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2025-05-09 17:21:58, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001145065 6205 bp mRNA linear PRI 15-JUN-2013
DEFINITION Homo sapiens coiled-coil serine-rich protein 1 (CCSER1), transcript
variant 1, mRNA.
ACCESSION NM_001145065
VERSION NM_001145065.1 GI:222831646
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 6205)
AUTHORS Luykx,J.J., Bakker,S.C., Lentjes,E., Neeleman,M., Strengman,E.,
Mentink,L., Deyoung,J., de Jong,S., Sul,J.H., Eskin,E., van
Eijk,K., van Setten,J., Buizer-Voskamp,J.E., Cantor,R.M., Lu,A.,
van Amerongen,M., van Dongen,E.P., Keijzers,P., Kappen,T.,
Borgdorff,P., Bruins,P., Derks,E.M., Kahn,R.S. and Ophoff,R.A.
TITLE Genome-wide association study of monoamine metabolite levels in
human cerebrospinal fluid
JOURNAL Mol. Psychiatry (2013) In press
PUBMED 23319000
REMARK Publication Status: Available-Online prior to print
REFERENCE 2 (bases 1 to 6205)
AUTHORS Hart,A.B., Engelhardt,B.E., Wardle,M.C., Sokoloff,G., Stephens,M.,
de Wit,H. and Palmer,A.A.
TITLE Genome-wide association study of d-amphetamine response in healthy
volunteers identifies putative associations, including cadherin 13
(CDH13)
JOURNAL PLoS ONE 7 (8), E42646 (2012)
PUBMED 22952603
REFERENCE 3 (bases 1 to 6205)
AUTHORS Lantieri,F., Glessner,J.T., Hakonarson,H., Elia,J. and Devoto,M.
TITLE Analysis of GWAS top hits in ADHD suggests association to two
polymorphisms located in genes expressed in the cerebellum
JOURNAL Am. J. Med. Genet. B Neuropsychiatr. Genet. 153B (6), 1127-1133
(2010)
PUBMED 20607790
REMARK GeneRIF: Two SNPs located in genes coding for as yet
uncharacterized proteins expressed in the cerebellum, XKR4 in
8q12.1, and FAM190A in 4q22.1 suggest association with association
with attention deficit hyperactivity disorder. [FAM190A]
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
DB027029.1, AB051467.1 and AC110774.3.
Transcript Variant: This variant (1) encodes the longer isoform
(1).
##Evidence-Data-START##
Transcript exon combination :: AB051467.1 [ECO:0000332]
RNAseq introns :: mixed/partial sample support
ERS025081, ERS025082 [ECO:0000350]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-52 DB027029.1 1-52
53-4316 AB051467.1 1-4264
4317-6205 AC110774.3 57075-58963
FEATURES Location/Qualifiers
source 1..6205
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="4"
/map="4q22.1"
gene 1..6205
/gene="CCSER1"
/gene_synonym="FAM190A"
/note="coiled-coil serine-rich protein 1"
/db_xref="GeneID:401145"
/db_xref="HGNC:29349"
exon 1..299
/gene="CCSER1"
/gene_synonym="FAM190A"
/inference="alignment:Splign:1.39.8"
variation 37..38
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace=""
/replace="ct"
/db_xref="dbSNP:142199213"
variation 259
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:187161303"
variation 261
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="g"
/db_xref="dbSNP:190422682"
exon 300..1664
/gene="CCSER1"
/gene_synonym="FAM190A"
/inference="alignment:Splign:1.39.8"
variation 318
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="t"
/db_xref="dbSNP:375470349"
misc_feature 332..334
/gene="CCSER1"
/gene_synonym="FAM190A"
/note="upstream in-frame stop codon"
variation 335
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:28592243"
variation 338
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:200716258"
CDS 341..3043
/gene="CCSER1"
/gene_synonym="FAM190A"
/note="isoform 1 is encoded by transcript variant 1;
protein FAM190A; family with sequence similarity 190,
member A; serine-rich coiled-coil domain-containing
protein 1"
/codon_start=1
/product="serine-rich coiled-coil domain-containing
protein 1 isoform 1"
/protein_id="NP_001138537.1"
/db_xref="GI:222831647"
/db_xref="CCDS:CCDS47099.1"
/db_xref="GeneID:401145"
/db_xref="HGNC:29349"
/translation="
MGDSGSRRSTLVSRLPIFRRSINRRHDSLPSSPSSSNTVGVHSSSPSSTNSSSGSTGKRRSIFRTPSISFHHKKGSEPKQEPTNQNLSISNGAQPGHSNMQKLSLEEHIKTRGRHSVGFSSSRNKKITRSLTEDFEREKEHSTNKNVFINCLSSGKSEGDDSGFTEDQTRRSVKQSTRKLLPKSFSSHYKFSKPVLQSQSISLVQQSEFSLEVTQYQEREPVLVRASPSCSVDVTERAGSSLQSPLLSADLTTAQTPSEFLALTEDSVSEMDAFSKSGSMASHCDNFGHNDSTSQMSLNSAAVTKTTTELTGTVPCAIMSPGKYRLEGQCSTESNSLPETSAANQKEVLLQIAELPATSVSHSESNLPADSEREENIGLQNGETMLGTNSPRKLGFYEQHKAIAEHVKGIHPISDSKIIPTSGDHHIFNKTSHGYEANPAKVLASSLSPFREGRFIERRLRSSSEGTAGSSRMILKPKDGNIEEVNSLRKQRAGSSSSKMNSLDVLNNLGSCELDEDDLMLDLEFLEEQSLHPSVCREDSYHSVVSCAAVVLTPMEPMIEMKKREEPEFPEPSKQNLSLKLTKDVDQEARCSHISRMPNSPSADWPLQGVEENGGIDSLPFRLMLQDCTAVKTLLLKMKRVLQESADMSPASSTTSLPVSPLTEEPVPFKDIMKDECSMLKLQLKEKDELISQLQEELGKVRHLQKAFASRVDKSTQTELLCYDGLNLKRLETVQGGREATYRNRIVSQNLSTRDRKAIHTPTEDRFRYSAADQTSPYKNKTCQLPSLCLSNFLKDKELAEVIKHSRGTYETLTSDVTQNLRATVGQSSLKPTAKTEGLSTFLEKPKDQVATARQHSTFTGRFGQPPRGPISLHMYSRKNVFLHHNLHSTELQTLGQQDG
