ver.2
Home
|
Help
|
Advanced search
Previous release (v1)
2024-05-04 10:48:12, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001277200 822 bp mRNA linear PRI 08-JAN-2023
DEFINITION Homo sapiens cornichon family AMPA receptor auxiliary protein 4
(CNIH4), transcript variant 5, mRNA.
ACCESSION NM_001277200
VERSION NM_001277200.2
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 822)
AUTHORS Zhang H, Lin Y, Zhuang M, Zhu L, Dai Y and Lin M.
TITLE Screening and identification of CNIH4 gene associated with cell
proliferation in gastric cancer based on a large-scale CRISPR-Cas9
screening database DepMap
JOURNAL Gene 850, 146961 (2023)
PUBMED 36220450
REMARK GeneRIF: Screening and identification of CNIH4 gene associated with
cell proliferation in gastric cancer based on a large-scale
CRISPR-Cas9 screening database DepMap.
REFERENCE 2 (bases 1 to 822)
AUTHORS Liu H and Li Y.
TITLE Potential roles of Cornichon Family AMPA Receptor Auxiliary Protein
4 (CNIH4) in head and neck squamous cell carcinoma
JOURNAL Cancer Biomark 35 (4), 439-450 (2022)
PUBMED 36404537
REMARK GeneRIF: Potential roles of Cornichon Family AMPA Receptor
Auxiliary Protein 4 (CNIH4) in head and neck squamous cell
carcinoma.
REFERENCE 3 (bases 1 to 822)
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 4 (bases 1 to 822)
AUTHORS Chen S, Li T, Zhao Q, Xiao B and Guo J.
TITLE Using circular RNA hsa_circ_0000190 as a new biomarker in the
diagnosis of gastric cancer
JOURNAL Clin Chim Acta 466, 167-171 (2017)
PUBMED 28130019
REMARK GeneRIF: hsa_circ_0000190 (gene symbol is CNIH4) may be a novel
non-invasive biomarker for the diagnosis of gastric cancer
REFERENCE 5 (bases 1 to 822)
AUTHORS Sauvageau E, Rochdi MD, Oueslati M, Hamdan FF, Percherancier Y,
Simpson JC, Pepperkok R and Bouvier M.
TITLE CNIH4 interacts with newly synthesized GPCR and controls their
export from the endoplasmic reticulum
JOURNAL Traffic 15 (4), 383-400 (2014)
PUBMED 24405750
REFERENCE 6 (bases 1 to 822)
AUTHORS Wray NR, Pergadia ML, Blackwood DH, Penninx BW, Gordon SD, Nyholt
DR, Ripke S, MacIntyre DJ, McGhee KA, Maclean AW, Smit JH, Hottenga
JJ, Willemsen G, Middeldorp CM, de Geus EJ, Lewis CM, McGuffin P,
Hickie IB, van den Oord EJ, Liu JZ, Macgregor S, McEvoy BP, Byrne
EM, Medland SE, Statham DJ, Henders AK, Heath AC, Montgomery GW,
Martin NG, Boomsma DI, Madden PA and Sullivan PF.
TITLE Genome-wide association study of major depressive disorder: new
results, meta-analysis, and lessons learned
JOURNAL Mol Psychiatry 17 (1), 36-48 (2012)
PUBMED 21042317
REFERENCE 7 (bases 1 to 822)
AUTHORS Simpson JC, Wellenreuther R, Poustka A, Pepperkok R and Wiemann S.
TITLE Systematic subcellular localization of novel proteins identified by
large-scale cDNA sequencing
JOURNAL EMBO Rep 1 (3), 287-292 (2000)
PUBMED 11256614
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
DA185135.1, HY145928.1 and BQ575976.1.
On Jun 1, 2019 this sequence version replaced NM_001277200.1.
Transcript Variant: This variant (5) uses an alternate downstream
exon in place of the last exon of variant 1. The resulting isoform
(5) has a shorter and distinct C-terminus compared to isoform 1.
