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2024-04-24 20:36:52, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_020882 4187 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens collagen, type XX, alpha 1 (COL20A1), mRNA.
ACCESSION NM_020882 XM_028834
VERSION NM_020882.2 GI:112734844
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 4187)
AUTHORS Deloukas,P., Matthews,L.H., Ashurst,J., Burton,J., Gilbert,J.G.,
Jones,M., Stavrides,G., Almeida,J.P., Babbage,A.K., Bagguley,C.L.,
Bailey,J., Barlow,K.F., Bates,K.N., Beard,L.M., Beare,D.M.,
Beasley,O.P., Bird,C.P., Blakey,S.E., Bridgeman,A.M., Brown,A.J.,
Buck,D., Burrill,W., Butler,A.P., Carder,C., Carter,N.P.,
Chapman,J.C., Clamp,M., Clark,G., Clark,L.N., Clark,S.Y.,
Clee,C.M., Clegg,S., Cobley,V.E., Collier,R.E., Connor,R.,
Corby,N.R., Coulson,A., Coville,G.J., Deadman,R., Dhami,P.,
Dunn,M., Ellington,A.G., Frankland,J.A., Fraser,A., French,L.,
Garner,P., Grafham,D.V., Griffiths,C., Griffiths,M.N., Gwilliam,R.,
Hall,R.E., Hammond,S., Harley,J.L., Heath,P.D., Ho,S., Holden,J.L.,
Howden,P.J., Huckle,E., Hunt,A.R., Hunt,S.E., Jekosch,K.,
Johnson,C.M., Johnson,D., Kay,M.P., Kimberley,A.M., King,A.,
Knights,A., Laird,G.K., Lawlor,S., Lehvaslaiho,M.H., Leversha,M.,
Lloyd,C., Lloyd,D.M., Lovell,J.D., Marsh,V.L., Martin,S.L.,
McConnachie,L.J., McLay,K., McMurray,A.A., Milne,S., Mistry,D.,
Moore,M.J., Mullikin,J.C., Nickerson,T., Oliver,K., Parker,A.,
Patel,R., Pearce,T.A., Peck,A.I., Phillimore,B.J.,
Prathalingam,S.R., Plumb,R.W., Ramsay,H., Rice,C.M., Ross,M.T.,
Scott,C.E., Sehra,H.K., Shownkeen,R., Sims,S., Skuce,C.D.,
Smith,M.L., Soderlund,C., Steward,C.A., Sulston,J.E., Swann,M.,
Sycamore,N., Taylor,R., Tee,L., Thomas,D.W., Thorpe,A., Tracey,A.,
Tromans,A.C., Vaudin,M., Wall,M., Wallis,J.M., Whitehead,S.L.,
Whittaker,P., Willey,D.L., Williams,L., Williams,S.A., Wilming,L.,
Wray,P.W., Hubbard,T., Durbin,R.M., Bentley,D.R., Beck,S. and
Rogers,J.
TITLE The DNA sequence and comparative analysis of human chromosome 20
JOURNAL Nature 414 (6866), 865-871 (2001)
PUBMED 11780052
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
BC043183.1, BC041767.1, AL121827.34 and AB040943.1.
On Aug 18, 2006 this sequence version replaced gi:44917609.
