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2024-04-26 02:22:47, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_152564 14025 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens vacuolar protein sorting 13 homolog B (yeast)
(VPS13B), transcript variant 1, mRNA.
ACCESSION NM_152564
VERSION NM_152564.4 GI:384551659
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 14025)
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 14025)
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 14025)
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 14025)
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 14025)
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 14025)
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 14025)
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 14025)
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 14025)
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 14025)
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 AY223815.1, AC105195.5,
AC023933.9 and AC105328.13.
On Apr 19, 2012 this sequence version replaced gi:35493700.
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 (1) lacks one alternate in-frame
exon and includes a different in-frame exon, compared to variant 5.
The resulting isoform (1) is shorter and varies within this region
of the protein, but has the same C- and N-termini, compared to
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 :: AY223815.1, AJ608773.1 [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 AY223815.1 1-1667
1668-1668 AC105195.5 119108-119108
1669-1740 AY223815.1 1669-1740
1741-1741 AC105195.5 120112-120112
1742-1962 AY223815.1 1742-1962
1963-1963 AC105195.5 131230-131230
1964-5053 AY223815.1 1964-5053
5054-5054 AC023933.9 83192-83192
5055-9602 AY223815.1 5055-9602
9603-9603 AC105328.13 112032-112032 c
9604-14018 AY223815.1 9604-14018
14019-14025 AC105328.13 66976-66982 c
FEATURES Location/Qualifiers
source 1..14025
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="8"
/map="8q22.2"
gene 1..14025
/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..12105
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/note="isoform 1 is encoded by transcript variant 1;
vacuolar protein sorting-associated protein 13B"
/codon_start=1
/product="vacuolar protein sorting-associated protein 13B
isoform 1"
/protein_id="NP_689777.3"
/db_xref="GI:35493701"
/db_xref="CCDS:CCDS6281.1"
/db_xref="GeneID:157680"
/db_xref="HGNC:2183"
/db_xref="MIM:607817"
/translation="
MLESYVTPILMSYVNRYIKNLKPSDLQLSLWGGDVVLSKLELKLDVLEQELKLPFTFLSGHIHELRIHVPWTKLGSEPVVITINTMECILKLKDGIQDDHESCGSNSTNRSTAESTKSSIKPRRMQQAAPTDPDLPPGYVQSLIRRVVNNVNIVINNLILKYVEDDIVLSVNITSAECYTVGELWDRAFMDISATDLVLRKVINFSDCTVCLDKRNASGKIEFYQDPLLYKCSFRTRLHFTYENLNSKMPSVIKIHTLVESLKLSITDQQLPMFIRIMQLGIALYYGEIGNFKEGEIEDLTCHNKDMLGNITGSEDETRIDMQYPAQHKGQELYSQQDEEQPQGWVSWAWSFVPAIVSYDDGEEDFVGNDPASTMHQQKAQTLKDPIVSIGFYCTKATVTFKLTEMQVESSYYSPQKVKSKEVLCWEQEGTTVEALMMGEPFFDCQIGFVGCRAMCLKGIMGVKDFEENMNRSETEACFFICGDNLSTKGFTYLTNSLFDYRSPENNGTRAEFILDSTHHKETYTEIAGMQRFGAFYMDYLYTMENTSGKGSTNQQDFSSGKSEDLGTVQEKSTKSLVIGPLDFRLDSSAVHRILKMIVCALEHEYEPYSRLKSDIKDENETILNPEEVALLEEYIPTRHTSVTLLKCTCTISMAEFNLLDHLLPVIMGEKNSSNFMNTTNFQSLRPLPSIRILVDKINLEHSVPMYAEQLVHVVSSLTQPSDNLLHYCYVHCYLKIFGFQAGLTSLDCSGSYCLPVPVIPSFSTALYGKLLKLPTCWTKRSQIAITEGIFELPNLTIQATRAQTLLLQAIYQSWSHLGNVSSSAVIEALINEIFLSIGVKSKNPLPTLEGSIQNVELKYCSTSLVKCASGTMGSIKICAKAPVDSGKEKLIPLLQGPSDTKDLHSTKWLNESRKPESLLAPDLMAFTIQVPQYIDYCHNSGAVLLCSIQGLAVNIDPILYTWLIYQPQKRTSRHMQQQPVVAVPLVMPVCRRKEDEVSIGSAPLAKQQSYQASEYASSPVKTKTVTESRPLSVPVKAMLNISESCRSPEERMKEFIGIVWNAVKHLTLQLEVQSCCVFIPNDSLPSPSTIVSGDIPGTVRSWYHGQTSMPGTLVLCLPQIKIISAGHKYMEPLQEIPFVIPRPILEEGDAFPWTISLHNFSIYTLLGKQVTLCLVEPMGCTSTLAVTSQKLLATGPDTRHSFVVCLHVDLESLEIKCSNPQVQLFYELTDIMNKVWNKIQKRGNLNLSPTSPETMAGPVPTSPVRSSIGTAPPDTSTCSPSADIGTTTEGDSIQAGEESPFSDSVTLEQTTSNIGGTSGRVSLWMQWVLPKITIKLFAPDPENKGTEVCMVSELEDLSASIDVQDVYTKVKCKIESFNIDHYRSRPGEGWQSGHFEGVFLQCKEKSVTTTKLLDGTHQQHGFLSLTYTKAVTKNVRHKLTSRNERRSFHKLSEGLMDGSPHFLHEILLSAQAFDIVLYFPLLNAIASIFQAKLPKTQKEKRKSPGQPMRTHTLTSRNLPLIYVNTSVIRIFIPKTEEMQPTVEANQAAKEDTVVLKIGSVAMAPQADNPLGRSVLRKDIYQRALNLGILRDPGSEIEDRQYQIDLQSINIGTAQWHQLKPEKESVSGGVVTETERNSQNPALEWNMASSIRRHQERRAILTPVLTDFSVRITGAPAVIFTKVVSPENLHTEEILVCGHSLEVNITTNLDFFLSVAQVQLLHQLIVANMTGLEPSNKAAEISKQEQKKVDIFDGGMAETSSRYSGAQDSGIGSDSVKIRIVQIEQHSGASQHRIARPSRQSSIVKNLNFIPFDIFITASRISLMTYSCMALSKSKSQEQKNNEKTDKSSLNLPEVDSDVAKPNQACISTVTAEDLLRSSISFPSGKKIGVLSLESLHASTRSSARQALGITIVRQPGRRGTGDLQLEPFLYFIVSQPSLLLSCHHRKQRVEVSIFDAVLKGVASDYKCIDPGKTLPEALDYCTVWLQTVPGEIDSKSGIPPSFITLQIKDFLNGPADVNLDISKPLKANLSFTKLDQINLFLKKIKNAHSLAHSEETSAMSNTMVNKDDLPVSKYYRGKLSKPKIHGDGVQKISAQENMWRAVSCFQKISVQTTQIVISMETVPHTSKPCLLASLSNLNGSLSVKATQKVPGIILGSSFLLSINDFLLKTSLKERSRILIGPCCATANLEAKWCKHSGNPGPEQSIPKISIDLRGGLLQVFWGQEHLNCLVLLHELLNGYLNEEGNFEVQVSEPVPQMSSPVEKNQTFKSEQSSDDLRTGLFQYVQDAESLKLPGVYEVLFYNETEDCPGMMLWRYPEPRVLTLVRITPVPFNTTEDPDISTADLGDVLQVPCSLEYWDELQKVFVAFREFNLSESKVCELQLPDINLVNDQKKLVSSDLWRIVLNSSQNGADDQSSASESGSQSTCDPLVTPTALAACTRVDSCFTPWFVPSLCVSFQFAHLEFHLCHHLDQLGTAAPQYLQPFVSDRNMPSELEYMIVSFREPHMYLRQWNNGSVCQEIQFLAQADCKLLECRNVTMQSVVKPFSIFGQMAVSSDVVEKLLDCTVIVDSVFVNLGQHVVHSLNTAIQAWQQNKCPEVEELVFSHFVICNDTQETLRFGQVDTDENILLASLHSHQYSWRSHKSPQLLHICIEGWGNWRWSEPFSVDHAGTFIRTIQYRGRTASLIIKVQQLNGVQKQIIICGRQIICSYLSQSIELKVVQHYIGQDGQAVVREHFDCLTAKQKLPSYILENNELTELCVKAKGDEDWSRDVCLESKAPEYSIVIQVPSSNSSIIYVWCTVLTLEPNSQVQQRMIVFSPLFIMRSHLPDPIIIHLEKRSLGLSETQIIPGKGQEKPLQNIEPDLVHHLTFQAREEYDPSDCAVPISTSLIKQIATKVHPGGTVNQILDEFYGPEKSLQPIWPYNKKDSDRNEQLSQWDSPMRVKLSIWKPYVRTLLIELLPWALLINESKWDLWLFEGEKIVLQVPAGKIIIPPNFQEAFQIGIYWANTNTVHKSVAIKLVHNLTSPKWKDGGNGEVVTLDEEAFVDTEIRLGAFPGHQKLCQFCISSMVQQGIQIIQIEDKTTIINNTPYQIFYKPQLSVCNPHSGKEYFRVPDSATFSICPGGEQPAMKSSSLPCWDLMPDISQSVLDASLLQKQIMLGFSPAPGADSSQCWSLPAIVRPEFPRQSVAVPLGNFRENGFCTRAIVLTYQEHLGVTYLTLSEDPSPRVIIHNRCPVKMLIKENIKDIPKFEVYCKKIPSECSIHHELYHQISSYPDCKTKDLLPSLLLRVEPLDEVTTEWSDAIDINSQGTQVVFLTGFGYVYVDVVHQCGTVFITVAPEGKAGPILTNTNRAPEKIVTFKMFITQLSLAVFDDLTHHKASAELLRLTLDNIFLCVAPGAGPLPGEEPVAALFELYCVEICCGDLQLDNQLYNKSNFHFAVLVCQGEKAEPIQCSKMQSLLISNKELEEYKEKCFIKLCITLNEGKSILCDINEFSFELKPARLYVEDTFVYYIKTLFDTYLPNSRLAGHSTHLSGGKQVLPMQVTQHARALVNPVKLRKLVIQPVNLLVSIHASLKLYIASDHTPLSFSVFERGPIFTTARQLVHALAMHYAAGALFRAGWVVGSLDILGSPASLVRSIGNGVADFFRLPYEGLTRGPGAFVSGVSRGTTSFVKHISKGTLTSITNLATSLARNMDRLSLDEEHYNRQEEWRRQLPESLGEGLRQGLSRLGISLLGAIAGIVDQPMQNFQKTSEAQASAGHKAKGVISGVGKGIMGVFTKPIGGAAELVSQTGYGILHGAGLSQLPKQRHQPSDLHADQAPNSHVKYVWKMLQSLGRPEVHMALDVVLVRGSGQEHEGCLLLTSEVLFVVSVSEDTQQQAFPVTEIDCAQDSKQNNLLTVQLKQPRVACDVEVDGVRERLSEQQYNRLVDYITKTSCHLAPSCSSMQIPCPVVAAEPPPSTVKTYHYLVDPHFAQVFLSKFTMVKNKALRKGFP
