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Previous release (v1)
2024-05-19 12:21:20, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_033377 693 bp mRNA linear PRI 29-DEC-2022
DEFINITION Homo sapiens chorionic gonadotropin subunit beta 1 (CGB1),
transcript variant 1, mRNA.
ACCESSION NM_033377
VERSION NM_033377.2
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 693)
AUTHORS Wu W, Gao H, Li X, Peng S, Yu J, Liu N, Zhan G, Zhu Y, Wang K and
Guo X.
TITLE beta-hCG promotes epithelial ovarian cancer metastasis through
ERK/MMP2 signaling pathway
JOURNAL Cell Cycle 18 (1), 46-59 (2019)
PUBMED 30582718
REMARK GeneRIF: these data provide new insight into the roles and
mechanisms of b-hCG in regulating Epithelial ovarian cancer (EOC
metastasis through ERK/MMP2 signaling pathway and may become a new
target for therapeutic intervention.
REFERENCE 2 (bases 1 to 693)
AUTHORS Burczynska BB, Kobrouly L, Butler SA, Naase M and Iles RK.
TITLE Novel insights into the expression of CGB1 & 2 genes by epithelial
cancer cell lines secreting ectopic free hCGbeta
JOURNAL Anticancer Res 34 (5), 2239-2248 (2014)
PUBMED 24778026
REFERENCE 3 (bases 1 to 693)
AUTHORS Kubiczak M, Walkowiak GP, Nowak-Markwitz E and Jankowska A.
TITLE Human chorionic gonadotropin beta subunit genes CGB1 and CGB2 are
transcriptionally active in ovarian cancer
JOURNAL Int J Mol Sci 14 (6), 12650-12660 (2013)
PUBMED 23774837
REMARK GeneRIF: The presence of CGB1 and CGB2 transcripts in 41% of
analyzed ovarian cancer cases, is reported.
Publication Status: Online-Only
REFERENCE 4 (bases 1 to 693)
AUTHORS Goto-Kazeto R, Kazeto Y and Trant JM.
TITLE Molecular cloning, characterization and expression of
thyroid-stimulating hormone receptor in channel catfish
JOURNAL Gen Comp Endocrinol 161 (3), 313-319 (2009)
PUBMED 19523396
REFERENCE 5 (bases 1 to 693)
AUTHORS Rull K, Hallast P, Uuskula L, Jackson J, Punab M, Salumets A,
Campbell RK and Laan M.
TITLE Fine-scale quantification of HCG beta gene transcription in human
trophoblastic and non-malignant non-trophoblastic tissues
JOURNAL Mol Hum Reprod 14 (1), 23-31 (2008)
PUBMED 18048458
REFERENCE 6 (bases 1 to 693)
AUTHORS Bo M and Boime I.
TITLE Identification of the transcriptionally active genes of the
chorionic gonadotropin beta gene cluster in vivo
JOURNAL J Biol Chem 267 (5), 3179-3184 (1992)
PUBMED 1371113
REFERENCE 7 (bases 1 to 693)
AUTHORS Jameson JL and Lindell CM.
TITLE Isolation and characterization of the human chorionic gonadotropin
beta subunit (CG beta) gene cluster: regulation of
transcriptionally active CG beta gene by cyclic AMP
JOURNAL Mol Cell Biol 8 (12), 5100-5107 (1988)
PUBMED 2468994
REFERENCE 8 (bases 1 to 693)
AUTHORS Policastro,P.F., Daniels-McQueen,S., Carle,G. and Boime,I.
TITLE A map of the hCG beta-LH beta gene cluster
JOURNAL J Biol Chem 261 (13), 5907-5916 (1986)
PUBMED 2422163
REFERENCE 9 (bases 1 to 693)
AUTHORS Julier,C., Weil,D., Couillin,P., Cote,J.C., Nguyen,V.C.,
Foubert,C., Boue,A., Thirion,J.P., Kaplan,J.C. and Junien,C.