"
variation 360
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:199614921"
variation 370
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:200195268"
variation 402
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:368150393"
variation 416
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="c"
/db_xref="dbSNP:371755465"
variation 458
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="g"
/db_xref="dbSNP:192580573"
variation 459
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:76979602"
variation 472
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="g"
/db_xref="dbSNP:34706417"
variation 516
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:200969775"
variation 522
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="g"
/db_xref="dbSNP:184253075"
variation 542
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:369591675"
variation 555
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:373213361"
variation 561
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="t"
/db_xref="dbSNP:377147993"
variation 584
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:370619679"
variation 589
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="g"
/db_xref="dbSNP:373060209"
variation 608
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:377402944"
variation 655
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:371138602"
variation 662
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:200481128"
variation 675
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:368224537"
variation 714
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:142325447"
variation 717
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="c"
/db_xref="dbSNP:371096921"
variation 731
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:76123304"
variation 737
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="g"
/db_xref="dbSNP:114592140"
variation 851
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:199696987"
variation 971
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:202076608"
variation 1049
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:200732825"
variation 1054
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:146032287"
variation 1078
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:375348353"
variation 1099
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="c"
/db_xref="dbSNP:35038198"
variation 1272
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:372404975"
variation 1273
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:200529705"
variation 1276
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="t"
/db_xref="dbSNP:369314240"
variation 1284
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:372893740"
variation 1291
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:377342558"
variation 1292
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:368884423"
variation 1312
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:34445159"
variation 1321
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:35057072"
variation 1342
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:371219201"
variation 1344
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:375167122"
variation 1353
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:202060801"
variation 1354
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:370616330"
variation 1373
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="g"
/db_xref="dbSNP:374058079"
variation 1384
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:368109569"
variation 1385
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="t"
/db_xref="dbSNP:72659490"
variation 1398
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:373844112"
variation 1426
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="g"
/db_xref="dbSNP:372479561"
variation 1435
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:368828745"
