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Previous release (v1)
2024-04-26 11:42:35, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001866 2444 bp mRNA linear PRI 11-NOV-2023
DEFINITION Homo sapiens cytochrome c oxidase subunit 7B (COX7B), mRNA; nuclear
gene for mitochondrial product.
ACCESSION NM_001866
VERSION NM_001866.3
KEYWORDS RefSeq; MANE Select.
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 2444)
AUTHORS Luck K, Kim DK, Lambourne L, Spirohn K, Begg BE, Bian W, Brignall
R, Cafarelli T, Campos-Laborie FJ, Charloteaux B, Choi D, Cote AG,
Daley M, Deimling S, Desbuleux A, Dricot A, Gebbia M, Hardy MF,
Kishore N, Knapp JJ, Kovacs IA, Lemmens I, Mee MW, Mellor JC,
Pollis C, Pons C, Richardson AD, Schlabach S, Teeking B, Yadav A,
Babor M, Balcha D, Basha O, Bowman-Colin C, Chin SF, Choi SG,
Colabella C, Coppin G, D'Amata C, De Ridder D, De Rouck S,
Duran-Frigola M, Ennajdaoui H, Goebels F, Goehring L, Gopal A,
Haddad G, Hatchi E, Helmy M, Jacob Y, Kassa Y, Landini S, Li R, van
Lieshout N, MacWilliams A, Markey D, Paulson JN, Rangarajan S,
Rasla J, Rayhan A, Rolland T, San-Miguel A, Shen Y, Sheykhkarimli
D, Sheynkman GM, Simonovsky E, Tasan M, Tejeda A, Tropepe V,
Twizere JC, Wang Y, Weatheritt RJ, Weile J, Xia Y, Yang X,
Yeger-Lotem E, Zhong Q, Aloy P, Bader GD, De Las Rivas J, Gaudet S,
Hao T, Rak J, Tavernier J, Hill DE, Vidal M, Roth FP and Calderwood
MA.
TITLE A reference map of the human binary protein interactome
JOURNAL Nature 580 (7803), 402-408 (2020)
PUBMED 32296183
REFERENCE 2 (bases 1 to 2444)
AUTHORS Tanaka N, Katayama S, Reddy A, Nishimura K, Niwa N, Hongo H,
Ogihara K, Kosaka T, Mizuno R, Kikuchi E, Mikami S, Miyakawa A,
Arenas E, Kere J, Oya M and Uhlen P.
TITLE Single-cell RNA-seq analysis reveals the platinum resistance gene
COX7B and the surrogate marker CD63
JOURNAL Cancer Med 7 (12), 6193-6204 (2018)
PUBMED 30367559
REMARK GeneRIF: Our results offer a new transcriptome landscape of
platinum-resistance that provides valuable insights into
chemosensitivity and drug resistance in cancers, and we identify a
novel platinum resistance gene, COX7B, and a surrogate marker,
CD63.
REFERENCE 3 (bases 1 to 2444)
AUTHORS Zong S, Wu M, Gu J, Liu T, Guo R and Yang M.
TITLE Structure of the intact 14-subunit human cytochrome c oxidase
JOURNAL Cell Res 28 (10), 1026-1034 (2018)
PUBMED 30030519
REFERENCE 4 (bases 1 to 2444)
AUTHORS Indrieri A, van Rahden VA, Tiranti V, Morleo M, Iaconis D, Tammaro
R, D'Amato I, Conte I, Maystadt I, Demuth S, Zvulunov A, Kutsche K,
Zeviani M and Franco B.
TITLE Mutations in COX7B cause microphthalmia with linear skin lesions,
an unconventional mitochondrial disease
JOURNAL Am J Hum Genet 91 (5), 942-949 (2012)
PUBMED 23122588
REMARK GeneRIF: study analyzed the X-linked COX7B and found deleterious de
novo mutations in two simplex cases of microphthalmia with linear
skin lesions and a nonsense mutation, which segregates with the
disease, in a familial case
REFERENCE 5 (bases 1 to 2444)
AUTHORS Possekel S, Marsac C and Kadenbach B.
TITLE Biochemical analysis of fibroblasts from patients with cytochrome c
oxidase-associated Leigh syndrome
JOURNAL Biochim Biophys Acta 1316 (3), 153-159 (1996)
PUBMED 8781533
REFERENCE 6 (bases 1 to 2444)
AUTHORS Sadlock JE, Lightowlers RN, Capaldi RA and Schon EA.
TITLE Isolation of a cDNA specifying subunit VIIb of human cytochrome c
oxidase
JOURNAL Biochim Biophys Acta 1172 (1-2), 223-225 (1993)
PUBMED 8382530
REFERENCE 7 (bases 1 to 2444)
AUTHORS Morleo,M. and Franco,B.
TITLE Microphthalmia with Linear Skin Defects Syndrome
JOURNAL (in) Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH,
Gripp KW and Amemiya A (Eds.);
GENEREVIEWS(R);
(1993)
PUBMED 20301767
REFERENCE 8 (bases 1 to 2444)
AUTHORS Longoni,M., Pober,B.R. and High,F.A.
