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2024-04-26 10:01:24, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_017890 14100 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens vacuolar protein sorting 13 homolog B (yeast)
(VPS13B), transcript variant 5, mRNA.
ACCESSION NM_017890
VERSION NM_017890.4 GI:384551660
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 14100)
AUTHORS Melville SA, Buros J, Parrado AR, Vardarajan B, Logue MW, Shen L,
Risacher SL, Kim S, Jun G, DeCarli C, Lunetta KL, Baldwin CT,
Saykin AJ and Farrer LA.
CONSRTM Alzheimer's Disease Neuroimaging Initiative
TITLE Multiple loci influencing hippocampal degeneration identified by
genome scan
JOURNAL Ann. Neurol. 72 (1), 65-75 (2012)
PUBMED 22745009
REFERENCE 2 (bases 1 to 14100)
AUTHORS Seifert,W., Kuhnisch,J., Maritzen,T., Horn,D., Haucke,V. and
Hennies,H.C.
TITLE Cohen syndrome-associated protein, COH1, is a novel, giant Golgi
matrix protein required for Golgi integrity
JOURNAL J. Biol. Chem. 286 (43), 37665-37675 (2011)
PUBMED 21865173
REMARK GeneRIF: COH1 as a Golgi-associated matrix protein required for
Golgi integrity.
REFERENCE 3 (bases 1 to 14100)
AUTHORS Balikova,I., de Ravel,T., Ayuso,C., Thienpont,B., Casteels,I.,
Villaverde,C., Devriendt,K., Fryns,J.P. and Vermeesch,J.R.
TITLE High frequency of submicroscopic chromosomal deletions in patients
with idiopathic congenital eye malformations
JOURNAL Am. J. Ophthalmol. 151 (6), 1087-1094 (2011)
PUBMED 21353197
REMARK GeneRIF: This high frequency of causal submicroscopic chromosomal
aberrations in patients with congenital ocular malformation
warrants implementation of array comparative genomic hybridization
in the diagnostic work-up of these patients.
REFERENCE 4 (bases 1 to 14100)
AUTHORS Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B,
Yusuf S, Gerstein HC, Engert JC 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 5 (bases 1 to 14100)
AUTHORS El Chehadeh,S., Aral,B., Gigot,N., Thauvin-Robinet,C., Donzel,A.,
Delrue,M.A., Lacombe,D., David,A., Burglen,L., Philip,N.,
Moncla,A., Cormier-Daire,V., Rio,M., Edery,P., Verloes,A.,
Bonneau,D., Afenjar,A., Jacquette,A., Heron,D., Sarda,P.,
Pinson,L., Doray,B., Vigneron,J., Leheup,B., Frances-Guidet,A.M.,
Dienne,G., Holder,M., Masurel-Paulet,A., Huet,F., Teyssier,J.R. and
Faivre,L.
TITLE Search for the best indicators for the presence of a VPS13B gene
mutation and confirmation of diagnostic criteria in a series of 34
patients genotyped for suspected Cohen syndrome
JOURNAL J. Med. Genet. 47 (8), 549-553 (2010)
PUBMED 20656880
REMARK GeneRIF: VPS13B screening is not indicated in the absence of
chorioretinal dystrophy or neutropenia in patients aged over 5
years.
REFERENCE 6 (bases 1 to 14100)
AUTHORS Hennies,H.C., Rauch,A., Seifert,W., Schumi,C., Moser,E.,
Al-Taji,E., Tariverdian,G., Chrzanowska,K.H., Krajewska-Walasek,M.,
Rajab,A., Giugliani,R., Neumann,T.E., Eckl,K.M., Karbasiyan,M.,
Reis,A. and Horn,D.
TITLE Allelic heterogeneity in the COH1 gene explains clinical
variability in Cohen syndrome
JOURNAL Am. J. Hum. Genet. 75 (1), 138-145 (2004)
PUBMED 15154116
REMARK GeneRIF: Allelic heterogeneity in the COH1 gene explains clinical
variability in Cohen syndrome
REFERENCE 7 (bases 1 to 14100)
AUTHORS Kolehmainen,J., Wilkinson,R., Lehesjoki,A.E., Chandler,K.,
Kivitie-Kallio,S., Clayton-Smith,J., Traskelin,A.L., Waris,L.,
Saarinen,A., Khan,J., Gross-Tsur,V., Traboulsi,E.I., Warburg,M.,
Fryns,J.P., Norio,R., Black,G.C. and Manson,F.D.
TITLE Delineation of Cohen syndrome following a large-scale
genotype-phenotype screen
JOURNAL Am. J. Hum. Genet. 75 (1), 122-127 (2004)
PUBMED 15141358
REMARK GeneRIF: COH1 mutations is associated with Cohen syndrome
REFERENCE 8 (bases 1 to 14100)
AUTHORS Kolehmainen,J., Black,G.C., Saarinen,A., Chandler,K.,
Clayton-Smith,J., Traskelin,A.L., Perveen,R., Kivitie-Kallio,S.,
Norio,R., Warburg,M., Fryns,J.P., de la Chapelle,A. and
Lehesjoki,A.E.
TITLE Cohen syndrome is caused by mutations in a novel gene, COH1,
encoding a transmembrane protein with a presumed role in
vesicle-mediated sorting and intracellular protein transport
JOURNAL Am. J. Hum. Genet. 72 (6), 1359-1369 (2003)
PUBMED 12730828
REMARK GeneRIF: A mutated gene on chromosome 8q22 found by haplotype
analysis in patients with this syndrome.
REFERENCE 9 (bases 1 to 14100)
AUTHORS Kolehmainen,J., Norio,R., Kivitie-Kallio,S., Tahvanainen,E., de la
Chapelle,A. and Lehesjoki,A.E.
TITLE Refined mapping of the Cohen syndrome gene by linkage
disequilibrium
JOURNAL Eur. J. Hum. Genet. 5 (4), 206-213 (1997)
PUBMED 9359041
REFERENCE 10 (bases 1 to 14100)
AUTHORS Tahvanainen,E., Norio,R., Karila,E., Ranta,S., Weissenbach,J.,
Sistonen,P. and de la Chapelle,A.
TITLE Cohen syndrome gene assigned to the long arm of chromosome 8 by
linkage analysis
JOURNAL Nat. Genet. 7 (2), 201-204 (1994)
PUBMED 7920642
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AY223814.1, AC105195.5,
AC026827.6, AC023933.9 and AC105328.13.
This sequence is a reference standard in the RefSeqGene project.
On Apr 19, 2012 this sequence version replaced gi:35493712.
Summary: This gene encodes a potential transmembrane protein that
may function in vesicle-mediated transport and sorting of proteins
within the cell. This protein may play a role in the development
and the function of the eye, hematological system, and central
nervous system. Mutations in this gene have been associated with
Cohen syndrome. Multiple splice variants encoding distinct isoforms
have been identified for this gene. [provided by RefSeq, Jul 2008].
Transcript Variant: This variant (5) encodes the longest isoform
(5).
