Home |
Help |
Advanced search
2024-04-26 08:45:34, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_016343 10316 bp mRNA linear PRI 09-JUN-2013
DEFINITION Homo sapiens centromere protein F, 350/400kDa (CENPF), mRNA.
ACCESSION NM_016343 NM_005196
VERSION NM_016343.3 GI:55770833
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 10316)
AUTHORS Jodoin,J.N., Shboul,M., Sitaram,P., Zein-Sabatto,H., Reversade,B.,
Lee,E. and Lee,L.A.
TITLE Human Asunder promotes dynein recruitment and centrosomal tethering
to the nucleus at mitotic entry
JOURNAL Mol. Biol. Cell 23 (24), 4713-4724 (2012)
PUBMED 23097494
REMARK GeneRIF: Data suggest that ASUN promotes perinuclear enrichment of
dynein at G2/M that facilitates BICD2- and CENP-F-mediated
anchoring of dynein to nuclear pore complexes.
REFERENCE 2 (bases 1 to 10316)
AUTHORS Kim,H.E., Kim,D.G., Lee,K.J., Son,J.G., Song,M.Y., Park,Y.M.,
Kim,J.J., Cho,S.W., Chi,S.G., Cheong,H.S., Shin,H.D., Lee,S.W. and
Lee,J.K.
TITLE Frequent amplification of CENPF, GMNN and CDK13 genes in
hepatocellular carcinomas
JOURNAL PLoS ONE 7 (8), E43223 (2012)
PUBMED 22912832
REMARK GeneRIF: Coincidently amplified CDK13, GMNN, and CENPF genes can
play a role as common cancer-driver genes in human cancers.
REFERENCE 3 (bases 1 to 10316)
AUTHORS Serio,G., Margaria,V., Jensen,S., Oldani,A., Bartek,J.,
Bussolino,F. and Lanzetti,L.
TITLE Small GTPase Rab5 participates in chromosome congression and
regulates localization of the centromere-associated protein CENP-F
to kinetochores
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 108 (42), 17337-17342 (2011)
PUBMED 21987812
REMARK GeneRIF: Rab5 forms a complex with a subset of CENP-F in mitotic
cells and regulates the kinetics of release of CENP-F from the
nuclear envelope and its accumulation on kinetochores.
REFERENCE 4 (bases 1 to 10316)
AUTHORS Wade,R., Di Bernardo,M.C., Richards,S., Rossi,D.,
Crowther-Swanepoel,D., Gaidano,G., Oscier,D.G., Catovsky,D. and
Houlston,R.S.
TITLE Association between single nucleotide polymorphism-genotype and
outcome of patients with chronic lymphocytic leukemia in a
randomized chemotherapy trial
JOURNAL Haematologica 96 (10), 1496-1503 (2011)
PUBMED 21659360
REFERENCE 5 (bases 1 to 10316)
AUTHORS Chen,W.B., Cheng,X.B., Ding,W., Wang,Y.J., Chen,D., Wang,J.H. and
Fei,R.S.
TITLE Centromere protein F and survivin are associated with high risk and
a poor prognosis in colorectal gastrointestinal stromal tumours
JOURNAL J. Clin. Pathol. 64 (9), 751-755 (2011)
PUBMED 21613637
REMARK GeneRIF: Centromere protein F and survivin are malignant behaviour
markers for colorectal gastrointestinal stromal tumours.
REFERENCE 6 (bases 1 to 10316)
AUTHORS Zhu,X., Mancini,M.A., Chang,K.H., Liu,C.Y., Chen,C.F., Shan,B.,
Jones,D., Yang-Feng,T.L. and Lee,W.H.
TITLE Characterization of a novel 350-kilodalton nuclear phosphoprotein
that is specifically involved in mitotic-phase progression
JOURNAL Mol. Cell. Biol. 15 (9), 5017-5029 (1995)
PUBMED 7651420
REFERENCE 7 (bases 1 to 10316)
AUTHORS Zhu,X., Chang,K.H., He,D., Mancini,M.A., Brinkley,W.R. and Lee,W.H.
TITLE The C terminus of mitosin is essential for its nuclear
localization, centromere/kinetochore targeting, and dimerization
JOURNAL J. Biol. Chem. 270 (33), 19545-19550 (1995)
PUBMED 7642639
REFERENCE 8 (bases 1 to 10316)
AUTHORS Liao,H., Winkfein,R.J., Mack,G., Rattner,J.B. and Yen,T.J.
TITLE CENP-F is a protein of the nuclear matrix that assembles onto
kinetochores at late G2 and is rapidly degraded after mitosis
JOURNAL J. Cell Biol. 130 (3), 507-518 (1995)
PUBMED 7542657
REFERENCE 9 (bases 1 to 10316)
AUTHORS Li,Q., Ke,Y., Kapp,J.A., Fertig,N., Medsger,T.A. Jr. and Joshi,H.C.
TITLE A novel cell-cycle-dependent 350-kDa nuclear protein: C-terminal
domain sufficient for nuclear localization
JOURNAL Biochem. Biophys. Res. Commun. 212 (1), 220-228 (1995)
PUBMED 7612011
REFERENCE 10 (bases 1 to 10316)
AUTHORS Testa,J.R., Zhou,J.Y., Bell,D.W. and Yen,T.J.
TITLE Chromosomal localization of the genes encoding the kinetochore
proteins CENPE and CENPF to human chromosomes 4q24-->q25 and
1q32-->q41, respectively, by fluorescence in situ hybridization
JOURNAL Genomics 23 (3), 691-693 (1994)
PUBMED 7851898
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from BU662228.1, U30872.1,
BU155312.1, CD654009.1, BG680819.1 and BQ774943.1.
On or before Nov 15, 2004 this sequence version replaced
gi:4885132, gi:14670380.
Summary: This gene encodes a protein that associates with the
centromere-kinetochore complex. The protein is a component of the
nuclear matrix during the G2 phase of interphase. In late G2 the
protein associates with the kinetochore and maintains this
association through early anaphase. It localizes to the spindle
midzone and the intracellular bridge in late anaphase and
telophase, respectively, and is thought to be subsequently
degraded. The localization of this protein suggests that it may
play a role in chromosome segregation during mitotis. It is thought
to form either a homodimer or heterodimer. Autoantibodies against
this protein have been found in patients with cancer or graft
versus host disease. [provided by RefSeq, Jul 2008].