TITLE Congenital Diaphragmatic Hernia Overview
JOURNAL (in) Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH,
Gripp KW and Amemiya A (Eds.);
GENEREVIEWS(R);
(1993)
PUBMED 20301533
REFERENCE 9 (bases 1 to 2444)
AUTHORS Van Kuilenburg AB, Van Beeumen JJ, Van der Meer NM and Muijsers AO.
TITLE Subunits VIIa,b,c of human cytochrome c oxidase. Identification of
both 'heart-type' and 'liver-type' isoforms of subunit VIIa in
human heart
JOURNAL Eur J Biochem 203 (1-2), 193-199 (1992)
PUBMED 1309697
REFERENCE 10 (bases 1 to 2444)
AUTHORS Stroh,A. and Kadenbach,B.
TITLE Tissue-specific and species-specific distribution of -SH groups in
cytochrome c oxidase subunits
JOURNAL Eur J Biochem 156 (1), 199-204 (1986)
PUBMED 3007143
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from Z14244.1 and AL356235.22.
This sequence is a reference standard in the RefSeqGene project.
On Jul 13, 2018 this sequence version replaced NM_001866.2.
Summary: Cytochrome c oxidase (COX), the terminal component of the
mitochondrial respiratory chain, catalyzes the electron transfer
from reduced cytochrome c to oxygen. This component is a
heteromeric complex consisting of 3 catalytic subunits encoded by
mitochondrial genes and multiple structural subunits encoded by
nuclear genes. The mitochondrially-encoded subunits function in
electron transfer, and the nuclear-encoded subunits may function in
the regulation and assembly of the complex. This nuclear gene
encodes subunit VIIb, which is highly similar to bovine COX VIIb
protein and is found in all tissues. This gene may have several
pseudogenes on chromosomes 1, 2, 20 and 22. [provided by RefSeq,
Jun 2011].
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: DA173495.1, SRR3476690.694958.1
[ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1965299, SAMEA1966682
[ECO:0000348]
##Evidence-Data-END##
##RefSeq-Attributes-START##
gene product(s) localized to mito. :: reported by MitoCarta
MANE Ensembl match :: ENST00000650309.2/
ENSP00000497474.1
RefSeq Select criteria :: based on single
protein-coding transcript
##RefSeq-Attributes-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-452 Z14244.1 17-468
453-2444 AL356235.22 32749-34740
FEATURES Location/Qualifiers
source 1..2444
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="X"
/map="Xq21.1"
gene 1..2444
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/note="cytochrome c oxidase subunit 7B"
/db_xref="GeneID:1349"
/db_xref="HGNC:HGNC:2291"
/db_xref="MIM:300885"
exon 1..126
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/inference="alignment:Splign:2.1.0"
variation 2
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077114955"
variation 3
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077114965"
variation 8
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1280846573"
variation 10
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077114987"
variation 12
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1411168042"
variation 14
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1354597946"
variation 15
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1328857950"
variation 16..17
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="g"
/db_xref="dbSNP:372770371"
variation 16
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1408644197"
variation 17
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1404814798"
variation 21
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077115059"
variation 22
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1177536032"
variation 24
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782112788"
variation 25
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782647960"
variation 26
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077115099"
misc_feature 27..29
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/note="upstream in-frame stop codon"
variation 27
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:963709282"
variation 30
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1603366738"
variation 33
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1184582569"
variation 37
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1472995139"
variation 39
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1232372681"
variation 40
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:374052875"
variation 45
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:782793919"
variation 48
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077115196"
variation 49
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557220448"
variation 52
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:368265984"
variation 53
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557220449"
variation 54
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322525515"
variation 55
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:946919889"
variation 57
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557220453"
variation 58
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782568175"
variation 59..60
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:2077115261"
variation 61
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:782703625"
variation 63
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:924139812"
variation 65
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077115297"
variation 66
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:11552077"
variation 67
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077115312"
variation 70
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:781788728"
variation 75..76
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1440673337"
variation 80
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:782488046"
variation 81
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782600544"
variation 86
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557220461"
CDS 87..329
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/EC_number="7.1.1.9"
/note="cytochrome-c oxidase chain VIIb; cytochrome c
oxidase subunit 7B, mitochondrial; cytochrome c oxidase
polypeptide VIIb; cytochrome c oxidase subunit VIIb"
/codon_start=1
/product="cytochrome c oxidase subunit 7B, mitochondrial
precursor"
/protein_id="NP_001857.1"
/db_xref="CCDS:CCDS14437.1"
/db_xref="GeneID:1349"
/db_xref="HGNC:HGNC:2291"
/db_xref="MIM:300885"
/translation="
MFPLVKSALNRLQVRSIQQTMARQSHQKRTPDFHDKYGNAVLASGATFCIVTWTYVATQVGIEWNLSPVGRVTPKEWRNQ"
misc_feature 87..323
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/note="Cytochrome C oxidase chain VIIB; Region: COX7B;
pfam05392"
/db_xref="CDD:428452"
transit_peptide 87..158
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/note="Mitochondrion.
/evidence=ECO:0000269|PubMed:1309697; propagated from
UniProtKB/Swiss-Prot (P24311.2)"
mat_peptide 159..326
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/product="Cytochrome c oxidase subunit 7B, mitochondrial.
