2024-05-03 06:35:54, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001170747 1605 bp mRNA linear PRI 10-MAY-2023 DEFINITION Homo sapiens peptidylprolyl cis/trans isomerase, NIMA-interacting 4 (PIN4), transcript variant 2, mRNA. ACCESSION NM_001170747 VERSION NM_001170747.1 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 1605) AUTHORS Naito M, Ikeda K, Aoyama S, Kanamoto M, Akasaka Y, Kido Y, Nakanishi M, Kanna M, Yamamotoya T, Matsubara A, Hinata N, Asano T and Nakatsu Y. TITLE Par14 interacts with the androgen receptor, augmenting both its transcriptional activity and prostate cancer proliferation JOURNAL Cancer Med 12 (7), 8464-8475 (2023) PUBMED 36583514 REMARK GeneRIF: Par14 interacts with the androgen receptor, augmenting both its transcriptional activity and prostate cancer proliferation. REFERENCE 2 (bases 1 to 1605) AUTHORS Fragoza R, Das J, Wierbowski SD, Liang J, Tran TN, Liang S, Beltran JF, Rivera-Erick CA, Ye K, Wang TY, Yao L, Mort M, Stenson PD, Cooper DN, Wei X, Keinan A, Schimenti JC, Clark AG and Yu H. TITLE Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations JOURNAL Nat Commun 10 (1), 4141 (2019) PUBMED 31515488 REMARK Publication Status: Online-Only REFERENCE 3 (bases 1 to 1605) AUTHORS Saeed U, Kim J, Piracha ZZ, Kwon H, Jung J, Chwae YJ, Park S, Shin HJ and Kim K. TITLE Parvulin 14 and Parvulin 17 Bind to HBx and cccDNA and Upregulate Hepatitis B Virus Replication from cccDNA to Virion in an HBx-Dependent Manner JOURNAL J Virol 93 (6), e01840-18 (2019) PUBMED 30567987 REMARK GeneRIF: In the presence of HBx, the Par14 and Par17 proteins bound to cccDNA. Publication Status: Online-Only REFERENCE 4 (bases 1 to 1605) AUTHORS Kessler D, Papatheodorou P, Stratmann T, Dian EA, Hartmann-Fatu C, Rassow J, Bayer P and Mueller JW. TITLE The DNA binding parvulin Par17 is targeted to the mitochondrial matrix by a recently evolved prepeptide uniquely present in Hominidae JOURNAL BMC Biol 5, 37 (2007) PUBMED 17875217 REMARK Publication Status: Online-Only REFERENCE 5 (bases 1 to 1605) AUTHORS Mueller JW, Kessler D, Neumann D, Stratmann T, Papatheodorou P, Hartmann-Fatu C and Bayer P. TITLE Characterization of novel elongated Parvulin isoforms that are ubiquitously expressed in human tissues and originate from alternative transcription initiation JOURNAL BMC Mol Biol 7, 9 (2006) PUBMED 16522211 REMARK GeneRIF: Identification of a longer Parvulin isoform (Par17) that has an extension at the 5' end including a 75 bp extended open reading frame. Publication Status: Online-Only REFERENCE 6 (bases 1 to 1605) AUTHORS Surmacz TA, Bayer E, Rahfeld JU, Fischer G and Bayer P. TITLE The N-terminal basic domain of human parvulin hPar14 is responsible for the entry to the nucleus and high-affinity DNA-binding JOURNAL J Mol Biol 321 (2), 235-247 (2002) PUBMED 12144781 REMARK GeneRIF: The N-terminal basic domain of human parvulin hPar14 is responsible for the entry to the nucleus and high-affinity DNA-binding. REFERENCE 7 (bases 1 to 1605) AUTHORS Fujiyama S, Yanagida M, Hayano T, Miura Y, Isobe T, Fujimori F, Uchida T and Takahashi N. TITLE Isolation and proteomic characterization of human Parvulin-associating preribosomal ribonucleoprotein complexes JOURNAL J Biol Chem 277 (26), 23773-23780 (2002) PUBMED 11960984 REMARK Erratum:[J Biol Chem. 2002 Nov 1;277(44):42418.] REFERENCE 8 (bases 1 to 1605) AUTHORS Terada T, Shirouzu M, Fukumori Y, Fujimori F, Ito Y, Kigawa T, Yokoyama S and Uchida T. TITLE Solution structure of the human parvulin-like peptidyl prolyl cis/trans isomerase, hPar14 JOURNAL J Mol Biol 305 (4), 917-926 (2001) PUBMED 11162102 REFERENCE 9 (bases 1 to 1605) AUTHORS Rulten S, Thorpe J and Kay J. TITLE Identification of eukaryotic parvulin homologues: a new subfamily of peptidylprolyl cis-trans isomerases JOURNAL Biochem Biophys Res Commun 259 (3), 557-562 (1999) PUBMED 10364457 REFERENCE 10 (bases 1 to 1605) AUTHORS Uchida T, Fujimori F, Tradler T, Fischer G and Rahfeld JU. TITLE Identification and characterization of a 14 kDa human protein as a novel parvulin-like peptidyl prolyl cis/trans isomerase JOURNAL FEBS Lett 446 (2-3), 278-282 (1999) PUBMED 10100858 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AU098526.1, AV709926.2 and AK127605.1. Summary: This gene encodes a member of the parvulin subfamily of the peptidyl-prolyl cis/trans isomerase protein family. The encoded protein catalyzes the isomerization of peptidylprolyl bonds, and may play a role in the cell cycle, chromatin remodeling, and/or ribosome biogenesis. The encoded protein may play an additional role in the mitochondria. [provided by RefSeq, Dec 2009]. Transcript Variant: This variant (2) differs in the 3' coding region and 3' UTR, compared to variant 1. The resulting isoform (2) has a distinct C-terminus and is shorter than isoform 1. 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 :: SRR1660803.27994.1, AK127605.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1968540, SAMEA1968832 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## gene product(s) localized to mito. :: PMID: 10364457, 17875217 ##RefSeq-Attributes-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-81 AU098526.1 1-81 82-89 AV709926.2 31-38 90-1605 AK127605.1 1-1516 FEATURES Location/Qualifiers source 1..1605 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="X" /map="Xq13.1" gene 1..1605 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /note="peptidylprolyl cis/trans isomerase, NIMA-interacting 4" /db_xref="GeneID:5303" /db_xref="HGNC:HGNC:8992" /db_xref="MIM:300252" exon 1..153 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /inference="alignment:Splign:2.1.0" variation 2 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1313617752" variation 3 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:776608845" variation 8 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:1330583765" variation 10 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2042672614" variation 11 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:2042672629" variation 12 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:748908858" variation 18 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:765394055" variation 21 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:2042672704" variation 22 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1290839298" variation 23 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2042672750" variation 27 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1207293988" variation 29 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1232154214" misc_feature 30..32 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /note="upstream in-frame stop codon" variation 30 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:2042672814" CDS 36..437 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /EC_number="5.2.1.8" /note="isoform 2 is encoded by transcript variant 2; peptidyl-prolyl cis-trans isomerase NIMA-interacting 4; rotamase PIN4; PPIase PIN4; parvulin-14; parvulin-17; eukaryotic parvulin homolog; protein (peptidylprolyl cis/trans isomerase) NIMA-interacting, 4 (parvulin); peptidyl-prolyl cis-trans isomerase Pin4; peptidyl-prolyl cis/trans isomerase EPVH" /codon_start=1 /product="peptidyl-prolyl cis-trans isomerase NIMA-interacting 4 isoform 2" /protein_id="NP_001164218.1" /db_xref="CCDS:CCDS55447.1" /db_xref="GeneID:5303" /db_xref="HGNC:HGNC:8992" /db_xref="MIM:300252" /translation="