TITLE The beta chorionic gonadotropin-beta luteinizing gene cluster maps
to human chromosome 19
JOURNAL Hum Genet 67 (2), 174-177 (1984)
PUBMED 6204923
REFERENCE 10 (bases 1 to 693)
AUTHORS Policastro,P., Ovitt,C.E., Hoshina,M., Fukuoka,H., Boothby,M.R. and
Boime,I.
TITLE The beta subunit of human chorionic gonadotropin is encoded by
multiple genes
JOURNAL J Biol Chem 258 (19), 11492-11499 (1983)
PUBMED 6194155
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AC008687.5.
On May 6, 2020 this sequence version replaced NM_033377.1.
Summary: The beta subunit of chorionic gonadotropin (CGB) is
encoded by six highly homologous and structurally similar genes
that are arranged in tandem and inverted pairs on chromosome
19q13.3, and contiguous with the luteinizing hormone beta (LHB)
subunit gene. The CGB genes are primarily distinguished by
differences in the 5' untranscribed region. This gene was
originally thought to be one of the two pseudogenes (CGB1 and CGB2)
of CGB subunit, however, detection of CGB1 and CGB2 transcripts in
vivo, and their presence on the polysomes, suggested that these
transcripts are translated. To date, a protein product
corresponding to CGB1 has not been isolated. The deduced sequence
of the hypothetical protein of 132 aa does not share any similarity
with that of functional CGB subunits (PMID:8954017). However, a 155
aa protein, translated from a different frame, is about the same
size, and shares 98% identity with other CGB subunits. [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 :: BC126460.1, GE745564.1 [ECO:0000332]
RNAseq introns :: mixed sample support SAMEA1968968,
SAMEA2148874 [ECO:0006172]
##Evidence-Data-END##
##RefSeq-Attributes-START##
MANE Ensembl match :: ENST00000301407.8/ ENSP00000301407.6
RefSeq Select criteria :: based on manual assertion, conservation,
expression, longest protein
##RefSeq-Attributes-END##
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-193 AC008687.5 48011-48203 c
194-361 AC008687.5 47444-47611 c
362-693 AC008687.5 46877-47208 c
FEATURES Location/Qualifiers
source 1..693
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="19"
/map="19q13.33"
gene 1..693
/gene="CGB1"
/note="chorionic gonadotropin subunit beta 1"
/db_xref="GeneID:114335"
/db_xref="HGNC:HGNC:16721"
/db_xref="MIM:608823"
exon 1..193
/gene="CGB1"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231819631"
variation 3
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:536700356"
variation 4
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1488096349"
variation 6
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:569421954"
variation 7
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039828600"
variation 8
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:551501295"
variation 9
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1262313547"
variation 10
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:532769722"
variation 11
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1162522223"
variation 12..13
/gene="CGB1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1308150352"
variation 12
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039828465"
variation 13..18
/gene="CGB1"
/replace="agggga"
/replace="aggggagggga"
/db_xref="dbSNP:202189266"
variation 13..14
/gene="CGB1"
/replace="ag"
/replace="agtggag"
/db_xref="dbSNP:1290022585"
variation 13
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:185491599"
variation 14..17
/gene="CGB1"
/replace="gggg"
/replace="ggggcgggg"
/db_xref="dbSNP:2122150436"
variation 14
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:900948651"
variation 15
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:942506736"
variation 17
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1372541577"
variation 20
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048265754"
variation 22
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:929929757"
variation 23
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:575971914"
variation 24
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039828117"
variation 25
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039828094"
variation 26
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:377385500"
variation 27
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:919258507"
variation 28..36
/gene="CGB1"
/replace="gagagag"
/replace="gagagagag"
/replace="gagagagagag"
/db_xref="dbSNP:1185637314"
variation 28
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122150376"
variation 30
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:972497937"
variation 32
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039827959"
variation 33
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1600224459"
variation 34
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1386376438"
variation 35
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:960808642"
variation 36
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:868818970"
variation 37
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039827755"
variation 38
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:928009459"
variation 43
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:980898105"
variation 44
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:969506134"
variation 45
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1405321829"
variation 48
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1159195121"
variation 51
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:34291483"
variation 52
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:373044257"
variation 53
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:34228596"
variation 54
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:956980716"
variation 55
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1030646237"
variation 56
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1198195794"
variation 58
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039827242"
variation 59
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1345735543"
variation 60..61
/gene="CGB1"
/replace=""
/replace="tg"
/db_xref="dbSNP:1555806967"
variation 60
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:10853805"
variation 61..62
/gene="CGB1"
/replace=""
/replace="gg"
/db_xref="dbSNP:1555806966"
variation 61
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039827098"
variation 62
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:35533886"
variation 63
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:900856459"
variation 64
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039826914"
variation 65
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:369471697"
variation 67
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1006650939"
variation 71
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:571679811"
variation 72
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451977649"
variation 73
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:182402915"
variation 74
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039826679"
variation 75
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1048255288"
variation 76
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039826622"
variation 77
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1211192571"
variation 78
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1327253886"
variation 79
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:929877689"
variation 80
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:377556920"
variation 81
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231941928"
variation 82
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1326505487"
variation 86
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039826427"
variation 87
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039826399"
variation 88
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:373088178"
