brca.iarc.fr rapport :   Visitez le site


Titre:cancer susceptibility (including unclassified variants) salt lake city, utah

La description :patient care academics & research español refer a patient about us giving newsroom directions jobs contact us publications disclaimer huntsman cancer institute / research / cancer genetics / cance...

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Server:Apache/2.4.18 (Ubunt...

L'adresse IP principale: 193.51.164.193,Votre serveur France,Lyon ISP:International Agency for Research on Cancer  TLD:fr Code postal:fr

Ce rapport est mis à jour en 09-May-2019

Created Date:1995-01-01
Changed Date:2016-12-31
Expires Date:2017-12-31

Données techniques du brca.iarc.fr


Geo IP vous fournit comme la latitude, la longitude et l'ISP (Internet Service Provider) etc. informations. Notre service GeoIP a trouvé l'hôte brca.iarc.fr.Actuellement, hébergé dans France et son fournisseur de services est International Agency for Research on Cancer .

Latitude: 45.748458862305
Longitude: 4.8467102050781
Pays: France (fr)
Ville: Lyon
Région: Rhone-Alpes
ISP: International Agency for Research on Cancer

Analyse d'en-tête HTTP


Les informations d'en-tête HTTP font partie du protocole HTTP que le navigateur d'un utilisateur envoie à appelé Apache/2.4.18 (Ubuntu) contenant les détails de ce que le navigateur veut et acceptera de nouveau du serveur Web.

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Date:Thu, 09 May 2019 06:34:52 GMT
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DNS

cname:parbat.iarc.fr.
ipv4:IP:193.51.164.193
ASN:2200
OWNER:FR-RENATER Reseau National de telecommunications pour la Technologie, FR
Country:FR

HtmlToText

patient care academics & research español refer a patient about us giving newsroom directions jobs contact us publications disclaimer huntsman cancer institute / research / cancer genetics / cancer susceptibility (including unclassified variance) cancer susceptibility (including unclassified variants) genetic variant databases link directly to databases >>> when testing a gene, many different types of genetic changes are identified. some genetic changes clearly impair the function of the gene (that is, they are pathogenic) and may cause disease. other genetic changes are benign – causing no problems with the gene and creating no medical problems for the individual. however, some genetic changes are not easily classified as either pathogenic or benign. these genetic changes are called unclassified variants. unclassified variants present a dilemma for researchers, clinicians, and patients – all of whom are seeking clear, informative genetic test results. when an unclassified variant is identified in a patient’s genetic test results, it is unknown whether or not that variant has caused or could cause disease in the patient (or his/her family members). many researchers are working to gain more information about variants to definitively classify them as benign or pathogenic. however, this research takes time. until a variant can be classified, care for patients and their relatives is typically planned using what is definitely known – with tailored treatment and screening recommendations based on the patient’s personal and family history rather than the genetic variant. researchers at huntsman cancer institute at the university of utah (hci) have been involved with unclassified variant research for many years. their research has focused on classifying variants in genes associated with hereditary cancer risk, including brca1 and brca 2 and the mismatch repair genes. to increase access to genetic variant information, we have created this portal. by following the links below, you can access multiple internal and external databases full of information on variants in genes associated with hereditary cancer. you can also review powerpoint slides, videos, and articles on the topic of genetic variants. these databases are updated frequently, so we encourage you to check back regularly. if you have questions on genetic variant research, please contact sean.tavtigian@hci.utah.edu . if you or one of your patients has received a genetic test result containing an unclassified variant and you are looking for additional clinical guidance, please contact the family cancer assessment clinic at hci at 801-587-9555. one of the genetic counselors can assist you. huntsman cancer institute and university of utah managed sites resource genes resource description hci brca1/2 classified variant database brca1/2 hci-exlovd.hci.utah.edu curated published data on variants hci brca1/2 prior probabilities database brca1/2 http://priors.hci.utah.edu/priors/ data on all possible single nucleotide substitutions in brca1/2 hci mmr: prior probabilities and classified variants database mismatch repair (mlh1, msh2, pms2, msh6) hci-lovd.hci.utah.edu/home.php data on all possible single nucleotide substitutions in the mmr genes external managed sites resource genes resource description lovd-for paraganglioma genes (fh, sdhx) lovd-for paraganglioma genes (fh, sdhx) chromium.liacs.nl/lovd_sdh/home.php curated published data on variants iarc tp53 tp53 p53.iarc.fr/ curated published data on germline and tumor variants insight mismatch repair/apc/cdh1 www.insight-group.org/variants/database/ curated published data on germline variants breast cancer information core brca1/2 research.nhgri.nih.gov/bic/ database of submitted vus information from researchers and clinicians, classifications if available evidence-based network for the interpretation of germline alleles (enigma) multiple enigmaconsortium.org/ submit variants for research publications clinical resources at huntsman cancer institute family cancer assessment clinic (fcac) - providing clinical genetics evaluations and hereditary cancer risk assessment for patients research resources at huntsman cancer institute cancer genetics study (cgs) - enrolling patients with personal or family histories that suggest increased cancer risk to gain and refine knowledge about hereditary cancer contact information huntsman cancer institute 2000 circle of hope salt lake city, ut 84112 cancer hospital 801-585-0100 general 801-585-0303 quick links about us find a doctor careers circle of hope blog news & events directions & parking giving site information patient rights & responsibilities disclaimer privacy statement non-discrimination policy copyright and trademarks all clinical services and programs are part of university of utah health hospitals and clinics © 2018 huntsman cancer institute at the university of utah social media

Informations Whois


Whois est un protocole qui permet d'accéder aux informations d'enregistrement.Vous pouvez atteindre quand le site Web a été enregistré, quand il va expirer, quelles sont les coordonnées du site avec les informations suivantes. En un mot, il comprend ces informations;

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hold: NO
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tech-c: GR1378-FRNIC
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Expiry Date: 31/12/2017
created: 01/01/1995
last-update: 31/12/2016
source: FRNIC

ns-list: NSL50420-FRNIC
nserver: ns1.iarc.fr [193.51.164.138]
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nserver: ccpntc3.in2p3.fr [134.158.69.191]
nserver: ccpnvx.in2p3.fr [134.158.69.104]
source: FRNIC

registrar: GIP RENATER
type: Isp Option 1
address: 23-25 Rue Daviel
address: PARIS
country: FR
phone: +33 1 53 94 20 30
fax-no: +33 1 53 94 20 31
e-mail: domaine@renater.fr
website: http://www.renater.fr
anonymous: NO
registered: 01/01/1998
source: FRNIC

nic-hdl: IAFR1-FRNIC
type: ORGANIZATION
contact: International Agency for Research on Cancer
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nic-hdl: MS5771-FRNIC
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registrar: GIP RENATER
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anonymous: NO
obsoleted: NO
source: FRNIC


  REFERRER http://www.nic.fr

  REGISTRAR AFNIC

SERVERS

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ADDRESS
International Agency for Research on Cancer
150, cours Albert Thomas
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ADDRESS
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TROUBLE
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TECH-C
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OWNER

  HANDLE IAFR1-FRNIC

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  CONTACT International Agency for Research on Cancer

ADDRESS
150, cours Albert Thomas
69372 Lyon Cedex 8

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DOMAIN

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NSERVER

  NS1.IARC.FR 193.51.164.138

  DNSEXT.IARC.FR 193.51.164.142

  CCPNTC3.IN2P3.FR 134.158.69.191

  CCPNVX.IN2P3.FR 134.158.69.104

  NAME iarc.fr

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