variation 1467
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:372304488"
variation 1476
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:200176834"
variation 1484
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:12647859"
variation 1510
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:369643100"
variation 1539
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:191663649"
variation 1551
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:372007893"
variation 1554
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="t"
/db_xref="dbSNP:200137337"
variation 1568
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="t"
/db_xref="dbSNP:376784766"
variation 1595
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="t"
/db_xref="dbSNP:202091224"
variation 1598
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:184476624"
variation 1617
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:111729858"
variation 1618
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:188755217"
variation 1627
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:369959947"
variation 1659
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:373458356"
exon 1665..1849
/gene="CCSER1"
/gene_synonym="FAM190A"
/inference="alignment:Splign:1.39.8"
variation 1675
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:187564848"
variation 1701
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:373593209"
variation 1702
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="t"
/db_xref="dbSNP:367744361"
variation 1769
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:142352144"
variation 1787
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:200976407"
variation 1798
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:368916233"
exon 1850..1943
/gene="CCSER1"
/gene_synonym="FAM190A"
/inference="alignment:Splign:1.39.8"
variation 1866
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace=""
/replace="t"
/db_xref="dbSNP:35235945"
variation 1938
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="c"
/db_xref="dbSNP:369051250"
exon 1944..2064
/gene="CCSER1"
/gene_synonym="FAM190A"
/inference="alignment:Splign:1.39.8"
variation 1968
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="g"
/db_xref="dbSNP:370139962"
variation 1973
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:374464125"
variation 1984
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:182106294"
variation 1987
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:150977627"
variation 2003
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:187207325"
exon 2065..2272
/gene="CCSER1"
/gene_synonym="FAM190A"
/inference="alignment:Splign:1.39.8"
variation 2070
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:371946210"
variation 2078
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:375334932"
variation 2089
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:200539996"
variation 2091
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:368111669"
variation 2127
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:371365258"
variation 2133
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:201505045"
variation 2143
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:375966943"
variation 2149
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:369689377"
variation 2177
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="c"
/db_xref="dbSNP:202243228"
variation 2206
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:369064746"
variation 2239
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:375090018"
variation 2246
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:369597376"
variation 2250
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:373209732"
exon 2273..2350
/gene="CCSER1"
/gene_synonym="FAM190A"
/inference="alignment:Splign:1.39.8"
variation 2274
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:200214194"
variation 2313
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:371145987"
variation 2316
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:376190647"
variation 2322
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:201489889"
exon 2351..2434
/gene="CCSER1"
/gene_synonym="FAM190A"
/inference="alignment:Splign:1.39.8"
variation 2354
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:61743906"
