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2019-03-25 15:16:15, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001184776            6348 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens seizure related 6 homolog (mouse)-like (SEZ6L),
            transcript variant 5, mRNA.
ACCESSION   NM_001184776
VERSION     NM_001184776.1  GI:296179441
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 6348)
  AUTHORS   Wilk,J.B., Shrine,N.R., Loehr,L.R., Zhao,J.H., Manichaikul,A.,
            Lopez,L.M., Smith,A.V., Heckbert,S.R., Smolonska,J., Tang,W.,
            Loth,D.W., Curjuric,I., Hui,J., Cho,M.H., Latourelle,J.C.,
            Henry,A.P., Aldrich,M., Bakke,P., Beaty,T.H., Bentley,A.R.,
            Borecki,I.B., Brusselle,G.G., Burkart,K.M., Chen,T.H., Couper,D.,
            Crapo,J.D., Davies,G., Dupuis,J., Franceschini,N., Gulsvik,A.,
            Hancock,D.B., Harris,T.B., Hofman,A., Imboden,M., James,A.L.,
            Khaw,K.T., Lahousse,L., Launer,L.J., Litonjua,A., Liu,Y.,
            Lohman,K.K., Lomas,D.A., Lumley,T., Marciante,K.D., McArdle,W.L.,
            Meibohm,B., Morrison,A.C., Musk,A.W., Myers,R.H., North,K.E.,
            Postma,D.S., Psaty,B.M., Rich,S.S., Rivadeneira,F., Rochat,T.,
            Rotter,J.I., Artigas,M.S., Starr,J.M., Uitterlinden,A.G.,
            Wareham,N.J., Wijmenga,C., Zanen,P., Province,M.A., Silverman,E.K.,
            Deary,I.J., Palmer,L.J., Cassano,P.A., Gudnason,V., Barr,R.G.,
            Loos,R.J., Strachan,D.P., London,S.J., Boezen,H.M.,
            Probst-Hensch,N., Gharib,S.A., Hall,I.P., O'Connor,G.T., Tobin,M.D.
            and Stricker,B.H.
  TITLE     Genome-wide association studies identify CHRNA5/3 and HTR4 in the
            development of airflow obstruction
  JOURNAL   Am. J. Respir. Crit. Care Med. 186 (7), 622-632 (2012)
   PUBMED   22837378
REFERENCE   2  (bases 1 to 6348)
  AUTHORS   Irvin,M.R., Wineinger,N.E., Rice,T.K., Pajewski,N.M.,
            Kabagambe,E.K., Gu,C.C., Pankow,J., North,K.E., Wilk,J.B.,
            Freedman,B.I., Franceschini,N., Broeckel,U., Tiwari,H.K. and
            Arnett,D.K.
  TITLE     Genome-wide detection of allele specific copy number variation
            associated with insulin resistance in African Americans from the
            HyperGEN study
  JOURNAL   PLoS ONE 6 (8), E24052 (2011)
   PUBMED   21901158
REFERENCE   3  (bases 1 to 6348)
  AUTHORS   Bailey,S.D., Xie,C., Do,R., Montpetit,A., Diaz,R., Mohan,V.,
            Keavney,B., Yusuf,S., Gerstein,H.C., Engert,J.C. and Anand,S.
  CONSRTM   DREAM investigators
  TITLE     Variation at the NFATC2 locus increases the risk of
            thiazolidinedione-induced edema in the Diabetes REduction
            Assessment with ramipril and rosiglitazone Medication (DREAM) study
  JOURNAL   Diabetes Care 33 (10), 2250-2253 (2010)
   PUBMED   20628086
  REMARK    GeneRIF: Observational study of gene-disease association,
            gene-environment interaction, and pharmacogenomic / toxicogenomic.
            (HuGE Navigator)
REFERENCE   4  (bases 1 to 6348)
  AUTHORS   Raji,O.Y., Agbaje,O.F., Duffy,S.W., Cassidy,A. and Field,J.K.
  TITLE     Incorporation of a genetic factor into an epidemiologic model for
            prediction of individual risk of lung cancer: the Liverpool Lung
            Project
  JOURNAL   Cancer Prev Res (Phila) 3 (5), 664-669 (2010)
   PUBMED   20424129
  REMARK    GeneRIF: the addition of SEZ6L improved the performance of the
            Liverpool Lung Project risk model.