##Evidence-Data-START##
Transcript exon combination :: BC043183.1 [ECO:0000332]
RNAseq introns :: mixed/partial sample support
ERS025084, ERS025088 [ECO:0000350]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-136 BC043183.1 6-141
137-1205 BC041767.1 99-1167
1206-1377 BC043183.1 1211-1382
1378-1379 AL121827.34 79897-79898
1380-1903 BC041767.1 1345-1868
1904-2869 BC043183.1 1909-2874
2870-3114 AB040943.1 2322-2566
3115-3158 AL121827.34 89639-89682
3159-3671 BC043183.1 3164-3676
3672-3673 AB040943.1 3124-3125
3674-3810 BC043183.1 3679-3815
3811-3812 AB040943.1 3281-3282
3813-4187 BC043183.1 3818-4192
FEATURES Location/Qualifiers
source 1..4187
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="20"
/map="20q13.33"
gene 1..4187
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="collagen, type XX, alpha 1"
/db_xref="GeneID:57642"
/db_xref="HGNC:14670"
exon 1..90
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
misc_feature 2..4
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="upstream in-frame stop codon"
variation 6
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:373583822"
variation 53
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:190626448"
variation 65
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:192362734"
exon 91..182
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 93
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:183105977"
CDS 101..3955
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="collagen-like protein; collagen alpha-1(XX) chain"
/codon_start=1
/product="collagen alpha-1(XX) chain precursor"
/protein_id="NP_065933.2"
/db_xref="GI:112734845"
/db_xref="CCDS:CCDS46628.1"
/db_xref="GeneID:57642"
/db_xref="HGNC:14670"
/translation="
MSSGDPAHLGLCLWLWLGATLGREQVQASGLLRLAVLPEDRLQMKWRESEGSGLGYLVQVKPMAGDSEQEVILTTKTPKATVGGLSPSKGYTLQIFELTGSGRFLLARREFVIEDLKSSSLDRSSQRPLGSGAPEPTPSHTGSPDPEQASEPQVAFTPSQDPRTPAGPQFRCLPPVPADMVFLVDGSWSIGHSHFQQVKDFLASVIAPFEIGPDKVQVGLTQYSGDAQTEWDLNSLSTKEQVLAAVRRLRYKGGNTFTGLALTHVLGQNLQPAAGLRPEAAKVVILVTDGKSQDDVHTAARVLKDLGVNVFAVGVKNADEAELRLLASPPRDITVHSVLDFLQLGALAGLLSRLICQRLQGGSPRQGPAAAPALDTLPAPTSLVLSQVTSSSIRLSWTPAPRHPLKYLIVWRASRGGTPREVVVEGPAASTELHNLASRTEYLVSVFPIYEGGVGEGLRGLVTTAPLPPPRALTLAAVTPRTVHLTWQPSAGATHYLVRCSPASPKGEEEEREVQVGRPEVLLDGLEPGRDYEVSVQSLRGPEGSEARGIRARTPTLAPPRHLGFSDVSHDAARVFWEGAPRPVRLVRVTYVSSEGGHSGQTEAPGNATSATLGPLSSSTTYTVRVTCLYPGGGSSTLTGRVTTKKAPSPSQLSMTELPGDAVQLAWVAAAPSGVLVYQITWTPLGEGKAHEISVPGNLGTAVLPGLGRHTEYDVTILAYYRDGARSDPVSLRYTPSTVSRSPPSNLALASETPDSLQVSWTPPLGRVLHYWLTYAPASGLGPEKSVSVPGARSHVTLPDLQAATKYRVLVSAIYAAGRSEAVSATGQTACPALRPDGSLPGFDLMVAFSLVEKAYASIRGVAMEPSAFGGTPTFTLFKDAQLTRRVSDVYPAPLPPEHTIVFLVRLLPETPREAFALWQMTAEDFQPLLGVLLDAGKKSLTYFHRDPRAALQEATFDPQEVRKIFFGSFHKVHVAVGRSKVRLYVDCRKVAERPLGEMGSPPAAGFVTLGRLAKARGPRSSSAAFQLQMLQIVCSDTWADEDRCCELPASRDGETCPAFVSACSCSSETPGPPGPQGPPGLPGRNGTPGEQGFPGPRGPPGVKGEKGDHGLPGLQGHPGHQGIPGRVGLQGPKGMRGLEGTAGLPGPPGPRGFQGMAGARGTSGERGPPGTVGPTGLPGPKGERGEKGEPQSLATLYQLVSQASHVSKFDSFHENTRPPMPILEQKLEPGTEPLGSPGTRSKALVPGEWGRGGRHLEGRGEPGAVGQMGSPGQQGASTQGLWE
"
sig_peptide 101..166
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
mat_peptide 167..3952
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/product="Collagen alpha-1(XX) chain"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9P218.4)"
misc_feature 215..406
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="Fibronectin type 3 domain; One of three types of
internal repeats found in the plasma protein fibronectin.
Its tenth fibronectin type III repeat contains an RGD cell
recognition sequence in a flexible loop between 2 strands.
Approximately 2% of all...; Region: FN3; cl00065"
/db_xref="CDD:206813"
misc_feature 632..1123
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="Collagen: The extracellular matrix represents a
complex alloy of variable members of diverse protein
families defining structural integrity and various
physiological functions. The most abundant family is the
collagens with more than 20 different...; Region:
vWA_collagen_alphaI-XII-like; cd01482"
/db_xref="CDD:29255"
misc_feature order(653..655,659..661,665..667,866..868,965..967)
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="metal ion-dependent adhesion site (MIDAS); other
site"
/db_xref="CDD:29255"
misc_feature order(659..667,671..673,866..868)
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="integrin-collagen binding site; other site"
/db_xref="CDD:29255"
misc_feature 1277..1438
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="Fibronectin type 3 domain; One of three types of
internal repeats found in the plasma protein fibronectin.
