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Previous release (v1)
2024-05-01 21:00:53, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_033187 1165 bp RNA linear PRI 31-MAY-2023
DEFINITION Homo sapiens peptidylprolyl cis/trans isomerase, NIMA-interacting 4
(PIN4), transcript variant 3, non-coding RNA.
ACCESSION NR_033187
VERSION NR_033187.2
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 1165)
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 1165)
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 1165)
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 1165)
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 1165)
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 1165)
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 1165)
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 1165)
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 1165)
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 1165)
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 AV709926.2, BC112281.1,
BE504461.1 and BC111394.1.
On Jul 12, 2019 this sequence version replaced NR_033187.1.
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 (3) lacks an alternate internal
exon, compared to variant 1. This variant is represented as
non-coding because the use of the 5'-most supported translational
start codon, as used in variant 1, renders the transcript a
candidate for nonsense-mediated mRNA decay (NMD).
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 :: DW429727.1, BM894296.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1965299, SAMEA1968189
[ECO:0000348]
##Evidence-Data-END##
##RefSeq-Attributes-START##
gene product(s) localized to mito. :: PMID: 10364457, 17875217
##RefSeq-Attributes-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-8 AV709926.2 31-38
9-72 BC112281.1 87-150
73-433 BC112281.1 225-585
434-480 BE504461.1 437-483 c
481-1165 BC111394.1 556-1240
FEATURES Location/Qualifiers
source 1..1165
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="X"
/map="Xq13.1"
gene 1..1165
/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"
misc_RNA 1..1165
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/product="peptidylprolyl cis/trans isomerase,
NIMA-interacting 4, transcript variant 3"
/db_xref="GeneID:5303"
/db_xref="HGNC:HGNC:8992"
/db_xref="MIM:300252"
exon 1..72
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:6525589"
variation 3
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:776253818"
variation 8
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:7058353"
variation 9
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769563285"
variation 14
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:140494564"
variation 16
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1248894800"
variation 17
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:764456398"
variation 18
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1356496363"
variation 22
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1198053299"
variation 26
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1161859993"
variation 27
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:774679844"
misc_feature 30..92
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/inference="COORDINATES:
alignment:Blast2seq::RefSeq|NM_006223.4"
/note="primary ORF has stop codon >50 nucleotides from the
terminal splice site; nonsense-mediated decay (NMD)
candidate"
variation 32
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:928957074"
variation 33
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761901303"
variation 34
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:767947505"
variation 35
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042674116"
variation 36
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396116235"
variation 37
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:750693487"
variation 38
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:972910933"
variation 41
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:756647963"
variation 42
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:766793709"
variation 43
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042674272"
variation 44
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1282237271"
variation 45
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042674317"
variation 48
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:752263746"
variation 50
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1602423545"
variation 51
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042674403"
variation 54
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1406000209"
variation 55
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:919695845"
variation 58
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:757882457"
variation 62
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042674505"
variation 63
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274971838"
variation 64
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:376742840"
variation 65
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2042674568"
variation 66
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1389483169"
variation 67
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2042674636"
variation 71
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:2042674656"
exon 73..192
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/inference="alignment:Splign:2.1.0"
variation 75
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:2042768419"
variation 77
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212456427"
variation 78
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1489194758"
variation 81
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:758379340"
variation 87
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186725109"
variation 93
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208971104"
variation 99
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1263638121"
variation 101
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042768627"
variation 102
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1356830897"
variation 108
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:777869803"
variation 110
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:747218626"
variation 118
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1418507010"
variation 123
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1602431274"
variation 125..129
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="agtta"
/replace="agttagtta"
/db_xref="dbSNP:1462890104"
variation 125
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:771087340"
variation 126
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:776986443"
variation 129
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:367799837"
variation 136
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042768901"
variation 139
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1454539015"
variation 144
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:371560354"
variation 147
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2042768952"
variation 149
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042768987"
variation 150
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042769012"
variation 153
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:775826431"
variation 159
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:11415"
variation 160
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:144390339"
variation 163
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:772719143"
variation 164
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1227047935"
variation 175
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:760407590"
variation 177
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1327836879"
variation 178
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:761536707"
variation 181
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:376285927"
variation 183
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1178733216"
variation 184
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010056637"
exon 193..1165
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/inference="alignment:Splign:2.1.0"
variation 193
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:987800721"
variation 194
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1354853451"
variation 196
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:769139448"
variation 199
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1486526891"
variation 202
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1327148409"
variation 204
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:772664721"
variation 209
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1311831095"
variation 213
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2042772300"
variation 214
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250999628"
variation 223
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:760247738"
variation 226
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042772395"
variation 228
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:766182674"
variation 233
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1423088655"