variation 89
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380971474"
variation 90
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039826306"
variation 91
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1340305554"
variation 95
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1313831281"
variation 96
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:897107347"
variation 98
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039826183"
variation 101..112
/gene="CGB1"
/replace="gtctcactcccc"
/replace="gtctcactccccgtctcactcccc"
/db_xref="dbSNP:1462610580"
variation 101
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039826154"
variation 103
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1348503251"
variation 104
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1057060606"
variation 106
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1436845047"
variation 110
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1270624555"
variation 111
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:191756795"
variation 112
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369942258"
variation 113
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1600224361"
variation 115
/gene="CGB1"
/replace=""
/replace="c"
/db_xref="dbSNP:1600224356"
variation 115
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600224353"
variation 116
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:573599743"
variation 119
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:373660013"
variation 120
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:774444681"
variation 121
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039825739"
variation 122
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1466780913"
variation 123
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:375233005"
variation 124
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:927988907"
variation 127
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:981230197"
variation 130
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371968536"
variation 134
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:34566775"
variation 135
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:569543184"
variation 136
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039825520"
variation 137
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:377327911"
variation 139
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039825446"
variation 141
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039825429"
variation 143
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192328032"
variation 144
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:766762733"
variation 146
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:541595731"
variation 147
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039825289"
variation 149
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:751016313"
variation 150
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1484721212"
variation 152
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:766140640"
variation 153
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039825169"
variation 154
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1031649274"
variation 155
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1648715505"
variation 157
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1240170111"
variation 158
/gene="CGB1"
/replace="c"
/replace="ccc"
/db_xref="dbSNP:2122149797"
variation 158
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1260481965"
variation 159
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:762625218"
variation 160
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:373873835"
variation 162
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:769475713"
variation 164
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1233529193"
variation 165
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:765647516"
variation 166
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568660258"
variation 167
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:186958845"
variation 168..170
/gene="CGB1"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2039824813"
variation 168
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:777235070"
variation 170
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1382985885"
variation 171
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:769039759"
misc_feature 173..175
/gene="CGB1"
/note="upstream in-frame stop codon"
variation 173
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775492190"
variation 174..175
/gene="CGB1"
/replace=""
/replace="aa"
/db_xref="dbSNP:1332199875"
variation 176
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1215113238"
variation 179
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:772289035"
variation 180
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:746052565"
variation 181
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:777570430"
variation 182
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378558958"
variation 184
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039824503"
CDS 185..652
/gene="CGB1"
/note="isoform 1 precursor is encoded by transcript
variant 1; chorionic gonadotropin, beta polypeptide 1;
chorionic gonadotropin beta subunit 1"
/codon_start=1
/product="choriogonadotropin subunit beta variant 1
isoform 1 precursor"
/protein_id="NP_203695.2"
/db_xref="CCDS:CCDS12751.2"
/db_xref="GeneID:114335"
/db_xref="HGNC:HGNC:16721"
/db_xref="MIM:608823"
/translation="
MSKRLLLLLLLSMGGTWASKEPLRPRCRPINATLAVEKEGCPVCITVNTTICAGYCPTMTRVLQGVLPALPQVVCNYRDVRFESIRLPGCPRGVNPVVSYAVALSCQCALCRRSTTDCGGPKDHPLTCDDPRFQDSSSSKAPPPSLPSPSRLPGP"
sig_peptide 185..238
/gene="CGB1"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
misc_feature 251..571
/gene="CGB1"
/note="Glycoprotein hormone beta chain homologues; Region:
GHB; smart00068"
/db_xref="CDD:214502"
misc_feature order(263..265,338..340,350..352,407..409,500..502,
506..508)
/gene="CGB1"
/note="cysteine knot motif; other site"
/db_xref="CDD:200450"
misc_feature order(284..286,293..295,335..376,404..409,515..517,
521..523,530..547)
/gene="CGB1"
/note="dimer interface [polypeptide binding]; other site"
/db_xref="CDD:200450"
misc_feature order(374..376,521..526,533..535,539..547)
/gene="CGB1"
/note="receptor binding site [polypeptide binding]; other
site"
/db_xref="CDD:200450"
variation 185
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1201548329"
variation 187
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1233593844"
variation 188
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:769630365"
variation 190
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1568660224"
variation 192
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:375110238"
variation 193
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781245225"
exon 194..361
/gene="CGB1"
/inference="alignment:Splign:2.1.0"
variation 194
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:62126040"
variation 195
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1457305022"
variation 196
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:746779481"
variation 197
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1311038616"
variation 200
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1200221979"
variation 201..211
/gene="CGB1"
/replace="tgctgttgctg"
/replace="tgctgttgctgttgctg"
/db_xref="dbSNP:765624542"
variation 202
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332430658"
variation 203
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:572197136"
variation 205
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1228003059"
variation 207
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1270512752"
variation 208
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1357119887"
variation 210
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039816765"