MPMAGLLKGLVRQLERFSVQQQASKMPPKGKSGSGKAGKGGAASGSDSADKKAQGPKGGGNAVKVRHILCEKHGKIMEAMEKLKSGMRFNEVAAQYSEDKARQGIPSLQQHAGHHRDLRSTLISLVSYLQTTP"
misc_feature 186..>338 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /note="PPIC-type PPIASE domain; Region: Rotamase_2; cl29122" /db_xref="CDD:452928" variation 36 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:1244901284" variation 38 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:775386803" variation 41 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:763284331" variation 42 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:764405239" variation 43 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:867298070" variation 45 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1168175194" variation 46 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1380863526" variation 49 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:2042673041" variation 50 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:757670554" variation 52 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:942264130" variation 53 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:767946061" variation 55 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1349812122" variation 57 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:750970887" variation 59 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:756529299" variation 62 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:2042673261" variation 63 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1372508561" variation 66 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1225770176" variation 68 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:1392562085" variation 69 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:375360841" variation 70 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1342685978" variation 73 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:758115612" variation 75 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:777392941" variation 76 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="" /replace="t" /db_xref="dbSNP:1569487831" variation 76 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:140834424" variation 80 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1287391920" variation 82 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:6525589" variation 84 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:776253818" variation 89 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:7058353" variation 90 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:769563285" variation 95 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:140494564" variation 97 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:1248894800" variation 98 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:764456398" variation 99 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1356496363" variation 103 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1198053299" variation 107 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:1161859993" variation 108 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:774679844" variation 113 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:928957074" variation 114 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:761901303" variation 115 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:767947505" variation 116 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2042674116" variation 117 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1396116235" variation 118 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:750693487" variation 119 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:972910933" variation 122 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:756647963" variation 123 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:766793709" variation 124 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:2042674272" variation 125 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1282237271" variation 126 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2042674317" variation 129 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:752263746" variation 131 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:1602423545" variation 132 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2042674403" variation 135 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:1406000209" variation 136 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:919695845" variation 139 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:757882457" variation 143 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2042674505" variation 144 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1274971838" variation 145 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:376742840" variation 146 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2042674568" variation 147 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:1389483169" variation 148 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:2042674636" variation 152 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:2042674656" exon 154..227 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /inference="alignment:Splign:2.1.0" variation 154 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:889080355" variation 158 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:771318018" variation 159 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:1000835180" variation 160 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:371226434" variation 161 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:760052937" variation 164 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1354887405" variation 167 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1209742577" variation 168 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:1266101192" variation 172 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2042704083" variation 179 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2042704119" variation 180 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:914083195" variation 181 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2042704179" variation 185 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1184254268" variation 186..191 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="aag" /replace="aagaag" /db_xref="dbSNP:1473857391" variation 187 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:754347273" variation 