variation 234
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042772482"
variation 238
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1354538511"
variation 241
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285035008"
variation 247
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:776392747"
variation 264..265
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1174467156"
variation 279
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:143295755"
variation 288
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:148339434"
variation 290
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042772692"
variation 296
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:752479921"
variation 297
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1044552"
variation 298
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:945815294"
variation 299
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1373543056"
variation 300
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201381459"
variation 301
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1299431242"
variation 305
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042772823"
variation 310
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:751700739"
variation 323
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1439793400"
variation 324..332
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="tattat"
/replace="tattattat"
/db_xref="dbSNP:1291112739"
variation 324
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:35470967"
variation 325
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2147576297"
variation 326
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:781205028"
variation 331
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:750663705"
variation 332
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042773029"
variation 333
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:959476923"
variation 334
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1667663132"
variation 336
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:937788922"
variation 337
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:756299765"
variation 340
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1272123247"
variation 347
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488868680"
variation 356..359
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="at"
/replace="atat"
/db_xref="dbSNP:754858466"
variation 356
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773189"
variation 358
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:376487600"
variation 370
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:369019391"
variation 371
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1194570777"
variation 373
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:769101076"
variation 383
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1569488931"
variation 384..387
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="tt"
/replace="tttt"
/db_xref="dbSNP:756508072"
variation 394
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:779452784"
variation 400
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773393"
variation 403
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773420"
variation 408
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:2042773447"
variation 427
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1321537358"
variation 430
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1290831636"
variation 433
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1569488932"
variation 434
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1230302948"
variation 438
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409325654"
variation 443
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773565"
variation 444
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1056320924"
variation 451..455
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:2147576386"
variation 451
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778253319"
variation 455
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1012235097"
variation 458
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773665"
variation 459
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:2042773689"
variation 465
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1159890837"
variation 468
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1569488935"
variation 472
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1602431789"
variation 474
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2042773775"
variation 476
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:749719040"
variation 480
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773821"
variation 482
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:187578610"
variation 485
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773873"
variation 491
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773899"
variation 493
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1418653034"
variation 494
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042773940"
variation 495
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1303364642"
variation 500
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042774004"
variation 512
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:191822305"
variation 523
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042774048"
variation 529
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:878886192"
variation 538
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1349141102"
variation 539
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042774131"
variation 545
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1017383723"
variation 546
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:962765281"
variation 548
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:747010973"
variation 549
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1421037070"
variation 554
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:887097938"
variation 558..567
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="tcagtc"
/replace="tcagtcagtc"
/db_xref="dbSNP:201724035"
variation 567
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042774327"
variation 574..576
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:1190029718"
variation 575
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042774353"
variation 576..580
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="aga"
/replace="agaga"
/db_xref="dbSNP:2042774383"
variation 582
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1373902318"
variation 590
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:994214495"
variation 599
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025731243"
variation 604
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042774449"
variation 606
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1569488943"
variation 607
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042774491"
variation 610
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2147576493"
variation 611
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2147576498"
variation 617
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:183989280"
variation 621
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:187600228"
variation 626
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2147576509"
variation 628
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1219288448"
variation 632
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2042774575"
variation 636..640
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="ctc"
/replace="ctctc"
/db_xref="dbSNP:1320151265"
variation 650
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1602431880"
variation 651
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:192028442"
variation 653
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1602431894"
variation 654
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1385071582"
variation 660
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2041668432"
variation 662
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:964676337"
variation 671
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:768901954"
variation 679
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042774729"
variation 690
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2147576549"
variation 694
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042774752"
variation 697
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2042774786"
variation 703
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303755683"
variation 704
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042774832"
variation 707
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353065086"
variation 714
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438369222"
variation 722
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042774897"
variation 725
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:772969634"
variation 733
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:2042774945"
variation 737
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247081390"
variation 751
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace=""
/replace="t"