            GeneRIF: Observational study of gene-disease association and
            gene-environment interaction. (HuGE Navigator)
REFERENCE   5  (bases 1 to 6348)
  AUTHORS   Talmud,P.J., Drenos,F., Shah,S., Shah,T., Palmen,J., Verzilli,C.,
            Gaunt,T.R., Pallas,J., Lovering,R., Li,K., Casas,J.P., Sofat,R.,
            Kumari,M., Rodriguez,S., Johnson,T., Newhouse,S.J., Dominiczak,A.,
            Samani,N.J., Caulfield,M., Sever,P., Stanton,A., Shields,D.C.,
            Padmanabhan,S., Melander,O., Hastie,C., Delles,C., Ebrahim,S.,
            Marmot,M.G., Smith,G.D., Lawlor,D.A., Munroe,P.B., Day,I.N.,
            Kivimaki,M., Whittaker,J., Humphries,S.E. and Hingorani,A.D.
  CONSRTM   ASCOT investigators; NORDIL investigators; BRIGHT Consortium
  TITLE     Gene-centric association signals for lipids and apolipoproteins
            identified via the HumanCVD BeadChip
  JOURNAL   Am. J. Hum. Genet. 85 (5), 628-642 (2009)
   PUBMED   19913121
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   6  (bases 1 to 6348)
  AUTHORS   Gorlov,I.P., Meyer,P., Liloglou,T., Myles,J., Boettger,M.B.,
            Cassidy,A., Girard,L., Minna,J.D., Fischer,R., Duffy,S.,
            Spitz,M.R., Haeussinger,K., Kammerer,S., Cantor,C., Dierkesmann,R.,
            Field,J.K. and Amos,C.I.
  TITLE     Seizure 6-like (SEZ6L) gene and risk for lung cancer
  JOURNAL   Cancer Res. 67 (17), 8406-8411 (2007)
   PUBMED   17804757
  REMARK    GeneRIF: A role of the SEZ6L Met430Ile polymorphic variant in
            increasing lung cancer risk.
            GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   7  (bases 1 to 6348)
  AUTHORS   Nishioka,M., Kohno,T., Takahashi,M., Niki,T., Yamada,T., Sone,S.
            and Yokota,J.
  TITLE     Identification of a 428-kb homozygously deleted region disrupting
            the SEZ6L gene at 22q12.1 in a lung cancer cell line
  JOURNAL   Oncogene 19 (54), 6251-6260 (2000)
   PUBMED   11175339
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AY358405.1, AB023144.2, AB041736.1 and AL078460.6.
            
            Transcript Variant: This variant (5) lacks two alternate, in-frame
            segments in the coding region, compared to variant 1. The resulting
            protein (isoform 5) is shorter when it is compared to isoform 1.
            
            Sequence Note: This RefSeq record was created from transcript and
            genomic sequence data to make the sequence consistent with the
            reference genome assembly. The genomic coordinates used for the
            transcript record were based on transcript alignments.
            
            ##Evidence-Data-START##
            Transcript exon combination :: AB023144.2 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025084 [ECO:0000348]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-40                AY358405.1         1-40
            41-756              AB023144.2         1-716
            757-1031            AB041736.1         561-835
            1032-1614           AB023144.2         992-1574
            1615-1710           AB041736.1         1419-1514
            1711-3016           AB023144.2         1671-2976
            3017-6348           AL078460.6         524-3855
FEATURES             Location/Qualifiers
     source          1..6348
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="22"
                     /map="22q12.1"
     gene            1..6348
                     /gene="SEZ6L"
                     /note="seizure related 6 homolog (mouse)-like"
                     /db_xref="GeneID:23544"
                     /db_xref="HGNC:10763"
                     /db_xref="MIM:607021"
     exon            1..290
                     /gene="SEZ6L"
                     /inference="alignment:Splign:1.39.8"
     CDS             197..3046
                     /gene="SEZ6L"
                     /note="isoform 5 precursor is encoded by transcript
                     variant 5; seizure related gene 6-like; seizure 6-like
                     protein"
                     /codon_start=1
                     /product="seizure 6-like protein isoform 5 precursor"
                     /protein_id="NP_001171705.1"
                     /db_xref="GI:296179442"
                     /db_xref="CCDS:CCDS54511.1"
                     /db_xref="GeneID:23544"
                     /db_xref="HGNC:10763"
                     /db_xref="MIM:607021"
                     /translation="
MPAARPPAAGLRGISLFLALLLGSPAAALERDALPEGDASPLGPYLLPSGAPERGSPGKEHPEERVVTAPPSSSQSAEVLGELVLDGTAPSAHHDIPALSPLLPEEARPKHALPPKKKLPSLKQVNSARKQLRPKATSAATVQRAGSQPASQGLDLLSSSTEKPGPPGDPDPIVASEEASEVPLWLDRKESAVPTTPAPLQISPFTSQPYVAHTLPQRPEPGEPGPDMAQEAPQEDTSPMALMDKGENELTGSASEESQETTTSTIITTTVITTEQAPALCSVSFSNPEGYIDSSDYPLLPLNNFLECTYNVTVYTGYGVELQVKSVNLSDGELLSIRGVDGPTLTVLANQTLLVEGQVIRSPTNTISVYFRTFQDDGLGTFQLHYQAFMLSCNFPRRPDSGDVTVMDLHSGGVAHFHCHLGYELQGAKMLTCINASKPHWSSQEPICSAPCGGAVHNATIGRVLSPSYPENTNGSQFCIWTIEAPEGQKLHLHFERLLLHDKDRMTVHSGQTNKSALLYDSLQTESVPFEGLLSEGNTIRIEFTSDQARAASTFNIRFEAFEKGHCYEPYIQNGNFTTSDPTYNIGTIVEFTCDPGHSLEQGPAIIECINVRDPYWNDTEPLCRAMCGGELSAVAGVVLSPNWPEPYVEGEDCIWKIHVGEEKRIFLDIQFLNLSNSDILTIYDGDEVMPHILGQYLGNSGPQKLYSSTPDLTIQFHSDPAGLIFGKGQGFIMNYIEVSRNDSCSDLPEIQNGWKTTSHTELVRGARITYQCDPGYDIVGSDTLTCQWDLSWSSDPPFCEKTEESLACDNPGLPENGYQILYKRLYLPGESLTFMCYEGFELMGEVTIRCILGQPSHWNGPLPVCKVAEAAAETSLEGGNMALAIFIPVLIISLLLGGAYIYITRCRYYSNLRLPLMYSHPYSQITVETEFDNPIYETGETREYEVSI
"
     sig_peptide     197..280
                     /gene="SEZ6L"
                     /inference="COORDINATES: ab initio prediction:SignalP:4.0"
     misc_feature    1037..1360
                     /gene="SEZ6L"
                     /note="CUB domain; extracellular domain; present in
                     proteins mostly known to be involved in development; not
                     found in prokaryotes, plants and yeast; Region: CUB;
                     cd00041"
                     /db_xref="CDD:28922"
     misc_feature    order(1061..1063,1067..1069,1073..1075,1157..1159,
                     1172..1174,1271..1273,1343..1345,1349..1351,1355..1360)
                     /gene="SEZ6L"
                     /note="heterodimerization interface [polypeptide binding];