"
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 <7930..>8154
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/note="Protein of unknown function (DUF1162); Region:
DUF1162; pfam06650"
/db_xref="CDD:203492"
misc_feature 11251..11514
/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..4335
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 4279
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369731827"
variation 4280
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:372350591"
exon 4336..4744
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 4359
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202048397"
variation 4365
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:201349007"
variation 4370
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834084"
variation 4371
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376118865"
variation 4373
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371961155"
variation 4432..4433
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834085"
variation 4435
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:143566455"
variation 4447
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834086"
variation 4467
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:61754112"
variation 4507
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:120074151"
variation 4510
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834087"
variation 4516..4518
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ctt"
/db_xref="dbSNP:386834088"
variation 4563
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148033080"
variation 4567
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370519991"
variation 4573
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:373919780"
variation 4608..4609
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834089"
variation 4628
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140797231"
variation 4660
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375652507"
variation 4662
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:150376603"
variation 4681
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:200774003"
variation 4708
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:200815297"
exon 4745..4856
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 4764
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368552225"
variation 4784
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:138417551"
variation 4846
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:142708735"
exon 4857..5060
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 4868
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147342579"
variation 4879
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371397733"
variation 4915..4916
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="aat"
/db_xref="dbSNP:180177359"
variation 4916..4917
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ata"
/db_xref="dbSNP:386834092"
variation 4940
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201587931"
variation 4959
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:180177360"
variation 4987
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138577821"
variation 4991
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:180177361"
variation 5001
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144069822"
variation 5054
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373351609"
exon 5061..5187
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 5065
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376467374"
variation 5066
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138148013"
variation 5067
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:192128754"
variation 5070
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:182877520"
variation 5086
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200014322"
variation 5097
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148773425"
variation 5100
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:142380266"
variation 5105
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:150857730"
variation 5106
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139586722"
variation 5108
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:373695822"
variation 5122
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834093"
variation 5176
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:192416968"
variation 5180
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:202135519"
exon 5188..5331
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 5204
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:368362777"
variation 5234
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200878381"
variation 5248
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:187596259"
variation 5251..5268
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="agtgtggctcaagttcaa"
/db_xref="dbSNP:180177362"
variation 5284
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371963567"
exon 5332..6019
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 5334
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:144223843"
variation 5367..5368
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="t"
/db_xref="dbSNP:386834094"
variation 5380
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146540735"
variation 5406
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139459037"
variation 5463..5464
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ag"
/db_xref="dbSNP:180177363"
variation 5496
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371961319"
variation 5497..5498
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="c"
/db_xref="dbSNP:180177364"
variation 5498
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201737428"
variation 5528
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:149954671"
variation 5610
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145048987"
variation 5612
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144257406"
variation 5613
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143115716"
variation 5628
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61742808"
variation 5639
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:141211386"
variation 5649..5650
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="t"
/db_xref="dbSNP:386834095"
variation 5717