/db_xref="dbSNP:2042775012"
variation 762
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1602431914"
variation 765
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:184474327"
variation 766
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:914281688"
variation 767
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:945741790"
variation 770..775
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="aca"
/replace="acaaca"
/db_xref="dbSNP:1221234465"
variation 771
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1041495818"
variation 778
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1433045777"
variation 786
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1233998408"
variation 787
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1602431935"
variation 799
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2042775238"
variation 800
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042775263"
variation 804
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193237409"
variation 811
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1029803076"
variation 813
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:928424044"
variation 814
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:2042775364"
variation 819
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:938547889"
variation 826
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1056059235"
variation 827
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:894384309"
variation 830
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:988282416"
variation 847
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006591018"
variation 848
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1038293724"
variation 852
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1163523336"
variation 854
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:143233900"
variation 855
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403413347"
variation 860
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1220707153"
variation 868
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163755801"
variation 873
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:774348069"
variation 874
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042775628"
variation 878
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2147576701"
variation 879
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1448983565"
variation 880
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1447149646"
variation 886
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1329225580"
variation 891
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042775714"
variation 893
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042775737"
variation 895
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1300508199"
variation 902
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042775765"
variation 903
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042775784"
variation 904
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465129571"
variation 905
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:190749180"
variation 906
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1378680798"
variation 907
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042775861"
variation 908..913
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:979124188"
variation 909
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042775887"
variation 937
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1438202695"
variation 939
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1380140557"
variation 940
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042775957"
variation 943
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1179654206"
variation 948
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace=""
/replace="a"
/db_xref="dbSNP:926492764"
variation 948
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042775995"
variation 949
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042776037"
variation 952
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:767086808"
variation 954
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025700115"
variation 955
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042776093"
variation 962
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:752296762"
variation 963
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042776147"
variation 980
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:955477282"
variation 983
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1199899582"
variation 992
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042776212"
variation 1002
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:937926043"
variation 1005
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042776260"
variation 1011
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256492081"
variation 1017
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042776306"
variation 1018
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042776322"
variation 1021
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1056288083"
variation 1024
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042776375"
variation 1030
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008381055"
variation 1032
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:745343572"
variation 1035
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1602432032"
variation 1039
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213007704"
variation 1040
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042776473"
variation 1051..1052
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace=""
/replace="tt"
/db_xref="dbSNP:917740392"
variation 1055
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042776521"
variation 1056
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042776538"
variation 1057
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042776555"
variation 1058
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1569488983"
variation 1060
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:929186001"
variation 1061
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:769356424"
variation 1071
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1337113038"
variation 1076
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1310182148"
variation 1078
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1394918103"
variation 1085..1100
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="catat"
/replace="catatttatgacatat"
/db_xref="dbSNP:760382674"
variation 1086
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:2147576898"
variation 1094
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1305101967"
variation 1095
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:763902424"
variation 1096
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:990813025"
variation 1097..1101
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="ata"
/replace="atata"
/db_xref="dbSNP:1274084941"
variation 1100
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace=""
/replace="t"
/db_xref="dbSNP:2042776852"
variation 1100
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042776825"
variation 1108
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042776878"
variation 1111
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:754254826"
variation 1117
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242348603"
variation 1128..1137
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="atact"
/replace="atactatact"
/db_xref="dbSNP:2042776958"
variation 1134..1138
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace=""
/replace="tactg"
/db_xref="dbSNP:2042776989"
variation 1154
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042777007"
variation 1157
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042777020"
variation 1158
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042777044"
variation 1162
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441961302"
ORIGIN
ggttcagcgttcaacaacaagcttccaagatgccgcccaaaggaaaaagtggttctggaaaagcggggaaaggtcagacacattctatgtgaaaaacatggcaaaatcatggaagccatggaaaagttaaagtctgggatgagattcaatgaagtggccgcacagtatagtgaagataaagccaggcaagggggtgacttgggttggatgaccagagggtccatggtgggaccatttcaagaagcagcatttgccttgcctgtaagtgggatggataagcctgtgtttacagacccaccggttaagacaaaatttggatatcatattattatggtcgaaggaagaaaataaaatcatatgaaagactgaataagttttatacattttgtttctttaaaaggtattacatattcttttgagctggagctgcaaggaaatacaaaaatttttaaaaagaaaagatattggatgctccttgtattctgtgaaagctctaagtatgggtttgtaggtgtaagagagggtggggctaagtgaatgtcaactgtagtaggtattcagtcagtctttctcaaagagaagtcaagcagactccctttaacctgtattctctttcctcccagaactatatctgactctcagtctgtcccataaattaattcagaaaccatcttcaggggaagcagatatcaactcacactattcacacaactgaaaatattgggcatcaaatagattagtgtgtgagaatcataaaataagttcctagacaacatttgttttacatgttagtcaactctgatcttccaggacaggtggtattagctccactgtcttaacatagtacgtggcacgttatgcctttcagtgttaactcctttctttttaaataaatgtttattggaggaaaaaagcactcagttgttccatgagttgttttgtactagactaaccgagtgctggttaaagggagggatgtcagcataaaaatgtcattccctcatcttcagtgtatgggttacattaagactgtcctttccagggccaatgttctgtgcatctaaatttttaaaatttaaaatgccatatttatgacatataaaaaagtataaagattactaatataaatactatactgcttcaaaaataaaactttgccaacaca
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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