                     other site"
                     /db_xref="CDD:28922"
     misc_feature    1373..1540
                     /gene="SEZ6L"
                     /note="Complement control protein (CCP) modules (aka short
                     consensus repeats SCRs or SUSHI repeats) have been
                     identified in several proteins of the complement system;
                     Region: CCP; cd00033"
                     /db_xref="CDD:153056"
     misc_feature    order(1403..1405,1454..1456)
                     /gene="SEZ6L"
                     /note="receptor-ligand interactions; other site"
                     /db_xref="CDD:153056"
     misc_feature    1550..1879
                     /gene="SEZ6L"
                     /note="CUB domain; extracellular domain; present in
                     proteins mostly known to be involved in development; not
                     found in prokaryotes, plants and yeast; Region: CUB;
                     cd00041"
                     /db_xref="CDD:28922"
     misc_feature    order(1577..1579,1583..1585,1589..1591,1670..1672,
                     1685..1687,1787..1789,1862..1864,1868..1870,1874..1879)
                     /gene="SEZ6L"
                     /note="heterodimerization interface [polypeptide binding];
                     other site"
                     /db_xref="CDD:28922"
     misc_feature    1895..2071
                     /gene="SEZ6L"
                     /note="Complement control protein (CCP) modules (aka short
                     consensus repeats SCRs or SUSHI repeats) have been
                     identified in several proteins of the complement system;
                     Region: CCP; cd00033"
                     /db_xref="CDD:153056"
     misc_feature    order(1922..1924,1979..1981)
                     /gene="SEZ6L"
                     /note="receptor-ligand interactions; other site"
                     /db_xref="CDD:153056"
     misc_feature    2078..2404
                     /gene="SEZ6L"
                     /note="CUB domain; extracellular domain; present in
                     proteins mostly known to be involved in development; not
                     found in prokaryotes, plants and yeast; Region: CUB;
                     cd00041"
                     /db_xref="CDD:28922"
     misc_feature    order(2102..2104,2108..2110,2114..2116,2195..2197,
                     2210..2212,2309..2311,2393..2395,2399..2401)
                     /gene="SEZ6L"
                     /note="heterodimerization interface [polypeptide binding];
                     other site"
                     /db_xref="CDD:28922"
     misc_feature    2429..2599
                     /gene="SEZ6L"
                     /note="Complement control protein (CCP) modules (aka short
                     consensus repeats SCRs or SUSHI repeats) have been
                     identified in several proteins of the complement system;
                     Region: CCP; cd00033"
                     /db_xref="CDD:153056"
     misc_feature    order(2459..2461,2516..2518)
                     /gene="SEZ6L"
                     /note="receptor-ligand interactions; other site"
                     /db_xref="CDD:153056"
     misc_feature    2621..2797
                     /gene="SEZ6L"
                     /note="Complement control protein (CCP) modules (aka short
                     consensus repeats SCRs or SUSHI repeats) have been
                     identified in several proteins of the complement system;
                     Region: CCP; cd00033"
                     /db_xref="CDD:153056"
     misc_feature    order(2651..2653,2708..2710)
                     /gene="SEZ6L"
                     /note="receptor-ligand interactions; other site"
                     /db_xref="CDD:153056"
     variation       247
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:199592259"
     variation       259
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150514257"
     exon            291..1031
                     /gene="SEZ6L"
                     /inference="alignment:Splign:1.39.8"
     variation       296
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200131802"
     variation       301
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201233214"
     variation       302
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373985470"
     variation       307
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:35377445"
     variation       320
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:16981666"
     variation       323
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:144848715"
     variation       332
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:140163670"
     variation       337
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375944877"
     variation       351
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6004989"
     variation       357
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201583563"
     variation       403
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145637105"
     variation       423
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367686525"
     variation       427
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371822368"
     variation       461
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376609269"
     variation       473
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:147727804"
     variation       478
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372902970"
     variation       489
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201824145"
     variation       499
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:140909448"
     variation       540
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:144766472"
     variation       558
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151261975"
     variation       559
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376407598"
     variation       610
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369680345"
     variation       611
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140450910"