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:117148013"
variation 5718
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368851580"
variation 5773..5774
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834096"
variation 5782
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:137901436"
variation 5786
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="c"
/db_xref="dbSNP:386834097"
variation 5833
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:35625719"
variation 5845..5846
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="at"
/db_xref="dbSNP:386834098"
variation 5851
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:141608582"
variation 5852
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150272676"
variation 5863
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834099"
variation 5872
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112749780"
variation 5914
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:138930771"
variation 5922
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:201448190"
variation 5923
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:186741842"
variation 5943
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372340783"
variation 5956
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:180177365"
variation 5995
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:375399419"
variation 5996
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149408318"
variation 6001
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148704031"
variation 6016
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139640224"
exon 6020..6157
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 6024..6025
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="g"
/db_xref="dbSNP:34054236"
variation 6032
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201494346"
variation 6075
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373595694"
exon 6158..6565
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 6158
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199837195"
variation 6159
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200691718"
variation 6169
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:377724023"
variation 6183
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142850229"
variation 6214
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:146073786"
variation 6236
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:371364257"
variation 6289
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200711677"
variation 6301
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200554315"
variation 6422
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374298481"
variation 6435
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:140028547"
variation 6456..6457
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ga"
/db_xref="dbSNP:386834101"
variation 6512
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:367838871"
variation 6527
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142248228"
variation 6561
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:61910727"
exon 6566..6768
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 6567
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:141845131"
variation 6614
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:120074149"
variation 6641
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147099791"
variation 6657
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374153644"
variation 6702..6703
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="g"
/db_xref="dbSNP:34813150"
variation 6713
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149727474"
variation 6723
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834102"
variation 6742
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:369932118"
variation 6756
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:147817990"
exon 6769..6976
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 6779
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:189948782"
variation 6824
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141275433"
variation 6825
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375613057"
variation 6838
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:146960401"
variation 6863
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147576864"
variation 6897
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369708908"
variation 6900
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:373927754"
variation 6968
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200713917"
variation 6973
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201909199"
exon 6977..7161
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 7037
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373240775"
variation 7058
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:386834104"
variation 7074
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61753724"
variation 7087
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:120074150"
variation 7088
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61754113"
variation 7158
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201133836"
exon 7162..7358
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 7189
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:180177368"
variation 7196
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148385830"
variation 7257
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="g"
/db_xref="dbSNP:386834105"
variation 7262
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:183874686"
variation 7263
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61753725"
variation 7267
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370689956"
variation 7275
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374136243"
variation 7278
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145846582"
variation 7305
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112496457"
variation 7358
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="gg"
/db_xref="dbSNP:180177367"
exon 7359..7540
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 7402
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138405323"
variation 7417
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200065297"
variation 7441
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373779146"
variation 7449
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:150771329"