##Evidence-Data-START##
Transcript exon combination :: BQ575976.1, BI196635.1 [ECO:0000332]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-8 DA185135.1 69-76
9-494 HY145928.1 2-487
495-822 BQ575976.1 16-343 c
FEATURES Location/Qualifiers
source 1..822
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="1"
/map="1q42.11"
gene 1..822
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/note="cornichon family AMPA receptor auxiliary protein 4"
/db_xref="GeneID:29097"
/db_xref="HGNC:HGNC:25013"
/db_xref="MIM:617483"
exon 1..115
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="t"
/db_xref="dbSNP:1178098067"
variation 2
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="t"
/db_xref="dbSNP:1156331026"
variation 3
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1672126086"
variation 5
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:777482220"
variation 7
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:756893076"
variation 8
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:868263888"
variation 9..11
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:747077136"
variation 9
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:902322076"
variation 10
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672126550"
variation 11
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:745335191"
variation 12
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1462831043"
variation 13
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1672126666"
misc_feature 14..16
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/note="upstream in-frame stop codon"
variation 14
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1672126727"
variation 15
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:999373921"
variation 17
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1394925801"
variation 18
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1391388274"
variation 19
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1330023862"
variation 21
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672127405"
variation 22
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:559260881"
variation 23
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:1672127544"
variation 25
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1352665559"
variation 26
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779449187"
variation 27
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1672127833"
variation 30
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748630041"
variation 32
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:772710126"
variation 33
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745341397"
variation 34
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:2102844290"
variation 35
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1558392558"
variation 36..53
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="ggaggaggaggatggagg"
/replace="ggaggaggaggatggaggaggaggatggagg"
/db_xref="dbSNP:1672128500"
variation 36..47
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="ggaggagga"
/replace="ggaggaggagga"
/replace="ggaggaggaggagga"
/db_xref="dbSNP:768665444"
variation 36
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:936885361"
variation 37
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:773706546"
variation 39
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1197947671"
variation 40
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:530246814"
variation 43
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163239009"
variation 44
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:771248464"
variation 45
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1181926021"
variation 46
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672129086"
CDS 47..460
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/note="isoform 5 is encoded by transcript variant 5;
protein cornichon homolog 4"
/codon_start=1
/product="protein cornichon homolog 4 isoform 5"
/protein_id="NP_001264129.1"
/db_xref="CCDS:CCDS60429.1"
/db_xref="GeneID:29097"
/db_xref="HGNC:HGNC:25013"
/db_xref="MIM:617483"
/translation="
MEAVVFVFSLLDCCALIFLSVYFIITLSDLECDYINARSCCSKLNKWVIPELIGHTIVTVLLLMSLHWFIFLLNLPVATWNIYRYIMVPSGNMGVFDPTEIHNRGQLKSHMKEAMIKLGFHLLCFFMYLYSGSNCPC"
misc_feature 53..436
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/note="Cornichon protein; Region: Cornichon; pfam03311"
/db_xref="CDD:427237"
misc_feature 59..121
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/note="propagated from UniProtKB/Swiss-Prot (Q9P003.1);
transmembrane region"
misc_feature 215..277
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/note="propagated from UniProtKB/Swiss-Prot (Q9P003.1);
transmembrane region"
variation 47
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201055685"
variation 49
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1672129276"
variation 51
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:1012204347"
variation 53
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:776873507"
variation 54
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:12123896"
variation 55..56
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1672129928"
variation 55
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752728512"
variation 56
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:1177831448"
variation 57
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1672130094"
variation 58
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1406119227"
variation 59
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:942741263"
variation 60
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:372251807"
variation 62
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199803522"
variation 64
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:367704082"
variation 67
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1310706780"
variation 68
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:2102844413"
variation 69..76
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="tctctctc"
/replace="tctctctctc"
/db_xref="dbSNP:776910171"
variation 70
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750040168"
variation 72
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:755731202"
variation 74
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779548938"
variation 76
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748814839"
variation 79
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:141928208"
variation 81
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:141888425"
variation 82
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1558392688"
variation 85
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:114855926"
variation 86
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:776872569"
variation 87
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672132179"
variation 88
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:780233335"
variation 89
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1286818383"
variation 91
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1432264233"
variation 94
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769981324"
variation 97
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:1558392715"
variation 98..99
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace=""
/replace="tt"
/db_xref="dbSNP:1558392722"
variation 100
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:775629488"
variation 101..105
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="ctctc"
/replace="ctctctc"
/db_xref="dbSNP:1558392733"
variation 101
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1477713911"
variation 103
