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2025-05-09 17:18:22, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001373 13788 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens dynein, axonemal, heavy chain 14 (DNAH14), transcript
variant 1, mRNA.
ACCESSION NM_001373
VERSION NM_001373.1 GI:223555934
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 13788)
AUTHORS Venter,J.C., Adams,M.D., Myers,E.W., Li,P.W., Mural,R.J.,
Sutton,G.G., Smith,H.O., Yandell,M., Evans,C.A., Holt,R.A.,
Gocayne,J.D., Amanatides,P., Ballew,R.M., Huson,D.H., Wortman,J.R.,
Zhang,Q., Kodira,C.D., Zheng,X.H., Chen,L., Skupski,M.,
Subramanian,G., Thomas,P.D., Zhang,J., Gabor Miklos,G.L.,
Nelson,C., Broder,S., Clark,A.G., Nadeau,J., McKusick,V.A.,
Zinder,N., Levine,A.J., Roberts,R.J., Simon,M., Slayman,C.,
Hunkapiller,M., Bolanos,R., Delcher,A., Dew,I., Fasulo,D.,
Flanigan,M., Florea,L., Halpern,A., Hannenhalli,S., Kravitz,S.,
Levy,S., Mobarry,C., Reinert,K., Remington,K., Abu-Threideh,J.,
Beasley,E., Biddick,K., Bonazzi,V., Brandon,R., Cargill,M.,
Chandramouliswaran,I., Charlab,R., Chaturvedi,K., Deng,Z., Di
Francesco,V., Dunn,P., Eilbeck,K., Evangelista,C., Gabrielian,A.E.,
Gan,W., Ge,W., Gong,F., Gu,Z., Guan,P., Heiman,T.J., Higgins,M.E.,
Ji,R.R., Ke,Z., Ketchum,K.A., Lai,Z., Lei,Y., Li,Z., Li,J.,
Liang,Y., Lin,X., Lu,F., Merkulov,G.V., Milshina,N., Moore,H.M.,
Naik,A.K., Narayan,V.A., Neelam,B., Nusskern,D., Rusch,D.B.,
Salzberg,S., Shao,W., Shue,B., Sun,J., Wang,Z., Wang,A., Wang,X.,
Wang,J., Wei,M., Wides,R., Xiao,C., Yan,C., Yao,A., Ye,J., Zhan,M.,
Zhang,W., Zhang,H., Zhao,Q., Zheng,L., Zhong,F., Zhong,W., Zhu,S.,
Zhao,S., Gilbert,D., Baumhueter,S., Spier,G., Carter,C.,
Cravchik,A., Woodage,T., Ali,F., An,H., Awe,A., Baldwin,D.,
Baden,H., Barnstead,M., Barrow,I., Beeson,K., Busam,D., Carver,A.,
Center,A., Cheng,M.L., Curry,L., Danaher,S., Davenport,L.,
Desilets,R., Dietz,S., Dodson,K., Doup,L., Ferriera,S., Garg,N.,
Gluecksmann,A., Hart,B., Haynes,J., Haynes,C., Heiner,C.,
Hladun,S., Hostin,D., Houck,J., Howland,T., Ibegwam,C., Johnson,J.,
Kalush,F., Kline,L., Koduru,S., Love,A., Mann,F., May,D.,
McCawley,S., McIntosh,T., McMullen,I., Moy,M., Moy,L., Murphy,B.,
Nelson,K., Pfannkoch,C., Pratts,E., Puri,V., Qureshi,H.,
Reardon,M., Rodriguez,R., Rogers,Y.H., Romblad,D., Ruhfel,B.,
Scott,R., Sitter,C., Smallwood,M., Stewart,E., Strong,R., Suh,E.,
Thomas,R., Tint,N.N., Tse,S., Vech,C., Wang,G., Wetter,J.,
Williams,S., Williams,M., Windsor,S., Winn-Deen,E., Wolfe,K.,
Zaveri,J., Zaveri,K., Abril,J.F., Guigo,R., Campbell,M.J.,
Sjolander,K.V., Karlak,B., Kejariwal,A., Mi,H., Lazareva,B.,
Hatton,T., Narechania,A., Diemer,K., Muruganujan,A., Guo,N.,
Sato,S., Bafna,V., Istrail,S., Lippert,R., Schwartz,R., Walenz,B.,
Yooseph,S., Allen,D., Basu,A., Baxendale,J., Blick,L., Caminha,M.,
Carnes-Stine,J., Caulk,P., Chiang,Y.H., Coyne,M., Dahlke,C.,
Mays,A., Dombroski,M., Donnelly,M., Ely,D., Esparham,S., Fosler,C.,
Gire,H., Glanowski,S., Glasser,K., Glodek,A., Gorokhov,M.,
Graham,K., Gropman,B., Harris,M., Heil,J., Henderson,S., Hoover,J.,
Jennings,D., Jordan,C., Jordan,J., Kasha,J., Kagan,L., Kraft,C.,
Levitsky,A., Lewis,M., Liu,X., Lopez,J., Ma,D., Majoros,W.,
McDaniel,J., Murphy,S., Newman,M., Nguyen,T., Nguyen,N., Nodell,M.,
Pan,S., Peck,J., Peterson,M., Rowe,W., Sanders,R., Scott,J.,
Simpson,M., Smith,T., Sprague,A., Stockwell,T., Turner,R.,
Venter,E., Wang,M., Wen,M., Wu,D., Wu,M., Xia,A., Zandieh,A. and
Zhu,X.