     variation       646
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150393362"
     variation       672
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373898124"
     variation       678
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201671037"
     variation       696
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200003656"
     variation       697
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192283519"
     variation       713
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:201060309"
     variation       715
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376527866"
     variation       716
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149306304"
     variation       724
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371054914"
     variation       725
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370632181"
     variation       730
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:374087121"
     variation       750
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:137203"
     variation       753
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111570897"
     variation       757
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17304075"
     variation       759
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146205533"
     variation       771
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138721720"
     variation       772
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368342681"
     variation       783
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:141695407"
     variation       816
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200293457"
     variation       817
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143504590"
     variation       835
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:371017350"
     variation       841
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374380587"
     variation       859
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202064668"
     variation       867
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368564640"
     variation       875
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147999138"
     variation       906
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199597034"
     variation       928
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:141642477"
     variation       965
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:150517564"
     variation       972
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201779919"
     variation       974
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:193920876"
     variation       979
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370951707"
     variation       981
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375502842"
     variation       983
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367558456"
     variation       993
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368299217"
     variation       1005
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371478865"
     variation       1013
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372123102"
     variation       1018
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376019482"
     variation       1024
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17395296"
     exon            1032..1165
                     /gene="SEZ6L"
                     /inference="alignment:Splign:1.39.8"
     variation       1063
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:56042239"
     variation       1082
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200380172"
     variation       1083
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:372813703"
     variation       1107
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376420402"
     variation       1129
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151335289"
     variation       1130
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375396789"
     exon            1166..1358
                     /gene="SEZ6L"
                     /inference="alignment:Splign:1.39.8"
     variation       1166
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201889766"
     variation       1174
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147324317"
     variation       1187
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200655803"
     variation       1225
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140372463"
     variation       1228
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375660013"
     variation       1234
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112422707"
     variation       1235
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370293421"
     variation       1267
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200005508"
     variation       1284
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200639264"
     variation       1301
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144740621"
     variation       1311
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148526431"
     variation       1324
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371203903"
     variation       1325
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:142863810"
     variation       1338
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:146559583"
     exon            1359..1544
                     /gene="SEZ6L"
                     /inference="alignment:Splign:1.39.8"
     variation       1359
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200415298"
     variation       1377
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141216329"
     variation       1384
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199849358"
     variation       1411
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143488032"
     variation       1418
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201236913"
     variation       1462
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:146744873"
     variation       1466