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 :: U30872.1 [ECO:0000332]
RNAseq introns :: mixed/partial sample support
ERS025081, ERS025082 [ECO:0000350]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-655 BU662228.1 28-682
656-1998 U30872.1 554-1896
1999-2013 BU155312.1 305-319
2014-5312 U30872.1 1909-5207
5313-5322 CD654009.1 502-511
5323-8996 U30872.1 5218-8891
8997-9005 BG680819.1 531-539
9006-9487 U30872.1 8901-9382
9488-9497 BQ774943.1 332-341 c
9498-10316 U30872.1 9393-10211
FEATURES Location/Qualifiers
source 1..10316
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="1"
/map="1q41"
gene 1..10316
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/note="centromere protein F, 350/400kDa"
/db_xref="GeneID:1063"
/db_xref="HGNC:1857"
/db_xref="MIM:600236"
exon 1..133
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 76
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:3748691"
variation 115
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:1467083"
variation 115
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace=""
/replace="t"
/db_xref="dbSNP:377078645"
variation 118
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:1467084"
exon 134..336
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 141
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:376037426"
variation 144
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:111454498"
misc_feature 157..159
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/note="upstream in-frame stop codon"
CDS 175..9519
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/note="centromere protein F, 350/400ka (mitosin);
centromere protein F, 350/400kDa (mitosin); CENP-F
kinetochore protein; AH antigen; cell-cycle-dependent 350K
nuclear protein; kinetochore protein CENPF"
/codon_start=1
/product="centromere protein F"
/protein_id="NP_057427.3"
/db_xref="GI:55770834"
/db_xref="CCDS:CCDS31023.1"
/db_xref="GeneID:1063"
/db_xref="HGNC:1857"
/db_xref="MIM:600236"
/translation="
MSWALEEWKEGLPTRALQKIQELEGQLDKLKKEKQQRQFQLDSLEAALQKQKQKVENEKTEGTNLKRENQRLMEICESLEKTKQKISHELQVKESQVNFQEGQLNSGKKQIEKLEQELKRCKSELERSQQAAQSADVSLNPCNTPQKIFTTPLTPSQYYSGSKYEDLKEKYNKEVEERKRLEAEVKALQAKKASQTLPQATMNHRDIARHQASSSVFSWQQEKTPSHLSSNSQRTPIRRDFSASYFSGEQEVTPSRSTLQIGKRDANSSFFDNSSSPHLLDQLKAQNQELRNKINELELRLQGHEKEMKGQVNKFQELQLQLEKAKVELIEKEKVLNKCRDELVRTTAQYDQASTKYTALEQKLKKLTEDLSCQRQNAESARCSLEQKIKEKEKEFQEELSRQQRSFQTLDQECIQMKARLTQELQQAKNMHNVLQAELDKLTSVKQQLENNLEEFKQKLCRAEQAFQASQIKENELRRSMEEMKKENNLLKSHSEQKAREVCHLEAELKNIKQCLNQSQNFAEEMKAKNTSQETMLRDLQEKINQQENSLTLEKLKLAVADLEKQRDCSQDLLKKREHHIEQLNDKLSKTEKESKALLSALELKKKEYEELKEEKTLFSCWKSENEKLLTQMESEKENLQSKINHLETCLKTQQIKSHEYNERVRTLEMDRENLSVEIRNLHNVLDSKSVEVETQKLAYMELQQKAEFSDQKHQKEIENMCLKTSQLTGQVEDLEHKLQLLSNEIMDKDRCYQDLHAEYESLRDLLKSKDASLVTNEDHQRSLLAFDQQPAMHHSFANIIGEQGSMPSERSECRLEADQSPKNSAILQNRVDSLEFSLESQKQMNSDLQKQCEELVQIKGEIEENLMKAEQMHQSFVAETSQRISKLQEDTSAHQNVVAETLSALENKEKELQLLNDKVETEQAEIQELKKSNHLLEDSLKELQLLSETLSLEKKEMSSIISLNKREIEELTQENGTLKEINASLNQEKMNLIQKSESFANYIDEREKSISELSDQYKQEKLILLQRCEETGNAYEDLSQKYKAAQEKNSKLECLLNECTSLCENRKNELEQLKEAFAKEHQEFLTKLAFAEERNQNLMLELETVQQALRSEMTDNQNNSKSEAGGLKQEIMTLKEEQNKMQKEVNDLLQENEQLMKVMKTKHECQNLESEPIRNSVKERESERNQCNFKPQMDLEVKEISLDSYNAQLVQLEAMLRNKELKLQESEKEKECLQHELQTIRGDLETSNLQDMQSQEISGLKDCEIDAEEKYISGPHELSTSQNDNAHLQCSLQTTMNKLNELEKICEILQAEKYELVTELNDSRSECITATRKMAEEVGKLLNEVKILNDDSGLLHGELVEDIPGGEFGEQPNEQHPVSLAPLDESNSYEHLTLSDKEVQMHFAELQEKFLSLQSEHKILHDQHCQMSSKMSELQTYVDSLKAENLVLSTNLRNFQGDLVKEMQLGLEEGLVPSLSSSCVPDSSSLSSLGDSSFYRALLEQTGDMSLLSNLEGAVSANQCSVDEVFCSSLQEENLTRKETPSAPAKGVEELESLCEVYRQSLEKLEEKMESQGIMKNKEIQELEQLLSSERQELDCLRKQYLSENEQWQQKLTSVTLEMESKLAAEKKQTEQLSLELEVARLQLQGLDLSSRSLLGIDTEDAIQGRNESCDISKEHTSETTERTPKHDVHQICDKDAQQDLNLDIEKITETGAVKPTGECSGEQSPDTNYEPPGEDKTQGSSECISELSFSGPNALVPMDFLGNQEDIHNLQLRVKETSNENLRLLHVIEDRDRKVESLLNEMKELDSKLHLQEVQLMTKIEACIELEKIVGELKKENSDLSEKLEYFSCDHQELLQRVETSEGLNSDLEMHADKSSREDIGDNVAKVNDSWKERFLDVENELSRIRSEKASIEHEALYLEADLEVVQTEKLCLEKDNENKQKVIVCLEEELSVVTSERNQLRGELDTMSKKTTALDQLSEKMKEKTQELESHQSECLHCIQVAEAEVKEKTELLQTLSSDVSELLKDKTHLQEKLQSLEKDSQALSLTKCELENQIAQLNKEKELLVKESESLQARLSESDYEKLNVSKALEAALVEKGEFALRLSSTQEEVHQLRRGIEKLRVRIEADEKKQLHIAEKLKERERENDSLKDKVENLERELQMSEENQELVILDAENSKAEVETLKTQIEEMARSLKVFELDLVTLRSEKENLTKQIQEKQGQLSELDKLLSSFKSLLEEKEQAEIQIKEESKTAVEMLQNQLKELNEAVAALCGDQEIMKATEQSLDPPIEEEHQLRNSIEKLRARLEADEKKQLCVLQQLKESEHHADLLKGRVENLERELEIARTNQEHAALEAENSKGEVETLKAKIEGMTQSLRGLELDVVTIRSEKENLTNELQKEQERISELEIINSSFENILQEKEQEKVQMKEKSSTAMEMLQTQLKELNERVAALHNDQEACKAKEQNLSSQVECLELEKAQLLQGLDEAKNNYIVLQSSVNGLIQEVEDGKQKLEKKDEEISRLKNQIQDQEQLVSKLSQVEGEHQLWKEQNLELRNLTVELEQKIQVLQSKNASLQDTLEVLQSSYKNLENELELTKMDKMSFVEKVNKMTAKETELQREMHEMAQKTAELQEELSGEKNRLAGELQLLLEEIKSSKDQLKELTLENSELKKSLDCMHKDQVEKEGKVREEIAEYQLRLHEAEKKHQALLLDTNKQYEVEIQTYREKLTSKEECLSSQKLEIDLLKSSKEELNNSLKATTQILEELKKTKMDNLKYVNQLKKENERAQGKMKLLIKSCKQLEEEKEILQKELSQLQAAQEKQKTGTVMDTKVDELTTEIKELKETLEEKTKEADEYLDKYCSLLISHEKLEKAKEMLETQVAHLCSQQSKQDSRGSPLLGPVVPGPSPIPSVTEKRLSSGQNKASGKRQRSSGIWENGRGPTPATPESFSKKSKKAVMSGIHPAEDTEGTEFEPEGLPEVVKKGFADIPTGKTSPYILRRTTMATRTSPRLAAQKLALSPLSLGKENLAESSKPTAGGSRSQKVKVAQRSPVDSGTILREPTTKSVPVNNLPERSPTDSPREGLRVKRGRLVPSPKAGLESNGSENCKVQ
"
misc_feature 175..1038
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/note="Cenp-F N-terminal domain; Region: Cenp-F_N;
pfam10481"
/db_xref="CDD:119001"
misc_feature 2635..2637
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 3937..3939
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 4018..4020
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 4144..4146
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 5125..5127
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 5134..5136
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 5848..5850
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 6028..8448
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/note="chromosome segregation protein SMC, common
bacterial type; Region: SMC_prok_B; TIGR02168"
/db_xref="CDD:162739"
misc_feature 6565..6984
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/note="Leucine-rich repeats of kinetochore protein
Cenp-F/LEK1; Region: Cenp-F_leu_zip; pfam10473"
/db_xref="CDD:151039"
misc_feature 7111..7530
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/note="Leucine-rich repeats of kinetochore protein
Cenp-F/LEK1; Region: Cenp-F_leu_zip; pfam10473"
/db_xref="CDD:151039"
misc_feature 7423..7425
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 7798..7800
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 8863..8865
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 8872..8874
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 8905..8907
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 8917..8919
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 9067..9213
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/note="Rb-binding domain of kinetochore protein
Cenp-F/LEK1; Region: Rb-bdg_C_Cenp-F; pfam10490"
/db_xref="CDD:119010"
misc_feature 9166..9168
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 9241..9243
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 9241..9243
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 9334..9336
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 9409..9411
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 9421..9423
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 9505..9507
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="prenylation site; modified site"
/db_xref="HPRD:00607"
misc_feature 9505..9507
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
/note="prenylation site; modified site"
/db_xref="HPRD:00608"
variation 207
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070064"
variation 214
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:138690504"
variation 307
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:368361514"
variation 314
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:372352745"
exon 337..533
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 353
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:371121070"
variation 377
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:371576824"
variation 391
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:375887256"
variation 394
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:368853837"
variation 409
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:199586456"
variation 466
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:146920776"
variation 467
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:146340205"
variation 468
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:372336545"
variation 481
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:199558501"
variation 486
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:139296855"
variation 504
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:144231687"
exon 534..655
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 542
