
variation 1048..1052
/gene="CCS"
/replace=""
/replace="gtttt"
/db_xref="dbSNP:2495356338"
variation 1048
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2134987495"
variation 1049..1052
/gene="CCS"
/replace="tt"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:952231144"
variation 1049..1050
/gene="CCS"
/replace=""
/replace="aaaac"
/db_xref="dbSNP:2495356348"
variation 1049
/gene="CCS"
/replace="c"
/replace="t"
/db_xref="dbSNP:969464081"
variation 1051
/gene="CCS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1858653692"
variation 1052..1053
/gene="CCS"
/replace=""
/replace="c"
/db_xref="dbSNP:2495356366"
variation 1052
/gene="CCS"
/replace="g"
/replace="t"
/db_xref="dbSNP:2495356363"
variation 1053
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1858653740"
variation 1058
/gene="CCS"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:908092681"
variation 1059
/gene="CCS"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1289143310"
variation 1063..1065
/gene="CCS"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:2495356379"
variation 1064
/gene="CCS"
/replace="a"
/replace="g"
/db_xref="dbSNP:771207391"
polyA_site 1066
/gene="CCS"
/note="major polyA site"
ORIGIN
agtccccgcgacgccgcgctggttggtgctcctgcgccggaggagttctgcgtctcggggtggtgactgggtccagaatggcttcggattcggggaaccaggggaccctctgcacgttggagttcgcggtgcagatgacctgtcagagctgtgtggacgcggtgcgcaaatccctgcaaggggtggcaggtgtccaggatgtggaggtgcacttggaggaccagatggtcttggtacacaccactctacccagccaggaggtgcaggctctcctggaaggcacggggcggcaggcggtactcaagggcatgggcagcggccagttgcagaatctgggggcagcagtggccatcctgggggggcctggcaccgtgcagggggtggtgcgcttcctacagctgacccctgagcgctgcctcatcgagggaactattgacggcctggagcctgggctgcatggactccacgtccatcagtacggggaccttacaaacaactgcaacagctgtgggaatcactttaaccctgatggagcatctcatgggggcccccaggactctgaccggcaccgcggagacctgggcaatgtccgtgctgatgctgacggccgcgccatcttcagaatggaggatgagcagctgaaggtgtgggatgtgattggccgcagcctgattattgatgagggagaagatgacctgggccggggaggccatcccttatccaagatcacagggaactccggggagaggttggcctgtggcatcattgcacgctccgctggccttttccagaaccccaagcagatctgctcttgcgatggcctcaccatctgggaggagcgaggccggcccatcgctggcaagggccgaaaggagtcagcgcagccccctgcccacctttgagcaggacctcaccttggctctgttgctgtcctccagggcgagcactttccacttccagagggggccagagggactttgcctgcccagtctttggagagctcagtacagggcaggagctgctgtggtgttcccttggcaaatgaaagttttattttcgtttggga
//
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]