variation 7477
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201963516"
exon 7541..7890
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 7545
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373550277"
variation 7582
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:375004684"
variation 7639
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834107"
variation 7640
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146092684"
variation 7646
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:386834108"
variation 7690
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369062407"
variation 7691
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373512013"
variation 7750
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140061281"
variation 7756
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:377498258"
variation 7758
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:112634620"
variation 7771
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:202226215"
variation 7779
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370903187"
variation 7786
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:144668374"
variation 7787
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:7833870"
variation 7788
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373165767"
variation 7789
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:111751379"
variation 7806
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:114038492"
variation 7807
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200302943"
variation 7810
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:186294088"
variation 7819
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140179844"
variation 7823
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145208175"
variation 7829
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199528303"
variation 7848
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147593451"
variation 7863
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201735478"
exon 7891..8052
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 7897
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:200941251"
variation 7903
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:202238616"
variation 7912
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144350008"
variation 7931
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370370264"
variation 7970
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:120074153"
variation 7972
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="c"
/db_xref="dbSNP:386834109"
variation 8004
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145460276"
variation 8035
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:377379862"
exon 8053..8208
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 8061
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:61754503"
variation 8106
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:149017920"
variation 8109
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199941415"
variation 8121
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376062743"
variation 8151
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:145899918"
variation 8155
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834110"
variation 8170
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369100428"
variation 8172
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201866766"
exon 8209..8472
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 8212
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374805472"
variation 8213
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:189689493"
variation 8244
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373542052"
variation 8270
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369898130"
variation 8271
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373348061"
variation 8282
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138453594"
variation 8284
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201127443"
variation 8288
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376283724"
variation 8312
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370701337"
variation 8328
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:180177369"
variation 8354
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:180177370"
variation 8355
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:182347753"
variation 8377
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="c"
/db_xref="dbSNP:386834111"
variation 8377
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:141360806"
variation 8391
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145090492"
variation 8405
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372979537"
variation 8464
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:377170629"
exon 8473..8556
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 8485
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:374369731"
variation 8492
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:146553331"
variation 8495
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:120074155"
variation 8497
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368143021"
variation 8501
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371325199"
variation 8508
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:386834112"
variation 8534
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368357351"
variation 8551
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834113"
variation 8552
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148333124"
exon 8557..8732
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 8557
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373961820"
variation 8647
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834114"
variation 8681
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145890213"
variation 8686
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:371609624"
exon 8733..8903
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 8748
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:150836518"
variation 8772
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199552885"
variation 8779
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:138140174"
variation 8788
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:79389009"
variation 8803
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200611924"