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:144933281"
variation 563
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:371726811"
variation 569
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:140106255"
variation 570
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:373652018"
variation 581
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:145538443"
exon 656..747
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 686
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:140195013"
variation 690
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:144898977"
variation 706
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:199800194"
variation 707..708
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace=""
/replace="a"
/db_xref="dbSNP:375674714"
variation 712
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:149042046"
variation 736
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:61732049"
exon 748..1039
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 790
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:376653860"
variation 791
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:373857309"
variation 793
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:141779900"
variation 799
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:148125567"
variation 809
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:141892982"
variation 817
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:369501655"
variation 825
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:201702404"
variation 869
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:372789993"
variation 905
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:139700147"
variation 923
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:1050065"
variation 940
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:377444877"
variation 941
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:147545168"
variation 978
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:370239629"
variation 989
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:1050066"
variation 991
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:145606920"
variation 1028
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:375031145"
variation 1029
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:114104425"
exon 1040..1242
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 1072
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:17023281"
variation 1107
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:146767943"
variation 1139
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:140399039"
variation 1162
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:370955098"
variation 1204
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:375201684"
variation 1217
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:150363473"
variation 1224
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:113096414"
variation 1228
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:368264741"
variation 1229
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:6697155"
variation 1233
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:372173425"
exon 1243..1368
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 1244
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:138247858"
variation 1248
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:113017521"
variation 1264
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:199872430"
variation 1319
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:114338555"
variation 1333
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:202217426"
variation 1363
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:371315575"
exon 1369..1497
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 1372
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:139908163"
variation 1392
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:139919911"
variation 1417
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:61999278"
variation 1431
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:149792761"
variation 1434
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:374647912"
variation 1469
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:368665391"
variation 1473
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:139190120"
variation 1474
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:189714127"
exon 1498..1620
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 1553
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:200286242"
variation 1572
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:139822426"
variation 1595
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:201692235"
exon 1621..1756
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 1656
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:2070065"
variation 1657
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:371547901"
variation 1691
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:140375946"
variation 1696
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:148373466"
variation 1704
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:373344151"
variation 1732
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:377380966"
variation 1735
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:370775342"
exon 1757..5160
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 1760
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:143280998"
variation 1768
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:146202877"
variation 1776
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:372374310"
variation 1815
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:201426172"
variation 1821
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:149872585"
STS 1838..1987
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/standard_name="SHGC-33480"
/db_xref="UniSTS:76342"
STS 1843..1973
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/standard_name="RH16564"
/db_xref="UniSTS:36617"
variation 1856
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:200431234"
variation 1908
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:373784639"
variation 1918
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:367624766"
variation 1932
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:372883869"
variation 1971
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:201978958"
variation 1980
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:2070066"
variation 1991
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:147826307"
variation 2016
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:147543346"
variation 2052
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:141295897"
variation 2058
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:147687208"
variation 2069
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:140953760"
variation 2071
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:200802393"
variation 2094
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:138983504"
variation 2142
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:200262272"
variation 2169
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:376676752"
variation 2174
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:375816558"
variation 2175
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:145859186"
variation 2188
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:61732045"
variation 2205
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:368651584"
variation 2206
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:371979886"
variation 2245
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:376964760"
variation 2262
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:199610174"
variation 2275
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:3795524"
variation 2323
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:369218990"
variation 2327
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:370332295"
variation 2425
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:199832648"
variation 2426
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:77399701"
variation 2434
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:3795523"
variation 2445
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:111676558"
variation 2448
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:372008067"
variation 2546
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:368928145"
variation 2552
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:61732042"
variation 2572
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:144034954"
variation 2576
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:142089181"
variation 2618
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:3795522"
variation 2631