/id=PRO_0000006158"
/note="propagated from UniProtKB/Swiss-Prot (P24311.2)"
misc_feature 183..263
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/note="propagated from UniProtKB/Swiss-Prot (P24311.2);
transmembrane region"
misc_feature order(186..191,201..203,228..233,243..245,273..275,
288..290,294..296,300..302,306..317)
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/note="Subunit IV/VIIb interface [polypeptide binding];
other site"
/db_xref="CDD:238696"
misc_feature 276..281
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/note="Subunit I/VIIb interfae [polypeptide binding];
other site"
/db_xref="CDD:238696"
misc_feature 315..317
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/note="Subunit VIc/VIIb interface [polypeptide binding];
other site"
/db_xref="CDD:238696"
variation 93
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:370681452"
variation 95
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1557220463"
variation 100
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557220465"
variation 103
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1337924791"
variation 105
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1557220467"
variation 107
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:782218608"
variation 110
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077115425"
variation 111
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1557220469"
variation 117
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077115450"
exon 127..251
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/inference="alignment:Splign:2.1.0"
variation 127
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:781898266"
variation 130
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077123474"
variation 134
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:61752458"
variation 140
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782572549"
variation 141
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:397514585"
variation 147
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781794203"
variation 154
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374767785"
variation 157
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782609880"
variation 160
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1400071124"
variation 161
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782264229"
variation 171
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:367723477"
variation 172
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782685682"
variation 175
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782279552"
variation 177
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782303080"
variation 178
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:781962321"
variation 183
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077123722"
variation 191
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782074964"
variation 192
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1177820943"
variation 193
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782304953"
variation 197
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557220734"
variation 198
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:781987663"
variation 203
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782719518"
variation 206
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557220737"
variation 223
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557220738"
variation 224
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210386350"
variation 225
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2077123920"
variation 226
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:781928139"
variation 227
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557220740"
variation 230
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:371924096"
variation 234
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:781807328"
variation 239
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782050272"
variation 242
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:782763224"
variation 250
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1275827355"
variation 251
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:141779813"
exon 252..2444
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/inference="alignment:Splign:2.1.0"
variation 255
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:782772132"
variation 256
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557221011"
variation 259
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1695055814"
variation 260
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:781986371"
variation 266
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782173769"
variation 281..282
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:397514583"
variation 282
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:782099149"
variation 286
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077131067"
variation 287
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369762465"
variation 303
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1603367347"
variation 304
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1294019831"
variation 308
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077131100"
variation 311
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2149034194"
variation 318
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232699344"
variation 319
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1354758165"
variation 320
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557221017"
variation 321
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:781812051"
variation 325
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:782483005"
variation 328
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557221022"
variation 329
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077131235"
variation 334
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781818697"
variation 340
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557221025"
variation 341
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557221027"
variation 342
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:781863218"
variation 343
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557221030"
variation 344
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557221031"
variation 348
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077131363"
variation 358..360
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:782525847"
variation 361..366
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:1345550472"
variation 361
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373951997"
variation 366
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2077131437"
variation 370
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557221035"
variation 374
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1398558729"
variation 376
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782477129"
variation 377
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1569548490"
variation 378
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1557221039"
variation 379
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077131534"
variation 380
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1557221040"
variation 387
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782235659"
variation 395
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:3190122"
variation 396
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077131590"
variation 403
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077131603"
variation 408
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1603367360"
variation 411
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:41304464"
variation 414
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077131665"
variation 415
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1460411652"
variation 417
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416428829"
variation 418
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1188790593"
variation 423
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1557221045"
regulatory 430..435
/regulatory_class="polyA_signal_sequence"
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/note="hexamer: AATAAA"
variation 433
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2149034227"
variation 436
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1241864113"
variation 448
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1036220636"
polyA_site 453
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/note="major polyA site"
variation 453
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1273985439"
variation 458
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077131773"
variation 459
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1213148868"
variation 460
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332759932"
variation 462..468
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="ttt"
/replace="tttgttt"
/db_xref="dbSNP:2077131795"
variation 471
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077131811"
variation 474
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2077131823"
variation 476
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1557221047"
variation 483
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="c"
/db_xref="dbSNP:1271256842"
variation 484
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782483712"
variation 487
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077131874"
variation 491
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:933147444"
variation 498
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077131891"
variation 501
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:34170405"
variation 503
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1362443424"
variation 508
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2077131941"
variation 509
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077131954"
variation 514
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1269406275"
variation 518
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2077131977"