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140350607"
     variation       1481
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150343251"
     variation       1486
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:663048"
     variation       1513
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149068026"
     exon            1545..1710
                     /gene="SEZ6L"
                     /inference="alignment:Splign:1.39.8"
     variation       1577
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201513330"
     variation       1586
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373919244"
     variation       1588
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200212656"
     variation       1589
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201151950"
     variation       1615
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1210894"
     variation       1641
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138692969"
     variation       1642
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:142670064"
     variation       1698
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201913763"
     exon            1711..1877
                     /gene="SEZ6L"
                     /inference="alignment:Splign:1.39.8"
     variation       1716
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376866700"
     variation       1717
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371509981"
     variation       1726
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147328329"
     variation       1741
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:367751295"
     variation       1756
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199770989"
     variation       1771
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186497116"
     variation       1772
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:117917851"
     variation       1776
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200361966"
     variation       1809
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374078308"
     variation       1818
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142214073"
     variation       1820
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201153704"
     variation       1822
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144295883"
     variation       1830
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190114018"
     variation       1831
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368332411"
     variation       1835
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139354547"
     variation       1845
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150022206"
     variation       1848
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201841723"
     variation       1849
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146077946"
     variation       1855
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140029399"
     exon            1878..2072
                     /gene="SEZ6L"
                     /inference="alignment:Splign:1.39.8"
     variation       1878
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:143554731"
     variation       1879
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:199961565"
     variation       1900
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:146763740"
     variation       1942
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148910882"
     variation       1953
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201588335"
     variation       1962
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142677073"
     variation       1978
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370996675"
     variation       1984
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150994059"
     variation       1985
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375633558"
     variation       2008
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199713722"
     variation       2018
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370294088"
     variation       2036
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201869380"
     exon            2073..2211
                     /gene="SEZ6L"
                     /inference="alignment:Splign:1.39.8"
     variation       2109
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201292047"
     variation       2131
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375506025"
     variation       2140
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145294635"
     variation       2190
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150114413"
     variation       2209
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:586542"
     exon            2212..2408
                     /gene="SEZ6L"
                     /inference="alignment:Splign:1.39.8"
     variation       2245
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200764167"
     variation       2248
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138699202"
     variation       2254
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141142000"
     variation       2255
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201856091"
     variation       2257
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371326790"
     variation       2264
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376430157"
     variation       2296
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200138174"
     variation       2301
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376290581"
     exon            2409..2603
                     /gene="SEZ6L"
                     /inference="alignment:Splign:1.39.8"
     variation       2413
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149869184"
     variation       2469
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375559047"
     variation       2475
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:200745477"
     variation       2478
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199970754"
     variation       2493
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:137881901"