193 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1213489459" variation 196 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:946447218" variation 198 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1286399946" variation 199 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:2042704295" variation 201..203 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="cc" /replace="ccc" /db_xref="dbSNP:2147567048" variation 204 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1043439923" variation 208 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2042704348" variation 211 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:2147567063" variation 213 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1032364083" variation 217 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:145654350" variation 218 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:761204353" variation 222 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2042704489" variation 223 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2042704520" variation 226 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:956775117" exon 228..347 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /inference="alignment:Splign:2.1.0" variation 230 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:2042768419" variation 232 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1212456427" variation 233 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1489194758" variation 236 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:758379340" variation 242 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1186725109" variation 248 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1208971104" variation 254 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:1263638121" variation 256 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2042768627" variation 257 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1356830897" variation 263 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:777869803" variation 265 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:747218626" variation 273 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1418507010" variation 278 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:1602431274" variation 280..284 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="agtta" /replace="agttagtta" /db_xref="dbSNP:1462890104" variation 280 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:771087340" variation 281 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:776986443" variation 284 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:367799837" variation 291 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2042768901" variation 294 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:1454539015" variation 299 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:371560354" variation 302 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:2042768952" variation 304 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2042768987" variation 305 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2042769012" variation 308 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:775826431" variation 314 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:11415" variation 315 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:144390339" variation 318 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:772719143" variation 319 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1227047935" variation 330 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:760407590" variation 332 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:1327836879" variation 333 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:761536707" variation 336 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:376285927" variation 338 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1178733216" variation 339 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1010056637" exon 348..1605 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /inference="alignment:Splign:2.1.0" variation 358 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1342045906" variation 363 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:1242148710" variation 364 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:1013711408" variation 371 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043144507" variation 373 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:775005516" variation 374 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1356795521" variation 380 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:762569898" variation 387 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:1283827634" variation 388 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1487898860" variation 394 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1194526560" variation 402..403 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="" /replace="c" /db_xref="dbSNP:1306948689" variation 403 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:2043144625" variation 408 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1602465133" variation 409 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1265399524" variation 411 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:762232589" variation 413..417 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="at" /replace="atcat" /db_xref="dbSNP:1422343785" variation 413 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1187099255" variation 414 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:2043144737" variation 416 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1369202440" variation 422 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:187890537" variation 427 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:2043144779" variation 428 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1602465159" variation 438 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:751438160" variation 442 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043144833" polyA_site 453 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /note="major polyA site" variation 456 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043144852" variation 462 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:1360479983" variation 463 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:1420822611" variation 472 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043144913" variation 475 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:1426313235" variation 476 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043144941" variation 477 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:1010558375" variation 494 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:2043144984" variation 495 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1004852391" variation 496 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:2043145016" variation 