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1672133087"
variation 105
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:763071837"
variation 106
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1672133296"
variation 109
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432043863"
variation 115
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:1672133479"
exon 116..184
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/inference="alignment:Splign:2.1.0"
variation 116
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1353247400"
variation 118
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1366550493"
variation 123
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247011037"
variation 126..131
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="tg"
/replace="tgtctg"
/db_xref="dbSNP:767531867"
variation 127
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:113066197"
variation 136
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1394100063"
variation 139
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:761667696"
variation 141
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:767420548"
variation 143
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1672248515"
variation 145
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1233940121"
variation 146
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1672248688"
variation 147
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1481927460"
variation 154
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:773044988"
variation 155
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326505846"
variation 158
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672249023"
variation 163
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378008708"
variation 171
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1375072172"
variation 175
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438630250"
variation 180
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="t"
/db_xref="dbSNP:1672249724"
variation 181
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1163831807"
variation 183
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1572118385"
variation 184
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1194420525"
exon 185..297
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/inference="alignment:Splign:2.1.0"
variation 187
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1411530555"
variation 189
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:774998849"
variation 191
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:553640041"
variation 198
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:1672436931"
variation 199..206
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="attgattg"
/replace="attgattgattgattg"
/db_xref="dbSNP:753462863"
variation 202
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:371904070"
variation 205
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="t"
/db_xref="dbSNP:1672437225"
variation 206
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:74546314"
variation 213
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:774410620"
variation 215
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:748284957"
variation 216
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:2102857670"
variation 219
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1672437625"
variation 224
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:772022347"
variation 225
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1219454055"
variation 227
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:2102857682"
variation 230
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:569063391"
variation 236..237
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="at"
/replace="atat"
/db_xref="dbSNP:867611119"
variation 238
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:2102857691"
variation 246
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:2102857698"
variation 248
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="t"
/db_xref="dbSNP:1364528987"
variation 249
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345062328"
variation 250
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:773062618"
variation 256
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:760685072"
variation 259
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:1672438669"
variation 264
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:766032776"
variation 265
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043567917"
variation 267
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1324936188"
variation 268
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:776572379"
variation 270
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1264522692"
variation 273
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:1368410302"
variation 274
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1440288304"
variation 277
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1186412041"
variation 278
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242449359"
variation 282
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:903711158"
variation 284
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1672439655"
variation 287
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:1294041278"
variation 290
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:759258232"
variation 292
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1461458883"
variation 294
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:917486920"
variation 296
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:765043396"
variation 297..307
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="gatacattatg"
/replace="gatacattatgatacattatg"
/db_xref="dbSNP:2102857788"
variation 297
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:183720647"
exon 298..438
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/inference="alignment:Splign:2.1.0"
variation 298
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358766269"
variation 302
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1174282957"
variation 305
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672619598"
variation 306
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1435151278"
variation 308
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410435248"
variation 310
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:878923655"
variation 312
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1418163903"
variation 313
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1396381468"
variation 315
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:759458223"
variation 318
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:769543021"
variation 320
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:1407258071"
variation 321
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:775246064"
variation 323
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:762687236"
variation 324
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231845891"
variation 338
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:887392884"
variation 340
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:1672620849"
variation 341
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672620936"
variation 343
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:2102865519"
variation 345..347
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1279692809"
variation 346
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:372288762"
variation 349
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace=""
/replace="a"
/db_xref="dbSNP:1237525173"
variation 350