     variation       2521
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146425607"
     variation       2532
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200709491"
     variation       2533
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141377957"
     variation       2534
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375640180"
     variation       2536
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149442184"
     variation       2553
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144838560"
     variation       2590
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:116806899"
     variation       2597
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367783225"
     variation       2599
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141923405"
     exon            2604..2798
                     /gene="SEZ6L"
                     /inference="alignment:Splign:1.39.8"
     variation       2662
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:146764929"
     variation       2680
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:142020765"
     variation       2710
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146313552"
     variation       2740
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148908719"
     variation       2775
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139248080"
     variation       2776
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149968977"
     exon            2799..2913
                     /gene="SEZ6L"
                     /inference="alignment:Splign:1.39.8"
     variation       2808
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:376385912"
     variation       2809
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369690932"
     variation       2821
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146602479"
     variation       2828
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199913295"
     variation       2832
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200000489"
     variation       2838
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148666049"
     STS             2912..3021
                     /gene="SEZ6L"
                     /standard_name="D22S988E"
                     /db_xref="UniSTS:90244"
     exon            2914..3016
                     /gene="SEZ6L"
                     /inference="alignment:Splign:1.39.8"
     variation       2934
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201269295"
     variation       2999
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:190563242"
     variation       3007
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374094771"
     exon            3017..6348
                     /gene="SEZ6L"
                     /inference="alignment:Splign:1.39.8"
     variation       3031
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138281845"
     variation       3057
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:375371828"
     variation       3096
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:75138773"
     variation       3097
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:142360994"
     variation       3107
                     /gene="SEZ6L"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:144636647"
     variation       3166
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:5997084"
     variation       3247
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184914894"
     variation       3317
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:112693479"
     variation       3318
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113309050"
     variation       3585..3586
                     /gene="SEZ6L"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:151237595"
     variation       3646
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:79392905"
     variation       3665
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375923717"
     variation       3716
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:60383901"
     variation       3752
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189670414"
     variation       3764
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115524791"
     variation       3772
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370558030"
     variation       3806
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:183208392"
     variation       3810
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:5761503"
     variation       3879
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:587471"
     variation       3906
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:117888300"
     variation       3927
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:116578176"
     variation       3979
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138176320"
     variation       4138
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:188165461"
     variation       4160
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141792319"
     variation       4161
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:73879891"
     variation       4225
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:5752315"
     variation       4275
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191717454"
     variation       4416
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116906183"
     variation       4455
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:183544332"
     STS             4462..4584
                     /gene="SEZ6L"
                     /standard_name="D22S1013E"
                     /db_xref="UniSTS:85568"
     variation       4505
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:188874701"
     variation       4514
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:192366428"
     variation       4535
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115727743"
     variation       4580
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:482902"
     variation       4662
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:79154331"
     variation       4682