TITLE The sequence of the human genome
JOURNAL Science 291 (5507), 1304-1351 (2001)
PUBMED 11181995
REMARK Erratum:[Science 2001 Jun 5;292(5523):1838]
REFERENCE 2 (bases 1 to 13788)
AUTHORS Vaughan,K.T., Mikami,A., Paschal,B.M., Holzbaur,E.L., Hughes,S.M.,
Echeverri,C.J., Moore,K.J., Gilbert,D.J., Copeland,N.G.,
Jenkins,N.A. and Vallee,R.B.
TITLE Multiple mouse chromosomal loci for dynein-based motility
JOURNAL Genomics 36 (1), 29-38 (1996)
PUBMED 8812413
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AC093560.2, AL590547.3, AL645769.9, AL357912.10, AL162738.12,
AL596134.8 and AC092811.2.
Summary: Dyneins are microtubule-associated motor protein complexes
composed of several heavy, light, and intermediate chains. Two
major classes of dyneins, axonemal and cytoplasmic, have been
identified. DNAH14 is an axonemal dynein heavy chain (DHC) (Vaughan
et al., 1996 [PubMed 8812413]).[supplied by OMIM, Mar 2008].
Transcript Variant: This variant (1) encodes the longest isoform
(1).
Sequence Note: The RefSeq transcript and protein were derived from
genomic sequence to make the sequence consistent with the reference
genome assembly. The genomic coordinates used for the transcript
record were based on alignments.
##Evidence-Data-START##
RNAseq introns :: mixed/partial sample support ERS025081, ERS025082
[ECO:0000350]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-182 AC093560.2 122795-122976
183-292 AC093560.2 145811-145920
293-432 AC093560.2 148100-148239
433-582 AC093560.2 153294-153443
583-713 AC093560.2 157620-157750
714-866 AC093560.2 160572-160724
867-982 AC093560.2 161900-162015
983-1045 AC093560.2 167232-167294
1046-1190 AC093560.2 195924-196068
1191-1322 AL590547.3 2960-3091
1323-1573 AL590547.3 19162-19412
1574-1703 AL590547.3 34241-34370
1704-1983 AL590547.3 38382-38661
1984-2029 AL590547.3 39291-39336
2030-2127 AL590547.3 39433-39530
2128-2294 AL590547.3 45757-45923
2295-2639 AL590547.3 46998-47342
2640-2981 AL645769.9 15635-15976
2982-3351 AL645769.9 16807-17176
3352-3542 AL645769.9 18977-19167
3543-3788 AL645769.9 21972-22217
3789-3910 AL357912.10 9827-9948
3911-4082 AL357912.10 13422-13593
4083-4187 AL357912.10 30393-30497
4188-4306 AL357912.10 30590-30708
4307-4381 AL357912.10 31929-32003
4382-4672 AL357912.10 53440-53730
4673-4904 AL357912.10 57106-57337
4905-4958 AL357912.10 58035-58088
4959-5104 AL357912.10 59813-59958
5105-5173 AL357912.10 64714-64782
5174-5360 AL357912.10 65406-65592
5361-5437 AL357912.10 66459-66535
5438-5594 AL357912.10 72038-72194
5595-5684 AL357912.10 80648-80737
5685-5819 AL357912.10 98000-98134
5820-6035 AL357912.10 105405-105620
6036-6126 AL357912.10 116892-116982
6127-6335 AL357912.10 118680-118888
6336-6588 AL357912.10 119677-119929
6589-6667 AL162738.12 13825-13903
6668-6897 AL162738.12 23345-23574
6898-6945 AL162738.12 33408-33455
6946-7062 AL162738.12 35053-35169
7063-7221 AL162738.12 40712-40870
7222-7354 AL162738.12 41873-42005
7355-7419 AL162738.12 46949-47013
7420-7607 AL162738.12 47934-48121
7608-7736 AL162738.12 49393-49521
7737-7868 AL162738.12 53487-53618
7869-8036 AL162738.12 54658-54825
8037-8207 AL162738.12 55707-55877
8208-8405 AL162738.12 72637-72834
8406-8567 AL162738.12 83621-83782
8568-8759 AL162738.12 85908-86099
8760-8941 AL162738.12 87660-87841
8942-9050 AL162738.12 90213-90321
9051-9176 AL162738.12 91037-91162
9177-9271 AL162738.12 101335-101429
9272-9431 AL162738.12 105416-105575
9432-9563 AL162738.12 106974-107105
9564-9659 AL162738.12 107489-107584
9660-9800 AL162738.12 114189-114329
9801-10016 AL162738.12 116043-116258
10017-10247 AL162738.12 120018-120248
10248-10369 AL162738.12 120813-120934
10370-10614 AL596134.8 3381-3625
10615-11033 AC092811.2 185237-185655 c
11034-11232 AC092811.2 184963-185161 c
11233-11469 AC092811.2 179734-179970 c
11470-11555 AC092811.2 177729-177814 c
11556-11712 AC092811.2 172965-173121 c
11713-11923 AC092811.2 170726-170936 c
11924-12026 AC092811.2 166723-166825 c
12027-12254 AC092811.2 163585-163812 c
12255-12444 AC092811.2 156740-156929 c
12445-12625 AC092811.2 154181-154361 c
12626-12789 AC092811.2 151295-151458 c
12790-12986 AC092811.2 150038-150234 c
12987-13099 AC092811.2 143126-143238 c
13100-13239 AC092811.2 141744-141883 c
13240-13400 AC092811.2 139166-139326 c
13401-13547 AC092811.2 132951-133097 c
13548-13788 AC092811.2 132323-132563 c
FEATURES Location/Qualifiers
source 1..13788
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="1"
/map="1q42.12"
gene 1..13788
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/note="dynein, axonemal, heavy chain 14"
/db_xref="GeneID:127602"
/db_xref="HGNC:2945"
/db_xref="MIM:603341"
exon 1..182
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 15
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:189391711"
variation 88
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:373318095"
variation 99
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace=""
/replace="g"
/db_xref="dbSNP:34258633"
exon 183..292
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
misc_feature 195..197
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/note="upstream in-frame stop codon"
CDS 216..13763
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/note="isoform 1 is encoded by transcript variant 1;
dynein, axonemal, heavy polypeptide 14; dynein heavy chain
14, axonemal; ciliary dynein heavy chain 14; axonemal beta
dynein heavy chain 14"
/codon_start=1
/product="dynein heavy chain 14, axonemal isoform 1"
/protein_id="NP_001364.1"
/db_xref="GI:223555935"
/db_xref="GeneID:127602"
/db_xref="HGNC:2945"
/db_xref="MIM:603341"
/translation="
METFIPIDLTTENQEMDKEETKTKPRLLRYEEKKYEDVKPLETQPAEIAEKETLEYKTVRTFSESLKSEKTEDYLRESIIQQHMVSPEPASLKEKGKSRRKKDQTHACPNVRKARPVSYDRTEPKDDDVIRNIIRLREKLGWQTILPQHSLKYGSSKIAIQKITLKKPLEDDGEFVYCLPRKSPKSLYNPYDLQVVSAHTAKHCKEFWVITASFISKVINIVGSVKEVELIPTLEWLSERRHYYLLRQFKIFSDFRMNKAFVTWKLNVKRIKTEKSRSFLYHHLFLADDLFQTCLVYIRGLCEDAINLKNYNDHENNLSAICLVKLDSSRTYSLDEFCEEQLQQATQALKQLEDIRNKAISEMKSTFLKVAEKNEIKEYFESKLSEDDTTHFKLPKYRRLLETFFKFVMLVDYIFQELIRQLMNTAVTLLLELFNGSAGMPFSVEKKNENLIRTFKDNSFPTGKTTNDCEELVDNSKLHAISVQKSEVKTDTDINEILNSVEVGKDLRKTYAPIFEVNLCLRIPAESDSSENSKENFHESDQCPEECVMFEDEMSENKDNCVKKHSSEELLPKAKKSKEISYNLEDIISDTEIETEFENKYMYYEFPEFPTNLFIDPNRLEFSVKIQNMLTNMEKCITTITPLCQDPQLSIFIDLVSIMDLPNKTGSIIHYKEQTRWPDCHILFETDPAYQNIIVNLLTIIGNSMGLVNAYSHKFIKYCTMTEKAKIMSMKISSMGELTSKEFEAILNRFRNYFRHIVNMAIEKRIGIFNVVSLDYQSECLLYIDNVIHMSHTLIQSVIEKKNKNLLEVVESSLQQLECDPTEIEEFLEHFIFLNAISSKISKLEKEFLTMSQLYSVAKHHQIHISEEQIAIFQVLLLKFSQLKSSMKLSKINKDTAITKFRDNLEACISGLHVDVGNLKAKIRTPLLLCAGTQVSTAMEMIQTLSGEAASLTNKAKAYSHYQDCFSDSQSHMHSVNVEEITQIVLSEISDIEGDLTLRKKLWEAQEEWKRASWEWRNSSLQSIDVESVQRNVSKLMHIISVLEKGLPKSDMVTHLKQVVTEFKQELPIIIALGNPCLKPRHWEALQEIIGKSVPLDKNCKVENLLALKMFQYENEINDMSTSATNEAALEKMLFKIIDFWNTTPLPLILHHTEIYSIFIIPSIDDISAQLEESQVILATIKGSPHIGPIKDLVNEWDQNLTLFSYTLEEWMNCQRNWLYLEPVFHSSEIRRQLPAETELFSQVISMWKKIMSKIQNKQNALQITTSAGVLEILQNCNIHLEHIKKSLEDYLEVKRLIFPRFYFLSNAELLDILADSRNPESVQPHLVKCFENIKQLLIWKQDIGPPAVKMLISAEGEGLVLPKKIRVRSAVEQWLVNVEKSMFDVLKKERYIYNIILLFQSQIMFYNDCVKSFVSSYSREKLEKVHAGLMCHLEEVADLVVLDTSNSRTKAILGALLILYVHCRDIVINLLLKNIFNAEDFEWTRHLQYKWNEKQKLCYVSQGNASFTYGYEYLGCTSRLVITPLTDRCWLTLMEALHLNLGGCPAGPAGTGKTETVKDLAKSLGKHCVVFNCFEDLDYKIVRKFFFGLVQSGAWSCFDEFNLIDLEVLSVIASQILTIKAAKDNYSARFVLEGKEIRINMSCAVFITMNPRYGGGVELPDNLKSLFRPVAMMVPHYQMIAEIILFSFGFKSANSLSGKLTNLYELARKQLSQQDHYNFGLRSLKIVLIMAGTKKREFKCLSEADETLIVIEAIREASLPKCPPEDVPLFENIIGDIFPEVTVLKVNQLALEKVIYTATQQLGLQNWSSQKEKIIQFYNQLQVCVGVMLVGPTGGGKTTVRRILEKALTLLPIADFLSVAERKSASKISERKGKVDICVLNPKCVTLSELYGQLDPNTMEWTDGLLSATIRSYVYFNTPKNTKKDIDLRLKSRISDLSNVFKLDSSDTTETDDNIFEEIEKVVKIPENHNFDWQWIILDGPVDTFWVENLNSVLDDTRTLCLANSERIALTNKIRVIFEVDNLSQASPATVSRCAMVYMDPVDLGWEPYVKSWLLKTSKIISQSGVDCLEFMIKNSVTDGLQFIRNRQKFQPYPMEDITVVITLCRILDAFFDFMGKNGGFEQSDDLNDTSSKEANSQRESVTFKDIEKRDENTWYPEKNPDKLTKIIQKLFVFAFTWAFGGALNREDEHRENIPFCPSLEPDSLAKVTYDFDKLVHELFGNSSQVGWKHWGQSQGRRRKGNCINLPTGECSIFGYFVDIEQCEFIPWSDLVPNDQTLIQRGTSLLTNLQRSGGNFLKITECGECINYTATRDTTCLSFLMSLLLKNSCPVLLTGESGVGKTAAINQMLEKLEGPGAFDIKHGSILGDTLLYSEIKKSSSLKQNITILIPETHKTATGSSDNPTKKPEVRTNKKLLKNNDHKGVVVSTINFSTNVTAAKTKEMILKKLIRRTKDTLGAPKNNRILIFIDDMNMPVSDMYGAQPPLELIRQLLDLGGVYDTEKNTWKNIQDLSIVAACVPVVNDISPRLLKHFSMLVLPHPSQDILCTIFQAHLGIYFSINNFTPEVQKSKDQIISCSLAIYHQVRQNMLPTPTKCHYMFNLRDMFKLLLGLLQADRTVVNSKEMAALLFVHEATRVFHDRLIDFTDKSLFYRLLSRELENCFQIGIDGCGKKTCATLACYLTDNKLYRVPISHKCAYIEFKEVFKKVFIHAGLKGKPTVLMVPNLNIEQDSFLEDLNYIISSGRIPDLFENVELDSIAMKIRYLTEQSGHMDNRQSLLSFFQKRIYKNLHIFVIMSPEGPSFRQNCRVYPSMISSCTIDWYERWPEEALLIVANSFLKEKVNFENRENLKEKLAPTCVQIHKSMKDLNRKYFEETGRFYYTTPNSYLQFMETFAHILRAREEEMQTKRDRFHMGLSTILEATTLVTEMQEELLILGPQVEQKTKETETLMEKLRKDSQVVEKVQMLVKQDEEIVAEEVRIVEDYAQKTANELKSVLPAFDKAIVALNALDKADVAELRVYTRPPFLVLTVMNAVCILLQKKPNWATAKLLLSETGFLKKLINLDKDSIPDKVFVKLKKIVTLPDFNPHKISLVSVACCSLCQWVIALNNYHEVQKVVGPKQIQVAEAQNVLKIARQRLAEKQRGLQLVEEHLLFLQAAYKDTVAEKQLLANRKTMASRRFQCASVLLTVLEDEKTRWQETINQIDNKLEGILGDILLSAACIVYSGILTPEFRQLIVNKWETFCIENGISLSSKFSLIKVMAQKYEISRWHNQGLPHGQYSVENAILIKNGQQWPLLIDPHRQAHKWIRQMEGSRLQKLSIEDSNYTKKIENAMKTGGSVLLQNLLETLAPGLKAILKKDIYQKKGHYFIRVGDAEFEYNSNFRLYLSTEIDNPHFLPSVYNFVTMINFTVTFQGLQDQLLSTVVTHEVPHLEDQRSKLLESISLDAITLEELEEKTLNLLQKALGSILDDDKIVDTLRKSKMTSNEISKRIEATKKAESEIQAIRKNYLPIATRGALLYFLVADLTQINYMYQFSLDWFHQVFVSSVVSKSKEQEHSFKREKVSPKEVHEFISISKEPNLENEKNLLDKHIKSAIDMLTKSIFKVVSSALFNEDKLCFSFRLCTVIMQNNANGNLIQDDIGFLPEEEWNIFLYSGILINIKSALSQSRLTSTFEIGESQHLQWLSDSRWRQCQYVSTHLEPFSLLCKSLLSNVSQWDTFKNSKAVYSLISTPFSSENASLEENTKPPEETELLNENKETCNPINFPWEKLTSFQRLILVKVLRPESLNNSVRKFITEKMGNKYLQRTGVNLKDAYKGSNARTPLILIQTHGIDLTNILLRFAQELKGTTHHVTIISLGRDQAAKAEDLILKALTKTQQWVFLQNCHLATSFMPRLCTIVESFNSPNVTIDPEFRLWLSSKSYSSFPIPVLKKGLKIAVESPQGLKSNLLQTFGCTGSGEVTEEIFENPDCGQWWKKLLFSLCFFNAVINERKNYGILGWNIAYKFNSSDLGVAIKVLENSLRGQPSISWQALRYLIGEVIYGGRVIDNWDKRCLKTLLYKFCNPEVLKDDFSFSRSASIKDYIHIIQSLPDDDLPEVLGIHPEAIRSCWETQGEKFIENLIAMQPKTTTANLMIRPEQSKDELVMEILSDLLKRLPLTVEKEEIAVGTPSTLKSMMSSSIWESLSKNLKDHDPLIHCVLLTFLKQEIKRFDKLLFVIHKSLKDLQLAIKGEIILTQELEEIFNSFLNMRVPTLWQKHAYRSCKPLSSWIDDLIQRLNFFNTWAKVAYTAIQRRYMRFVTVWKQSIPSTSQKCKHPEDSENNFFEGFPSRYWLPAFFFPQAFLAAVLQDYGRSRGIAVDALTFTHHVISNTTDKDEKFSVFMPKKLNIVRRAFKGSASSHTGVYIFGLFIEGARWNREQKILEDSLPLEMCCDFPDIYFLPTKISTKTPNASNQTDSELYAFECPVYQTPERSRILATTGLPTNFLTSVYLSTKKPPSHWITMRVALLCEKNEK
"
misc_feature 3174..4382
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/note="Dynein heavy chain, N-terminal region 2; Region:
DHC_N2; pfam08393"
/db_xref="CDD:203929"
misc_feature 4743..5426
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/note="Hydrolytic ATP binding site of dynein motor region
D1; Region: AAA_6; pfam12774"
/db_xref="CDD:193250"
misc_feature 7464..8114
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/note="P-loop containing Nucleoside Triphosphate
Hydrolases; Region: P-loop_NTPase; cl09099"
/db_xref="CDD:213113"
misc_feature 8172..8909
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/note="P-loop containing Nucleoside Triphosphate
Hydrolases; Region: P-loop_NTPase; cl09099"
/db_xref="CDD:213113"
misc_feature 8943..9947
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/note="Microtubule-binding stalk of dynein motor; Region:
MT; pfam12777"
/db_xref="CDD:193253"
misc_feature 10014..10685
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/note="ATP-binding dynein motor region D5; Region: AAA_9;
pfam12781"
/db_xref="CDD:193257"
misc_feature 11262..13748
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/note="Dynein heavy chain and region D6 of dynein motor;
Region: Dynein_heavy; pfam03028"
/db_xref="CDD:145919"
variation 224
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:192193099"
variation 270
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:61745064"
variation 282
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:201634729"
exon 293..432
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 327
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:372136045"
variation 342
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:41267347"
variation 380
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:369460884"
variation 413
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:372589152"
variation 417
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:375259141"
exon 433..582
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 459
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:374296761"
variation 505
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:377514534"
variation 510
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:201089763"
variation 512
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:373709305"
variation 551
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:376453640"
variation 556
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:199833408"
variation 571
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:202149727"
exon 583..713
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 585
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:370168340"
variation 624
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:192345324"
variation 648
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:367728866"
variation 655
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:41267349"
variation 656
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:371936326"
variation 675
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:202121833"
variation 691
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:200184686"
variation 700
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:79645812"
variation 711
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:376849940"
exon 714..866
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 717