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.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: AY223814.1, AJ608772.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-1667 AY223814.1 1-1667
1668-1668 AC105195.5 119108-119108
1669-1740 AY223814.1 1669-1740
1741-1741 AC105195.5 120112-120112
1742-1962 AY223814.1 1742-1962
1963-1963 AC105195.5 131230-131230
1964-4270 AY223814.1 1964-4270
4271-4386 AC026827.6 137338-137453
4387-4409 AY223814.1 4387-4409
4410-4410 AC026827.6 137477-137477
4411-5128 AY223814.1 4411-5128
5129-5129 AC023933.9 83192-83192
5130-9677 AY223814.1 5130-9677
9678-9678 AC105328.13 112032-112032 c
9679-14093 AY223814.1 9679-14093
14094-14100 AC105328.13 66976-66982 c
FEATURES Location/Qualifiers
source 1..14100
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="8"
/map="8q22.2"
gene 1..14100
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/note="vacuolar protein sorting 13 homolog B (yeast)"
/db_xref="GeneID:157680"
/db_xref="HGNC:2183"
/db_xref="MIM:607817"
exon 1..82
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
exon 83..258
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 87
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374307844"
misc_feature 106..108
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/note="upstream in-frame stop codon"
CDS 112..12180
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/note="isoform 5 is encoded by transcript variant 5;
vacuolar protein sorting-associated protein 13B"
/codon_start=1
/product="vacuolar protein sorting-associated protein 13B
isoform 5"
/protein_id="NP_060360.3"
/db_xref="GI:35493713"
/db_xref="CCDS:CCDS6280.1"
/db_xref="GeneID:157680"
/db_xref="HGNC:2183"
/db_xref="MIM:607817"
/translation="
MLESYVTPILMSYVNRYIKNLKPSDLQLSLWGGDVVLSKLELKLDVLEQELKLPFTFLSGHIHELRIHVPWTKLGSEPVVITINTMECILKLKDGIQDDHESCGSNSTNRSTAESTKSSIKPRRMQQAAPTDPDLPPGYVQSLIRRVVNNVNIVINNLILKYVEDDIVLSVNITSAECYTVGELWDRAFMDISATDLVLRKVINFSDCTVCLDKRNASGKIEFYQDPLLYKCSFRTRLHFTYENLNSKMPSVIKIHTLVESLKLSITDQQLPMFIRIMQLGIALYYGEIGNFKEGEIEDLTCHNKDMLGNITGSEDETRIDMQYPAQHKGQELYSQQDEEQPQGWVSWAWSFVPAIVSYDDGEEDFVGNDPASTMHQQKAQTLKDPIVSIGFYCTKATVTFKLTEMQVESSYYSPQKVKSKEVLCWEQEGTTVEALMMGEPFFDCQIGFVGCRAMCLKGIMGVKDFEENMNRSETEACFFICGDNLSTKGFTYLTNSLFDYRSPENNGTRAEFILDSTHHKETYTEIAGMQRFGAFYMDYLYTMENTSGKGSTNQQDFSSGKSEDLGTVQEKSTKSLVIGPLDFRLDSSAVHRILKMIVCALEHEYEPYSRLKSDIKDENETILNPEEVALLEEYIPTRHTSVTLLKCTCTISMAEFNLLDHLLPVIMGEKNSSNFMNTTNFQSLRPLPSIRILVDKINLEHSVPMYAEQLVHVVSSLTQPSDNLLHYCYVHCYLKIFGFQAGLTSLDCSGSYCLPVPVIPSFSTALYGKLLKLPTCWTKRSQIAITEGIFELPNLTIQATRAQTLLLQAIYQSWSHLGNVSSSAVIEALINEIFLSIGVKSKNPLPTLEGSIQNVELKYCSTSLVKCASGTMGSIKICAKAPVDSGKEKLIPLLQGPSDTKDLHSTKWLNESRKPESLLAPDLMAFTIQVPQYIDYCHNSGAVLLCSIQGLAVNIDPILYTWLIYQPQKRTSRHMQQQPVVAVPLVMPVCRRKEDEVSIGSAPLAKQQSYQASEYASSPVKTKTVTESRPLSVPVKAMLNISESCRSPEERMKEFIGIVWNAVKHLTLQLEVQSCCVFIPNDSLPSPSTIVSGDIPGTVRSWYHGQTSMPGTLVLCLPQIKIISAGHKYMEPLQEIPFVIPRPILEEGDAFPWTISLHNFSIYTLLGKQVTLCLVEPMGCTSTLAVTSQKLLATGPDTRHSFVVCLHVDLESLEIKCSNPQVQLFYELTDIMNKVWNKIQKRGNLNLSPTSPETMAGPVPTSPVRSSIGTAPPDTSTCSPSADIGTTTEGDSIQAGEESPFSDSVTLEQTTSNIGGTSGRVSLWMQWVLPKITIKLFAPDPENKGTEVCMVSELEDLSASIDVQDVYTKVKCKIESFNIDHYRSSLGEECWSLGQCGGVFLSCTDKLNRRTLLVRPISKQDPFSNCSGFFPSTTTKLLDGTHQQHGFLSLTYTKAVTKNVRHKLTSRNERRSFHKLSEGLMDGSPHFLHEILLSAQAFDIVLYFPLLNAIASIFQAKLPKTQKEKRKSPGQPMRTHTLTSRNLPLIYVNTSVIRIFIPKTEEMQPTVEANQAAKEDTVVLKIGSVAMAPQADNPLGRSVLRKDIYQRALNLGILRDPGSEIEDRQYQIDLQSINIGTAQWHQLKPEKESVSGGVVTETERNSQNPALEWNMASSIRRHQERRAILTPVLTDFSVRITGAPAVIFTKVVSPENLHTEEILVCGHSLEVNITTNLDFFLSVAQVQLLHQLIVANMTGLEPSNKAAEISKQEQKKVDIFDGGMAETSSRYSGAQDSGIGSDSVKIRIVQIEQHSGASQHRIARPSRQSSIVKNLNFIPFDIFITASRISLMTYSCMALSKSKSQEQKNNEKTDKSSLNLPEVDSDVAKPNQACISTVTAEDLLRSSISFPSGKKIGVLSLESLHASTRSSARQALGITIVRQPGRRGTGDLQLEPFLYFIVSQPSLLLSCHHRKQRVEVSIFDAVLKGVASDYKCIDPGKTLPEALDYCTVWLQTVPGEIDSKSGIPPSFITLQIKDFLNGPADVNLDISKPLKANLSFTKLDQINLFLKKIKNAHSLAHSEETSAMSNTMVNKDDLPVSKYYRGKLSKPKIHGDGVQKISAQENMWRAVSCFQKISVQTTQIVISMETVPHTSKPCLLASLSNLNGSLSVKATQKVPGIILGSSFLLSINDFLLKTSLKERSRILIGPCCATANLEAKWCKHSGNPGPEQSIPKISIDLRGGLLQVFWGQEHLNCLVLLHELLNGYLNEEGNFEVQVSEPVPQMSSPVEKNQTFKSEQSSDDLRTGLFQYVQDAESLKLPGVYEVLFYNETEDCPGMMLWRYPEPRVLTLVRITPVPFNTTEDPDISTADLGDVLQVPCSLEYWDELQKVFVAFREFNLSESKVCELQLPDINLVNDQKKLVSSDLWRIVLNSSQNGADDQSSASESGSQSTCDPLVTPTALAACTRVDSCFTPWFVPSLCVSFQFAHLEFHLCHHLDQLGTAAPQYLQPFVSDRNMPSELEYMIVSFREPHMYLRQWNNGSVCQEIQFLAQADCKLLECRNVTMQSVVKPFSIFGQMAVSSDVVEKLLDCTVIVDSVFVNLGQHVVHSLNTAIQAWQQNKCPEVEELVFSHFVICNDTQETLRFGQVDTDENILLASLHSHQYSWRSHKSPQLLHICIEGWGNWRWSEPFSVDHAGTFIRTIQYRGRTASLIIKVQQLNGVQKQIIICGRQIICSYLSQSIELKVVQHYIGQDGQAVVREHFDCLTAKQKLPSYILENNELTELCVKAKGDEDWSRDVCLESKAPEYSIVIQVPSSNSSIIYVWCTVLTLEPNSQVQQRMIVFSPLFIMRSHLPDPIIIHLEKRSLGLSETQIIPGKGQEKPLQNIEPDLVHHLTFQAREEYDPSDCAVPISTSLIKQIATKVHPGGTVNQILDEFYGPEKSLQPIWPYNKKDSDRNEQLSQWDSPMRVKLSIWKPYVRTLLIELLPWALLINESKWDLWLFEGEKIVLQVPAGKIIIPPNFQEAFQIGIYWANTNTVHKSVAIKLVHNLTSPKWKDGGNGEVVTLDEEAFVDTEIRLGAFPGHQKLCQFCISSMVQQGIQIIQIEDKTTIINNTPYQIFYKPQLSVCNPHSGKEYFRVPDSATFSICPGGEQPAMKSSSLPCWDLMPDISQSVLDASLLQKQIMLGFSPAPGADSSQCWSLPAIVRPEFPRQSVAVPLGNFRENGFCTRAIVLTYQEHLGVTYLTLSEDPSPRVIIHNRCPVKMLIKENIKDIPKFEVYCKKIPSECSIHHELYHQISSYPDCKTKDLLPSLLLRVEPLDEVTTEWSDAIDINSQGTQVVFLTGFGYVYVDVVHQCGTVFITVAPEGKAGPILTNTNRAPEKIVTFKMFITQLSLAVFDDLTHHKASAELLRLTLDNIFLCVAPGAGPLPGEEPVAALFELYCVEICCGDLQLDNQLYNKSNFHFAVLVCQGEKAEPIQCSKMQSLLISNKELEEYKEKCFIKLCITLNEGKSILCDINEFSFELKPARLYVEDTFVYYIKTLFDTYLPNSRLAGHSTHLSGGKQVLPMQVTQHARALVNPVKLRKLVIQPVNLLVSIHASLKLYIASDHTPLSFSVFERGPIFTTARQLVHALAMHYAAGALFRAGWVVGSLDILGSPASLVRSIGNGVADFFRLPYEGLTRGPGAFVSGVSRGTTSFVKHISKGTLTSITNLATSLARNMDRLSLDEEHYNRQEEWRRQLPESLGEGLRQGLSRLGISLLGAIAGIVDQPMQNFQKTSEAQASAGHKAKGVISGVGKGIMGVFTKPIGGAAELVSQTGYGILHGAGLSQLPKQRHQPSDLHADQAPNSHVKYVWKMLQSLGRPEVHMALDVVLVRGSGQEHEGCLLLTSEVLFVVSVSEDTQQQAFPVTEIDCAQDSKQNNLLTVQLKQPRVACDVEVDGVRERLSEQQYNRLVDYITKTSCHLAPSCSSMQIPCPVVAAEPPPSTVKTYHYLVDPHFAQVFLSKFTMVKNKALRKGFP
"
misc_feature 115..414
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/note="N-terminal region of Chorein, a TM vesicle-mediated
sorter; Region: Chorein_N; pfam12624"
/db_xref="CDD:204985"
misc_feature 3106..3108
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 3115..3117
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature <8005..>8229
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/note="Protein of unknown function (DUF1162); Region:
DUF1162; pfam06650"
/db_xref="CDD:203492"
misc_feature 11326..11589
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/note="ATG C terminal domain; Region: ATG_C; pfam09333"
/db_xref="CDD:192254"
variation 133..134
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="cc"
/db_xref="dbSNP:386834076"
variation 167
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200327756"
variation 203
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:76932157"
exon 259..402
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 314
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368511311"
variation 321
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201517617"
variation 330..331
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="ac"
/replace="t"
/db_xref="dbSNP:386834075"
variation 345
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372597619"
exon 403..523
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 417
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:201568328"
variation 439
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368290618"
variation 440
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61754110"
variation 450
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:200619753"
variation 456
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372489158"
variation 469
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201147123"
variation 476
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201723380"
variation 477
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373340298"
variation 515..516
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="t"
/db_xref="dbSNP:386834083"
exon 524..691
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 542
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:200662439"
variation 547
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144539572"
variation 564
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148436198"
variation 578..581
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ataa"
/db_xref="dbSNP:386834090"
variation 586
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142560687"
variation 616
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:376498106"
variation 653
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370545250"
variation 668
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373678127"
variation 670
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:367561688"
variation 671
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150941426"
exon 692..873
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 722
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201363767"
variation 737..738
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ca"
/db_xref="dbSNP:386834100"
variation 820
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376296532"
variation 822
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140808736"
exon 874..1048
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 938
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:181021782"
variation 945
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201743982"
variation 996
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143112539"
variation 1008
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:146883974"
variation 1027..1028
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ga"
/db_xref="dbSNP:386834117"
variation 1032
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140709787"
exon 1049..1317
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 1094
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:181625846"
variation 1104
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374781096"
variation 1111
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:150464408"
variation 1136
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138271331"
variation 1152
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149176010"
variation 1153
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:78072232"
variation 1175
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:368837821"
variation 1184
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201965789"
variation 1193
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143295587"
variation 1198
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:116951775"
variation 1309
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139093635"
exon 1318..1413
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 1330
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834070"
variation 1336
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:386834071"