variation 2374
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:373571745"
exon 2435..2512
/gene="CCSER1"
/gene_synonym="FAM190A"
/inference="alignment:Splign:1.39.8"
exon 2513..2557
/gene="CCSER1"
/gene_synonym="FAM190A"
/inference="alignment:Splign:1.39.8"
variation 2541
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:76504638"
exon 2558..6205
/gene="CCSER1"
/gene_synonym="FAM190A"
/inference="alignment:Splign:1.39.8"
variation 2649
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:370719096"
variation 2807
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:199543790"
variation 2849
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:374138135"
variation 2878
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:377349774"
variation 2901
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:370398819"
variation 3054
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:374846974"
variation 3108
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:142684466"
variation 3161
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="g"
/db_xref="dbSNP:189219877"
variation 3189
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:72658064"
variation 3201
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:62311870"
variation 3246
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:368053715"
variation 3254
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="c"
/db_xref="dbSNP:9991015"
variation 3256
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:181969780"
variation 3262
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:375859720"
variation 3309
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:140819001"
variation 3319
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:368349378"
variation 3333
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:10013578"
variation 3502
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="t"
/db_xref="dbSNP:77808276"
variation 3513
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:186539249"
variation 3521
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:190716650"
variation 3663
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:372716124"
variation 3701
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:150133247"
variation 3741
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="c"
/db_xref="dbSNP:377313809"
variation 3776
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:372980376"
variation 3831
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:181963575"
variation 3833
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="t"
/db_xref="dbSNP:185203412"
variation 3877
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:10014070"
variation 3899
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="t"
/db_xref="dbSNP:57495859"
variation 3910
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:189627589"
variation 3953
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:182700147"
variation 3977
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:185435003"
variation 3981
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:191021457"
variation 4036
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:62311871"
variation 4079
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="g"
/db_xref="dbSNP:6841541"
variation 4103
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:147697678"
variation 4171
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:116651948"
variation 4263
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:183697283"
variation 4284
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:374737908"
variation 4301
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="c"
/db_xref="dbSNP:116108384"
variation 4317
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1516697"
variation 4322
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:188269688"
variation 4426
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:62311872"
variation 4434
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:112360537"
variation 4549
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:142390777"
variation 4589
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:73836298"
variation 4645
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="c"
/db_xref="dbSNP:192365520"
variation 4791..4794