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:182183699"
variation 2694
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:145907868"
variation 2745
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:374019549"
variation 2762
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:375479551"
variation 2769
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:142993088"
variation 2771
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:138860485"
variation 2791
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:371370612"
variation 2792
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:373161735"
variation 2847
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:61732041"
variation 2908
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:200976140"
variation 3018
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:147300870"
variation 3064
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:3795521"
variation 3075
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:3795520"
variation 3114
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:373190310"
variation 3119
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:376432730"
variation 3177
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:145269947"
variation 3195
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:376141874"
variation 3200
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:371042522"
variation 3204
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:201065588"
variation 3217
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:190391942"
variation 3226
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:3795519"
variation 3250
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:182151029"
variation 3271
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:3795518"
variation 3276
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:113783927"
variation 3287
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:111484686"
variation 3297
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:76696551"
variation 3307
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:146647521"
variation 3334
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:373954389"
variation 3354
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:367811235"
variation 3418
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:61732031"
variation 3441
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:371608412"
variation 3488
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:12067133"
variation 3511..3512
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace=""
/replace="ga"
/db_xref="dbSNP:201985722"
variation 3526
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:200341117"
variation 3527
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:375681596"
variation 3543
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:369791107"
variation 3550
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:142718897"
variation 3554
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:137861168"
variation 3578
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:144108767"
variation 3609
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:61732030"
variation 3627
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:139611178"
variation 3639
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:113670271"
variation 3667
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:368660042"
variation 3701
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:201954964"
variation 3704
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:372588481"
variation 3730
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:199839240"
variation 3791
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:144237457"
variation 3797
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:114717799"
variation 3798
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:145854163"
variation 3810
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:200477750"
variation 3811
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:143757664"
variation 3825
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:375228091"
variation 3827
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:369609081"
variation 3855
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:200042063"
variation 3863
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:199690817"
variation 3876
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:372468473"
variation 3877
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:375722599"
variation 3879
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:200820664"
variation 3894
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:141235377"
variation 3931
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:201651380"
variation 3968
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:137925834"
variation 3977
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:116055478"
variation 3985
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:62000407"
variation 4014
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:368221348"
variation 4027
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:139262804"
variation 4040
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:372144616"
variation 4060
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:146083083"
variation 4084
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:375214598"
variation 4086
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:142263675"
variation 4102
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:148517685"
variation 4107
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:201165677"
variation 4125
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:17023329"
variation 4143
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:369306542"
variation 4148
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:150048811"
variation 4166
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:371416739"
variation 4210
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:375735845"
variation 4216
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:367738298"
variation 4276
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:146963558"
variation 4298
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:146531387"
variation 4302
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:143023033"
variation 4304
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:190865579"
variation 4329
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:139914723"
variation 4344
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:143334997"
variation 4345
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:141352776"
variation 4356
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:150367049"
variation 4381
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:146731847"
variation 4383
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:369944054"
variation 4398
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:367938541"
variation 4409
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:3795517"
variation 4447
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:373356010"
variation 4457
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:189233892"
variation 4463
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:76231205"
variation 4487
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:142984971"
variation 4492
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:376287584"
variation 4506
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:372343987"
variation 4522
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:200151949"
variation 4526
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:147738481"
variation 4529
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:140952090"
variation 4538
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:376658652"
STS 4632..4776
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/standard_name="RH47698"
/db_xref="UniSTS:37145"
variation 4635
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:3795516"
variation 4644
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:112985127"
variation 4656
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:148816462"
variation 4691
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:186880898"
variation 4693
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:191767198"
variation 4694
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:145589304"
variation 4717
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:2666839"
variation 4741
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:376492439"
variation 4756
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:141472136"
variation 4786
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:138163000"
variation 4790
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:3795514"