variation 1359
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:143024324"
variation 1380..1384
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="attgt"
/db_xref="dbSNP:386834072"
variation 1392
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370660111"
variation 1400
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:147448147"
variation 1404
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:77759532"
exon 1414..1536
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
exon 1537..1674
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 1543
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371379631"
variation 1551
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:141324814"
variation 1574
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:150783688"
variation 1602
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:374276141"
variation 1615
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:180177354"
variation 1639
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139141291"
variation 1641
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149919865"
variation 1642
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368241718"
variation 1647
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145969836"
variation 1662
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:200635121"
variation 1665
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139849251"
variation 1670
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143205296"
variation 1674
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:180177355"
exon 1675..1762
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 1678
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146659631"
variation 1701
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200519753"
variation 1705
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369930405"
variation 1707
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:140746659"
variation 1708
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:199684925"
variation 1738
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372625091"
variation 1750
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142971568"
exon 1763..1954
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 1782
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:151105917"
variation 1811
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141046414"
variation 1815
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:190009435"
variation 1848
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369470068"
variation 1859
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368595026"
variation 1879
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140601319"
variation 1880
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:182397346"
variation 1882
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372593334"
variation 1893
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145648860"
variation 1936
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138171489"
variation 1943
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61754109"
exon 1955..2124
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 1976
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147043610"
variation 1998
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138291421"
variation 2092
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149334616"
exon 2125..2319
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 2126
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143606631"
variation 2149
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374124369"
variation 2158
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="c"
/db_xref="dbSNP:386834074"
variation 2159
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:372585253"
variation 2162
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:367999029"
variation 2167
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148047632"
variation 2180
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:141744983"
variation 2185
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:180177356"
variation 2186
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371500701"
variation 2202
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:376694328"
variation 2235
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201650333"
variation 2256
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369680212"
variation 2266
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372387373"
variation 2294
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370883635"
exon 2320..2444
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 2320
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369198846"
variation 2345
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199574731"
variation 2354
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145988999"
variation 2355
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:146450992"
variation 2359
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112858205"
variation 2386
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:140848350"
variation 2393
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:186644576"
variation 2433
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376216240"
exon 2445..2626
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 2461
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:370855171"
variation 2467
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:202052403"
variation 2488
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:141638933"
variation 2495
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376115412"
variation 2542
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:370570714"
variation 2549
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146195479"
variation 2562
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:114120664"
variation 2581
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:149866274"
variation 2582
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145419141"
variation 2584
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148788159"
variation 2585
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:376354130"
variation 2596
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61753721"
variation 2620
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:201872788"
variation 2623
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147924250"
exon 2627..2761
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 2629
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141694201"
variation 2645
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:147059568"
variation 2666
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147682334"
variation 2694
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199868590"
variation 2702
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:140936527"
variation 2707
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150185067"
variation 2716
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371800257"
variation 2720
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376044341"
variation 2729
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:112259211"
variation 2754
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:148777544"
variation 2757
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369124790"
exon 2762..2935
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 2778
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:369849286"
variation 2788
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:373346647"
variation 2789
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:188536125"
variation 2815
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149531438"
variation 2825
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376255480"
variation 2841..2842
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="gctc"
/db_xref="dbSNP:180177357"
variation 2859
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144830924"
variation 2862
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:192509060"
variation 2871
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138661755"
variation 2875
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371120818"
variation 2899
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372949456"
variation 2919
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:377174760"
variation 2934
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199881514"
variation 2935
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370336663"
exon 2936..3045
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 2939
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369198102"
variation 2964
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:374898875"
variation 2978
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:367603630"
variation 2988
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:371301713"
variation 3000
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:386834078"
variation 3014
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200724624"
variation 3022
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:120074152"
variation 3035
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376049764"
exon 3046..3193
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 3061
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:148422160"
variation 3110
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149970869"
variation 3117
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:201033083"
variation 3119
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371660958"
variation 3123
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199519352"
variation 3128
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201566948"
variation 3134
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369745645"
variation 3186
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141637316"
exon 3194..3321
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 3195
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150505597"
variation 3199
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374072699"
variation 3200
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:182764947"
variation 3205
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373538168"
variation 3227
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140015545"
variation 3239
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:376330680"
variation 3261
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144920754"
variation 3314
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:61753722"
variation 3315
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140090983"
exon 3322..3556
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 3331
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:186098421"
variation 3354
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:34961653"
variation 3366
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371674854"
variation 3373
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:373965494"
variation 3408
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:200982547"
variation 3444
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:367791771"
variation 3459..3460
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ct"
/db_xref="dbSNP:180177327"
variation 3472
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:199986963"
variation 3474
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:191099208"
variation 3490
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:117357319"
variation 3496
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371315874"
variation 3497
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61759485"
variation 3517
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199902569"
variation 3524
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:35342235"
variation 3538
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834080"
variation 3539
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112095679"
variation 3543
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375994361"
variation 3547
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:202015701"
exon 3557..3777
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 3627
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:118158347"
variation 3670
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:151247807"
variation 3675
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140905518"
variation 3678
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144895307"
variation 3680
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138729944"
variation 3709
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140353201"
variation 3710
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376524142"
variation 3717
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369539973"
variation 3729
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:386834081"
variation 3732
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373889030"
variation 3739
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:145417421"
variation 3761
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:138000928"
variation 3765
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200422365"
variation 3767
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:149478021"
exon 3778..3981
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 3780
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143905569"
variation 3855
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:16897391"
variation 3862
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:184693266"
variation 3895
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199872639"
variation 3922
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:142674934"
variation 3948
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:34941871"
variation 3977
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:145569846"
exon 3982..4153
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 3985
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150662496"
variation 4008
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139828348"
variation 4066
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374363141"
variation 4073
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200229383"
exon 4154..4268
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 4213
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372887370"
variation 4257
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:75493878"
variation 4259
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:367556418"
exon 4269..4410
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 4308
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149796549"
variation 4309
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374008116"
variation 4342
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376954713"
variation 4357
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145741622"
variation 4358
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:75933366"
variation 4391
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144187978"
exon 4411..4819
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 4434
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202048397"
variation 4440
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:201349007"
variation 4445
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834084"
variation 4446
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376118865"
variation 4448
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371961155"
variation 4507..4508
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834085"
variation 4510
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:143566455"
variation 4522
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834086"
variation 4542
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:61754112"
variation 4582
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:120074151"
variation 4585
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834087"
variation 4591..4593
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ctt"
/db_xref="dbSNP:386834088"
variation 4638
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148033080"
variation 4642
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370519991"
variation 4648
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:373919780"
variation 4683..4684
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834089"
variation 4703
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140797231"
variation 4735
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375652507"
variation 4737
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:150376603"
variation 4756
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:200774003"
variation 4783
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:200815297"
exon 4820..4931
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 4839
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368552225"
variation 4859
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:138417551"
variation 4921
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:142708735"
exon 4932..5135
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 4943
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147342579"
variation 4954
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371397733"
variation 4990..4991
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="aat"
/db_xref="dbSNP:180177359"
variation 4991..4992
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ata"
/db_xref="dbSNP:386834092"
variation 5015
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201587931"
variation 5034
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:180177360"
variation 5062
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138577821"
variation 5066
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:180177361"
variation 5076
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144069822"
variation 5129
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373351609"
exon 5136..5262
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 5140
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376467374"
variation 5141
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138148013"
variation 5142
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:192128754"
variation 5145
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:182877520"
variation 5161
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200014322"
variation 5172
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148773425"
variation 5175
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:142380266"
variation 5180
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:150857730"
variation 5181
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139586722"
variation 5183
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:373695822"
variation 5197
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834093"
variation 5251
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:192416968"
variation 5255
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:202135519"
exon 5263..5406
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 5279
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:368362777"
variation 5309
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200878381"
variation 5323
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:187596259"
variation 5326..5343
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="agtgtggctcaagttcaa"
/db_xref="dbSNP:180177362"
variation 5359
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371963567"
exon 5407..6094
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 5409
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:144223843"
variation 5442..5443
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="t"
/db_xref="dbSNP:386834094"
variation 5455
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146540735"
variation 5481
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139459037"
variation 5538..5539
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ag"
/db_xref="dbSNP:180177363"
variation 5571
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371961319"
variation 5572..5573
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="c"
/db_xref="dbSNP:180177364"
variation 5573
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201737428"
variation 5603
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:149954671"
variation 5685
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145048987"
variation 5687
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144257406"
variation 5688
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143115716"
variation 5703
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61742808"
variation 5714
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:141211386"
variation 5724..5725
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="t"
/db_xref="dbSNP:386834095"
variation 5792
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:117148013"
variation 5793
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368851580"
variation 5848..5849
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834096"
variation 5857
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:137901436"
variation 5861
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="c"
/db_xref="dbSNP:386834097"
variation 5908