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:183837315"
     variation       4736
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:601548"
     variation       4780
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377155701"
     variation       4797
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73415354"
     variation       4862
                     /gene="SEZ6L"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:143254900"
     variation       4919
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114145797"
     variation       4921..4922
                     /gene="SEZ6L"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:35212633"
     variation       4927
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:370264622"
     variation       4962
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:16981991"
     variation       4977
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372296472"
     variation       4995
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:186951974"
     variation       5008
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:77237339"
     variation       5018
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:76540571"
     variation       5019
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:78032966"
     variation       5020
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:74382755"
     variation       5032
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:149269258"
     variation       5051
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:146221536"
     variation       5070
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:5997085"
     variation       5112
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191420478"
     variation       5115
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:75170824"
     variation       5120
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:16981994"
     STS             5189..5299
                     /gene="SEZ6L"
                     /standard_name="D22S1017E"
                     /db_xref="UniSTS:150801"
     variation       5236
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:184889287"
     variation       5246
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:489363"
     variation       5260
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189787384"
     variation       5278
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181806723"
     variation       5294
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:7284717"
     variation       5349
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:139223070"
     variation       5356
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185094410"
     variation       5378
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:143967932"
     variation       5405
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145942215"
     variation       5489
                     /gene="SEZ6L"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:71758401"
     variation       5489
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:201703792"
     variation       5532
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:16981995"
     variation       5576
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:189355139"
     variation       5617
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375396060"
     variation       5638
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:182007069"
     variation       5771
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:369050660"
     variation       5819..5820
                     /gene="SEZ6L"
                     /replace=""
                     /replace="gc"
                     /db_xref="dbSNP:141631869"
     variation       5820
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77779362"
     variation       5821
                     /gene="SEZ6L"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:35749592"
     variation       5822
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:78604204"
     variation       5838
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:79458369"
     variation       5844
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:62224568"
     variation       5992
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:73158677"
     variation       6014
                     /gene="SEZ6L"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:140605651"
     variation       6037
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:2092744"
     variation       6038
                     /gene="SEZ6L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:16981998"
     STS             6117..6226
                     /gene="SEZ6L"
                     /standard_name="RH77725"
                     /db_xref="UniSTS:6770"
     variation       6125
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142481081"
     variation       6157
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:73415355"
     STS             6169..6328
                     /gene="SEZ6L"
                     /standard_name="A002S43"
                     /db_xref="UniSTS:62230"
     STS             6207..6345
                     /gene="SEZ6L"
                     /standard_name="WI-18670"
                     /db_xref="UniSTS:83301"
     variation       6216
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:8136212"
     variation       6255
                     /gene="SEZ6L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:186236660"
     variation       6266
                     /gene="SEZ6L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376337208"
ORIGIN      