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284961022"
variation 354
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:751081561"
variation 355
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1672621510"
variation 356
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:1359924899"
variation 357
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1211513330"
variation 359
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:377109185"
variation 360
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451035685"
variation 364
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:766928434"
variation 365
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1255033251"
variation 366
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:754179767"
variation 367
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:143487399"
variation 372
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1672622544"
variation 377
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:779278796"
variation 379..385
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="gaaagaa"
/replace="gaaagaaagaa"
/db_xref="dbSNP:780584986"
variation 383
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:752806168"
variation 387..388
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1278634437"
variation 388
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:1161866151"
variation 389
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:758653463"
variation 394
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369790169"
variation 396
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="t"
/db_xref="dbSNP:2102865618"
variation 397
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:770754845"
variation 398
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:781323491"
variation 402
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:745834213"
variation 409
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1362775552"
variation 413
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:141333468"
variation 414
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1553347711"
variation 415
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1672623992"
variation 420
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1019628519"
variation 421
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775436262"
variation 424
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:762443340"
variation 427
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:145122242"
variation 429
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1359977064"
variation 434
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1196311841"
variation 436
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1672625307"
variation 437
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="t"
/db_xref="dbSNP:761434887"
exon 439..822
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/inference="alignment:Splign:2.1.0"
variation 440
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1270241676"
variation 443
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672851906"
variation 444
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1299741907"
variation 446
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:1311806063"
variation 448
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:1672852088"
variation 452
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:200306692"
variation 456
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1399276012"
variation 457
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:149125195"
variation 460
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672852370"
variation 463
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672852434"
variation 465
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1046110536"
variation 466
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:926541157"
variation 468
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="t"
/db_xref="dbSNP:1672852641"
variation 469
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:780085863"
variation 471
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:1672852754"
variation 473
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:188007583"
variation 474
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:373829232"
variation 475
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1161603926"
variation 478
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:570344591"
variation 479..486
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="agaa"
/replace="agaaagaa"
/db_xref="dbSNP:1672853134"
variation 479
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1284276879"
variation 482..488
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="aaga"
/replace="aagaaga"
/db_xref="dbSNP:1672853187"
variation 485
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:2102875224"
variation 487
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1026766952"
variation 493
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:960945389"
variation 494
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353467737"
variation 495
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:754762448"
variation 500..501
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1672853501"
variation 502
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1345645062"
variation 504
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:1672853604"
variation 506
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1672853652"
variation 507
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1248934954"
variation 514
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1210757253"
variation 515
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1672853814"
variation 523
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:192279478"
variation 525
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358730799"
variation 535
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1572139616"
variation 546
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672854038"
variation 547
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:1672854090"
variation 548
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1004825395"
variation 554
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1015806360"
variation 556
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:966019763"
variation 558
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226079051"
variation 562..565
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="ca"
/replace="caca"
/db_xref="dbSNP:1362721928"
variation 562
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:1672854426"
variation 568..573
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace=""
/replace="ctacag"
/db_xref="dbSNP:1672854600"
variation 568..569
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace=""
/replace="ct"
/db_xref="dbSNP:1399366108"
variation 571..574
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace=""
/replace="cagt"
/db_xref="dbSNP:1276175334"
variation 572
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1380734123"
variation 573
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430690503"
variation 574
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="t"
/db_xref="dbSNP:1672854832"
variation 575
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386907701"
variation 576
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672854943"
variation 577
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:2102875290"
variation 579
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:945046769"
variation 584
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:1672855053"
variation 588
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1347183523"