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:35625719"
variation 5920..5921
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="at"
/db_xref="dbSNP:386834098"
variation 5926
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:141608582"
variation 5927
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150272676"
variation 5938
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834099"
variation 5947
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112749780"
variation 5989
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:138930771"
variation 5997
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:201448190"
variation 5998
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:186741842"
variation 6018
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372340783"
variation 6031
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:180177365"
variation 6070
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:375399419"
variation 6071
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149408318"
variation 6076
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148704031"
variation 6091
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139640224"
exon 6095..6232
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 6099..6100
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="g"
/db_xref="dbSNP:34054236"
variation 6107
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201494346"
variation 6150
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373595694"
exon 6233..6640
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 6233
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199837195"
variation 6234
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200691718"
variation 6244
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:377724023"
variation 6258
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142850229"
variation 6289
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:146073786"
variation 6311
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:371364257"
variation 6364
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200711677"
variation 6376
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200554315"
variation 6497
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374298481"
variation 6510
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:140028547"
variation 6531..6532
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ga"
/db_xref="dbSNP:386834101"
variation 6587
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:367838871"
variation 6602
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142248228"
variation 6636
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:61910727"
exon 6641..6843
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 6642
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:141845131"
variation 6689
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:120074149"
variation 6716
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147099791"
variation 6732
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374153644"
variation 6777..6778
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="g"
/db_xref="dbSNP:34813150"
variation 6788
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149727474"
variation 6798
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834102"
variation 6817
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:369932118"
variation 6831
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:147817990"
exon 6844..7051
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 6854
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:189948782"
variation 6899
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141275433"
variation 6900
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375613057"
variation 6913
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:146960401"
variation 6938
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147576864"
variation 6972
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369708908"
variation 6975
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:373927754"
variation 7043
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200713917"
variation 7048
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201909199"
exon 7052..7236
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 7112
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373240775"
variation 7133
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:386834104"
variation 7149
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61753724"
variation 7162
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:120074150"
variation 7163
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61754113"
variation 7233
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201133836"
exon 7237..7433
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 7264
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:180177368"
variation 7271
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148385830"
variation 7332
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="g"
/db_xref="dbSNP:386834105"
variation 7337
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:183874686"
variation 7338
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61753725"
variation 7342
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370689956"
variation 7350
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374136243"
variation 7353
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145846582"
variation 7380
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112496457"
variation 7433
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="gg"
/db_xref="dbSNP:180177367"
exon 7434..7615
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 7477
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138405323"
variation 7492
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200065297"
variation 7516
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373779146"
variation 7524
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:150771329"
variation 7552
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201963516"
exon 7616..7965
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 7620
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373550277"
variation 7657
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:375004684"
variation 7714
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834107"
variation 7715
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146092684"
variation 7721
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:386834108"
variation 7765
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369062407"
variation 7766
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373512013"
variation 7825
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140061281"
variation 7831
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:377498258"
variation 7833
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:112634620"
variation 7846
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:202226215"
variation 7854
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370903187"
variation 7861
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:144668374"
variation 7862
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:7833870"
variation 7863
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373165767"
variation 7864
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:111751379"
variation 7881
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:114038492"
variation 7882
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200302943"
variation 7885
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:186294088"
variation 7894
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140179844"
variation 7898
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145208175"
variation 7904
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199528303"
variation 7923
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147593451"
variation 7938
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201735478"
exon 7966..8127
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 7972
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:200941251"
variation 7978
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:202238616"
variation 7987
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144350008"
variation 8006
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370370264"
variation 8045
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:120074153"
variation 8047
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="c"
/db_xref="dbSNP:386834109"
variation 8079
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145460276"
variation 8110
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:377379862"
exon 8128..8283
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 8136
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:61754503"
variation 8181
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:149017920"
variation 8184
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199941415"
variation 8196
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376062743"
variation 8226
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:145899918"
variation 8230
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834110"
variation 8245
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369100428"
variation 8247
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201866766"
exon 8284..8547
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 8287
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374805472"
variation 8288
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:189689493"
variation 8319
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373542052"
variation 8345
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369898130"
variation 8346
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373348061"
variation 8357
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138453594"
variation 8359
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201127443"
variation 8363
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376283724"
variation 8387
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370701337"
variation 8403
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:180177369"
variation 8429
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:180177370"
variation 8430
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:182347753"
variation 8452
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="c"
/db_xref="dbSNP:386834111"
variation 8452
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:141360806"
variation 8466
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145090492"
variation 8480
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372979537"