Its tenth fibronectin type III repeat contains an RGD cell
recognition sequence in a flexible loop between 2 strands.
Approximately 2% of all...; Region: FN3; cl00065"
/db_xref="CDD:206813"
misc_feature 1541..1723
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="Fibronectin type 3 domain; One of three types of
internal repeats found in the plasma protein fibronectin.
Its tenth fibronectin type III repeat contains an RGD cell
recognition sequence in a flexible loop between 2 strands.
Approximately 2% of all...; Region: FN3; cl00065"
/db_xref="CDD:206813"
misc_feature 1775..2032
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="Fibronectin type 3 domain; One of three types of
internal repeats found in the plasma protein fibronectin.
Its tenth fibronectin type III repeat contains an RGD cell
recognition sequence in a flexible loop between 2 strands.
Approximately 2% of all...; Region: FN3; cd00063"
/db_xref="CDD:28945"
misc_feature order(1952..1954,1997..1999)
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="Interdomain contacts; other site"
/db_xref="CDD:28945"
misc_feature order(2000..2002,2006..2011)
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="Cytokine receptor motif; other site"
/db_xref="CDD:28945"
misc_feature 2042..2293
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="Fibronectin type 3 domain; One of three types of
internal repeats found in the plasma protein fibronectin.
Its tenth fibronectin type III repeat contains an RGD cell
recognition sequence in a flexible loop between 2 strands.
Approximately 2% of all...; Region: FN3; cd00063"
/db_xref="CDD:28945"
misc_feature order(2225..2227,2270..2272)
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="Interdomain contacts; other site"
/db_xref="CDD:28945"
misc_feature order(2276..2281,2285..2290)
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="Cytokine receptor motif; other site"
/db_xref="CDD:28945"
misc_feature 2324..2578
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="Fibronectin type 3 domain; One of three types of
internal repeats found in the plasma protein fibronectin.
Its tenth fibronectin type III repeat contains an RGD cell
recognition sequence in a flexible loop between 2 strands.
Approximately 2% of all...; Region: FN3; cd00063"
/db_xref="CDD:28945"
misc_feature order(2507..2509,2552..2554)
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="Interdomain contacts; other site"
/db_xref="CDD:28945"
misc_feature order(2555..2560,2564..2569)
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="Cytokine receptor motif; other site"
/db_xref="CDD:28945"
misc_feature 2624..3208
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="Laminin G domain; Laminin G-like domains are
usually Ca++ mediated receptors that can have binding
sites for steroids, beta1 integrins, heparin, sulfatides,
fibulin-1, and alpha-dystroglycans. Proteins that contain
LamG domains serve a variety of...; Region: LamG; cl00102"
/db_xref="CDD:206838"
misc_feature 3359..3583
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/note="Collagen triple helix repeat (20 copies); Region:
Collagen; pfam01391"
/db_xref="CDD:189968"
variation 120
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:370140638"
variation 122
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:376830125"
variation 127
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:369025538"
variation 173
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:372419078"
exon 183..293
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 203
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:373850387"
variation 221
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:376288950"
variation 222
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:369131228"
variation 226
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:372981936"
variation 269
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="c"
/db_xref="dbSNP:144861412"
exon 294..437
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 335..336
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace=""
/replace="a"
/db_xref="dbSNP:34773333"
variation 346
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="g"
/replace="t"
/db_xref="dbSNP:201791689"
variation 388
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:371649528"
variation 389
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201366483"
variation 393
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="t"
/db_xref="dbSNP:368040086"
variation 413
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:377096032"
variation 420
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="c"
/db_xref="dbSNP:371961933"
exon 438..596
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 442
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:6090355"
variation 458
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="t"
/db_xref="dbSNP:201013661"
variation 481
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:369730137"
variation 487
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:372429110"
variation 489
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:376722969"
variation 501
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:753686"
variation 523
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:145631155"
variation 545
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201968872"
variation 559
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201480381"
variation 561
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:200460257"
exon 597..755
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 598
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="c"
/db_xref="dbSNP:3746373"
variation 599
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201827276"
variation 611
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:200049003"
variation 626
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:75604641"
variation 644
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="g"
/replace="t"
/db_xref="dbSNP:367630708"
variation 648
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:200736608"
variation 661
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:370768995"
variation 674
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:374717534"
variation 704
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:368508298"
variation 718
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:372458260"
variation 722
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:375441222"
variation 733
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:200569624"
variation 734
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:374109084"
exon 756..875