gcgcccggcgcagctcggccagagcgaccgcggggctgagcgcgcgtccgcccagggggctccggaagctgccccggcccgcggcctcctccctcgctcccgcttcccctttctcgctcaccgccgccctccttccccagctccctcgccgtccgcccgccccacagccagcggctccgcgccccctgcagccacgatgcccgcggcccggccgcccgccgcgggactccgcgggatctcgctgttcctcgctctgctcctggggagcccggcggcagcgctggagcgagatgctcttcccgagggagatgctagccctttgggtccttacctcctgccctcaggagccccggagagaggcagtcctggcaaagagcaccctgaagagagagtggtaacagcgccccccagttcctcacagtcggcggaagtgctgggcgagctggtgctggatgggaccgcaccctctgcacatcacgacatcccagccctgtcaccgctgcttccagaggaggcccgccccaagcacgccttgccccccaagaagaaactgccttcgctcaagcaggtgaactctgccaggaagcagctgaggcccaaggccacctccgcagccactgtccaaagggcagggtcccagccagcgtcccagggcctagatctcctctcctcctccacggagaagcctggcccaccgggggacccggaccccatcgtggcctccgaggaggcatcagaagtgcccctttggctggaccgaaaggagagtgcggtccctacaacacccgcacccctgcaaatctcccccttcacttcgcagccctatgtggcccacacactcccccagaggccagaacccggggagcctgggcctgacatggcccaggaggccccccaggaggacaccagccccatggccctgatggacaaaggtgagaatgagctgactgggtcagcctcagaggagagccaggagaccactacctccaccattatcaccaccacggtcatcaccaccgagcaggcaccagctctctgcagtgtgagcttctccaatcctgaggggtacattgactccagcgactacccactgctgcccctcaacaactttctggagtgcacatacaacgtgacagtctacactggctatggggtggagctccaggtgaagagtgtgaacctgtccgatggggaactgctctccatccgcggggtggacggccctaccctgaccgtcctggccaaccagacactcctggtggaggggcaggtaatccgaagccccaccaacaccatctccgtctacttccggaccttccaggacgacggccttgggaccttccagcttcactaccaggccttcatgctgagctgcaactttccccgccggcctgactctggggatgtcacggtgatggacctgcactcaggtggggtggcccactttcactgccacctgggctatgagctccagggcgctaagatgctgacatgcatcaatgcctccaagccgcactggagcagccaggagcccatctgctcagctccttgtggaggggcagtgcacaatgccaccatcggccgcgtcctctccccaagttaccctgaaaacacaaatgggagccaattctgcatctggacgattgaagctccagagggccagaagctgcacctgcactttgagaggctgttgctgcatgacaaggacaggatgacggttcacagcgggcagaccaacaagtcagctcttctctacgactcccttcaaaccgagagtgtcccttttgagggcctgctgagcgaaggcaacaccatccgcatcgagttcacgtccgaccaggcccgggcggcctccaccttcaacatccgatttgaagcgtttgagaaaggccactgctatgagccctacatccagaatgggaacttcactacatccgacccgacctataacattgggactatagtggagttcacctgcgaccccggccactccctggagcagggcccggccatcatcgaatgcatcaatgtgcgggacccatactggaatgacacagagcccctgtgcagagccatgtgtggtggggagctctctgctgtggctggggtggtattgtccccaaactggcccgagccctacgtggaaggtgaagattgtatctggaagatccacgtgggagaagagaaacggatcttcttagatatccagttcctgaatctgagcaacagtgacatcttgaccatctacgatggcgacgaggtcatgccccacatcttggggcagtaccttgggaacagtggcccccagaaactgtactcctccacgccagacttaaccatccagttccattcggaccctgctggcctcatctttggaaagggccagggatttatcatgaactacatagaggtatcaaggaatgactcctgctcggatttacccgagatccagaatggctggaaaaccacttctcacacggagttggtgcggggagccagaatcacctaccagtgtgaccccggctatgacatcgtggggagtgacaccctcacctgccagtgggacctcagctggagcagcgaccccccattttgtgagaaaacggaggagtccctggcatgtgacaacccagggctgcctgaaaatggataccaaatcctgtacaagcgactctacctgccaggagagtccctcaccttcatgtgctacgaaggctttgagctcatgggtgaagtgaccatccgctgcatcctgggacagccatcccactggaacgggcccctgcccgtgtgtaaagtagcagaagcggcagcagagacgtcgctggaaggggggaacatggccctggctatcttcatcccggtcctcatcatctccttactgctgggaggagcctacatttacatcacaagatgtcgctactattccaacctccgcctgcctctgatgtactcccacccctacagccagatcaccgtggaaaccgagtttgacaaccccatttacgagacaggggaaaccagagagtatgaggtttctatctaaagagagctacacttgagaaggggacttgtgaactcaaccacaatctcctcgagacattcatccagagaccatgtggcacttgattgaaaccccagaatgtcgactgtcttttgtttagactctttatcaaaggtttactgttttcttccctgtatttattatatttaaaagtgaaataggtgtgggtttggatgtttcgcggcctcagccaaattcatgttacagcctcaattctgaaggcaggtggaagacttgcaaaatggcaaaccgcggcagcaaaaacacaaaacagcagatggagtttctcccatcagcaatgccatgctaaggctgcattgaattgcatgcatctttgggaaccatgcccatgatgttttcagtacaaatctaagtcccaagattaggttggaaagggtatttcttgttggcttagtttgggttggaatttagcatgggtacttaaacccatttggagagctgtgctcctaaacaaattctgtgtcctctcttcccattttgccagcttctgaaaggtttttccacagcccctccctctcacggttcttctgaaggtagcaaaggtgttatataaacattgtcttttaccactctggcctcgctggacagtgacaaaacaagaaaacgttttctttctagaaaggtgataaacgaccaaaggcaatttttcagagacaaatgagagatttgagagttccaatgaagaattgggtgagggggatcattgggtaagggaattgggttaaaatgttcttttctttgacactctttcaatgatgaaagagcgtgtaatttatgctacaagtgccagaatcgatcaccatgttcagcaagccactctcaagctgtggtaataaacacacaggcttgggaggcaccagcggccccactcatacagtgacaaggatttgtgatgggaaaaaggaggtgccatgtttggaaatgcaggggtgagctctggtttctcctggggttctggaatatctcagccctcaaaatagaggagactcaagtgcactgattctctaaaaggtgtcatcttcagaatatacttgccatcaagtatttcagggggcgggagggtcccatgagaagaaactatttttctattctccaaagctgtctggatgttggagggtggtgtgaatgctgactgaggaggtgcagagaacaggggcaggggattttaaatcacagcagaccatccagtggaatcctgtatcatctgatctgaacatcaatgaagacagagagaggaatttcattcagaaaggattccatagccccacatctagtcacacgggcattcctcttattttatcagggtctgttttcccccaacccagtgaaaccggtgagtgtgtaactcttgggaagattcttttctaaatacaggtataaagagaaggtggagggtgcgggtgcatggaagaaatactatgtgtgaagcagattcaccttcctgggaccggtgacatggtggtgacagtcaatggcttggacagacagacgggcacagtggcatttggaaccctctttggtgccctcccattctctctggaattgtttcaagtctgctggttttcaaacaagaaaagacctttctggccatagggagaatagcagggagtctatgttttggtggttacattggaaacatcttaagcaagatagggaaagttgattttaggcacacatgtaccctccttgacagcaggaactcagacttcaatcttgggggtctaagaccagaatattttccttctgccagaaaagaatcttgcacatatactcctgaaggcatgagtgtgtggtccatggcaagaaatagctaaaggctgctttccaggacccaaagccccatttaatgcaagaaccagagaagtgttctaggccattagtggacaatgtcatgtttggagaaagataacaacacaaataatgtaacctttccttaaaaggcagaactcaatccattttatttgatgcttattctaaccctaaccctgggtcacctggaatgaagaactctatgaataatatttgattttacaacgtgttatggttatgtgaaaactaaacatttgccttttataaagactgacaaaatataaatctttattctaaccctatccccaaaactagccaggccacaccccagatgttcttattgactattggaaagatagaaaaggcgttgtgttttttgtttttttgttgttgttgtcattgttgtttttttcagaagaccagtgtctcagttctgtcttagtagtaccacacccgtaaccgtgttttaaaagtttgttttagcctagagacagatcatacgagttcaacaatgtacagtgtgattgaaaagacaggttggtgtctatttttctttttaaaatatctgaatgtgtatttgtaatacgtaaaggtaaaaaaaaatagtgccaaaaatgtgcaaggcatctcattacagctcatgtacgtctgtttttataagatcaatattaaaacccattgggattaaatatttttgaataggatacactcttgagaaactcgagaatggactgagccttcctacaagccactctttgtttttaaaacagtggggaaatacgtttacagagattgtgagcttcagagaatgcatgtgatggtgtgtattacatgctaattcatataagctgtatctgtcagctaccaccctgtgctttaaaaatgcacacactcaaccctctttagcttggagctcagctttttgcttttttttttttttttttgtagaattatttagctaacataagtattctgattgctacctgatggccattcttacttagtttcatagatgtgctttaactatgatcctttgaagctcaccccttggagagcctacagaacctcaggctgatagctttgaagactgccaaacagcccagaaggaagcaaagcatctgcataatcaggagggttgtataacaagtagtgatttggcaaatatgtgggtagctttaggctgaggcacgggcctcaggcaaaaatgcccttcgagtgaatccgaagggcatgatcttcctatgtccttgactaggcatgacgagtcatttgaggtcagatattatttgagttgttcagcacccccaaaggtaggcattctcctgggaaattttcatttccattttatcgccaaacaaaataaaaagcaaaacaaactttctaagctagaataatgaaattaagtcattttccactttgtatatattgatgctaataaaacagatgaaaaagac
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:23544 -> Cellular component: GO:0005789 [endoplasmic reticulum membrane] evidence: IEA
            GeneID:23544 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA

by @meso_cacase at DBCLS
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