497 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:750117506" variation 505 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:755728711" variation 507 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:971737709" variation 510 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:982093323" variation 522 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:2043145104" variation 530 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:1602465184" variation 532 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1602465187" variation 537..545 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="acaaa" /replace="acaaacaaa" /db_xref="dbSNP:2043145155" variation 551 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1481672961" variation 561 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1235772501" variation 564 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1207946246" variation 566 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:1435813260" variation 578 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:1311476814" variation 579 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043145240" variation 580 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:1602465196" variation 584 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043145269" variation 587 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043145284" variation 591 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043145301" variation 597 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043145318" variation 599 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:963664720" variation 605 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:996711928" variation 606 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043145365" variation 607 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:1326688684" variation 612 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1287297874" variation 621 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1408142105" variation 627 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1029194252" variation 629 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043145441" variation 633 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:927956490" variation 634..636 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="ggg" /replace="gggg" /db_xref="dbSNP:2043145472" variation 634 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:954609293" variation 643 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1376164035" variation 658 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1360234068" variation 661 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:959436280" variation 665 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:990942051" variation 669..685 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="atttgttca" /replace="atttgttcatttgttca" /db_xref="dbSNP:368197858" variation 676 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1411631568" variation 678 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1160225905" variation 679 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043145612" variation 690 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1421041263" variation 702 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043145634" variation 703 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:910031644" variation 708 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1885484" variation 709 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1037625548" variation 710 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:1482924236" variation 712 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:1899187679" variation 716 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1243646806" variation 732 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1602465244" variation 736 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:2043145782" variation 738 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2043145795" variation 742 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1205384695" variation 743 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:967014535" variation 748 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:918808626" variation 750..752 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="t" /replace="tat" /db_xref="dbSNP:1569493732" variation 752 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:978429420" variation 756 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:1208970161" variation 758 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:28710154" variation 762 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:190801378" variation 764 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:2043145937" variation 769 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="" /replace="t" /db_xref="dbSNP:1310026472" variation 769 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:925829886" variation 770..774 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="ggggg" /replace="gggggg" /db_xref="dbSNP:937308365" variation 773 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2043146010" variation 774 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:113497493" variation 784 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:991730500" variation 788 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1388376048" variation 793 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043146054" variation 795 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043146072" variation 796 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043146084" variation 803 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1050711088" variation 804 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="" /replace="t" /db_xref="dbSNP:2043146117" variation 807 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:113967040" variation 808 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1337791307" variation 813 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:942438102" variation 822 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:755277424" variation 825 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1281622050" variation 827 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043146231" variation 832 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:779439353" variation 834 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:2043146262" variation 848 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:2043146280" variation 849 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1387112707" variation 852 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:892902620" variation 858 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:2043146320" variation 859 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1046434860" variation 863 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043146361" variation 