variation 8539
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:377170629"
exon 8548..8631
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 8560
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:374369731"
variation 8567
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:146553331"
variation 8570
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:120074155"
variation 8572
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368143021"
variation 8576
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371325199"
variation 8583
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:386834112"
variation 8609
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368357351"
variation 8626
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834113"
variation 8627
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148333124"
exon 8632..8807
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 8632
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373961820"
variation 8722
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834114"
variation 8756
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145890213"
variation 8761
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:371609624"
exon 8808..8978
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 8823
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:150836518"
variation 8847
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199552885"
variation 8854
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:138140174"
variation 8863
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:79389009"
variation 8878
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200611924"
variation 8883
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375911218"
variation 8913
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201517365"
variation 8914
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143787982"
variation 8927
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147437490"
variation 8936
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139732310"
exon 8979..9180
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 8993
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372334983"
variation 9028
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145265055"
variation 9039
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147187040"
variation 9089
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:28940272"
variation 9098
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:375393153"
variation 9157
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:56413739"
exon 9181..9369
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 9199
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142110082"
variation 9209
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:6992059"
variation 9275
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:151159090"
variation 9280
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:140095832"
variation 9317
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:376652526"
exon 9370..9516
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 9370..9371
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="t"
/db_xref="dbSNP:180177329"
variation 9371..9372
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="t"
/db_xref="dbSNP:386834118"
variation 9378
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:376291996"
variation 9412
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201801811"
variation 9486
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:143974238"
exon 9517..9800
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 9518
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:199704158"
variation 9524
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141408531"
variation 9525
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:78277780"
variation 9535
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:113671330"
variation 9586
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138889735"
variation 9607
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373968887"
STS 9615..9633
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/db_xref="UniSTS:98954"
variation 9667
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201494563"
variation 9678
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:36074608"
variation 9716
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199559979"
variation 9733
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:143712369"
variation 9759
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:189680814"
variation 9778
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149842139"
exon 9801..9928
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 9817
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="t"
/db_xref="dbSNP:386834121"
variation 9831
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373968888"
variation 9842
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834122"
variation 9848
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:143852398"
variation 9918
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200883029"
exon 9929..10128
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 9969
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147242148"
variation 9972
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138221649"
variation 10016
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:141138612"
variation 10062
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:143728471"
variation 10089
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150573530"
variation 10103
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139575184"
variation 10112
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149285017"
exon 10129..10247
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 10129
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:116746734"
variation 10154
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376549169"
variation 10161
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369522130"
variation 10171
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:77308610"
variation 10179
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201746251"
variation 10187..10188
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ca"
/db_xref="dbSNP:386834054"
variation 10235
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138127778"
variation 10238
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:111353525"
exon 10248..11053
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 10250
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199931583"
variation 10251
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:61753726"
variation 10267..10268
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834055"
variation 10270
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140204523"
variation 10289
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:377348581"
variation 10302
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371573594"
variation 10321
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:377394274"
variation 10328
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:113335470"
variation 10338
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:374129601"
variation 10341
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:115369860"
variation 10342
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202113184"
variation 10385
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368041601"
variation 10386
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:151315104"
variation 10405
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:6468694"
variation 10421
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:112045467"
variation 10423
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:79324124"
variation 10426
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145279584"
variation 10427
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:142411465"
variation 10441
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:188030143"
variation 10444
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:191174682"
variation 10446
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200788631"
variation 10496
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200268089"
variation 10499
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146460917"
variation 10541
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:200491378"
variation 10567..10568
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ag"
/db_xref="dbSNP:180177371"
STS 10583..10684
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="A008R07"
/db_xref="UniSTS:6974"
variation 10627
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373773690"
variation 10634
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:367609176"
variation 10651
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112785599"
variation 10656
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:372875604"
variation 10708
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142957181"
variation 10710
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375804595"
variation 10713
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:113120767"
variation 10735
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143187571"
variation 10764
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:148265212"
variation 10770
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141266642"
variation 10798
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150767461"
variation 10812
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139227281"
variation 10836
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372367817"
variation 10867
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200232124"
variation 10889
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376964635"
variation 10900
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369258469"
variation 10930
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145547375"
variation 10941
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145950999"
variation 10952..10955
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tctc"
/db_xref="dbSNP:386834056"
variation 10988
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:28600803"
variation 10999
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:120074154"
variation 11010
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:114818249"
variation 11032
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149659649"
variation 11038
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373605057"
variation 11043
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:183080498"
exon 11054..11230
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 11057