variation 8808
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375911218"
variation 8838
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201517365"
variation 8839
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143787982"
variation 8852
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147437490"
variation 8861
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139732310"
exon 8904..9105
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 8918
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372334983"
variation 8953
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145265055"
variation 8964
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147187040"
variation 9014
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:28940272"
variation 9023
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:375393153"
variation 9082
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:56413739"
exon 9106..9294
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 9124
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142110082"
variation 9134
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:6992059"
variation 9200
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:151159090"
variation 9205
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:140095832"
variation 9242
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:376652526"
exon 9295..9441
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 9295..9296
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="t"
/db_xref="dbSNP:180177329"
variation 9296..9297
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="t"
/db_xref="dbSNP:386834118"
variation 9303
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:376291996"
variation 9337
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201801811"
variation 9411
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:143974238"
exon 9442..9725
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 9443
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:199704158"
variation 9449
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141408531"
variation 9450
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:78277780"
variation 9460
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:113671330"
variation 9511
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138889735"
variation 9532
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373968887"
STS 9540..9558
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/db_xref="UniSTS:98954"
variation 9592
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201494563"
variation 9603
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:36074608"
variation 9641
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199559979"
variation 9658
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:143712369"
variation 9684
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:189680814"
variation 9703
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149842139"
exon 9726..9853
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 9742
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="t"
/db_xref="dbSNP:386834121"
variation 9756
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373968888"
variation 9767
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834122"
variation 9773
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:143852398"
variation 9843
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200883029"
exon 9854..10053
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 9894
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147242148"
variation 9897
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138221649"
variation 9941
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:141138612"
variation 9987
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:143728471"
variation 10014
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150573530"
variation 10028
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139575184"
variation 10037
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149285017"
exon 10054..10172
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 10054
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:116746734"
variation 10079
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376549169"
variation 10086
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369522130"
variation 10096
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:77308610"
variation 10104
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201746251"
variation 10112..10113
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ca"
/db_xref="dbSNP:386834054"
variation 10160
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138127778"
variation 10163
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:111353525"
exon 10173..10978
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 10175
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199931583"
variation 10176
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:61753726"
variation 10192..10193
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834055"
variation 10195
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140204523"
variation 10214
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:377348581"
variation 10227
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371573594"
variation 10246
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:377394274"
variation 10253
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:113335470"
variation 10263
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:374129601"
variation 10266
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:115369860"
variation 10267
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202113184"
variation 10310
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368041601"
variation 10311
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:151315104"
variation 10330
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:6468694"
variation 10346
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:112045467"
variation 10348
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:79324124"
variation 10351
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145279584"
variation 10352
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:142411465"
variation 10366
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:188030143"
variation 10369
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:191174682"