variation 4798
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:370575486"
variation 4802
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:141012292"
variation 4804
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:148549570"
variation 4811
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:373708395"
variation 4853
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:188197039"
variation 4864
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:202135057"
variation 4893
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:202180444"
variation 4926
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:200241672"
variation 4946
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:376889332"
variation 5022
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:371328968"
variation 5032
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:192798222"
variation 5048
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:369404379"
variation 5049
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:201550181"
variation 5052
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:201352796"
variation 5091
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:202126235"
variation 5092
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:368361831"
variation 5099
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:373295400"
variation 5128
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:144881375"
variation 5146
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:200595760"
variation 5157
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:372352425"
exon 5161..8004
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 5173
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:375014198"
variation 5174
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:201574754"
variation 5205
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:111841607"
variation 5219
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:142125418"
variation 5255
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:151163618"
variation 5278
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:200540325"
variation 5282
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:11811736"
variation 5344
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:199873182"
variation 5416
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:146063444"
variation 5473
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:186165747"
variation 5476
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:3748692"
variation 5480
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:371989257"
variation 5484
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:3748693"
variation 5493
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:113247432"
variation 5507
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:368885520"
variation 5520
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:372338929"
variation 5537
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:199853658"
variation 5538
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:377252456"
variation 5551
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:375398134"
variation 5552
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:143725699"
variation 5567
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:369681198"
variation 5581
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:373138290"
variation 5615
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:111943005"
variation 5624
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:369331042"
variation 5635
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:368639269"
variation 5636
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:201865220"
variation 5663
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:201216907"
variation 5674
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:143876429"
variation 5712
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:41277190"
variation 5745
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:143325962"
variation 5748
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:147528881"
variation 5749
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:150031364"
variation 5768
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:372479804"
variation 5790
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:373268175"
variation 5796
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:376264816"
variation 5809
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:61732022"
STS 5812..6071
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/standard_name="D1S3278"
/db_xref="UniSTS:67960"
variation 5814
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:370241377"
variation 5845
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:201030011"
variation 5872
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:140761754"
variation 5878
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:376299939"
variation 5888
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:143508339"
variation 5928
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:377730723"
variation 5939
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:200650945"
variation 5973
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:202213228"
variation 6036
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:150348132"
variation 6058
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:113750787"
variation 6062
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:200344014"
variation 6064
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:139947449"
variation 6065
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:78580151"
variation 6081
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:374322005"
variation 6082
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:7544538"
variation 6096
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:368250246"
variation 6098
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:79313448"
variation 6107
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:3790646"
variation 6125
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:61741924"
variation 6159
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:199575719"
variation 6173
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:148462791"
variation 6200
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:202092147"
variation 6203
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:374691880"
variation 6206
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:3790647"
variation 6212
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:150986314"
variation 6252
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:146606492"
variation 6266
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:367836265"
variation 6287
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:142561288"
variation 6305
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:7533166"
variation 6329
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:201573129"
variation 6388
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:3748694"
variation 6389
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:74639538"
variation 6403
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:140780578"
variation 6419
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:199883439"
variation 6460
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:371317728"
variation 6564
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:200126499"
variation 6565
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:181293702"
variation 6585
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:138973447"
variation 6589
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:3748695"
variation 6607
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:114218080"
variation 6613
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:150719864"
variation 6614
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:201823371"
variation 6617
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:368661421"
variation 6647
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:376037863"
variation 6681
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:149961822"
variation 6705
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:200117793"
variation 6706
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:140541780"
variation 6724
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:62623663"
variation 6788
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:143686774"
variation 6794
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:185852220"
variation 6815
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:151039850"
variation 6842
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:150277836"
variation 6844
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:375601206"