variation 589
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:77770374"
variation 595
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:1572139656"
variation 599
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace=""
/replace="g"
/db_xref="dbSNP:573343321"
variation 599
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1672855309"
variation 602
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:2102875316"
variation 613
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1162987349"
variation 618
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:925046353"
variation 621
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="t"
/db_xref="dbSNP:1672855508"
variation 623
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:921281639"
variation 624
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1558403651"
variation 625
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:954068187"
variation 626
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1182347598"
variation 627
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1310144736"
variation 631
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1672855865"
variation 634
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1246128511"
variation 636
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:577313325"
variation 636
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1190194657"
variation 638
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:1217484233"
variation 640
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1572139689"
variation 643
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:182702979"
variation 645
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="t"
/db_xref="dbSNP:1218987598"
variation 647
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322964188"
variation 650
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1290050082"
variation 657
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:1214486369"
variation 659
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1363574364"
variation 660
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1672856414"
variation 662
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1300457758"
variation 663
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:891375559"
variation 664
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672856590"
variation 665
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1370746187"
variation 670
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:766598599"
variation 672
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:4654037"
variation 679
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:574457869"
variation 681
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1169754370"
variation 682
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192204866"
variation 686
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672857528"
variation 688
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:897122187"
variation 689
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:2102875397"
variation 691
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424882212"
variation 694
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1431708907"
variation 704
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:995527777"
variation 713
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:372410465"
variation 714
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1672857910"
variation 720
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:1027045094"
variation 721
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672858019"
variation 724
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:2102875429"
variation 726
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1388201832"
variation 728
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672858136"
variation 731
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1170437960"
variation 732
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:1672858265"
variation 744
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:970577855"
variation 745
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1672858387"
variation 752..753
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2102875451"
variation 752
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1345888802"
variation 759
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1002039789"
variation 760
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1033962398"
variation 761
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/db_xref="dbSNP:1296283392"
variation 765
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672858681"
variation 766
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:376679830"
variation 768
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1672858795"
variation 770..774
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="taaca"
/replace="taacataaca"
/db_xref="dbSNP:1672858933"
variation 770
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1052707292"
variation 772..776
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="aca"
/replace="acaca"
/db_xref="dbSNP:1672858994"
variation 774
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace=""
/replace="a"
/db_xref="dbSNP:1339496319"
variation 789
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="c"
/db_xref="dbSNP:2102875484"
regulatory 794..799
/regulatory_class="polyA_signal_sequence"
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/note="hexamer: AATAAA"
variation 795
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:755405690"
variation 796
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1672859507"
variation 797..799
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:372916692"
variation 801
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="g"
/replace="t"
/db_xref="dbSNP:1672859607"
variation 802..811
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace=""
/replace="attgttgagt"
/db_xref="dbSNP:781646534"
variation 804
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:12724850"
variation 805
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1672859838"
variation 810
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1299728609"
variation 813
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1388899114"
variation 814
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274092876"
variation 818
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="g"
/db_xref="dbSNP:913839321"
variation 819
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="c"
/replace="t"
/db_xref="dbSNP:1225160181"
variation 820
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/replace="a"
/replace="t"
/db_xref="dbSNP:1408024342"
polyA_site 822
/gene="CNIH4"
/gene_synonym="CNIH-4; CNIH2; HSPC163"
/note="major polyA site"
ORIGIN
atccgagcgggtttgacggaaggagcggcggcgacggaggaggaggatggaggcggtggtgttcgtcttctctctcctcgattgttgcgcgctcatcttcctctcggtctacttcataattacattgtctgatttagaatgtgattacattaatgctagatcatgttgctcaaaattaaacaagtgggtaattccagaattgattggccataccattgtcactgtattactgctcatgtcattgcactggttcatcttccttctcaacttacctgttgccacttggaatatatatcgatacattatggtgccgagtggtaacatgggagtgtttgatccaacagaaatacacaatcgagggcagctgaagtcacacatgaaagaagccatgatcaagcttggtttccacttgctctgcttcttcatgtatctttatagtggtagcaactgcccttgctaatcaccgtaacctcggctgagaaagaagaggaagcgaaatccaagatgcagctcagttcatcaaagcctagcaggtcccctcagctgccttttcatgcctgccacagactacagtaggacaaaacctgacctggtctttgaagttaagagctaagaaagcttcctatagtagtatctcccatggcacttaccacattctatctggtattacagttatttgtatgcaattaatcactcttagattgtatgttcctggagggcagaatatgcccattcatatttgtatcttcttccttctgctcttggcacctaacacagtgccttgcacacaaacaataaatgattgttgagtgaataagtaaa
//
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.
[Full Text]