variation 10371
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200788631"
variation 10421
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200268089"
variation 10424
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146460917"
variation 10466
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:200491378"
variation 10492..10493
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ag"
/db_xref="dbSNP:180177371"
STS 10508..10609
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="A008R07"
/db_xref="UniSTS:6974"
variation 10552
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373773690"
variation 10559
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:367609176"
variation 10576
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112785599"
variation 10581
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:372875604"
variation 10633
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142957181"
variation 10635
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375804595"
variation 10638
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:113120767"
variation 10660
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143187571"
variation 10689
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:148265212"
variation 10695
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141266642"
variation 10723
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150767461"
variation 10737
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139227281"
variation 10761
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372367817"
variation 10792
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200232124"
variation 10814
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376964635"
variation 10825
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369258469"
variation 10855
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145547375"
variation 10866
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145950999"
variation 10877..10880
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tctc"
/db_xref="dbSNP:386834056"
variation 10913
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:28600803"
variation 10924
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:120074154"
variation 10935
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:114818249"
variation 10957
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149659649"
variation 10963
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373605057"
variation 10968
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:183080498"
exon 10979..11155
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 10982
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:386834057"
variation 11016
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:61754107"
variation 11035
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148582416"
variation 11044
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61754108"
variation 11085
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:375117356"
variation 11087
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370507425"
variation 11089
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373947421"
variation 11091
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:142939294"
variation 11104
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:151089043"
variation 11112
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:367797468"
variation 11120
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370172252"
variation 11133
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375676564"
variation 11151
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199748413"
exon 11156..11326
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 11156
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:367940320"
variation 11161
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="c"
/db_xref="dbSNP:386834058"
variation 11163
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:373428916"
variation 11181
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:185477101"
variation 11182
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142476821"
variation 11188
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:146571766"
variation 11197
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147891367"
variation 11208..11209
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ggac"
/db_xref="dbSNP:386834059"
variation 11225
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:376308074"
variation 11252
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:386834060"
variation 11255
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141566041"
variation 11269
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150393340"
variation 11281
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:180177372"
variation 11292
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138667007"
variation 11299
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201448515"
variation 11306
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149318176"
exon 11327..11503
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 11350
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:386834061"
variation 11355
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375229257"
variation 11377
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138012121"
variation 11423
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:142516047"
variation 11428
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145970185"
variation 11449
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:138565077"
exon 11504..11606
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 11541
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834062"
variation 11545
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369891888"
variation 11582
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:75996587"
variation 11585
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199741560"
variation 11592..11593
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="t"
/db_xref="dbSNP:386834063"
variation 11595
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:370697316"
variation 11600..11601
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="at"
/db_xref="dbSNP:180177373"
variation 11600
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834064"
exon 11607..11856
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 11634