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:375791690"
variation 756
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:370187831"
variation 757
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:201807754"
variation 806
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:61732752"
variation 825
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:199814205"
variation 843
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:370749461"
variation 858
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:372706704"
exon 867..982
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 954
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:374672388"
exon 983..1045
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 1024
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:374048564"
variation 1045
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:192523416"
exon 1046..1190
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 1046
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:80297033"
variation 1057
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:201201605"
variation 1132
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:189576156"
exon 1191..1322
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 1220
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:149893393"
variation 1270
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:183952944"
variation 1294
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:74149431"
exon 1323..1573
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 1366
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:181331399"
variation 1428
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:75568712"
variation 1486
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:376817319"
variation 1531
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:185076105"
exon 1574..1703
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
exon 1704..1983
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 1763
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:201098114"
variation 1775
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:2501107"
variation 1796
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:12059619"
variation 1947
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:376558673"
variation 1953
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:145346250"
variation 1974
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:371575718"
exon 1984..2029
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
exon 2030..2127
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 2036
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:140788075"
exon 2128..2294
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 2152
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:191493695"
variation 2166
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:78320839"
exon 2295..2639
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 2328
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:140164319"
exon 2640..2981
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 2697
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:3105559"
variation 2759
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:182582660"
variation 2763
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:58506089"
variation 2768
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:185235980"
variation 2797
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:12081290"
variation 2849
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:375285772"
exon 2982..3351
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 2986
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:373262464"
variation 3007
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:115366080"
variation 3015
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:188000179"
variation 3064
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:369341655"
variation 3125
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:372916173"
variation 3186
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:113707090"
variation 3195
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:73133544"
variation 3244
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:3128651"
variation 3247
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:3128652"
variation 3294..3295
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace=""
/replace="a"
/db_xref="dbSNP:34842437"
variation 3328
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:115240788"
variation 3337
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:370909788"
exon 3352..3542
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 3420
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:202046747"
variation 3510
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:3128655"
variation 3525
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:201015646"
exon 3543..3788
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 3545
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:3128658"
variation 3620
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:367566298"
variation 3624
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:201011780"
exon 3789..3910
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 3862
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:371522012"
exon 3911..4082
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 4030
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:3105571"
exon 4083..4187
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
exon 4188..4306
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 4232
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:375097364"
variation 4286
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:74147113"
variation 4296
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:113651787"
exon 4307..4381
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 4315
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:372412698"
variation 4345
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:199634734"
variation 4367
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:150618371"
exon 4382..4672
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 4387
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:202118490"
variation 4388..4389
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace=""
/replace="at"
/db_xref="dbSNP:138066581"
variation 4389
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:75827633"
variation 4453
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:201843941"
variation 4493
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:116052053"
variation 4498
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:200017807"