867 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043146374" variation 874 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1247197577" variation 880 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1205487515" variation 887 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:41303713" variation 888 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:1220249641" variation 892 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043146444" variation 902 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043146474" variation 909 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043146524" variation 916 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:763808141" variation 918 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:2043146569" variation 923 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="" /replace="a" /db_xref="dbSNP:1359575938" variation 924 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1602465301" variation 933..939 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="agt" /replace="agttagt" /db_xref="dbSNP:1293244259" variation 938 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1020537770" variation 939 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1226859253" variation 943 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:2043146690" variation 944 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:2043146715" variation 945 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:753738969" variation 953 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:1253451038" variation 954 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:886543645" variation 957 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2147621379" variation 958 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1384245501" variation 973..977 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="aaaa" /replace="aaaaa" /db_xref="dbSNP:2043146834" variation 978 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:907082593" variation 986 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043146893" variation 988 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1203570758" variation 989 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043146947" variation 994 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043146974" variation 998 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1193375942" variation 1002..1004 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="aaa" /db_xref="dbSNP:2043147038" variation 1003 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1374593618" variation 1005 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043147104" variation 1010 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043147127" variation 1021..1023 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="gg" /replace="ggg" /db_xref="dbSNP:2043147152" variation 1028 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:2043147176" variation 1036 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1166731197" variation 1040 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1427804277" variation 1045 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043147223" variation 1047 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1003234550" variation 1048 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1035015799" variation 1051 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1430057410" variation 1059..1060 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="" /replace="gcc" /db_xref="dbSNP:2043147313" variation 1060 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:2043147337" variation 1062 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:2043147358" variation 1064..1069 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="ca" /replace="cattca" /db_xref="dbSNP:1695622940" variation 1064 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1264956012" variation 1078 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1190281375" variation 1079 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1037672520" variation 1080 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:899402563" variation 1081 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:182755506" variation 1082 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:990888221" variation 1083 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043147576" variation 1096 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:1602465337" variation 1117 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1395655105" variation 1126 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1602465345" variation 1127 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:150708239" variation 1138 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:1569493751" variation 1165 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:2043147735" variation 1168 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:749998776" variation 1171 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:1310840228" variation 1173 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1029555834" variation 1189 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1405794968" variation 1198 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043147854" variation 1200 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:2043147879" variation 1206 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:963122859" variation 1212 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:890602294" variation 1215 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:187721538" variation 1220 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:918784732" variation 1221 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043148014" variation 1225 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:746675363" variation 1227 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:1020007779" variation 1232 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1325082515" variation 1247 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1375737134" variation 1248 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:1228184171" variation 1249 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:1304600738" variation 1250 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:2043148187" variation 1251 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:967129383" variation 1259 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1350759795" variation 1267 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:5958776" variation 1278 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043148336" variation 1282 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:2043148357" variation 1283 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:987038681" variation 1284 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:910877426" variation 1290 