variation 523
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1428323849"
variation 528..538
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="gct"
/replace="gctgtgcagct"
/db_xref="dbSNP:1372738837"
variation 529
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1603367372"
variation 533
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1755507287"
variation 536..538
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="gct"
/db_xref="dbSNP:2077132039"
variation 540
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1603367374"
variation 545
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557221057"
variation 547
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="a"
/db_xref="dbSNP:2077132092"
variation 547
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2077132081"
variation 547
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2149034250"
variation 548..549
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2077132123"
variation 548
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1603367376"
variation 549
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1173217901"
variation 550..576
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="tttttttt"
/replace="ttttttttttt"
/replace="tttttttttttt"
/replace="ttttttttttttt"
/replace="tttttttttttttt"
/replace="ttttttttttttttt"
/replace="tttttttttttttttt"
/replace="ttttttttttttttttt"
/replace="tttttttttttttttttt"
/replace="ttttttttttttttttttt"
/replace="tttttttttttttttttttt"
/replace="ttttttttttttttttttttt"
/replace="tttttttttttttttttttttt"
/replace="ttttttttttttttttttttttt"
/replace="tttttttttttttttttttttttt"
/replace="ttttttttttttttttttttttttt"
/replace="tttttttttttttttttttttttttt"
/replace="ttttttttttttttttttttttttttt"
/replace="tttttttttttttttttttttttttttt"
/replace="ttttttttttttttttttttttttttttt"
/replace="tttttttttttttttttttttttttttttt"
/replace="ttttttttttttttttttttttttttttttt"
/replace="tttttttttttttttttttttttttttttttt"
/replace="ttttttttttttttttttttttttttttttttttt"
/db_xref="dbSNP:rs34296412"
variation 550
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557221059"
variation 552..553
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="g"
/db_xref="dbSNP:2077132305"
variation 553
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1349769578"
variation 554..555
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="g"
/db_xref="dbSNP:1557221064"
variation 555..556
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="g"
/db_xref="dbSNP:1439673582"
variation 555
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1847380770"
variation 556
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1368290065"
variation 557
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077132368"
variation 558
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077132379"
variation 559..560
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="g"
/db_xref="dbSNP:2077132413"
variation 559
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:113844181"
variation 560
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1051958504"
variation 561
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077132434"
variation 562
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077132449"
variation 564
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077132460"
variation 567..577
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="ttttttttttg"
/db_xref="dbSNP:2077132479"
variation 571..577
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="ttttttg"
/db_xref="dbSNP:1803122689"
variation 573..577
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="ttttg"
/db_xref="dbSNP:2077132488"
variation 574
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077132504"
variation 575..577
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="ttg"
/db_xref="dbSNP:1646156467"
variation 575
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:888832331"
variation 576..577
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="tg"
/replace="ttg"
/replace="tttg"
/db_xref="dbSNP:1491331761"
variation 576..577
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="tg"
/db_xref="dbSNP:1491487258"
variation 576
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007655319"
variation 577..579
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1396045407"
variation 577
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1173291205"
variation 578
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1603367386"
variation 580
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="a"
/db_xref="dbSNP:1452840959"
variation 580
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077132617"
variation 581
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077132637"
variation 582
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410372215"
variation 585
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077132671"
variation 587
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2149034277"
variation 589
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2149034278"
variation 595
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1177864801"
variation 601
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1480310067"
variation 602
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1232293341"
variation 603..604
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:34245696"
variation 603
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1031976969"
variation 610..612
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="gtg"
/replace="gtgtg"
/db_xref="dbSNP:1280825428"
variation 612
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1233232919"
variation 613
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1345311626"
variation 630
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1308614971"
variation 633
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1223921517"
variation 635
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077132812"
variation 637
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077132824"
variation 638
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:781806514"
variation 643
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077132851"
variation 646
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:147413588"
variation 648
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1557221073"
variation 654
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370974511"
variation 658
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1376551124"
variation 666
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782385284"
variation 669
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2077132937"
variation 672..675
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="tc"
/replace="tctc"
/db_xref="dbSNP:1433180518"
variation 678
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077132957"
variation 683
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:967549286"
variation 684
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077132985"
variation 688
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077132995"
variation 691
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:981571057"
variation 693
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1160095507"
variation 694
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1418631485"
variation 697
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077133050"
variation 699
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1405850610"
variation 705
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077133072"
variation 706
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557221079"
variation 711
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1190112135"
variation 712
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077133112"
variation 713
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="g"
/db_xref="dbSNP:2077133124"
variation 715
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1476161689"
variation 716
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077133146"
variation 719
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1036203671"
variation 725
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077133172"
variation 726..739
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="ttttttttt"
/replace="ttttttttttt"
/replace="tttttttttttt"
/replace="ttttttttttttt"
/replace="tttttttttttttt"
/replace="ttttttttttttttt"
/replace="tttttttttttttttt"
/db_xref="dbSNP:rs782016968"
variation 740
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1216035855"
variation 741
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2077133226"
variation 744
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1315852630"
variation 745
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285948645"
variation 746
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2149034308"
variation 750..756
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="ctc"
/replace="ctcactc"
/db_xref="dbSNP:1234534910"
variation 752
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1356668213"
variation 756
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077133273"
variation 758
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077133282"
variation 761
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1293140646"
variation 765
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077133313"
variation 772
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077133329"
variation 782
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1413391619"
variation 783
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1364499584"
variation 790
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1289712233"
variation 791
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:958790286"
variation 794
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077133397"
variation 801
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1343609766"
variation 805
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077133425"
variation 806
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1167209526"
variation 807
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:991970624"
variation 809
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:113865300"