exon 4673..4904
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 4701
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:148730700"
variation 4752
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:372717757"
variation 4786
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:201873499"
variation 4787
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:73133596"
variation 4857
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:41307682"
variation 4870
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:142356826"
exon 4905..4958
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
exon 4959..5104
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 5056
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:370823006"
variation 5072
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:374704151"
variation 5077
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace=""
/replace="ttaa"
/db_xref="dbSNP:80023327"
variation 5092
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:149056614"
exon 5105..5173
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 5130
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:115743416"
variation 5143
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:78335375"
exon 5174..5360
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 5185
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:17578819"
variation 5195
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:188496398"
variation 5211
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:375432909"
variation 5220
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:191860318"
variation 5339
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:139949596"
variation 5340
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:183567269"
variation 5341
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:143916022"
exon 5361..5437
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 5382
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:190061594"
variation 5416
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:369373571"
exon 5438..5594
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 5480
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:190863487"
exon 5595..5684
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 5670
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:78614986"
exon 5685..5819
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 5723
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:374309666"
variation 5764
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:61851487"
variation 5765
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:371171947"
variation 5775
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:150319745"
variation 5793
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:6679852"
variation 5797
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:370410795"
exon 5820..6035
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 5820
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:143317903"
variation 5834..5835
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace=""
/replace="g"
/db_xref="dbSNP:35786206"
variation 5885
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:200638575"
variation 5960
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:187487970"
variation 5984..5987
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace=""
/replace="aaag"
/db_xref="dbSNP:144339803"
variation 5986
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:191528375"
variation 5999
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:184059928"
variation 6025
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:146658863"
exon 6036..6126
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 6063
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:373487478"
variation 6074
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:192601701"
variation 6102..6104
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace=""
/replace="gtt"
/db_xref="dbSNP:148326046"
exon 6127..6335
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 6169
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:367559558"
variation 6215
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:370179144"
variation 6282
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:143058170"
exon 6336..6588
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 6455
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:368687409"
variation 6478
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:191968010"
variation 6514
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:375449724"
variation 6557
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:200519891"
exon 6589..6667
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 6608
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:370991538"
variation 6667
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:370328139"
exon 6668..6897
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 6722
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:201526391"
variation 6723
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:200064799"
variation 6735
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:184912210"
variation 6788
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:189747207"
variation 6868
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:371854981"
variation 6872
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:180868605"
exon 6898..6945
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 6930
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:374859085"
variation 6931
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:190087833"
variation 6941
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:181105903"
exon 6946..7062
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 6954
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:376690622"
exon 7063..7221
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 7098
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:149061712"
variation 7145
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:370676245"
variation 7221
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:373790753"
exon 7222..7354
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 7237
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:41303311"
variation 7238
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:79504221"
variation 7285
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:187694467"
exon 7355..7419
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
exon 7420..7607
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 7503
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:201372112"
variation 7519
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:76767146"