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:2043148429" variation 1292 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:942343422" variation 1293 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:991451986" variation 1299 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="" /replace="c" /db_xref="dbSNP:1482529012" variation 1300 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2071385237" variation 1303 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043148511" variation 1304 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:2043148561" variation 1311 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043148574" variation 1315 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043148589" variation 1333 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1054070569" variation 1346 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:892845156" variation 1363 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043148633" variation 1367 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:747226625" variation 1368 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:781478339" variation 1371 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:375691100" variation 1380 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043148721" variation 1390 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:771133411" variation 1396 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:1463242139" variation 1397 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:776693984" variation 1399..1401 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="" /replace="cca" /db_xref="dbSNP:2043148824" variation 1403 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:907069214" variation 1407 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="g" /db_xref="dbSNP:982581002" variation 1408 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:370116044" variation 1409 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:1471119428" variation 1410 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:907931614" variation 1411 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043148946" variation 1415 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1470105267" variation 1417..1418 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="gg" /db_xref="dbSNP:1431095052" variation 1418 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043149037" variation 1419 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:2043149061" variation 1442 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1002772136" variation 1449 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:940810452" variation 1452 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:1602465460" variation 1453 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1034297069" variation 1464 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:894409792" variation 1476 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:1472021008" variation 1481 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:2043149250" variation 1485 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:2043149277" variation 1494 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2147621532" variation 1496 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:3012639" variation 1499 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:144179196" variation 1510 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:1038102509" variation 1529 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="g" /replace="t" /db_xref="dbSNP:1160342900" variation 1530 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="c" /db_xref="dbSNP:1383139844" variation 1531 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:962820833" variation 1532 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:1434633811" variation 1533 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:1327078950" variation 1541..1547 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="aaaaaa" /replace="aaaaaaa" /replace="aaaaaaaa" /db_xref="dbSNP:773245894" variation 1543 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:2043149574" variation 1548 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="" /replace="g" /db_xref="dbSNP:2147621554" variation 1548 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1602465495" regulatory 1556..1561 /regulatory_class="polyA_signal_sequence" /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /note="hexamer: ATTAAA" variation 1556 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1602465498" variation 1575 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:2043149622" polyA_site 1576 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" variation 1580 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1204763637" variation 1582 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="t" /db_xref="dbSNP:1462952044" variation 1583 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:973268708" variation 1589 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="a" /replace="g" /db_xref="dbSNP:1208363317" variation 1591 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1351661309" variation 1601 /gene="PIN4" /gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17" /replace="c" /replace="t" /db_xref="dbSNP:1281418364" ORIGIN
aattgagatgcggctttcaggcatttgtttaggacatgcccatggcggggcttctaaaggggcttgtacggcaactggagcggttcagcgttcaacaacaagcttccaagatgccgcccaaaggaaaaagtggttctggaaaagcggggaaagggggagcagcctctgggagtgacagtgctgacaagaaggctcaaggtcccaaaggtggtggcaatgcagtaaaggtcagacacattctatgtgaaaaacatggcaaaatcatggaagccatggaaaagttaaagtctgggatgagattcaatgaagtggccgcacagtatagtgaagataaagccaggcaagggattcccagcctgcagcaacatgctggtcaccatagagacctgagaagcaccctcatctcattggtatcatatttacaaaccaccccttaaagtggattattttgcagatggctgatctcatctattcaatgttgattctattagttccaatttcagaaggtgacattttctgactttgtccccttaagcacaaacaaaaactatggatttttgtttttgttttcagaaaagagaaagtacaaggtgtgcttggggaacagcaaggaaaccagacagatgtgggggcgggtttgtaggggaactgctggatgtacctcattaatttgttcatttgttcagcacccacagggtgccagtgaacgggctaggtgctggggatagagtggtgaacaagatgagccttatgcacctcacagtctcctgggggagacagccaaatagacaattttaatacaatgtggcaaattctatgatgggaagaagagagaaatggtgtgtgtgagtccctcaccttcccagaggtttcccaggggaagcaacgtttcagctgagacctgaaggatggatgacagtccaccagaaaaaagttagtggagcggggacaagcagggttgcagagtggaagaaaaatgttcctgtgagaagaaactgtccaaagagtctgaagagaaaagggaacagggtgaatttgaggccctacaagaaaaacaggagaccattcaacaggagacgcccagggagcaggtggctttgtgggcctgatgtccaagaaagaagtcgtggtggtaaacagagacttgggattgcaagctactgttgtctttctattgaaaaaatagctgagcaccacactagggaggccttgcaaggacagcccaaagaatttgaacttgattctacaggcagtgattttgaacaagaggttttgaagagaacgtgacacacgtcaagctgagctctagggagtgggcagcagcctgcagaagagggactaggctaggagcacagaaagtagcccacggcagaggtagcagaaggaatggaggagtgcccatgtgaggggtactgaggtggcacacttgccagaatcagggcagcctgcttggtctcataccagctggaaccagttcctaccagctcccaagggctaattgttaaactttcaggaattttctcagcattcattaaaaatgaaaaaaagtatcaatattaaaaatatttttgctggacatggtgtctcaggcctgtaatcccagct
//
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]