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:386834057"
variation 11091
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:61754107"
variation 11110
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148582416"
variation 11119
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61754108"
variation 11160
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:375117356"
variation 11162
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370507425"
variation 11164
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373947421"
variation 11166
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:142939294"
variation 11179
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:151089043"
variation 11187
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:367797468"
variation 11195
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370172252"
variation 11208
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375676564"
variation 11226
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199748413"
exon 11231..11401
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 11231
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:367940320"
variation 11236
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="c"
/db_xref="dbSNP:386834058"
variation 11238
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:373428916"
variation 11256
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:185477101"
variation 11257
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142476821"
variation 11263
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:146571766"
variation 11272
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147891367"
variation 11283..11284
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ggac"
/db_xref="dbSNP:386834059"
variation 11300
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:376308074"
variation 11327
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:386834060"
variation 11330
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141566041"
variation 11344
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150393340"
variation 11356
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:180177372"
variation 11367
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138667007"
variation 11374
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201448515"
variation 11381
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149318176"
exon 11402..11578
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 11425
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834061"
variation 11430
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375229257"
variation 11452
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138012121"
variation 11498
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:142516047"
variation 11503
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145970185"
variation 11524
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:138565077"
exon 11579..11681
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 11616
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834062"
variation 11620
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369891888"
variation 11657
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:75996587"
variation 11660
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199741560"
variation 11667..11668
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="t"
/db_xref="dbSNP:386834063"
variation 11670
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:370697316"
variation 11675..11676
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="at"
/db_xref="dbSNP:180177373"
variation 11675
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834064"
exon 11682..11931
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 11709
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834065"
variation 11751
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:7844645"
variation 11756
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150713892"
variation 11760
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:368385004"
variation 11799
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139436386"
variation 11805
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:113454700"
variation 11806..11809
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="agtg"
/db_xref="dbSNP:386834066"
variation 11824
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147315245"
variation 11841
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368092348"
variation 11842
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141793014"
variation 11877
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:371985144"
variation 11891..11895
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="aa"
/replace="cagtg"
/db_xref="dbSNP:386834067"
variation 11893
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:144797111"
exon 11932..14100
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 11938..11939
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="atg"
/db_xref="dbSNP:386834068"
variation 11945
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147907236"
variation 11948
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368729107"
variation 11971
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148950784"
variation 11973
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147710096"
variation 11976
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:184614305"
STS 11982..12095
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="G34962"
/db_xref="UniSTS:117672"
STS 11982..12095
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="RH67322"
/db_xref="UniSTS:90383"
variation 12017..12026
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ccagctgttc"
/db_xref="dbSNP:386834069"
variation 12018..12019
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="c"
/db_xref="dbSNP:180177374"
variation 12038
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:73273219"
variation 12070
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201483764"
variation 12083
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:117934093"
variation 12103
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140216842"
variation 12169
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369435007"
variation 12196
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369670017"
variation 12208..12209
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tg"
/db_xref="dbSNP:201268463"
variation 12211..12212
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tgat"
/db_xref="dbSNP:141587726"
variation 12212..12213
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="gatt"
/db_xref="dbSNP:373852425"
variation 12217
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:201520925"
variation 12228
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373141658"
variation 12241
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:189939258"
variation 12334..12356
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="gccaccataaagggctgcatttt"
/db_xref="dbSNP:374682407"
variation 12382
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:201566966"
variation 12427..12428
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="caa"
/db_xref="dbSNP:71572048"
variation 12428..12429
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="aacaaca"
/replace="caa"
/db_xref="dbSNP:72291496"
variation 12429..12430
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="aca"
/db_xref="dbSNP:71274940"
variation 12485
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149912942"
variation 12554..12557
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="attt"
/db_xref="dbSNP:374440758"
variation 12579
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:62534630"
variation 12592
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375699554"
variation 12609..12611
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tat"
/db_xref="dbSNP:10537000"
variation 12611..12613
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tta"
/db_xref="dbSNP:10542428"
variation 12613..12615
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tta"
/db_xref="dbSNP:72544630"
variation 12703
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:144940198"
variation 12704
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:78526364"
variation 12775..12776
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tt"
/db_xref="dbSNP:35963691"
variation 12779..12780
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tt"
/db_xref="dbSNP:367738027"
variation 12835
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:78305289"
variation 12879..12881
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tga"
/db_xref="dbSNP:10542429"
variation 12880..12882
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="gat"
/db_xref="dbSNP:60078732"
variation 12881..12882
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="t"
/db_xref="dbSNP:200421894"
variation 12923
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:144603951"
variation 12925
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:138761680"
STS 12977..13076
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="D8S1427E"
/db_xref="UniSTS:151216"
variation 12994
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:181526774"
variation 13047..13048
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="c"
/db_xref="dbSNP:34615311"
STS 13085..13260
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="A006N10"
/db_xref="UniSTS:61015"
variation 13104
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:186225330"
variation 13221
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:140374149"
variation 13381
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:189427010"
variation 13387
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:182082022"
variation 13391..13392
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tctc"
/db_xref="dbSNP:60544715"
variation 13392..13393
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tctc"
/db_xref="dbSNP:368674871"
variation 13396..13397
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tctc"
/db_xref="dbSNP:71981100"
variation 13598
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145470065"
variation 13697..13698
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tgt"
/db_xref="dbSNP:146221403"
variation 13719
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:80237506"
variation 13720
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148026916"
variation 13750
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:186440514"
variation 13762
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:75181119"
variation 13765
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:190613136"
variation 13774
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:182902606"