variation 813
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375779946"
variation 814
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:971989079"
variation 815
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:112317103"
variation 816
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077133500"
variation 823
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1263546378"
variation 824
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1186849409"
variation 825
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1485352996"
variation 831
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077133555"
variation 843
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1265784519"
variation 844
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1215018798"
variation 845
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:781932188"
variation 846
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:5912528"
variation 848
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1309741639"
variation 853
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2077133649"
variation 856
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077133656"
variation 859
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296775132"
variation 868
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1603367415"
variation 869
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:782753110"
variation 870
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077133689"
variation 871
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077133695"
variation 873
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2149034344"
variation 881
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1363292114"
variation 882
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1328168902"
variation 884
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441811727"
variation 886
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077133736"
variation 887
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393804435"
variation 893
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1164173830"
variation 896..900
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1374675163"
variation 896
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1051580445"
variation 904
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:781975345"
variation 906
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1245883032"
variation 908
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1195095618"
variation 909
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557221110"
variation 910
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:943160254"
variation 912
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1251874041"
variation 913
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:371154733"
variation 922
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077133856"
variation 929
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782387241"
variation 935
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1252335430"
variation 936
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557221115"
variation 940
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1227244099"
variation 941
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1340465456"
variation 943
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1305962372"
variation 954
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077133966"
variation 955
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077133977"
variation 956
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1603367428"
variation 957
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235257389"
variation 962
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370474139"
variation 972
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134020"
variation 975
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077134030"
variation 976
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782808597"
variation 982
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1321693183"
variation 989
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134063"
variation 990
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2077134073"
variation 999
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393154010"
variation 1004
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:182439104"
variation 1007..1015
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="ccg"
/replace="ccgtgcccg"
/db_xref="dbSNP:1891498838"
variation 1008
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782606518"
variation 1009
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:903415408"
variation 1012
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1388062136"
variation 1013
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077134122"
variation 1014
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1175241426"
variation 1015
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1003057262"
variation 1019
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1394043968"
variation 1025
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134155"
variation 1029
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1196142515"
variation 1041
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077134170"
variation 1042..1043
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="ag"
/db_xref="dbSNP:2077134182"
variation 1042
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134175"
variation 1044
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:782232649"
variation 1045
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:959110180"
variation 1046
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:782313731"
variation 1048
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:782461448"
variation 1053
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1482303068"
variation 1061
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1282948866"
variation 1073
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134258"
variation 1075
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1211981809"
variation 1080
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1347445369"
variation 1081
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1273232814"
variation 1083
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077134292"
variation 1094..1095
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1241354419"
variation 1095
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374108380"
variation 1096
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307673677"
variation 1098
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:781841335"
variation 1100
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1368581805"
variation 1101
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1314510184"
variation 1109
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1435034705"
variation 1110
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1401140863"
variation 1113
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134374"
variation 1117
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1170433487"
variation 1119
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:963356300"
variation 1121
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134397"
variation 1124
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1470907185"
variation 1126
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077134415"
variation 1128
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1363843065"
variation 1130
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2048360436"
variation 1132
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077134432"
variation 1133
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:149547415"
variation 1135
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077134462"
variation 1137
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782532641"
variation 1140
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2149034411"
variation 1141
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:954598889"
variation 1142
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782659451"
variation 1143
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134500"
variation 1145
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134507"
variation 1147
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077134516"
variation 1153
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1212048198"
variation 1158
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134533"
variation 1164
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1485544803"
variation 1168
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077134548"
variation 1171
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1276840544"
variation 1173
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077134567"
variation 1174
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1207093814"
variation 1176
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557221137"
variation 1190
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1351543114"
variation 1194
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1260244975"
variation 1200
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077134602"
variation 1205
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:76994739"
variation 1211
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134620"
variation 1220
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:187063502"
variation 1223
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:191984170"
variation 1224
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2149034431"
variation 1231
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557221142"
variation 1233
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077134655"
variation 1234
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2077134667"
variation 1235
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134678"
variation 1246
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557221144"
variation 1248
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782421236"
variation 1249