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="a"
/db_xref="dbSNP:386834065"
variation 11676
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:7844645"
variation 11681
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150713892"
variation 11685
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:368385004"
variation 11724
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139436386"
variation 11730
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:113454700"
variation 11731..11734
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="agtg"
/db_xref="dbSNP:386834066"
variation 11749
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147315245"
variation 11766
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368092348"
variation 11767
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141793014"
variation 11802
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:371985144"
variation 11816..11820
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="aa"
/replace="cagtg"
/db_xref="dbSNP:386834067"
variation 11818
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:144797111"
exon 11857..14025
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/inference="alignment:Splign:1.39.8"
variation 11863..11864
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="atg"
/db_xref="dbSNP:386834068"
variation 11870
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147907236"
variation 11873
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368729107"
variation 11896
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148950784"
variation 11898
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147710096"
variation 11901
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:184614305"
STS 11907..12020
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="G34962"
/db_xref="UniSTS:117672"
STS 11907..12020
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="RH67322"
/db_xref="UniSTS:90383"
variation 11942..11951
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="ccagctgttc"
/db_xref="dbSNP:386834069"
variation 11943..11944
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="c"
/db_xref="dbSNP:180177374"
variation 11963
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:73273219"
variation 11995
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201483764"
variation 12008
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:117934093"
variation 12028
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140216842"
variation 12094
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369435007"
variation 12121
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369670017"
variation 12133..12134
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tg"
/db_xref="dbSNP:201268463"
variation 12136..12137
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tgat"
/db_xref="dbSNP:141587726"
variation 12137..12138
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="gatt"
/db_xref="dbSNP:373852425"
variation 12142
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:201520925"
variation 12153
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373141658"
variation 12166
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:189939258"
variation 12259..12281
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="gccaccataaagggctgcatttt"
/db_xref="dbSNP:374682407"
variation 12307
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:201566966"
variation 12352..12353
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="caa"
/db_xref="dbSNP:71572048"
variation 12353..12354
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="aacaaca"
/replace="caa"
/db_xref="dbSNP:72291496"
variation 12354..12355
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="aca"
/db_xref="dbSNP:71274940"
variation 12410
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149912942"
variation 12479..12482
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="attt"
/db_xref="dbSNP:374440758"
variation 12504
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:62534630"
variation 12517
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375699554"
variation 12534..12536
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tat"
/db_xref="dbSNP:10537000"
variation 12536..12538
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tta"
/db_xref="dbSNP:10542428"
variation 12538..12540
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tta"
/db_xref="dbSNP:72544630"
variation 12628
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:144940198"
variation 12629
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="t"
/db_xref="dbSNP:78526364"
variation 12700..12701
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tt"
/db_xref="dbSNP:35963691"
variation 12704..12705
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tt"
/db_xref="dbSNP:367738027"
variation 12760
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:78305289"
variation 12804..12806
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tga"
/db_xref="dbSNP:10542429"
variation 12805..12807
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="gat"
/db_xref="dbSNP:60078732"
variation 12806..12807
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="t"
/db_xref="dbSNP:200421894"
variation 12848
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:144603951"
variation 12850
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:138761680"
STS 12902..13001
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="D8S1427E"
/db_xref="UniSTS:151216"
variation 12919
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:181526774"
variation 12972..12973
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="c"
/db_xref="dbSNP:34615311"
STS 13010..13185
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="A006N10"
/db_xref="UniSTS:61015"
variation 13029
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:186225330"
variation 13146
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:140374149"
variation 13306
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:189427010"
variation 13312
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="g"
/db_xref="dbSNP:182082022"
variation 13316..13317
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tctc"
/db_xref="dbSNP:60544715"
variation 13317..13318
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tctc"
/db_xref="dbSNP:368674871"
variation 13321..13322
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tctc"
/db_xref="dbSNP:71981100"