variation 6848
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:12058704"
variation 6861
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:190762057"
variation 6873
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:149273910"
variation 6950
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:144478326"
variation 6959
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:369704485"
variation 6980
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:372963039"
variation 7000
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:141620633"
variation 7004
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:147776688"
variation 7018
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:61732016"
variation 7052
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:199997097"
variation 7065
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:11537813"
variation 7079
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:79923436"
variation 7082
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:146901951"
variation 7099
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:187123117"
variation 7100
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:145858780"
variation 7111
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:138428805"
variation 7143
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:74825176"
variation 7153
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:373698029"
variation 7156
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:372969150"
variation 7158
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:41277192"
variation 7164
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:138610661"
variation 7181
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:368991604"
variation 7223
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:373288161"
variation 7241
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:3748696"
variation 7281
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:142607504"
variation 7340
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:142605836"
variation 7347
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:201719243"
variation 7360
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:3748697"
variation 7367
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:140475132"
variation 7393
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:376076886"
variation 7453
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:377346261"
variation 7463
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:371330347"
variation 7467
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:146914457"
variation 7472
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:373848264"
variation 7500
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:75093097"
variation 7504
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:376823962"
variation 7526
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:138083875"
variation 7560
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:3748698"
variation 7604
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:371168964"
variation 7632
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:371119679"
variation 7647
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:148654343"
variation 7649
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:374129418"
variation 7680
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:76222303"
variation 7698
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:368045972"
variation 7718
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:62636593"
variation 7726
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:151128805"
variation 7729
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:149416779"
variation 7755
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:3790648"
variation 7764
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:200834057"
variation 7785
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:3790649"
variation 7807
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:189941961"
variation 7819
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:199813442"
variation 7831
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:117254535"
variation 7895
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:201477597"
variation 7927
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:62636591"
variation 7949
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:141793562"
variation 7951
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:370320022"
variation 7963
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:141721649"
variation 7970
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:111738354"
variation 8000
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:372442138"
exon 8005..8157
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 8064
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:141827306"
variation 8088
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:201700529"
variation 8109
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:146342844"
variation 8111
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:367604303"
variation 8131
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:142818960"
variation 8154
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:192234581"
exon 8158..8334
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 8222
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:376688044"
variation 8245
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:368484890"
variation 8257
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:200235175"
variation 8260
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:372430358"
variation 8278
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:376987914"
variation 8280
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:369254043"
variation 8293
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:144238914"
variation 8310
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:373593773"
exon 8335..8496
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 8352
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:190493764"
variation 8360
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:335524"
variation 8403
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:141235225"
variation 8439
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:144902806"
variation 8452
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:149025776"
variation 8485
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:201630285"
variation 8496
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:148269041"
exon 8497..8659
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 8502
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:61732051"
variation 8515
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:201359209"
variation 8523
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:142868556"
variation 8543
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:369765741"
variation 8550
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:373154133"
variation 8569
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:376139073"
variation 8654
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:370503334"
exon 8660..9136
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 8683
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:138734779"
variation 8753
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:370367881"
variation 8785
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:377015058"
variation 8786
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:149345652"
variation 8809
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:374750625"
variation 8821
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:145612869"
variation 8848
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:112918413"
variation 8871
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:368848952"
variation 8910
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:140887866"
variation 8924
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:372199261"
variation 8942
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:375747320"
variation 8964
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:189461485"
variation 8975
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:150951834"
variation 8976
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:72759668"
variation 8996
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:200366505"
variation 9001
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:438034"
variation 9087
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:149079161"
variation 9089
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:373916262"
exon 9137..9315
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 9138
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace=""