variation 211
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039816692"
variation 215
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:775626611"
variation 219
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:772131200"
variation 220
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1332650382"
variation 222
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745374910"
variation 223
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402369392"
variation 224
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:147731004"
variation 226
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1322428206"
variation 227
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304075768"
variation 230
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748849664"
variation 233
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600223869"
variation 235
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415312784"
variation 236
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:553812864"
variation 238
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:756480507"
variation 240
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380774679"
variation 241
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:768020387"
variation 242
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:755423976"
variation 243
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145503774"
variation 244
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:574448905"
variation 247
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1452477184"
variation 248
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1185137906"
variation 249
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773355851"
variation 250
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200371312"
variation 254
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1164418301"
variation 255
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:760613888"
variation 256
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039815790"
variation 257
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1310586210"
variation 258
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039815729"
variation 261
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1463048562"
variation 262
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242993940"
variation 263
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122147489"
variation 264
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:772147750"
variation 266
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1274689310"
variation 267
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:745750183"
variation 268
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1187529607"
variation 270
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039815499"
variation 273
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2122147444"
variation 274
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1351190630"
variation 275
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315800817"
variation 276
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:773940761"
variation 281
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1600223835"
variation 282
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202067695"
variation 283
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429863566"
variation 285
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:770384780"
variation 287
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1268216650"
variation 288
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:556214869"
variation 291
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:777344526"
variation 293
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:537693352"
variation 294..298
/gene="CGB1"
/replace="ag"
/replace="agaag"
/db_xref="dbSNP:759938269"
variation 294
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1478896026"
variation 295
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039815089"
variation 299
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1555806873"
variation 302
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:570339247"
variation 303
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1291309081"
variation 304
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:148640164"
variation 306
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1487983670"
variation 308
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:755513430"
variation 309
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1219412279"
variation 310
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:752048144"
variation 311
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:766888572"
variation 312
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:758466573"
variation 315
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415924632"
variation 319..334
/gene="CGB1"
/replace="cacc"
/replace="caccgtcaacaccacc"
/db_xref="dbSNP:777177662"
variation 319
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:750513213"
variation 322
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765381688"
variation 328..335
/gene="CGB1"
/replace="cacca"
/replace="caccacca"
/db_xref="dbSNP:1480444426"
variation 328
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1399064983"
variation 330
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762069467"
variation 331
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:752562285"
variation 332
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:767378543"
variation 333
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:759370769"
variation 334
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:889943275"
variation 335
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1176736924"
variation 337
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:774201663"
variation 340
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1417184280"
variation 341
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039814294"
variation 342
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:770884058"
variation 343
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1477649626"
variation 344
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1263989867"
variation 345
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1195851629"
variation 346
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1400360575"
variation 350
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1482324192"
variation 351
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:762432991"
variation 352
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211475929"
variation 353
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284292258"
variation 354
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1049923872"
variation 356
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039813919"
variation 357
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:558208220"
variation 358
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:540021521"
variation 359
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1256625036"
variation 360
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769462042"
variation 361
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:747762967"
exon 362..693
/gene="CGB1"
/inference="alignment:Splign:2.1.0"
variation 364
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1458468311"
variation 365
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1240464080"
variation 366
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1600223510"
variation 367
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:940301796"
variation 368
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039809609"
variation 369
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1207689861"
variation 370
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:747339118"
variation 374