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace=""
/replace="tttc"
/db_xref="dbSNP:148742254"
variation 4864
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:78673189"
variation 4974..4977
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace=""
/replace="atta"
/db_xref="dbSNP:144720566"
variation 5134
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:146363069"
variation 5155
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="g"
/db_xref="dbSNP:183323025"
variation 5158
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:139023511"
variation 5318
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace=""
/replace="t"
/db_xref="dbSNP:35647723"
variation 5341
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:186910767"
variation 5433
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:73836299"
variation 5466
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:143349832"
variation 5486..5487
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace=""
/replace="t"
/db_xref="dbSNP:376345641"
variation 5561
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:372471250"
variation 5615
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:1914240"
variation 5656
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:191426308"
variation 5740
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:143806543"
variation 5895
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:148159189"
variation 5912
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="c"
/replace="t"
/db_xref="dbSNP:369849530"
variation 5930
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="c"
/db_xref="dbSNP:183623288"
variation 5937
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="c"
/db_xref="dbSNP:187178477"
STS 6025..6108
/gene="CCSER1"
/gene_synonym="FAM190A"
/standard_name="1150"
/db_xref="UniSTS:28046"
variation 6070..6071
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace=""
/replace="a"
/db_xref="dbSNP:148066440"
variation 6076
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:374024992"
variation 6077
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:192601124"
variation 6083
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="g"
/replace="t"
/db_xref="dbSNP:370280119"
variation 6193
/gene="CCSER1"
/gene_synonym="FAM190A"
/replace="a"
/replace="g"
/db_xref="dbSNP:72886336"
ORIGIN
acaaatagtcgccgacctactgccaatccgcctctcctctctctctctctctgtctcaacatgactgactgggaagcggtggctcgggcagagcagctccgctggcgcaggcaggaggagcaggaggattattaaataacgcagctggactctgtgcaactgggagtggagaggagcccaacagccgagaaggggagggagggcagaggagggggaccaggaaggacacccccgtgccccgaagacataaatccctgagtgcccgggaggagccttaacaagcgcacggagccctcaaggctgcaaagttggctttcacagtgcaagcctttgattcccaatgggggactcaggatcaagacgatctaccctggtctcccggttgccaatattcagaagaagtattaacagaagacatgattctcttccttcttcaccttcttccagtaatacagttggtgtccacagttcctctccttccagcactaactcaagctcaggtagcacaggtaaacggaggagcatattccgtactccttccattagcttccaccataagaaggggagtgagcctaagcaagagcctaccaaccagaaccttagtatttcaaatggtgctcaacctggtcacagcaatatgcagaaactgagtttggaagaacatattaagaccaggggaagacattctgttggttttagtagttcacgaaataagaagataacaagatctttgacagaggattttgaaagggaaaaagagcactcaactaacaagaatgtctttataaattgtctaagttctggcaaaagtgaaggggatgattctggtttcacagaagaccaaactcgtcgttctgttaagcagtcaacaaggaagctactccctaaatctttttcatctcactataaattttctaagccagttctacagagccaatccatttcattggtacaacagtctgaattctcattggaagttacacagtaccaagagagagaacctgtattagtaagagcttcgccatcctgttctgtggatgtaacagaacgggcaggaagctctttacaatctcctttgctttctgctgatcttaccacagctcagacaccttcagaatttttagccttgactgaagattctgtgtctgaaatggatgcattttctaaaagtggaagcatggcatcccactgtgacaactttggccacaatgattctacctctcagatgtccctcaattctgctgctgttacaaagacaacaacagaacttacgggaactgttccctgtgcaattatgtctcctgggaaatataggttagagggtcaatgtagcactgaatctaattcattaccggaaacctctgctgctaatcagaaggaagtgttattacaaattgctgaactacctgctacaagtgtgagccactcagagagtaacctaccagcagatagtgaaagagaagaaaatatagggttacaaaatggtgaaacaatgctggggacaaactccccaaggaaacttggattttatgagcaacataaagcaatagcggaacatgtaaaagggatccatcctatttcagattcaaagataatacctacttctggtgatcatcatatttttaacaaaacatcacatggatatgaagcaaatcctgccaaagttcttgccagtagtctcagtccatttcgtgaaggaagatttatagagaggagactgcgatcctcgtcagaaggcactgcagggagtagcagaatgattttgaaaccgaaagatggaaatatagaagaagttaatagtttaagaaagcaaagagcaggttcttcatcttcaaaaatgaacagtttggatgttttgaataatttgggatcttgtgaactggatgaagatgatctaatgcttgatcttgaatttttagaggaacagagtcttcacccttctgtttgccgggaggactcatatcactctgtcgtctcatgtgccgcagtagttcttactcctatggaaccaatgatagaaatgaagaaaagagaagaaccagaatttcctgagccttccaaacagaatctttccctgaaattaacaaaggacgttgatcaagaagccaggtgttcccacatcagccgaatgcccaacagtccatctgcggattggcctctacaaggtgtggaagaaaacggaggcatagattctctgccattcagactgatgttacaggactgcacggcagtcaagacgttattattaaagatgaagagagttcttcaagagagtgcagacatgagtccagcaagcagtaccacgtcacttcctgttagtcctcttactgaagagccagtgcctttcaaggatataatgaaagatgaatgctcgatgctcaagctgcagctgaaagagaaggatgaactcatttcccaacttcaggaagagctgggaaaagtccggcatttacagaaggcttttgcttcaagagtagataaatccacacagactgaactactatgctatgatggtttaaacttgaaaagactagagacagtacaaggagggagagaggctacatatcgaaatcgaattgtgagccaaaatctcagcacaagggacagaaaagcaatacatactcccaccgaggaccgttttaggtattcggcagcggaccagacaagcccctacaaaaacaagacctgtcaactcccaagtctctgtttaagtaatttcctgaaggacaaggaactagcagaagttatcaaacattcaagaggaacttatgaaaccctcacttcagacgttacacagaacttacgggccaccgttgggcagagctctctgaagccaacagctaagacagaagggctctccacgttcttagagaaaccaaaggaccaagttgctacggcccgacagcattcgacctttacaggcaggtttggacagccacccagagggccaatctctttacacatgtacagcaggaagaatgtgtttctccaccacaatttacacagcactgagctgcaaactctaggccagcaggatgggtaattaaatcaccgtattcctgtctttgggtaggataaagatggttagtgtttctcgtgcatagttcatattaaaattgtcatgtactttttcttacattttagttataaacagagttgtgttgttgggttttttttcttagtcataaacaaagacttgtgggttttttttttccaagagtgaaagtttgagcatgttaattgaactaggttgcattgccttgaagactttactatataggtgtataataaatgggaccatcatgatcgtttatatagtccataatttatttattttttatctctatcacttactgatatgcattaaggtttcagaagataatatcaaatagcaatctgttcactgttaatggtgttactataaaagtagacctgatgaaaaatagataaaggaattataaagaattttaaattatataattaatagaaggaggaaaaaagagaaatgttaacgtcttatatttggtggtatatttatttgaagaatgtggcttgcttgcatgtaacctagagatgtgtttgtctctattacatacattcaagctcatcttgtgatactagtaagggggaaatggctgtattttttttcctttaaacgtttagttcatactagttcacaaaggatttcagacagagtaattgctagccaaatagagaatgacagctctgatctttgaaaaattttgcttttagtttttgttattgatgttgaagtaccgtgacataacacaaggtgataaagttggttgaattttgtcagatgatgcataaatactgacatgctatattctttgagccactgtcatggcaatataaacattttttcaaaatttcaaggatgaaacatcctaagaaaattattctttttctttactttccttattttttaaaatgttcttttttatgtaaatccaattttggtttatatacatcaacccatatctataattttatgaactgaagaacagaaagtcagtattttagtagccagcatacaatattctgactatgcagaaatctagatttggaacaaaagtaaagtaaatgtgaacattggcaatttaatcttagaaataagcttctaacaggaatatttaaaacccatttgatggcaaatatttctctttgacaaataaggcccaaatatgttataatatgttatatacttatgtgcactttagatcaatatatgaattgatctatggataattccatcatgttcaattagtagcagagcagaatcaaagagtacaattgaatacataaataaataatttttaaaagactaataggaatcaaggctgcagttttcttatacacatcagagctgttaagtacatccacattagccatagtccatgcaaattgaaactgtcatacctactgcatgatctgtttcccttgcattttctaacagaatctgtcagcgtgcacaagcaagatgaacaaagggaaattgagatagcagttttagcatggcatctgacaacttgcttaaattaaagctgtgtgcaaaatgcatctcctattataaaaatgtatttgtgccctgtgctttggggaaaagccattagacactccacccctgagctttaactactgaactttgatacatttgcaaacttagattggaactgataaagtaaggagtcgagtggatatgttgtacttgtaattttggttttccaaaggaacacacatgtgcatcaaggcagacatttgccaaatgttttctttctttgcgtgtttgtaattctgccaaaagagaacaatatacactgcaaattgcttgacttaatgagattgccatctaaagttcccaccatactttggaagctataatgatcatgcagatatacactttgggctgggcaatatttaagaaatgataggaaaatagaaaaatcatgattattaattgtggaattcagcttgatttgtcctaaatgttggtgtctgttgctagagtattttaaatctgtacataaataagcatgataaaataatcaaggattttttcccaggatatggaagaactatgtatcacaaataatgtttttgatttggacttttggagttgatagttttgttttcctggaagatagacttttgaattatactttataaaaataatctatttatagaagatctgtcatttaatagacattttaagagatgttttaaacgctagtattttcttgaaaaatcttttttaaagctgaatcattcaaaagaaaacctggattaaacagttcgattttaaaaggaagggtattttttggaaatatcatcttaaagctgttttgtatcagtattttcaacattgttataatattatttgtaatactaagtgtaactcaggcctggagaaggtgtaagcccactatgctaatgtacatcagtaactgtaaaacaggggttctttgtaagttcctcttgtgtatatatagtaacttataacaatggcatgtgggcattctttcagtgaattgctttctttgtactaaaatctctagttttctaagacagttccatgtataaaaatgatttatgcatttctccaaggcggtacatatccaaagacatgacaccagggggaaaaagtgcttgtttttctgatggaagcagtggtcttttcttttctttcctctttcttttgtgcatgtgtatgtgtagctaagcctaaataaccctgtaaaatttctgctgcaaattgtctcttctgaatttagaatgtgttttaaaggaacacttaggaagagaaataccttgaagaaaagctgtttccacctgaaataaactgttcccatttttataattattggaacatgaaactgtatttctatgaactcaatgatttttttccataaaattatatgctaagagagtcaccacaaaactatgaattctctcccgaattatttttgcttctttggagcaccatagtctttgttcaaatcacaacatgaaactgttgctgcaatgctaaagatgtgaatccaccactatcaatacggtcagggtaaaacctggagccacatgttattcaagttatttttgttatctaatgattgacatgaaaataaaatagtaagccaatattaatttgtaggcatagttgccccacttaaagtgtttacaaaga
//
by
@meso_cacase at
DBCLS
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