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 766
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201264923"
variation 772
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:376138467"
variation 802
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:369163909"
variation 839
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:367571854"
variation 840
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:376683624"
variation 842
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:371357198"
variation 843
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:199535047"
variation 849
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:184180648"
variation 857
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:188732284"
variation 858
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="g"
/replace="t"
/db_xref="dbSNP:373562137"
variation 861
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:368044718"
variation 864
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:3746374"
exon 876..1040
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 911
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:140030199"
variation 916
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:375403697"
variation 918
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:368479169"
variation 919
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:200720576"
variation 930
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:374818195"
variation 964
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:200002318"
variation 968
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:372806374"
variation 982
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:377136576"
variation 983
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="g"
/replace="t"
/db_xref="dbSNP:369552635"
variation 1002
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:374662658"
variation 1004
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:368382733"
variation 1015
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:377731107"
variation 1033
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="c"
/db_xref="dbSNP:371146289"
variation 1034
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:373120786"
exon 1041..1205
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 1055
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:202054720"
variation 1132
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:370751464"
variation 1133
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:374160831"
variation 1177
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:111641640"
variation 1193
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:372211237"
exon 1206..1363
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 1210
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:377006506"
variation 1251..1252
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace=""
/replace="a"
/db_xref="dbSNP:34485195"
variation 1258
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:370160805"
variation 1268
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="t"
/db_xref="dbSNP:200924087"
variation 1281
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="g"
/replace="t"
/db_xref="dbSNP:201491872"
variation 1299
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:377073867"
variation 1305
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:368982947"
variation 1313
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="c"
/db_xref="dbSNP:186757692"
variation 1328
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:372938275"
variation 1347
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:375988776"
variation 1357
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="c"
/db_xref="dbSNP:370343751"
exon 1364..1493
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 1378
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:4809287"
variation 1381
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:201958902"
variation 1384
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:369936311"
variation 1385
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:370533858"
variation 1404
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:372294549"
variation 1416
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201043063"
variation 1437
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="t"
/db_xref="dbSNP:369917449"
variation 1449
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:372796994"
variation 1466
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201458379"
variation 1476
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="g"
/replace="t"
/db_xref="dbSNP:376053524"
exon 1494..1639
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 1506
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:202110157"
variation 1528
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:371105219"
variation 1531
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:3746376"
variation 1536
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:376721997"
variation 1540
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:371306583"
variation 1595
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:375157219"
exon 1640..1763
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 1648
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:372276775"
variation 1652
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:376817042"
variation 1702
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="c"
/db_xref="dbSNP:368310195"
variation 1704
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:113738403"
variation 1705
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:150167513"
variation 1715
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:6062886"
variation 1717
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="g"
/replace="t"
/db_xref="dbSNP:369260236"
variation 1718
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:372462239"
variation 1736
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:372388936"
variation 1752
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:6089877"
variation 1763
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:376114513"
exon 1764..1903
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 1779
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:184582863"
variation 1802
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:188950518"
variation 1804
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:200521357"
variation 1815
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:375504407"
variation 1816
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:374496650"