variation 7575
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:371011826"
exon 7608..7736
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 7640
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:138408664"
variation 7651
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:4653415"
exon 7737..7868
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 7808
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:200968726"
variation 7831
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:375530989"
variation 7842
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:143552249"
exon 7869..8036
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 7897
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:186548606"
variation 7972
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:368246646"
variation 7987
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:191923388"
variation 8022
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:201910052"
exon 8037..8207
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 8080
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:191811978"
variation 8140
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:375254049"
exon 8208..8405
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 8214
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:371563812"
variation 8349
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:374829542"
variation 8370
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:181126197"
variation 8379
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:369228896"
exon 8406..8567
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 8426
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:369507297"
variation 8493
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:373274946"
variation 8515
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:375908462"
variation 8537
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:369335225"
exon 8568..8759
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 8625
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:140066130"
variation 8682
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:371705535"
exon 8760..8941
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 8860
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:116490173"
variation 8865..8866
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace=""
/replace="c"
/db_xref="dbSNP:141365402"
variation 8917
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:189545024"
exon 8942..9050
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 8947
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:112172758"
variation 8963
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:377569460"
variation 8967
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:200518833"
exon 9051..9176
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 9067
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:369223685"
variation 9079
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:183261121"
exon 9177..9271
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 9186
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:10495237"
variation 9187
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:371972178"
variation 9221
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:374773665"
variation 9226
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:191667479"
variation 9261
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:140440496"
exon 9272..9431
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 9276
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:375847465"
variation 9289
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:200333099"
variation 9321
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:369930943"
variation 9324
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:371882986"
exon 9432..9563
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 9491
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:145601562"
exon 9564..9659
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 9594
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:373139697"
variation 9606
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:200310916"
variation 9619
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:145100008"
exon 9660..9800
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 9699
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:377611333"
variation 9702
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:78999515"
variation 9724
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:188862661"
variation 9733
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:41303992"
variation 9744
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:185348183"
exon 9801..10016
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 9874
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:113335252"
variation 9909
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:41268715"
exon 10017..10247
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 10024
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:199848334"
variation 10132
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:370139767"
variation 10137
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:374469779"
variation 10155
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:187150031"
variation 10163
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:367756955"
variation 10188
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:200311669"
exon 10248..10369
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 10349
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:56918103"
exon 10370..10614
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 10386
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:184094753"
variation 10394
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:3856145"
variation 10394
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace=""
/replace="c"
/db_xref="dbSNP:377250670"
variation 10400
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:115148958"
variation 10507
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:6686504"
variation 10551
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:12184324"
exon 10615..11033
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 10635
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:6667999"
variation 10682
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:12742757"
variation 10690
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:200532024"
variation 10694
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:374323375"
variation 10720
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:148023906"