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1226592359"
variation 1251
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1348566081"
variation 1252
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782564948"
variation 1253
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077134732"
variation 1258
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:987780232"
variation 1259
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415230025"
variation 1260
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1339631800"
variation 1284
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:910407960"
variation 1286
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:943193344"
variation 1287
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077134794"
variation 1289
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402118563"
variation 1295
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1385163704"
variation 1299
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134810"
variation 1305
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1157787856"
variation 1306
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:182827283"
variation 1309
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189248268"
variation 1311
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1475111544"
variation 1313
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1603367455"
variation 1315
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077134851"
variation 1321
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236052187"
variation 1322
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134859"
variation 1324
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077134865"
variation 1326
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134872"
variation 1335
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1195720897"
variation 1338
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:568997577"
variation 1343
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077134892"
variation 1349
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1447816420"
variation 1353
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1557221151"
variation 1357
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077134916"
variation 1369
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1603367459"
variation 1376..1385
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="aaa"
/replace="aaaacttaaa"
/db_xref="dbSNP:2077134937"
variation 1376
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134933"
variation 1378..1384
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="aa"
/replace="aacttaa"
/db_xref="dbSNP:1261224405"
variation 1378
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134946"
variation 1380
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2040034973"
variation 1383..1385
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="aa"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:782084868"
variation 1384..1394
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="aagtgtcacca"
/db_xref="dbSNP:2077134976"
variation 1384
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077134968"
variation 1387
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="t"
/replace="tttt"
/db_xref="dbSNP:1233794064"
variation 1400
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1355506781"
variation 1405
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:185627327"
variation 1406
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1432565638"
variation 1411
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077135033"
variation 1414
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077135045"
variation 1416
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1326660538"
variation 1424..1426
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1557221155"
variation 1429
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1319466167"
variation 1430
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:190089774"
variation 1434..1435
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2077135097"
variation 1435..1443
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="ctgtctgaa"
/db_xref="dbSNP:2077135122"
variation 1435
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1603367467"
variation 1437..1444
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="gtctgaag"
/db_xref="dbSNP:2077135133"
variation 1437
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782234876"
variation 1444
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:945044879"
variation 1446
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1767659985"
variation 1449
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077135152"
variation 1452
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1432328058"
variation 1454
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557221157"
variation 1456
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:782137660"
variation 1459
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557221158"
variation 1461
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557221159"
variation 1462
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077135225"
variation 1463..1464
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="a"
/db_xref="dbSNP:1405321530"
variation 1464
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1412190152"
variation 1465
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077135251"
variation 1467
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:782409270"
variation 1480
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077135289"
variation 1484
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077135298"
variation 1490
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1475944315"
variation 1491
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782040995"
variation 1493
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077135327"
variation 1503..1538
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="tttcatcatattagggatgtttatgatgttattaaa"
/db_xref="dbSNP:2077135334"
variation 1504..1508
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="t"
/replace="ttcat"
/db_xref="dbSNP:1247706336"
variation 1507
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1557221162"
variation 1516
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1186891006"
variation 1517
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1569548503"
variation 1522
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469912771"
variation 1531
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2077135387"
variation 1548
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077135396"
variation 1549
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1253742108"
variation 1558
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:906187010"
variation 1560
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077135431"
variation 1572
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1450975538"
variation 1573
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782052371"
variation 1574
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1216174428"
variation 1576
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:782732580"
variation 1579
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077135480"
variation 1580
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077135490"
variation 1582
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:781959870"
variation 1587
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1225689316"
variation 1591
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782102938"
variation 1594
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077135527"
variation 1595
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077135546"
variation 1599
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1557221170"
variation 1602
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1372669911"
variation 1603
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1057504314"
variation 1604
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077135585"
variation 1606
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:112445268"
variation 1607
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1013468435"
variation 1623..1631
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="attatt"
/replace="attattatt"
/db_xref="dbSNP:1557221173"
variation 1625
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1016303875"
variation 1632
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1331444083"
variation 1633
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557221177"
variation 1635
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410931884"
variation 1636..1641
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="tata"
/replace="tatata"
/db_xref="dbSNP:2149034524"
variation 1638
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077135678"
variation 1641
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:963406012"
variation 1644
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1167059076"
variation 1645
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:993472190"
variation 1648
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557221180"
variation 1654
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2077135728"
variation 1662
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2149034527"
variation 1665
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077135736"
variation 1673
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077135746"
variation 1675
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077135755"
variation 1681
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077135764"
variation 1682
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395856298"
variation 1683..1685
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:2077135777"
variation 1686
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1190686046"
variation 1691
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077135796"
variation 1692
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1477077353"
variation 1694..1700
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="ttt"
/replace="tttcttt"
/db_xref="dbSNP:2077135816"