variation 1821
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:73329169"
variation 1843
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:200123182"
variation 1854
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:375174903"
variation 1861
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:368464203"
variation 1865
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:371594397"
variation 1890
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201868354"
variation 1896
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:45465106"
exon 1904..2033
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 1929
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:201102423"
variation 1935
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:6011729"
variation 1936
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:377213715"
variation 1941
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:199662662"
variation 1942
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:374376106"
variation 1960
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:111272882"
variation 1967
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:202037894"
variation 1974
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201584342"
variation 1994
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:368905948"
variation 2010
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:200258845"
variation 2011
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:199552436"
variation 2021
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:201391388"
variation 2022
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:371561136"
exon 2034..2176
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 2046
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:199754091"
variation 2067
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:200873960"
variation 2083
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:4809530"
variation 2133
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:143321165"
variation 2142
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:373678411"
variation 2143
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:376373104"
variation 2146
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="g"
/replace="t"
/db_xref="dbSNP:369459285"
variation 2148
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:199774605"
exon 2177..2309
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 2197
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:375193228"
variation 2198
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:367897903"
variation 2202
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:113242150"
variation 2231
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:375390804"
variation 2242
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:201438584"
variation 2243
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:200875270"
variation 2254
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:199849682"
variation 2256
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:377187630"
variation 2264
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:369956737"
variation 2269
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:371862665"
variation 2273
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:376473959"
variation 2297
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:199598230"
exon 2310..2458
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 2313
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="c"
/db_xref="dbSNP:77576225"
variation 2314
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:368855968"
variation 2353
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:372563080"
variation 2362
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:376343023"
variation 2385
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:185636117"
variation 2392
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:373538527"
variation 2425
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:144975793"
variation 2431
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:148669802"
variation 2443
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:375149179"
variation 2445
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:199924678"
variation 2450
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:370151344"
variation 2452
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:41283002"
exon 2459..2588
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 2474
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:147670144"
variation 2480
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:369255661"
variation 2493
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:372380023"
variation 2497
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:374730380"
variation 2498
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:369095452"
variation 2506
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:373855748"
variation 2515
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:377014520"
variation 2525
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:371028614"
exon 2589..2624
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 2596
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:370290096"
variation 2604
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201818652"
variation 2611
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:368711881"
variation 2612
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201063299"
exon 2625..2763
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 2668
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:199530656"
variation 2670
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:375353757"
variation 2678..2679
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace=""
/replace="c"
/db_xref="dbSNP:34781242"
variation 2678
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:369054383"
variation 2680
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:371457012"
variation 2708
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:376634286"
variation 2727
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:139560899"
variation 2728
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:369912186"
exon 2764..2906
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 2768
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:199887430"
variation 2772
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:200830620"
variation 2789
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:200164977"
variation 2797
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:373710198"
variation 2803