variation 13523
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145470065"
variation 13622..13623
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace=""
/replace="tgt"
/db_xref="dbSNP:146221403"
variation 13644
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:80237506"
variation 13645
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148026916"
variation 13675
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="g"
/db_xref="dbSNP:186440514"
variation 13687
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="a"
/replace="c"
/db_xref="dbSNP:75181119"
variation 13690
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="g"
/replace="t"
/db_xref="dbSNP:190613136"
variation 13699
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:182902606"
STS 13738..13895
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="D8S1415E"
/db_xref="UniSTS:151205"
STS 13742..13989
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="A003B20"
/db_xref="UniSTS:9488"
STS 13868..13967
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="WI-14296"
/db_xref="UniSTS:36777"
STS 13879..13959
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/standard_name="1734"
/db_xref="UniSTS:60466"
variation 13888
/gene="VPS13B"
/gene_synonym="CHS1; COH1"
/replace="c"
/replace="t"
/db_xref="dbSNP:7157"
ORIGIN
ggcgcggtacaggagcagcactgccggcgggggcgggtgccagggacttggaggtggaggggacgcggcggtactctggcgtcttccgacttcgactccttaccttaaaagatgctggagtcatatgtaactccaattttaatgagctatgtgaatcgctacatcaagaacttaaagccgtcggatctacagctttcactatggggtggagacgtggtactcagcaagctcgagttaaagttggatgtgctggaacaggaactgaaattaccattcacttttttaagtggacatattcatgaattgaggattcatgtaccatggacaaaactgggttcagaaccagtggtaattaccatcaatactatggaatgcattttgaaacttaaggatgggatacaggatgaccatgaaagctgtggttctaattctaccaaccgtagtactgctgagagcacaaaatcatcaatcaaaccgcggagaatgcagcaggctgctcctacagatcctgacttaccaccaggttatgtgcagagtctgattagacgagttgtaaataatgtaaacattgtgataaataatctcatactaaaatatgttgaagatgatatcgtcctttccgtcaatatcacttctgcagaatgttatacagtaggtgaattatgggatcgtgcattcatggatatttctgcaactgatttggtgctgagaaaggttatcaatttttctgactgtacagtttgtcttgataaacggaatgccagtggtaaaatagaattttaccaggatcctttattatacaaatgttccttcagaactcgtcttcattttacatatgaaaacctaaattccaagatgccatctgttattaaaattcatactttagtggaaagtttgaaactttctatcacagatcaacaactgcctatgtttattcgtataatgcaacttggaattgctctttactatggagaaataggcaattttaaagaaggcgaaatagaggaccttacttgtcataataaagatatgctaggaaacattacaggttctgaagatgaaacaagaatagatatgcaatatcctgctcagcataaaggtcaagagttatattcacagcaagatgaggagcagccacagggatgggtgtcatgggcctggtcctttgtgcctgcaattgtgagttatgacgatggcgaggaagactttgttgggaacgatcctgcatcaaccatgcatcaacaaaaagcacagactttgaaggatcctattgtttctataggattttattgcacaaaggcaacggtgactttcaaactcacagaaatgcaagttgagagtagttattacagtccacagaaagtaaaatctaaagaagtattgtgttgggaacaagaaggaactacagttgaggcccttatgatgggagaacctttctttgattgccagattgggtttgttggttgcagagccatgtgccttaaaggaattatgggtgttaaagattttgaagagaatatgaatagaagtgaaactgaagcctgtttcttcatttgtggtgacaatttgagtacgaaaggtttcacataccttacaaattcattgtttgattaccgaagcccagaaaataatggtactcgcgcagaatttatcttggattcaactcatcataaggagacatacactgagatagctggaatgcaacggtttggggctttttatatggattacctgtatacaatggagaacactagtggcaaaggttccacaaatcaacaagacttttcttcagggaaaagtgaagatttgggaacagttcaggagaagtccaccaaaagccttgttataggtcctcttgattttcgtttggatagcagtgcggtgcataggattttgaaaatgattgtgtgtgccttggaacatgaatatgaaccatatagcaggctaaaatcagatattaaggatgaaaatgaaacaatactgaatcctgaagaggtggctcttctggaggaatatattcctactcgacatacaagtgttactctcctcaaatgtacctgcacaatttccatggctgaattcaacttgctggaccatttactacctgtcattatgggagaaaagaactcaagtaacttcatgaatactacaaacttccagtctcttcggcctttgccatccattcgaatattggtggataaaattaatctggaacattcagtgccaatgtatgctgaacagttggtgcatgtggtcagcagccttactcaaccttctgataacctgcttcattattgttatgtacactgctatcttaagatatttggtttccaggcaggactgacgtctttggattgcagtggatcttactgcttacctgtaccagttattccctctttcagcactgctctttatgggaaacttctgaaactccccacatgctggaccaaaagatctcagattgctataactgaaggtatatttgaacttccaaatctcacaattcaagctacaagagcacagacacttctcttgcaagcaatatatcaaagttggtctcatcttggaaatgtcagctcttccgcagtgattgaagctttgataaatgaaatcttcctaagtataggtgtgaaatctaagaatcccctgccaactcttgagggctcaatccagaatgttgaattgaagtactgcagcacatcattggtcaaatgtgcctctgggaccatgggatcaataaaaatttgtgccaaagccccagttgatagtggaaaagagaagttgattcccttgcttcagggtccttctgacactaaagaccttcatagcaccaagtggctcaatgagagtagaaagccagagtctctcttagctccagatttgatggccttcacaatccaagttccacaatatattgactactgccacaattccggtgctgtacttctttgcagtatacaaggactagcagttaatattgacccaatcttatatacgtggctcatctatcagcctcagaaacgaacaagtagacatatgcaacagcagcctgtggtagctgttcctcttgttatgccagtttgtagaaggaaagaggatgaggtgtctattggaagtgcccccttggcaaagcagcaatcatatcaggcctctgaatatgccagcagccctgtaaaaacaaaaacggtaacagaatcccgcccattgtcagttcctgttaaagccatgttgaatatatctgaaagctgtagaagtcctgaagaaagaatgaaggaatttattggaattgtttggaatgcagtgaagcatctcacactacagcttgaagtacaatcttgttgtgtgtttattccaaatgatagcctgccttccccaagtacaattgtatctggtgacattcctggaacagtaagaagttggtaccatggacaaaccagcatgccgggaacacttgtcctctgtttgcctcaaataaagattattagtgctgggcacaagtatatggaacctctgcaggagattccatttgttatcccacgacccatccttgaagaaggtgatgcttttccttggacgatcagcttgcataatttcagcatatatacccttcttggaaaacaagtgacactttgcctagtggaacctatgggttgcacctccactctagctgtcacgtctcaaaaactgcttgctacgggacctgatacacgacattcatttgttgtctgtctccatgttgacctagagtcactagagataaaatgctctaatccccaggtccagctcttctatgaactaactgatatcatgaataaggtctggaacaagattcagaagagaggcaatctcaacctatctccaacctctccagagaccatggcagggcctgttcctacttctccagttagaagcagtataggcacagctcctccagataccagcacatgcagcccatctgctgacattgggactactactgagggagattctatacaagcaggtgaggaatcaccattctcagattctgtgaccttggaacaaactacaagtaatattggaggaaccagtggacgtgttagtttatggatgcagtgggtgcttcccaaaattactataaagctctttgctccagatcctgaaaataaaggcacagaggtttgtatggtcagtgaactagaagatctcagtgcttccatagatgtccaggatgtatataccaaagtgaaatgtaaaatagagagtttcaatattgatcactatagaagcaggccaggggaaggttggcagtcaggacattttgaaggagtatttctacaatgcaaagaaaaatctgtgacaactacaaaacttctagatggcactcatcagcagcatggattcctctctctgacatacacaaaagctgtaacaaaaaatgtccgccacaagttaacatcaagaaatgagcgaagaagttttcataagttatctgaaggcctaatggatggttctcctcattttcttcatgaaattcttctttcagcacaagcttttgatattgttctttattttcctttacttaatgccattgcaagtatatttcaagcaaaactaccaaagacccaaaaagagaaaagaaaatctcctggtcagcccatgaggacccatacactgacatcccgcaatttacctttgatttatgtcaacacaagtgtaatcagaatttttattccaaaaacagaagaaatgcagccaactgttgaagctaatcaggcagcaaaagaagacactgtggttttgaagattggctctgttgccatggctccccaggctgacaatccccttggcagatctgtccttaggaaagatatttaccagagagccttgaacttaggaattcttcgagatcctggatcagaaatcgaagacagacaataccaaatagatctgcagtccatcaatattggtactgcacagtggcatcaactaaaaccagagaaggaaagtgtctcaggaggggt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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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