variation 1698..1704
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="ttt"
/replace="tttgttt"
/db_xref="dbSNP:1244965767"
variation 1699
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1206510917"
variation 1700
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1483282912"
variation 1702..1712
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="ttttt"
/replace="tttttcttttt"
/db_xref="dbSNP:2077135861"
variation 1707
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077135879"
variation 1708
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077135891"
variation 1717
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1273685795"
variation 1721
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2077135911"
variation 1724..1730
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="ctc"
/replace="ctcactc"
/db_xref="dbSNP:781871802"
variation 1730
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:782143426"
variation 1731..1733
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:2077135952"
variation 1737
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077135960"
variation 1740
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:536036772"
variation 1743
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1303688084"
variation 1745
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077135993"
variation 1752
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1218191706"
variation 1777
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077136015"
variation 1778
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1364848484"
variation 1787
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077136043"
variation 1788
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:987443315"
variation 1789
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370435494"
variation 1800
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1557221195"
variation 1801..1802
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:2077136087"
variation 1803
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077136100"
variation 1804
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557221198"
variation 1805
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306579519"
variation 1808
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1603367489"
variation 1809
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:910450905"
variation 1816
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077136138"
variation 1829..1830
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2077136150"
variation 1830
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077136159"
variation 1831
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1376362285"
variation 1834
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077136176"
variation 1835
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077136183"
variation 1840
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:964582581"
variation 1841
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:782800944"
variation 1842
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1472889703"
variation 1849
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250909195"
variation 1854
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1179834642"
variation 1856
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486522814"
variation 1857
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1256276939"
variation 1860
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1208955321"
variation 1861
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1310037915"
variation 1862
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1285778106"
variation 1863
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1223801389"
variation 1868
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2149034570"
variation 1871..1875
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:2077136294"
variation 1876
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1350413560"
variation 1877
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077136308"
variation 1883
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:781787116"
variation 1884
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2077136324"
variation 1887
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:945139266"
variation 1894
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782683429"
variation 1898
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077136352"
variation 1902
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077136365"
variation 1903
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302527919"
variation 1906
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077136385"
variation 1907
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077136392"
variation 1911
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1042144009"
variation 1919
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1464759811"
variation 1926
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557221209"
variation 1933
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:782065373"
variation 1934
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1159940457"
variation 1937
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782786451"
variation 1940
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1557221211"
variation 1941
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695157257"
variation 1964
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1603367501"
variation 1966
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1456773321"
variation 1967
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1603367502"
variation 1972
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077136499"
variation 1974
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1057385548"
variation 1983
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1156832516"
variation 1985
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1476088248"
variation 1986
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557221218"
variation 1987
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782444287"
variation 1988
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1013102491"
variation 1990
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1482080965"
variation 1991
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1208879084"
variation 1992
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782599468"
variation 1993
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:144154269"
variation 1997
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077136600"
variation 2001
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1603367512"
variation 2004
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782497922"
variation 2011
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:899326130"
variation 2012
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1312487783"
variation 2019
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077136646"
variation 2025
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:993565405"
variation 2026
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557221228"
variation 2028
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1364355517"
variation 2029..2048
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="gt"
/replace="gtctgtggtagttgttttgt"
/db_xref="dbSNP:1557221229"
variation 2036
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026352274"
variation 2038
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:890492940"
variation 2039..2044
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="gtt"
/replace="gttgtt"
/db_xref="dbSNP:201073519"
variation 2039
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077136731"
variation 2040..2056
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="ttgtttt"
/replace="ttgttttgtttt"
/replace="ttgttttgttttgtttt"
/db_xref="dbSNP:376638679"
variation 2041..2053
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="tgttttgttttgt"
/replace="tgttttgttttgtgttttgttttgt"
/db_xref="dbSNP:1368928437"
variation 2041
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1163815087"
variation 2042
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2149034611"
variation 2043..2063
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="ttttgtttt"
/replace="ttttgttttgttttttgtttt"
/db_xref="dbSNP:1421827747"
variation 2044
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077136826"
variation 2047
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1421276108"
variation 2052
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="g"
/db_xref="dbSNP:202036735"
variation 2052
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1464077918"
variation 2053..2058
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="tttttt"
/replace="ttttttt"
/db_xref="dbSNP:1188774932"
variation 2053
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1245700206"
variation 2054
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2077136900"
variation 2055
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1214960944"
variation 2059
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="g"
/db_xref="dbSNP:1489100198"
variation 2059
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1009278157"
variation 2060..2069
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="ttttttttt"
/replace="tttttttttt"
/replace="ttttttttttt"
/replace="tttttttttttt"
/db_xref="dbSNP:1265301963"
variation 2060
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1298659306"
variation 2064
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1017542410"
variation 2065
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1328026899"
variation 2070
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1387361646"
variation 2072
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:187902206"
variation 2078
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1391448197"
variation 2081
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1292855232"
variation 2084
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:964958725"
variation 2085
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1456241393"
variation 2087
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356026109"