/replace="g"
/db_xref="dbSNP:35210343"
variation 9182
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:376822086"
variation 9238
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:201909832"
variation 9255
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:74557452"
variation 9290
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:141439443"
variation 9308
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:369136400"
variation 9310
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:138255905"
variation 9311
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:371811978"
exon 9316..10296
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/inference="alignment:Splign:1.39.8"
variation 9331
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:140950062"
variation 9332
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:143976001"
variation 9359
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:79915399"
variation 9367
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:373341650"
variation 9375
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:148637528"
variation 9381
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:199989471"
variation 9382
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:139064536"
variation 9391
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:202111915"
variation 9407
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:144164373"
variation 9448
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:369478130"
variation 9492
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:7289"
variation 9503
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:372955906"
variation 9504
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="g"
/db_xref="dbSNP:201071952"
variation 9529
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="g"
/replace="t"
/db_xref="dbSNP:186883841"
variation 9544
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:14284"
variation 9558
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:373878385"
variation 9582
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:191783029"
variation 9592
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:11537814"
variation 9653
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:145285850"
STS 9658..9733
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/standard_name="SHGC-36458"
/db_xref="UniSTS:12153"
variation 9668
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:149168130"
variation 9703
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:183474592"
variation 9718
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:2290199"
variation 9740
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:188199052"
polyA_signal 9791..9796
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
polyA_site 9811
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/experiment="experimental evidence, no additional details
recorded"
variation 9829
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="t"
/db_xref="dbSNP:368338293"
variation 9847
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="c"
/db_xref="dbSNP:199936323"
variation 10051
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:77570585"
variation 10056
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:147882730"
variation 10105
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:141403573"
variation 10166
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="a"
/replace="g"
/db_xref="dbSNP:369111869"
polyA_signal 10268..10273
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
variation 10279
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
/replace="c"
/replace="t"
/db_xref="dbSNP:373066172"
polyA_site 10296
/gene="CENPF"
/gene_synonym="CENF; hcp-1; PRO1779"
ORIGIN
gagaccagaagcgggcgaattgggcaccggtggcggctgcgggcagtttgaattagactctgggctccagcccgccgaagccgcgccagaactgtactctccgagaggtcgttttcccgtccccgagagcaagtttatttacaaatgttggagtaataaagaaggcagaacaaaatgagctgggctttggaagaatggaaagaagggctgcctacaagagctcttcagaaaattcaagagcttgaaggacagcttgacaaactgaagaaggaaaagcagcaaaggcagtttcagcttgacagtctcgaggctgcgctgcagaagcaaaaacagaaggttgaaaatgaaaaaaccgagggtacaaacctgaaaagggagaatcaaagattgatggaaatatgtgaaagtctggagaaaactaagcagaagatttctcatgaacttcaagtcaaggagtcacaagtgaatttccaggaaggacaactgaattcaggcaaaaaacaaatagaaaaactggaacaggaacttaaaaggtgtaaatctgagcttgaaagaagccaacaagctgcgcagtctgcagatgtctctctgaatccatgcaatacaccacaaaaaatttttacaactccactaacaccaagtcaatattatagtggttccaagtatgaagatctaaaagaaaaatataataaagaggttgaagaacgaaaaagattagaggcagaggttaaagccttgcaggctaaaaaagcaagccagactcttccacaagccaccatgaatcaccgcgacattgcccggcatcaggcttcatcatctgtgttctcatggcagcaagagaagaccccaagtcatctttcatctaattctcaaagaactccaattaggagagatttctctgcatcttacttttctggggaacaagaggtgactccaagtcgatcaactttgcaaatagggaaaagagatgctaatagcagtttctttgacaattctagcagtcctcatcttttggatcaattaaaagcgcagaatcaagagctaagaaacaagattaatgagttggaactacgcctgcaaggacatgaaaaagaaatgaaaggccaagtgaataagtttcaagaactccaactccaactggagaaagcaaaagtggaattaattgaaaaagagaaagttttgaacaaatgtagggatgaactagtgagaacaacagcacaatacgaccaggcgtcaaccaagtatactgcattggaacaaaaactgaaaaaattgacggaagatttgagttgtcagcgacaaaatgcagaaagtgccagatgttctctggaacagaaaattaaggaaaaagaaaaggagtttcaagaggagctctcccgtcaacagcgttctttccaaacactggaccaggagtgcatccagatgaaggccagactcacccaggagttacagcaagccaagaatatgcacaacgtcctgcaggctgaactggataaactcacatcagtaaagcaacagctagaaaacaatttggaagagtttaagcaaaagttgtgcagagctgaacaggcgttccaggcgagtcagatcaaggagaatgagctgaggagaagcatggaggaaatgaagaaggaaaacaacctccttaagagtcactctgagcaaaaggccagagaagtctgccacctggaggcagaactcaagaacatcaaacagtgtttaaatcagagccagaattttgcagaagaaatgaaagcgaagaatacctctcaggaaaccatgttaagagatcttcaagaaaaaataaatcagcaagaaaactccttgactttagaaaaactgaagcttgctgtggctgatctggaaaagcagcgagattgttctcaagaccttttgaagaaaagagaacatcacattgaacaacttaatgataagttaagcaagacagagaaagagtccaaagccttgctgagtgctttagagttaaaaaagaaagaatatgaagaattgaaagaagagaaaactctgttttcttgttggaaaagtgaaaacgaaaaacttttaactcagatggaatcagaaaaggaaaacttgcagagtaaaattaatcacttggaaacttgtctgaagacacagcaaataaaaagtcatgaatacaacgagagagtaagaacgctggagatggacagagaaaacctaagtgtcgagatcagaaaccttcacaacgtgttagacagtaagtcagtggaggtagagacccagaaactagcttatatggagctacagcagaaagctgagttctcagatcagaaacatcagaaggaaatagaaaatatgtgtttgaagacttctcagcttactgggcaagttgaagatctagaacacaagcttcagttactgtcaaatgaaataatggacaaagaccggtgttaccaagacttgcatgccgaatatgagagcctcagggatctgctaaaatccaaagatgcttctctggtgacaaatgaagatcatcagagaagtcttttggcttttgatcagcagcctgccatgcatcattcctttgcaaatataattggagaacaaggaagcatgccttcagagaggagtgaatgtcgtttagaagcagaccaaagtccgaaaaattctgccatcctacaaaatagagttgattcacttgaattttcattagagtctcaaaaacagatgaactcagacctgcaaaagcagtgtgaagagttggtgcaaatcaaaggagaaatagaagaaaatctcatgaaagcagaacagatgcatcaaagttttgtggctgaaacaagtcagcgcattagtaagttacaggaagacacttctgctcaccagaatgttgttgctgaaaccttaagtgcccttgagaacaaggaaaaagagctgcaacttttaaatgataaggtagaaactgagcaggcagagattcaagaattaaaaaagagcaaccatctacttgaagactctctaaaggagctacaacttttatccgaaaccctaagcttggagaagaaagaaatgagttccatcatttctctaaataaaagggaaattgaagagctgacccaagagaatgggactcttaaggaaattaatgcatccttaaatcaagagaagatgaacttaatccagaaaagtgagagttttgcaaactatatagatgaaagggagaaaagcatttcagagttatctgatcagtacaagcaagaaaaacttattttactacaaagatgtgaagaaaccggaaatgcatatgaggatcttagtcaaaaatacaaagcagcacaggaaaagaattctaaattagaatgcttgctaaatgaatgcactagtctttgtgaaaataggaaaaatgagttggaacagctaaaggaagcatttgcaaaggaacaccaagaattcttaacaaaattagcatttgctgaagaaagaaatcagaatctgatgctagagttggagacagtgcagcaagctctgagatctgagatgacagataaccaaaacaattctaagagcgaggctggtggtttaaagcaagaaatcatgactttaaaggaagaacaaaacaaaatgcaaaaggaagttaatgacttattacaagagaatgaacagctgatgaaggtaatgaagactaaacatgaatgtcaaaatctagaatcagaaccaattaggaactctgtgaaagaaagagagagtgagagaaatcaatgtaattttaaacctcagatggatcttgaagttaaagaaatttctctagatagttataatgcgcagttggtgcaattagaagctatgctaagaaataaggaattaaaacttcaggaaagtgagaaggagaaggagtgcctgcagcatgaattacagacaattagaggagatcttgaaaccagcaatttgcaagacatgcagtcacaagaaattagtggccttaaagactgtgaaatagatgcggaagaaaagtatatttcagggcctcatgagttgtcaacaagtcaaaacgacaatgcacaccttcagtgctctctgcaaacaacaatgaacaagctgaatgagctagagaaaatatgtgaaatactgcaggctgaaaagtatgaactcgtaactgagctgaatgattcaaggtcagaatgtatcacagcaactaggaaaatggcagaagaggtagggaaactactaaatgaagttaaaatattaaatgatgacagtggtcttctccatggtgagttagtggaagacataccaggaggtgaatttggtgaacaaccaaatgaacagcaccctgtgtctttggctccattggacgagagtaattcctacgagcacttgacattgtcagacaaagaagttcaaatgcactttgccgaattgcaagagaaattcttatctttacaaagtgaacacaaaattttacatgatcagcactgtcagatgagctctaaaatgtcagagctgcagacctatgttgactcattaaaggccgaaaatttggtcttgtcaacgaatctgagaaactttcaaggtgacttggtgaaggagatgcagctgggcttggaggaggggctcgttccatccctgtcatcctcttgtgtgcctgacagctctagtcttagcagtttgggagactcctccttttacagagctcttttagaacagacaggagatatgtctcttttgagtaatttagaaggggctgtttcagcaaaccagtgcagtgtagatgaagtattttgcagcagtctgcaggaggagaatctgaccaggaaagaaaccccttcggccccagcgaagggtgttgaagagcttgagtccctctgtgaggtgtaccggcagtccctcgagaagctagaagagaaaatggaaagtcaagggattatgaaaaataaggaaattcaagagctcgagcagttattaagttctgaaaggcaagagcttgactgccttaggaagcagtatttgtcagaaaatgaacagtggcaacagaagctgacaagcgtgactctggagatggagtccaagttggcggcagaaaagaaacagacggaacaactgtcacttgagctggaagtagcacgactccagctacaaggtctggacttaagttctcggtctttgcttggcatcgacacagaagatgctattcaaggccgaaatgagagctgtgacatatcaaaagaacatacttcagaaactacagaaagaacaccaaagcatgatgttcatcagatttgtgataaagatgctcagcaggacctcaatctagacattgagaaaataactgagactggtgcagtgaaacccacaggagagtgctctggggaacagtccccagataccaattatgagcctccaggggaagataaaacccagggctcttcagaatgcatttctgaattgtcattttctggtcctaatgctttggtacctatggatttcctggggaatcaggaagatatccataatcttcaactgcgggtaaaagagacatcaaatgagaatttgagattacttcatgtgatagaggaccgtgacagaaaagttgaaagtttgctaaatgaaatgaaagaattagactcaaaactccatttacaggaggtacaactaatgaccaaaattgaagcatgcatagaattggaaaaaatagttggggaacttaagaaagaaaactcagatttaagtgaaaaattggaatatttttcttgtgatcaccaggagttactccagagagtagaaacttctgaaggcctcaattctgatttagaaatgcatgcagataaatcatcacgtgaagatattggagataatgtggccaaggtgaatgacagctggaaggagagatttcttgatgtggaaaatgagctgagtaggatcagatcggagaaagctagcattgagcatgaagccctctacctggaggctgacttagaggtagttcaaacagagaagctatgtttagaaaaagacaatgaaaataagcagaaggttattgtctgccttgaagaagaactctcagtggtcacaagtgagagaaaccagcttcgtggagaattagatactatgtcaaaaaaaaccacggcactggatcagttgtctgaaaaaatgaaggagaaaacacaagagcttgagtctcatcaaagtgagtgtctccattgcattcaggtggcagaggcagaggtgaaggaaaagacggaactccttcagactttgtcctctgatgtgagtgagctgttaaaagacaaaactcatctccaggaaaagctgcagagtttggaaaaggactcacaggcactgtctttgacaaaatgtgagctggaaaaccaaattgcacaactgaataaagagaaagaattgcttgtcaaggaatctgaaagcctgcaggccagactgagtgaatcagattatgaaaagctgaatgtctccaaggccttggaggccgcactggtggagaaaggtgagttcgcattgaggctgagctcaacacaggaggaagtgcatcagctgagaagaggcatcgagaaactgagagttcgcattgaggccgatgaaaagaagcagctgcacatcgcagagaaactgaaagaacgcgagcgggagaatgattcacttaaggataaagttgagaaccttgaaagggaattgcagatgtcagaagaaaaccaggagctagtgattcttgatgccgagaattccaaagcagaagtagagactctaaaaacacaaatagaagagatggccagaagcctgaaagtttttgaattagaccttgtcacgttaaggtctgaaaaagaaaatctgacaaaacaaatacaagaaaaacaaggtcagttgtcagaactagacaagttactctcttcatttaaaagtctgttagaagaaaaggagcaagcagagatacagatcaaagaagaatctaaaactgcagtggagatgcttcagaatcagttaaaggagctaaatgaggcagtagcagccttgtgtggtgaccaagaaattatgaaggccacagaacagagtctagacccaccaatagaggaagagcatcagctgagaaatagcattgaaaagctgagagcccgcctagaagctgatgaaaagaagcagctctgtgtcttacaacaactgaaggaaagtgagcatcatgcagatttacttaagggtagagtggagaaccttgaaagagagctagagatagccaggacaaaccaagagcatgcagctcttgaggcagagaattccaaaggagaggtagagaccctaaaagcaaaaatagaagggatgacccaaagtctgagaggtctggaattagatgttgttactataaggtcagaaaaagaaaatctgacaaatgaattacaaaaagagcaagagcgaatatctgaattagaaataataaattcatcatttgaaaatattttgcaagaaaaagagcaagagaaagtacagatgaaagaaaaatcaagcactgccatggagatgcttcaaacacaattaaaagagctcaatgagagagtggcagccctgcataatgaccaagaagcctgtaaggccaaagagcagaatcttagtagtcaagtagagtgtcttgaacttgagaaggctcagttgctacaaggccttgatgaggccaaaaataattatattgttttgcaatcttcagtgaatggcctcattcaagaagtagaagatggcaagcagaaactggagaagaaggatgaagaaatcagtagactgaaaaatcaaattcaagaccaagagcagcttgtctctaaactgtcccaggtggaaggagagcaccaactttggaaggagcaaaacttagaactgagaaatctgacagtggaattggagcagaagatccaagtgctacaatccaaaaatgcctctttgcaggacacattagaagtgctgcagagttcttacaagaatctagagaatgagcttgaattgacaaaaatggacaaaatgtcctttgttgaaaaagtaaacaaaatgactgcaaaggaaactgagctgcagagggaaatgcatgagatggcacagaaaacagcagagctgcaagaagaactcagtggagagaaaaataggctagctggagagttgcagttactgttggaagaaataaagagcagcaaagatcaattgaaggagctcacactagaaaatagtgaattgaagaagagcctagattgcatgcacaaagaccaggtggaaaaggaagggaaagtgagagaggaaatagctgaatatcagctacggcttcatgaagctgaaaagaaacaccaggctttgcttttggacacaaacaaacagtatgaagtagaaatccagacataccgagagaaattgacttctaaagaagaatgtctcagttcacagaagctggagatagaccttttaaagtctagtaaagaagagctcaataattcattgaaagctactactcagattttggaagaattgaagaaaaccaagatggacaatctaaaatatgtaaatcagttgaagaaggaaaatgaacgtgcccaggggaaaatgaagttgttgatcaaatcctgtaaacagctggaagaggaaaaggagatactgcagaaagaactctctcaacttcaagctgcacaggagaagcagaaaacaggtactgttatggataccaaggtcgatgaattaacaactgagatcaaagaactgaaagaaactcttgaagaaaaaaccaaggaggcagatgaatacttggataagtactgttccttgcttataagccatgaaaagttagagaaagctaaagagatgttagagacacaagtggcccatctgtgttcacagcaatctaaacaagattcccgagggtctcctttgctaggtccagttgttccaggaccatctccaatcccttctgttactgaaaagaggttatcatctggccaaaataaagcttcaggcaagaggcaaagatccagtggaatatgggagaatggtagaggaccaacacctgctaccccagagagcttttctaaaaaaagcaagaaagcagtcatgagtggtattcaccctgcagaagacacggaaggtactgagtttgagccagagggacttccagaagttgtaaagaaagggtttgctgacatcccgacaggaaagactagcccatatatcctgcgaagaacaaccatggcaactcggaccagcccccgcctggctgcacagaagttagcgctatccccactgagtctcggcaaagaaaatcttgcagagtcctccaaaccaacagctggtggcagcagatcacaaaaggtcaaagttgctcagcggagcccagtagattcaggcaccatcctccgagaacccaccacgaaatccgtcccagtcaataatcttcctgagagaagtccgactgacagccccagagagggcctgagggtcaagcgaggccgacttgtccccagccccaaagctggactggagtccaacggcagtgagaactgtaaggtccagtgaaggcactttgtgtgtcagtacccctgggaggtgccagtcattgaatagataaggctgtgcctacaggacttctctttagtcagggcatgctttattagtgaggagaaaacaattccttagaagtcttaaatatattgtactctttagatctcccatgtgtaggtattgaaaaagtttggaagcactgatcacctgttagcattgccattcctctactgcaatgtaaatagtataaagctatgtatataaagctttttggtaatatgttacaattaaaatgacaagcactatatcacaatctctgtttgtatgtgggttttacactaaaaaaatgcaaaacacattttattcttctaattaacagctcctaggaaaatgtagacttttgctttatgatattctatctgtagtatgaggcatggaatagttttgtatcgggaatttctcagagctgagtaaaatgaaggaaaagcatgttatgtgtttttaaggaaaatgtgcacacatatacatgtaggagtgtttatctttctcttacaatctgttttagacatctttgcttatgaaacctgtacatatgtgtgtgtgggtatgtgtttatttccagtgagggctgcaggcttcctagaggtgtgctataccatgcgtctgtcgttgtgcttttttctgtttttagaccaattttttacagttctttggtaagcattgtcgtatctggtgatggattaacatatagcctttgttttctaataaaatagtcgccttcgttttctgtaaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:1063 -> Molecular function: GO:0003682 [chromatin binding] evidence: NAS
GeneID:1063 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:1063 -> Molecular function: GO:0008022 [protein C-terminus binding] evidence: IPI
GeneID:1063 -> Molecular function: GO:0008134 [transcription factor binding] evidence: IPI
GeneID:1063 -> Molecular function: GO:0042803 [protein homodimerization activity] evidence: IPI
GeneID:1063 -> Molecular function: GO:0045502 [dynein binding] evidence: IDA
GeneID:1063 -> Biological process: GO:0000085 [G2 phase of mitotic cell cycle] evidence: IMP
GeneID:1063 -> Biological process: GO:0000087 [M phase of mitotic cell cycle] evidence: IDA
GeneID:1063 -> Biological process: GO:0000087 [M phase of mitotic cell cycle] evidence: IMP
GeneID:1063 -> Biological process: GO:0000278 [mitotic cell cycle] evidence: IMP
GeneID:1063 -> Biological process: GO:0000278 [mitotic cell cycle] evidence: TAS
GeneID:1063 -> Biological process: GO:0006260 [DNA replication] evidence: IEA
GeneID:1063 -> Biological process: GO:0007059 [chromosome segregation] evidence: IMP
GeneID:1063 -> Biological process: GO:0007059 [chromosome segregation] evidence: NAS
GeneID:1063 -> Biological process: GO:0007067 [mitosis] evidence: IEA
GeneID:1063 -> Biological process: GO:0007094 [mitotic spindle assembly checkpoint] evidence: NAS
GeneID:1063 -> Biological process: GO:0007517 [muscle organ development] evidence: IEA
GeneID:1063 -> Biological process: GO:0008283 [cell proliferation] evidence: NAS
GeneID:1063 -> Biological process: GO:0010389 [regulation of G2/M transition of mitotic cell cycle] evidence: IMP
GeneID:1063 -> Biological process: GO:0015031 [protein transport] evidence: IDA
GeneID:1063 -> Biological process: GO:0015031 [protein transport] evidence: IMP
GeneID:1063 -> Biological process: GO:0016202 [regulation of striated muscle tissue development] evidence: ISS
GeneID:1063 -> Biological process: GO:0030154 [cell differentiation] evidence: IEA
GeneID:1063 -> Biological process: GO:0042493 [response to drug] evidence: NAS
GeneID:1063 -> Biological process: GO:0045892 [negative regulation of transcription, DNA-dependent] evidence: IDA
GeneID:1063 -> Biological process: GO:0051301 [cell division] evidence: IEA
GeneID:1063 -> Biological process: GO:0051310 [metaphase plate congression] evidence: IDA
GeneID:1063 -> Biological process: GO:0051382 [kinetochore assembly] evidence: NAS
GeneID:1063 -> Cellular component: GO:0000775 [chromosome, centromeric region] evidence: IDA
GeneID:1063 -> Cellular component: GO:0000776 [kinetochore] evidence: IDA
GeneID:1063 -> Cellular component: GO:0000785 [chromatin] evidence: NAS
GeneID:1063 -> Cellular component: GO:0000922 [spindle pole] evidence: IDA
GeneID:1063 -> Cellular component: GO:0000940 [condensed chromosome outer kinetochore] evidence: IDA
GeneID:1063 -> Cellular component: GO:0000940 [condensed chromosome outer kinetochore] evidence: TAS
GeneID:1063 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:1063 -> Cellular component: GO:0005635 [nuclear envelope] evidence: IDA
GeneID:1063 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
GeneID:1063 -> Cellular component: GO:0005819 [spindle] evidence: IDA
GeneID:1063 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
GeneID:1063 -> Cellular component: GO:0016363 [nuclear matrix] evidence: IDA
GeneID:1063 -> Cellular component: GO:0030496 [midbody] evidence: IDA
GeneID:1063 -> Cellular component: GO:0045120 [pronucleus] evidence: IEA
GeneID:1063 -> Cellular component: GO:0048471 [perinuclear region of cytoplasm] evidence: IEA
by
@meso_cacase at
DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.