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039809517"
variation 375
/gene="CGB1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:760737028"
variation 375
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045834630"
variation 376
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1245486233"
variation 377
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223057392"
variation 378
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1350895730"
variation 379
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1917031560"
variation 380
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039809326"
variation 383
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285197170"
variation 387
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1308394303"
variation 388
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:541921440"
variation 389
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:574589925"
variation 391
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:556155690"
variation 392
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1054225655"
variation 393
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423857516"
variation 396
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039809103"
variation 399
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386013028"
variation 401
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:779529842"
variation 402
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039809016"
variation 405
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039808987"
variation 407
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600223464"
variation 409
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1294362608"
variation 411
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:544218520"
variation 415
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039808877"
variation 416
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753951799"
variation 417
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1158546357"
variation 418
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:778204464"
variation 419
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446116331"
variation 421..434
/gene="CGB1"
/replace="t"
/replace="tgtgcgcttcgagt"
/db_xref="dbSNP:773175443"
variation 421
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576811185"
variation 423
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039808655"
variation 424
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039808625"
variation 425
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:751337658"
variation 426
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1432984304"
variation 428
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039808507"
variation 430
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390883370"
variation 431
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758100273"
variation 435
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:750411436"
variation 437
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:765148068"
variation 440
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371128021"
variation 441
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1284750505"
variation 442
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:776054068"
variation 446
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355681618"
variation 447
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:763750280"
variation 448
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1393292136"
variation 454..456
/gene="CGB1"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:772368413"
variation 456
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1232195649"
variation 457
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568659618"
variation 458
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1331501646"
variation 459
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:539760342"
variation 460
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:775748503"
variation 463
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1180513505"
variation 464
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775053454"
variation 465
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1441666737"
variation 467
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1246303905"
variation 469
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:566235393"
variation 470
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1379146170"
variation 472
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:756326891"
variation 473
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201312433"
variation 474
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:781251303"
variation 478
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1465821820"
variation 481
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378616613"
variation 483
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1452013968"
variation 484
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750216960"
variation 485
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:765164331"
variation 487
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1262024856"
variation 488
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:377262139"
variation 492
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1448244749"
variation 499
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253945854"
variation 501
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199839749"
variation 502
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1345421914"
variation 503
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1197549618"
variation 505
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:753367928"
variation 506
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:535514659"
variation 507
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:568205173"
variation 508
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:987232053"
variation 509
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1179874353"
variation 510
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277824533"
variation 511
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1600223350"
variation 513
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:775256818"
variation 516
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039806754"
variation 518
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328312410"
variation 519
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1332739331"
variation 520
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1345340610"
variation 521
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:767060656"
variation 522
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:374210570"
variation 523
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039806573"
variation 525
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1600223341"
variation 526
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:774785916"
variation 528
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:771575126"
variation 529
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:749776099"
variation 531
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600223327"
variation 532
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568659539"
variation 535
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:773829110"
variation 536
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039806292"
variation 538
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200177766"
variation 539
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:748166776"
variation 543
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:199498446"
variation 544
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:745677072"
variation 545
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039806119"
variation 546
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:778631969"