variation 10767
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:369673460"
variation 10786
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:373712140"
variation 10812
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:74147200"
variation 10830
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:370632234"
variation 10861
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:201079664"
variation 10882
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:17522489"
variation 11010
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:200671919"
exon 11034..11232
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 11070
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:12565381"
variation 11095
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:7527925"
variation 11096
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:55725527"
variation 11145
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:187598699"
variation 11190
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:116404408"
variation 11200
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:73136911"
variation 11224
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:7535953"
exon 11233..11469
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 11247
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:12408617"
variation 11273
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:142089541"
variation 11360
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:368419004"
variation 11367..11368
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace=""
/replace="g"
/db_xref="dbSNP:34473543"
variation 11392
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:144674097"
exon 11470..11555
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 11498
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:192354509"
exon 11556..11712
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 11579
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:368426392"
variation 11649
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:190452224"
variation 11660
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:79877014"
variation 11690
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:373469864"
variation 11706
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:182215041"
exon 11713..11923
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 11747
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:370191299"
variation 11796
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:146438399"
variation 11820
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:141105896"
variation 11829
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:111504201"
variation 11835
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:373470844"
exon 11924..12026
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
exon 12027..12254
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 12032
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:11578981"
variation 12033
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:372806779"
variation 12039
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:141510580"
variation 12051
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:147045964"
variation 12122
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:12737248"
variation 12199
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:74149905"
exon 12255..12444
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 12265
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:112206346"
variation 12270
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:115803833"
variation 12309
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:374597184"
variation 12317
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:368211863"
variation 12340
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:201754277"
variation 12376
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:375272804"
variation 12394
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:199565083"
exon 12445..12625
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 12495
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:190428375"
variation 12502
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:3856154"
variation 12535..12536
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace=""
/replace="c"
/db_xref="dbSNP:369640978"
variation 12539
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:369062643"
variation 12552
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:75794192"
variation 12553
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:76375603"
variation 12560
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:3856155"
variation 12593
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:181625725"
exon 12626..12789
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 12635
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:74517776"
variation 12744
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:114941345"
exon 12790..12986
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 12799
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:141334390"
variation 12846
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:374542052"
variation 12908
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:150254532"
variation 12946
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:950210"
exon 12987..13099
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 12993
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:146075975"
variation 13045
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:370919219"
variation 13064
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:375801560"
exon 13100..13239
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 13126
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:190910110"
exon 13240..13400
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 13252
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:61739997"
variation 13273
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:371543296"
variation 13334
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:376675287"
variation 13340
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="g"
/db_xref="dbSNP:61738690"
variation 13356
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:372266024"
variation 13367
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:372569939"
variation 13385
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="c"
/replace="t"
/db_xref="dbSNP:2275600"
exon 13401..13547
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 13409
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:375100667"
variation 13453
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:41304131"
variation 13466
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="g"
/replace="t"
/db_xref="dbSNP:147317659"
variation 13481
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:181716749"
variation 13493
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:372710071"
variation 13546..13547
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace=""
/replace="g"
/db_xref="dbSNP:34522483"
exon 13548..13788
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/inference="alignment:Splign:1.39.8"
variation 13576
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:115162236"
variation 13599
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:115414058"
variation 13637
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:16844837"
variation 13693
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="c"
/db_xref="dbSNP:114514795"
variation 13763
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="t"
/db_xref="dbSNP:41305733"
variation 13770
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:77901289"
variation 13780
/gene="DNAH14"
/gene_synonym="C1orf67; Dnahc14; HL-18; HL18"
/replace="a"
/replace="g"
/db_xref="dbSNP:377610536"
ORIGIN
agggcgcaggcgtggctcttggtcaggcggttacggccaggaggcgtcggagcctggcgtggtagggctgtgctgcgcggtccttcccattcaccctagtctggcgctcgccggcgtgggcgggccggaccttcgccgcttccaggaagggccacaacggccgtcggaccacggcgcggcggccagttcctttatagttttgttcagaaaaacatatggagacgtttatacccattgatttgacaactgaaaatcaagagatggacaaggaggaaaccaagacaaaaccaagacttttaagatatgaagagaaaaaatatgaagatgtgaaaccattagagactcaaccagctgaaatagcagaaaaggaaacattggaatataaaacagttagaacattctctgaatctttgaagtcagagaaaacagaagattaccttagagaaagtataattcaacaacatatggtttctccagagccagcttcccttaaggagaaagggaagtcaaggagaaaaaaggatcaaactcatgcttgtccaaatgttaggaaagccaggcctgtgtcctatgatagaacagaaccaaaagatgatgatgtgataagaaatattattaggctacgagaaaagcttggttggcaaactatattaccgcagcacagtttgaaatacggaagctccaaaattgcaattcagaagattactttaaagaaacctttggaagatgatggagaatttgtttattgccttcctcggaaaagtcctaaatccctttacaatccatatgatcttcaggtagtatcggctcatactgctaaacattgcaaagaattttgggttattactgcttcatttatctcaaaggttattaatatagttggtagtgtaaaggaagtagaactcatacctactttggaatggctatcagaaagaagacattactatttattacggcaattcaagatattttctgatttccgaatgaataaagcatttgttacctggaaattgaatgttaaaagaattaagacagagaagagcaggtcatttttgtaccaccatctttttttggctgatgacttgtttcaaacctgtttggtttatataagaggactttgtgaagatgcaattaatctcaaaaattataatgaccatgaaaataatctatctgccatatgccttgtaaagctggatagttctcgaacatattctctagatgaattttgtgaagagcagttacagcaagctacccaggcattgaaacaacttgaggacatcaggaataaagcaatttcagagatgaaaagtacttttctaaaggttgcagaaaagaatgaaatcaaagagtattttgagtcaaaactctctgaagatgacacaacacatttcaagctgcctaaatatagacgtttattagaaacatttttcaagtttgtaatgctggttgactacatatttcaggaactcattcgtcaacttatgaacactgcagtcacactacttttggaattatttaatggttctgctggaatgccattttcagtggaaaaaaagaatgaaaatcttatcagaacattcaaggacaactcttttcctactggaaagacaacaaatgattgtgaagaacttgttgataattcaaagttacatgctatttctgttcaaaagtcagaagtaaaaacagacactgatattaatgagattttgaatagtgttgaagtggggaaggatttgagaaaaacatatgcaccaatatttgaagtaaatctatgcttgagaattcctgctgagagtgattcttcagaaaattctaaagagaactttcatgagtctgaccagtgccctgaagagtgtgtgatgtttgaagatgaaatgtcagaaaataaagacaattgtgtcaaaaaacactcaagtgaagaattgctcccaaaagccaagaaatcaaaagaaattagttacaatcttgaagatattatttcagacacagaaattgagactgagtttgagaataaatacatgtattatgaatttccagaatttcctacaaatctctttatagatcccaacagattggagttttcagtaaaaattcaaaatatgttgactaatatggaaaaatgtataaccacaattactcctctttgccaagatccccagctgtctatcttcattgatttggtttcaataatggatttacctaataagacaggaagcataatacattataaagagcagaccagatggccagattgtcacatcctttttgaaacagatcctgcctaccaaaatataattgtgaatctcctgactattattggtaattcaatgggcctagttaatgcttacagccacaagtttataaagtattgtaccatgacagaaaaggccaaaatcatgagtatgaaaatatcatctatgggagaattaacttcaaaagaatttgaagctattctaaatagattcagaaactattttagacatattgtgaatatggccattgagaagcgtattggtattttcaacgttgtaagtcttgattatcaatcagaatgcttactgtatattgacaacgtcatacatatgagccacaccctcatacaatctgtaattgaaaaaaagaacaaaaatttattggaagttgtggaatcatcattgcagcagctggaatgtgatcccactgaaatagaagaatttctggagcattttatttttttgaatgcaatttcctcaaaaatatctaaattagaaaaagagttcttaacaatgtctcagctatattctgttgcaaagcatcaccagatccatatttcagaagagcaaattgccatattccaagttcttcttcttaagtttagtcaactaaaatcatctatgaagttaagtaaaataaataaagacactgctataactaaattcagagataacttggaagcatgtatcagtggtctacatgttgatgttggcaatttaaaagccaagataagaactcctcttctgttatgtgctggtactcaagtgtcaacagcaatggaaatgatccagactctctcaggggaagctgcaagtttaactaacaaagctaaagcatattcacattatcaggattgtttcagtgattctcaatctcatatgcattctgttaatgtggaagaaattacacagattgtgctttcagagatctctgacattgaaggtgacttgactttgaggaaaaaactatgggaagcacaagaggagtggaagcgagcctcttgggaatggaggaatagttctcttcaaagtattgatgtagaatcagtacagagaaatgtttcaaaactgatgcacataatctcggtactagaaaaaggtttacctaaaagcgatatggtaacacatcttaagcaagtggtaacagagtttaaacaagagctgcctatcattatagctctgggaaatccctgtctcaagccaaggcattgggaggctctccaggagattattgggaagtcagttccgcttgataaaaactgtaaagtagagaatcttctagctctcaagatgtttcagtatgaaaatgaaataaatgatatgtcaacctcagcaactaatgaagctgctcttgaaaaaatgctatttaagattattgatttttggaacactactcctttgcctttaattcttcaccacacagagatttactctatcttcataattccatctatagatgacatatcagctcagttagaagagtctcaagtcatacttgcaacaattaaaggatctccccacattgggcccattaaggatcttgtgaatgaatgggatcaaaacttgactctcttctcttacacccttgaggaatggatgaattgtcaaagaaattggctttatcttgaaccagtctttcattcttcagaaatacgaaggcaactcccagcagaaacagaacttttctctcaagtgatttccatgtggaaaaaaataatgtcaaaaatacaaaacaaacagaatgctttgcagataaccacttctgcaggagtccttgaaattctgcaaaattgtaatatacatcttgaacatataaagaaaagccttgaggattaccttgaagttaaaagattaattttcccaagattttactttcttagcaatgccgagcttcttgatattctagctgatagcagaaatcctgagtctgtacagcctcatcttgtgaaatgctttgaaaatataaaacaattattgatatggaaacaagacattggccctcctgctgtaaaaatgctaatatctgctgaaggggaaggtctcgtgctgccaaagaaaattcgtgtaagaagtgctgtagaacagtggctggtaaatgtagaaaaaagcatgttcgatgtgctaaaaaaagagagatatatatataacattatcttactttttcagagccagatcatgttttataatgattgtgttaaaagttttgtgagttcttattcaagagaaaaattggaaaaagtccacgctggtctgatgtgtcatctagaagaggttgcagacctggtagtgctggatactagtaactctcgaacaaaagctatactaggggcattgcttatcctttatgttcactgcagagatatagtgataaatttactacttaaaaatatcttcaatgcagaggattttgagtggacaagacatttgcaatataaatggaatgaaaaacaaaagttgtgctatgtgtctcaaggaaatgccagctttacttatggctatgagtacttgggctgtacctcaagattggttattacgcctctcacagaccgatgctggctgactctcatggaagcactacacttgaatctaggaggctgtcctgccggtccagctggtacaggaaaaactgagactgtcaaagatctagcaaaatccttaggcaaacattgtgtggtcttcaactgttttgaggatttggattataagatagtgagaaaatttttctttggactagttcagtcaggagca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//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:127602 -> Molecular function: GO:0003777 [microtubule motor activity] evidence: IEA
GeneID:127602 -> Molecular function: GO:0005524 [ATP binding] evidence: IEA
GeneID:127602 -> Biological process: GO:0007018 [microtubule-based movement] evidence: IEA
GeneID:127602 -> Cellular component: GO:0005874 [microtubule] evidence: IEA
GeneID:127602 -> Cellular component: GO:0030286 [dynein complex] evidence: IEA
GeneID:127602 -> Cellular component: GO:0035085 [cilium axoneme] evidence: IEA
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