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:377419781"
variation 2827
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:202207738"
variation 2828
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="g"
/replace="t"
/db_xref="dbSNP:374617184"
variation 2830
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:368289920"
variation 2834
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:371998722"
variation 2838
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201266100"
variation 2848
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:116380821"
variation 2849
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:371663966"
variation 2850
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:374933120"
variation 2851
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:145173988"
variation 2867
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:370769673"
variation 2883
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:377282900"
variation 2888
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:200320542"
exon 2907..3016
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 2908
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:376469990"
variation 2909
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:202080315"
variation 2917
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:148231100"
variation 2936
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:368681298"
variation 2983
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="t"
/db_xref="dbSNP:369398342"
variation 2994
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="g"
/replace="t"
/db_xref="dbSNP:370480252"
exon 3017..3175
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 3019
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:376339971"
variation 3021
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="t"
/db_xref="dbSNP:371022180"
variation 3023
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:374063666"
variation 3066
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:376712737"
variation 3115
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:6089881"
variation 3125
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:373891406"
variation 3126
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:200056990"
variation 3127
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:368035015"
variation 3142
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:41309377"
variation 3158
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:200235715"
variation 3159
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:200857441"
variation 3173
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:367831166"
variation 3175
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201660444"
exon 3176..3253
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 3193
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:374723684"
variation 3199
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:369267534"
variation 3205
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:373367639"
variation 3220
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:371179357"
variation 3221
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:375718406"
variation 3230
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:184817651"
variation 3245
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:377531077"
variation 3252
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:370691431"
exon 3254..3340
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 3274
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:115782548"
variation 3287
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:377370525"
variation 3311
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:370492419"
exon 3341..3394
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 3386
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:371842330"
exon 3395..3448
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 3413
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201493226"
exon 3449..3502
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 3455
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:199703564"
variation 3456
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:370083784"
variation 3457
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:374363300"
variation 3483
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="g"
/replace="t"
/db_xref="dbSNP:376338171"
variation 3490
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:371001479"
exon 3503..3556
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 3504..3505
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace=""
/replace="g"
/db_xref="dbSNP:35625416"
variation 3524
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:199859698"
variation 3534
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:114790522"
variation 3541..3542
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace=""
/replace="c"
/db_xref="dbSNP:142285603"
variation 3542
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace=""
/replace="c"
/db_xref="dbSNP:67798234"
variation 3556
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:372675396"
exon 3557..3628
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 3565
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:181405962"
variation 3587
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:376946659"
variation 3594
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:200268522"
variation 3600
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:117846427"
variation 3616
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:146952253"
variation 3617
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:370233069"
exon 3629..3664
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 3654
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:199729752"
exon 3665..3713
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 3668
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:367621924"
variation 3694
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:199562369"
exon 3714..3881
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 3718
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2273495"
variation 3719
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:369702957"
variation 3743
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201339591"
variation 3750
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:112825381"
variation 3752
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:73921047"
variation 3765
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:143699396"
variation 3789
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:115749294"