variation 2088
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1168943585"
variation 2098
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557221245"
variation 2103
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448522513"
variation 2113
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:989385537"
variation 2131
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077137202"
variation 2137
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077137213"
variation 2140
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782498554"
variation 2142
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:192192967"
variation 2145
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077137254"
variation 2146
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1783483427"
variation 2153
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:966532058"
variation 2162
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782645845"
variation 2163
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:927666304"
variation 2171
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077137319"
variation 2176
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1208547378"
variation 2182
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1481883844"
variation 2185
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1275831882"
variation 2189
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1204818573"
variation 2190
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1340311684"
variation 2200
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077137402"
variation 2206
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:182740973"
variation 2209
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:990867161"
variation 2212
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1234124490"
variation 2213
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1557221258"
variation 2222
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:781819740"
variation 2224
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1330569799"
variation 2234
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077137458"
variation 2244
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1300551135"
variation 2251
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385035680"
variation 2255
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077137495"
variation 2256
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352204417"
variation 2257
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="t"
/db_xref="dbSNP:2077137537"
variation 2257
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1308424571"
variation 2266
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077137553"
variation 2270..2284
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="agttgcaagtttagt"
/replace="agttgcaagtttagttgcaagtttagt"
/db_xref="dbSNP:1428789225"
variation 2275
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368387270"
variation 2276
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077137605"
variation 2283
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077137620"
variation 2287
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1175105575"
variation 2288
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782582689"
variation 2289
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1376605304"
variation 2292
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077137688"
variation 2295
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1196071956"
variation 2300..2301
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="ct"
/db_xref="dbSNP:2077137720"
variation 2303
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2077137736"
variation 2308
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077137749"
variation 2318
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:916176544"
variation 2319
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1603367547"
variation 2320
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1253086986"
variation 2341
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1482272774"
variation 2342
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077137823"
variation 2348
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1282792481"
variation 2350
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:949016239"
variation 2356
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:782494173"
variation 2363
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077137874"
variation 2366
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1557221278"
variation 2367
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077137889"
variation 2368..2369
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="tt"
/db_xref="dbSNP:2077137908"
variation 2369
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1344525800"
variation 2370
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1254354329"
variation 2371..2379
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="ataca"
/replace="atacataca"
/db_xref="dbSNP:1241201129"
variation 2371
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077137928"
variation 2373
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352259918"
variation 2376
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1037899261"
variation 2377
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:782583898"
variation 2378
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2077137982"
variation 2380
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077138005"
variation 2381
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:929466736"
variation 2388
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:554247601"
variation 2389
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077138064"
variation 2390
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:890495014"
variation 2393
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077138095"
variation 2394
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1396273089"
variation 2395..2398
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="gaag"
/db_xref="dbSNP:1557221283"
variation 2397
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1008914359"
variation 2401..2407
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="aaa"
/replace="aaataaa"
/db_xref="dbSNP:2077138150"
regulatory 2402..2407
/regulatory_class="polyA_signal_sequence"
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/note="hexamer: AATAAA"
variation 2409..2410
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace=""
/replace="at"
/db_xref="dbSNP:1170306322"
variation 2409
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1458357819"
variation 2410
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077138208"
variation 2414
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077138225"
variation 2417
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1159042724"
variation 2419
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471836858"
variation 2423
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1260086659"
variation 2424
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:187665567"
polyA_site 2429
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
variation 2429
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1188616342"
variation 2430
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2077138285"
variation 2431
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077138303"
variation 2434
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2077138316"
variation 2439
/gene="COX7B"
/gene_synonym="APLCC; LSDMCA2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442074648"
ORIGIN
gtttttcagctcacttcaagggtacctgaagcgaattggcaccaaagcagcagctgtattgccgcagttctagcttcaccttcacgatgtttcccttggtcaaaagcgcactaaatcgtctccaagttcgaagcattcagcaaacaatggcaaggcagagccaccagaaacgtacacctgattttcatgacaaatacggtaatgctgtattagctagtggagccactttctgtattgttacatggacatatgtagcaacacaagtcggaatagaatggaacctgtcccctgttggcagagttaccccaaaggaatggaggaatcagtaatcatcccagctggtgtaataatgaattgtttaaaaaacagctcataattgatgccaaattaaagcactgtgtacccattaagatatggcattattgaagaaataaagtacatttgaaaccttcattgtaggttttgtttctttgtaaatgaaactaagcttgatcactttagcctttatgttaatattaaagtcaaatgctgtgcagcttcttaaataggtttttttttttttttttttttttttttgggacgaagtctcactttgtcccccaggctggagtgcagtggcaccatctcagctcactgcgacctctgcctcctgagttcaagtgattctcctgtctcagcctcccgagtagccagaactacaggcacatgccatgacgcccagctaattttttttttttttgagacggagtctcactctgttgcccaggctggaatgcaatggcgtgatctcggctcctgcaacctccgcctcccgggttcaagcgattctcctgtctcagccttccaagtagctgggattacaggtgcacgccaccaggcccggctaatttttgtatttttagtagagacggggtttcaccatgttggtcaggctggtctcgagctcctgatctcgtgatccacccaccttggtctcccaaagtgctgggattacaggtgtgagccaccgtgcccggcaatttttgtatttttagtagagacagggtttcaccatattggtcaggctggtttcaaactcacgacctcaggtgatccgcctgccttggcctcccaaagtggtaggattacaggcgtgagccacggcacccagcccttaaatggcttttatgaggtaatgtgaaaggaaaatttgcctttgacctggaagtcaactttatagtaagctgaaattataaataactgatcatggaactattgcagatcacctttgagccaaaaatttggcctggattttggttatgcctactactatgtgcctctcatttgtatttatacctggaattggcattattaactccttttcactcctgcctagaaaacttaaagtgtcaccagacccaagggcggagtggtcctataaaacaaactcgtagcctgtctgaagactagctactagctccttggctgttttggcatattcatcttgattatagctcttggtctttcatcatattagggatgtttatgatgttattaaagaaaatcttgtcaaatgcagtctgttcctagttatctactatcagtcacctgttgtataattataacaatgtttggatttgtggattattattttagtatataacattggattttatgtatgttacctgaagaagagcaatatctgtaccacatatttctttgtttttcttttttgagatgaagtctcactctgttgcccaggctggagtgcagtggtgtgatcttgacacactgcaacctttgcctcccggattcaagtgattctcctgtctcagcctccctagtaactggaattacaggcgcctgccaccatgcctggctaatttttgtatttttagtagagatggggtttcaccatgttggccaacctggtcttgaactcctgacctcaggcgatccacccacctcagcctcccaaagtgctaggcttacaggcatgagacaccgcgcccggcttatatatcattactttcttggctgagagctgtagtctgtggtagttgttttgttttgttttttgttttttttttgtagttttcttgatcgtgatcaattaagcagaaagtagaatttcagtcaggtaacctgtctatattagctaaattatcttttgcttattacatagagtgctagaagtatgctgtcatggcatatgtcctagtttctcatcaaatggaccaaagtcagtgattttatttgaagaggaaaaattgaacgtcattgtaaattaagttgcaagtttagtaaccatattgtaccactgtttgataaatttgaacgctttatggtatttcatatttagaatgttcaaaatagtactgaagtattcaaatacatacaaccctgagcgatattgaagtaaaataaacatgtatttaaggaagtgtcaaccttcaattatatac
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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