STS 13813..13970
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="D8S1415E"
/db_xref="UniSTS:151205"
STS 13817..14064
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="A003B20"
/db_xref="UniSTS:9488"
STS 13943..14042
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="WI-14296"
/db_xref="UniSTS:36777"
STS 13954..14034
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="1734"
/db_xref="UniSTS:60466"
variation 13963
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:7157"
ORIGIN
ggcgcggtacaggagcagcactgccggcgggggcgggtgccagggacttggaggtggaggggacgcggcggtactctggcgtcttccgacttcgactccttaccttaaaagatgctggagtcatatgtaactccaattttaatgagctatgtgaatcgctacatcaagaacttaaagccgtcggatctacagctttcactatggggtggagacgtggtactcagcaagctcgagttaaagttggatgtgctggaacaggaactgaaattaccattcacttttttaagtggacatattcatgaattgaggattcatgtaccatggacaaaactgggttcagaaccagtggtaattaccatcaatactatggaatgcattttgaaacttaaggatgggatacaggatgaccatgaaagctgtggttctaattctaccaaccgtagtactgctgagagcacaaaatcatcaatcaaaccgcggagaatgcagcaggctgctcctacagatcctgacttaccaccaggttatgtgcagagtctgattagacgagttgtaaataatgtaaacattgtgataaataatctcatactaaaatatgttgaagatgatatcgtcctttccgtcaatatcacttctgcagaatgttatacagtaggtgaattatgggatcgtgcattcatggatatttctgcaactgatttggtgctgagaaaggttatcaatttttctgactgtacagtttgtcttgataaacggaatgccagtggtaaaatagaattttaccaggatcctttattatacaaatgttccttcagaactcgtcttcattttacatatgaaaacctaaattccaagatgccatctgttattaaaattcatactttagtggaaagtttgaaactttctatcacagatcaacaactgcctatgtttattcgtataatgcaacttggaattgctctttactatggagaaataggcaattttaaagaaggcgaaatagaggaccttacttgtcataataaagatatgctaggaaacattacaggttctgaagatgaaacaagaatagatatgcaatatcctgctcagcataaaggtcaagagttatattcacagcaagatgaggagcagccacagggatgggtgtcatgggcctggtcctttgtgcctgcaattgtgagttatgacgatggcgaggaagactttgttgggaacgatcctgcatcaaccatgcatcaacaaaaagcacagactttgaaggatcctattgtttctataggattttattgcacaaaggcaacggtgactttcaaactcacagaaatgcaagttgagagtagttattacagtccacagaaagtaaaatctaaagaagtattgtgttgggaacaagaaggaactacagttgaggcccttatgatgggagaacctttctttgattgccagattgggtttgttggttgcagagccatgtgccttaaaggaattatgggtgttaaagattttgaagagaatatgaatagaagtgaaactgaagcctgtttcttcatttgtggtgacaatttgagtacgaaaggtttcacataccttacaaattcattgtttgattaccgaagcccagaaaataatggtactcgcgcagaatttatcttggattcaactcatcataaggagacatacactgagatagctggaatgcaacggtttggggctttttatatggattacctgtatacaatggagaacactagtggcaaaggttccacaaatcaacaagacttttcttcagggaaaagtgaagatttgggaacagttcaggagaagtccaccaaaagccttgttataggtcctcttgattttcgtttggatagcagtgcggtgcataggattttgaaaatgattgtgtgtgccttggaacatgaatatgaaccatatagcaggctaaaatcagatattaaggatgaaaatgaaacaatactgaatcctgaagaggtggctcttctggaggaatatattcctactcgacatacaagtgttactctcctcaaatgtacctgcacaatttccatggctgaattcaacttgctggaccatttactacctgtcattatgggagaaaagaactcaagtaacttcatgaatactacaaacttccagtctcttcggcctttgccatccattcgaatattggtggataaaattaatctggaacattcagtgccaatgtatgctgaacagttggtgcatgtggtcagcagccttactcaaccttctgataacctgcttcattattgttatgtacactgctatcttaagatatttggtttccaggcaggactgacgtctttggattgcagtggatcttactgcttacctgtaccagttattccctctttcagcactgctctttatgggaaacttctgaaactccccacatgctggaccaaaagatctcagattgctataactgaaggtatatttgaacttccaaatctcacaattcaagctacaagagcacagacacttctcttgcaagcaatatatcaaagttggtctcatcttggaaatgtcagctcttccgcagtgattgaagctttgataaatgaaatcttcctaagtataggtgtgaaatctaagaatcccctgccaactcttgagggctcaatccagaatgttgaattgaagtactgcagcacatcattggtcaaatgtgcctctgggaccatgggatcaataaaaatttgtgccaaagccccagttgatagtggaaaagagaagttgattcccttgcttcagggtccttctgacactaaagaccttcatagcaccaagtggctcaatgagagtagaaagccagagtctctcttagctccagatttgatggccttcacaatccaagttccacaatatattgactactgccacaattccggtgctgtacttctttgcagtatacaaggactagcagttaatattgacccaatcttatatacgtggctcatctatcagcctcagaaacgaacaagtagacatatgcaacagcagcctgtggtagctgttcctcttgttatgccagtttgtagaaggaaagaggatgaggtgtctattggaagtgcccccttggcaaagcagcaatcatatcaggcctctgaatatgccagcagccctgtaaaaacaaaaacggtaacagaatcccgcccattgtcagttcctgttaaagccatgttgaatatatctgaaagctgtagaagtcctgaagaaagaatgaaggaatttattggaattgtttggaatgcagtgaagcatctcacactacagcttgaagtacaatcttgttgtgtgtttattccaaatgatagcctgccttccccaagtacaattgtatctggtgacattcctggaacagtaagaagttggtaccatggacaaaccagcatgccgggaacacttgtcctctgtttgcctcaaataaagattattagtgctgggcacaagtatatggaacctctgcaggagattccatttgttatcccacgacccatccttgaagaaggtgatgcttttccttggacgatcagcttgcataatttcagcatatatacccttcttggaaaacaagtgacactttgcctagtggaacctatgggttgcacctccactctagctgtcacgtctcaaaaactgcttgctacgggacctgatacacgacattcatttgttgtctgtctccatgttgacctagagtcactagagataaaatgctctaatccccaggtccagctcttctatgaactaactgatatcatgaataaggtctggaacaagattcagaagagaggcaatctcaacctatctccaacctctccagagaccatggcagggcctgttcctacttctccagttagaagcagtataggcacagctcctccagataccagcacatgcagcccatctgctgacattgggactactactgagggagattctatacaagcaggtgaggaatcaccattctcagattctgtgaccttggaacaaactacaagtaatattggaggaaccagtggacgtgttagtttatggatgcagtgggtgcttcccaaaattactataaagctctttgctccagatcctgaaaataaaggcacagaggtttgtatggtcagtgaactagaagatctcagtgcttccatagatgtccaggatgtatataccaaagtgaaatgtaaaatagagagtttcaatattgatcactatagaagcagccttggggaagagtgttggtctttggggcaatgtggaggtgtcttcctttcctgtactgacaagctgaacagacgcaccttgttggttcgacccatcagcaagcaggaccctttcagtaattgctctggcttctttccttctacaactacaaaacttctagatggcactcatcagcagcatggattcctctctctgacatacacaaaagctgtaacaaaaaatgtccgccacaagttaacatcaagaaatgagcgaagaagttttcataagttatctgaaggcctaatggatggttctcctcattttcttcatgaaattcttctttcagcacaagcttttgatattgttctttattttcctttacttaatgccattgcaagtatatttcaagcaaaactaccaaagacccaaaaagagaaaagaaaatctcctggtcagcccatgaggacccatacactgacatcccgcaatttacctttgatttatgtcaacacaagtgtaatcagaatttttattccaaaaacagaagaaatgcagccaactgttgaagctaatcaggcagcaaaagaagacactgtggttttgaagattggctctgttgccatggctccccaggctgacaatccccttggcagatctgtccttaggaaagatatttaccagagagccttgaacttaggaattcttcgagatcctggatcagaaatcgaagacagacaataccaaatagatctgcagtccatcaatattggtactgcacagtggcatcaactaaaaccagagaaggaaagtgtctcaggaggggtggtaacagagactgaaaggaattctcaaaatccagcccttgagtggaatatggccagcagcatacggcggcatcaagaaaggagagcaattttgacccccgttttgacagatttttctgtccgaataactggagcacctgctgtcattttcaccaaagtagtttctccagaaaatttgcatactgaggagattttagtgtgtggccattccttagaagtgaatataaccacaaacctggacttcttcctaagtgtggctcaagttcaactcttacatcagttaatagtagcaaatatgactggactggaaccatcaaacaaggctgcagagatctctaaacaagaacagaaaaaagtggatatatttgatggaggcatggctgaaacctcatctcgctacagtggtgctcaggatagtggaattggcagtgacagtgttaaaatcagaatagtgcaaatagagcagcacagtggtgccagtcagcatcgcattgcccgtccctcacgccagtcatcaattgtaaaaaatctaaattttattccctttgacatatttattactgcaagtagaatctcactaatgacctattcctgtatggccttatccaaatcgaaatcacaagaacagaagaataatgaaaaaacagacaagagttcattaaatctcccagaagttgattcagatgttgctaagcccaaccaggcatgtatttccacggtgacagcagaagatctcttaaggagcagcatttcttttccttcagggaaaaaaataggggtcctctctcttgaaagtcttcatgcatccacaaggtcatctgctagacaagcacttggtataactattgttcggcagcctggtcgaagaggaactggtgacttacagctagagccttttctgtactttattgtgtcccagccttccttgcttctgagttgtcaccacagaaagcagcgagtggaagtatccatttttgatgctgtgcttaaaggggtggcctctgattacaaatgtatagatcctgggaagactctgcctgaagcccttgattattgcactgtttggctacagacagtgcctggagaaatagacagcaaaagtggtattccaccttcctttataacactacagattaaagactttctgaatggaccagcggatgtcaatttggatatatcaaagcctttgaaagcaaacctgagtttcaccaaactggatcagataaacctttttttaaagaagataaaaaatgcacacagtttggcacatagtgaagagacttcagccatgtccaacaccatggtgaataaggatgatcttccagtctccaaatattaccgtggaaagttgtctaaacccaaaattcatggtgatggagtgcaaaagatttcagctcaagaaaacatgtggagagctgtttcctgctttcaaaaaatttctgttcaaactactcagattgtgatctccatggaaactgtaccccataccagcaaaccatgcctgttagcatctctctcaaacctcaatggaagccttagtgtcaaggcaacacaaaaagtacctggcataattcttgggtcatcatttctactcagtataaacgattttctccttaaaacaagtctcaaagaaagaagccgcattctgataggaccatgttgtgctactgccaatctggaagctaagtggtgtaaacacagcgggaatccaggcccagaacaatccataccaaaaatatccattgacttaagaggaggtctactacaggtcttctggggtcaagaacatttgaattgtttagttcttctacatgaattactcaatggataccttaatgaggagggaaattttgaagtacaagtttctgaaccagtgcctcaaatgtcatctcctgtggaaaagaatcagacatttaaaagtgaacaaagttcagatgacctacggacaggtctatttcagtatgtacaggatgctgaatctttgaaattgcctggggtctatgaagtcttattttataatgaaactgaagattgcccagggatgatgttatggagatatccagaacctagagtactcacccttgtacgaataactcctgtaccttttaacaccacagaggatccagatattagcacagcagaccttggtgatgtgctacaggttccttgtagcttggaatactgggatgaactccagaaggtttttgttgcatttagagaatttaatctgtctgaaagcaaagtttgtgaactgcagttgccggatatcaatctcgtgaatgaccagaagaaattagtatcttcagatctttggagaattgtcttgaacagcagtcaaaatggagctgatgaccaaagctctgcaagtgagtctggttctcaaagcacttgtgatccacttgtgactccaacagccctggctgcctgtaccagagttgactcctgctttaccccatggtttgtcccatccctttgcgtttctttccagtttgctcacctggaattccatctttgtcatcaccttgaccaactaggcacagctgcaccacagtacctacagccatttgtttccgacagaaatatgccatctgaactagaatacatgattgtttccttcagagaaccacacatgtatcttcgacagtggaataatggttctgtctgtcaggagatccagttcttagctcaagcagactgtaaacttctagagtgcagaaatgtcactatgcaaagtgtggtgaaacccttcagcatcttcgggcagatggcagtttccagcgatgtagtggaaaagctgcttgactgcaccgtgatagttgattctgtatttgtaaaccttggacagcatgtagtccattcactaaacactgcaatacaagcttggcaacagaacaaatgccctgaggtagaggagttggtcttcagccattttgtgatctgtaatgacacacaggagacactgcggtttggccaggtggatactgatgaaaatattctgctggcgagtctccacagtcaccagtacagctggcgctctcacaaatccccacagctgttacacatctgtattgaaggttggggcaactggcgttggtcagagcctttcagtgtggaccatgccgggacttttattagaacaattcagtacaggggtcgaactgcttctctcatcatcaaggttcagcaactcaatggagtacaaaaacagattatcatctgtggaagacagatcatctgtagttacttgtctcaaagcatagaactaaaagtcgttcagcattacattggtcaagatggacaagctgtagttcgggaacattttgactgcctcacagccaaacagaaattgccttcgtacatactagaaaacaatgaactgacggagctgtgtgtgaaggccaaaggagatgaagactggtcaagagatgtgtgcctggaatccaaagcccctgagtacagcattgtcattcaggtgccatcttcaaacagttccattatttatgtctggtgcacagttttgactttagaacccaactctcaagtgcaacaacgaatgattgtgttcagccctctttttatcatgaggagtcatcttccagaccccattatcatacatttggagaaaaggagtctgggattgagtgaaacacaaattattccaggaaaagggcaggaaaaaccactgcaaaacatagaacctgaccttgtacatcacctgacattccaagcaagagaagaatatgatccttcagattgtgcagttcccatctcaacatccctcattaagcaaatagccactaaggtacaccctggaggcacagttaatcagatccttgacgaattctatgggccagaaaagtcgcttcaacccatatggccctataataagaaggattctgacaggaatgaacagctaagtcagtgggatagcccaatgcgagtgaagctgtcaatctggaagccatatgttagaactttgttgatagaacttctgccctgggccctgcttatcaatgaatccaaatgggacctctggctatttgaaggagagaaaattgttctacaggttcctgctggcaaaattattattcctcctaattttcaggaagcttttcaaattggaatatactgggcaaatacaaacactgtgcacaagtcagtagcaattaaactggtccataacctgacatctccaaagtggaaagatggaggtaatggtgaagttgtgacactggatgaagaagcgtttgttgatactgaaataagacttggtgcttttccaggacatcagaagttatgtcagttctgcatttcctccatggtacagcaaggtatacaaattattcagattgaagacaagactacaataatcaataatacaccatatcaaatattttataaaccacagctatctgtctgcaatccccattctggaaaggagtattttcgtgttccagacagtgctacttttagcatttgcccaggtggagagcagcctgctatgaaatccagctcccttccttgctgggacttgatgcctgacatcagtcagtcagtactggatgcatccctgcttcagaaacagatcatgctgggcttttctcctgccccaggtgctgacagctcacagtgctggagcctgccagctatagttagaccagagtttcccagacagagtgtggcagtacccctcgggaatttccgggaaaatggattctgtaccagggctatagtgctgacatatcaagaacacctcggagtgacttatttaaccctctcagaagaccctagtcctcgagtaattatccacaatagatgtccagtaaaaatgcttataaaggaaaacattaaagatattccaaagtttgaggtttattgcaaaaaaattccctccgagtgctcaattcatcatgagctgtatcatc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//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:157680 -> Biological process: GO:0015031 [protein transport] evidence: IEA
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@meso_cacase at
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