variation 3790
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:200097719"
variation 3810
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="c"
/db_xref="dbSNP:376331855"
variation 3821
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:371016549"
variation 3864
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:373532225"
exon 3882..3958
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 3906
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:6011740"
variation 3907
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:73921048"
variation 3914
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:372046790"
variation 3920
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:201640631"
variation 3922
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="g"
/replace="t"
/db_xref="dbSNP:369238688"
variation 3936
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:372971673"
variation 3939
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="t"
/db_xref="dbSNP:151293328"
variation 3952
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="g"
/db_xref="dbSNP:374721790"
exon 3959..4172
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/inference="alignment:Splign:1.39.8"
variation 3978
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:186542650"
variation 4019
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:190278278"
variation 4025
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:79986264"
variation 4108
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="a"
/replace="g"
/db_xref="dbSNP:115265086"
variation 4109
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:181138054"
variation 4124
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace="c"
/replace="t"
/db_xref="dbSNP:185399500"
variation 4158..4159
/gene="COL20A1"
/gene_synonym="bA261N11.4"
/replace=""
/replace="ct"
/db_xref="dbSNP:143325224"
ORIGIN
ataagctccagccttcctgtggccacagcaggaccagagtggaccagcacaccccaggagagaggactggggtcccaggagtaggaggagcccgagcaccatgagctccggagaccctgcacacctcggcctctgcctctggctgtggctgggcgccaccctgggaagagagcaagttcaagcaagcggtctcctgaggctggctgtgctgcctgaggaccggctgcagatgaagtggagagagtcggaggggagcggcctcggctacctggtgcaggtgaagcccatggcaggggactcggaacaggaggtgatactgaccaccaagacccctaaggccacagtggggggcctgagcccctccaagggctacaccttgcagatcttcgagctcactggctctgggcgcttcctgctagctcggagggagtttgtgattgaggatctgaagagtagctccctggacaggagcagccagaggcccctcggctctggagccccggagcccaccccctcccacacggggagcccagaccctgagcaggcttctgagccccaagttgccttcacaccaagccaggatccgcgcactcctgccggcccccagttccgctgcctgccccccgtgcctgctgacatggtcttcctggtggacgggtcctggagcattggccacagtcacttccagcaggtcaaggacttcctggccagtgtcatcgcaccctttgaaatcgggccggataaggtccaagtaggcctgactcagtacagcggggatgctcagactgagtgggacctgaactccctcagcaccaaggaacaggtgctggcagctgtgcgccgcctccgctacaagggggggaacacgttcacaggccttgccctgacccacgtgctggggcagaacctgcagccggcggctggcctccgtccagaggcagccaaggtggtgattctggtgacggacggcaagtcccaggacgatgtgcacactgctgcccgtgtcctcaaggacctgggcgtgaacgtcttcgctgtgggtgtgaagaacgccgatgaggctgagctgaggctcctggcgtccccgccgagggacatcaccgtccacagcgtgctggacttcctgcagctcggcgcgctggctggcctgctcagccgtctcatctgccagaggctccagggtgggagcccgcggcagggcccagcagcggctccagccctggacaccctccctgcccccaccagcctggtcctgagccaggtgacctcctccagcatccgcctgtcctggactccagccccccggcaccccctcaagtatctgatcgtttggcgagcctctagaggtggcacccccagggaggtggtggtggagggacccgccgcctccacggagctgcacaacctggcctcccgcacagagtacctggtctccgtgttccccatctatgagggcggggttggcgaaggcctgcggggcctggtgaccacagcacctctgcctccgccccgggcgctgaccctggccgcagtgacgcccagaaccgtccacctcacctggcagccctcggccggggccacccactacctggtgcgatgttctcctgcttcccccaagggtgaagaggaggagcgagaggtgcaggtcgggcggcccgaggtgctgctggatggcctggaacctggcagggactatgaggtctcggtgcagagcctgcgaggccctgagggcagcgaggcccggggcatccgtgccaggacccccaccctggcccccccgagacacctgggcttctcagacgtgagccacgacgcggcacgagtgttctgggagggtgccccgaggcctgtgcgcctggtcagggtcacctatgtgtccagcgagggtggacactcggggcagacagaggctcctgggaacgccacctcggccacgctggggcctctctcttcctccaccacctacactgtccgtgtcacctgcctctaccctgggggtggctcctctacgctgactggccgggtgaccaccaagaaagctcccagcccaagccagctgtccatgacggagctgccaggggatgcagtccagctggcgtgggtggccgcagccccgtctggcgtgcttgtctaccagatcacgtggacgcccctgggagaggggaaggctcacgagatctctgtcccagggaacctcggcacggccgtcctgcctggcctagggaggcacacagagtacgacgtcaccatcttggcctactacagggacggggcccgcagtgaccctgtgtccctccgctataccccctccacggtgagcaggagcccaccctccaacctggccctggcctcggagacccccgacagcctgcaggtcagctggacgcccccgcttggccgcgtgctccattactggctcacctacgcccccgcctctggcttgggacccgagaaatccgtctctgtgccaggagccaggagccacgtgacactgcccgacctgcaggcagccacgaagtacagggtcctggtctcagctatctatgcagcaggcaggagtgaggctgtgtctgccacgggccagacagcctgcccagccctccgccctgacggctccctcccagggtttgacctgatggtggccttcagcctggtggaaaaggcttatgcgtccatccggggcgtggccatggagccctctgccttcggtgggaccccgaccttcacgctcttcaaggacgcccagctgacaagacgggtcagtgacgtctacccagcccccctacctccagagcacaccatcgtcttccttgtgcgcctacttcccgagacaccccgtgaggccttcgcgctgtggcagatgacagccgaggacttccagcccctccttggggttctgctggatgccgggaagaagtccctgacctacttccaccgtgaccccagggctgccttgcaggaggccaccttcgacccgcaggaagtgaggaagattttcttcgggagcttccacaaggtgcacgtggctgtgggccgctccaaggtcaggctctatgtggactgccggaaggtggctgagcggccccttggggagatgggcagcccacccgctgcgggcttcgtcacgctggggaggctggccaaggccaggggcccccggagcagttcggccgcgtttcagctccagatgctgcagatcgtgtgcagtgacacctgggccgatgaggaccggtgctgtgagctccctgcctcgagggatggagagacctgccccgccttcgtgtctgcctgttcctgttcctcagagacccctgggcccccaggacctcaaggacccccaggcctccctgggaggaatggcaccccaggagagcagggcttcccagggcccaggggtccaccaggggtcaaaggagagaagggagaccatgggcttccaggcttgcagggccaccccggccaccagggcatccccgggagagttggcctccagggaccaaagggaatgagaggcctggagggaactgctggcctgcctggaccccctggccccagggggttccagggcatggcaggggccaggggcactagtggagagcgaggacctccagggaccgtggggcccacaggactgccagggcccaaaggggaacgaggagagaagggcgagccgcagtcccttgccaccctctaccagcttgtgagccaggcctcacacgtgtcaaagttcgactccttccacgagaacaccaggccccccatgcccatcttggagcagaagctggagccgggcactgagcccctggggtcccctggcacccgcagcaaggccctggttcctggagaatgggggcgtggtggccgccaccttgagggcagaggggagcctggagctgttggtcagatgggcagccctgggcagcagggggctagcacccagggcctctgggagtgacaggacattttctgcactgccccgaggaacgctgagccttcctccctgggtttgtctggacaccgagagcgaccacatcctggagaagccaggagaaaagctcaggaagagcctgcaggtggaaggagagggaagcagcggcctcggccaaggcccaccccatactcttggctctgtagcatttccaagttcagataaacccctgagtgctcacccaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:57642 -> Biological process: GO:0030198 [extracellular matrix organization] evidence: TAS
GeneID:57642 -> Cellular component: GO:0005576 [extracellular region] evidence: TAS
GeneID:57642 -> Cellular component: GO:0005581 [collagen] evidence: IEA
GeneID:57642 -> Cellular component: GO:0005615 [extracellular space] evidence: IEA
GeneID:57642 -> Cellular component: GO:0005788 [endoplasmic reticulum lumen] evidence: TAS
GeneID:57642 -> Cellular component: GO:0031012 [extracellular matrix] evidence: TAS
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