variation 547
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039806052"
variation 549
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1028339582"
variation 550
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376922188"
variation 552
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:753813017"
variation 556
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:777548163"
variation 558
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1219523475"
variation 563
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1399939084"
variation 572
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:755706231"
variation 573
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:752141739"
variation 574..578
/gene="CGB1"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1276406376"
variation 574
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:373128472"
variation 576
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:766894199"
variation 578
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:763390923"
variation 579
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367977437"
variation 583
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773830373"
variation 584
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1016217801"
variation 585
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:770198800"
variation 587
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:369301126"
variation 588
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:201231416"
variation 591
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039805299"
variation 593
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1247688792"
variation 594
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039805212"
variation 595
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:747191041"
variation 598
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039805157"
variation 599
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1162053395"
variation 601..603
/gene="CGB1"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1600223257"
variation 605
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1472850816"
variation 606
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780217968"
variation 607
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1388593246"
variation 608
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375388018"
variation 609
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039804877"
variation 610
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039804837"
variation 611..616
/gene="CGB1"
/replace="ccccc"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:1487932358"
variation 611
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373307100"
variation 613
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1350290889"
variation 614
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:755936073"
variation 615
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:752261004"
variation 616
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780516618"
variation 617
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568659471"
variation 619
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:200388907"
variation 620
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199785120"
variation 623
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:763481551"
variation 625
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2122145032"
variation 626
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:570788485"
variation 627
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:765789272"
variation 628
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:202114192"
variation 629
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1488200563"
variation 630
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:776805155"
variation 631
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768762805"
variation 633
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1347699604"
variation 634
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568659444"
variation 635
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:527614195"
variation 636
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:772276702"
variation 637
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:370143488"
variation 640
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1156748774"
variation 641
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:35371968"
variation 642
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380679945"
variation 643..646
/gene="CGB1"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:2122144824"
variation 643
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748079220"
variation 644
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1476931130"
variation 645
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:781171716"
variation 646
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1198471026"
variation 647
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1490527489"
variation 650
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:754596236"
variation 651
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:200329830"
variation 652
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:542056595"
variation 653
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1285587786"
variation 657
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:758068882"
variation 659
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:755082872"
variation 660
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:757610056"
variation 661
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1273850342"
variation 662
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:974126947"
variation 663
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:754350682"
variation 665
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:529956719"
variation 666
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1288631414"
variation 667
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775477990"
variation 668
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1295883640"
variation 669
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039803190"
variation 671
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:767737637"
regulatory 672..677
/regulatory_class="polyA_signal_sequence"
/gene="CGB1"
/note="hexamer: AATAAA"
variation 673
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1015752308"
variation 674
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:759624854"
variation 677
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1188343359"
variation 679
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:773087735"
variation 680
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1412512140"
variation 684
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:769530205"
variation 690
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:747965736"
variation 691
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:367968985"
variation 692
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:562568855"
polyA_site 693
/gene="CGB1"
/note="major polyA site"
ORIGIN
ctggagggaggaaggggaactgcatctgagagagagcagccaattgggtccgctgactctggccaggttcccgtgccgcgtccaacacccctcactccctgtctcactcccccacggagactcaatttactttccatgtccacattcccagtgcttgcggaagatatcccgctaagagagagacatgtcaaagaggctgctgctgttgctgctgctgagcatgggcgggacatgggcatccaaggagccgcttcggccacggtgccgccccatcaatgccaccctggctgtggagaaggagggctgccccgtgtgcatcaccgtcaacaccaccatctgtgccggctactgccccaccatgacccgcgtgctgcagggggtcctgccggccctgcctcaggtggtgtgcaactaccgcgatgtgcgcttcgagtccatccggctccctggctgcccgcgcggcgtgaaccccgtggtctcctacgccgtggctctcagctgtcaatgtgcactctgccgccgcagcaccactgactgcgggggtcccaaggaccaccccttgacctgtgatgacccccgcttccaggactcctcttcctcaaaggcccctccccccagccttccaagtccatcccgtctcccggggccctaggacaccccgatcctcccacaataaaggcttctcaatccgca
//
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]