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NR_109833.1(PRNCR1):n.11999A>G AND Familial prostate cancer

Germline classification:
association (1 submission)
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV001257962.1

Allele description [Variation Report for NR_109833.1(PRNCR1):n.11999A>G]

NR_109833.1(PRNCR1):n.11999A>G

Gene:
PRNCR1:prostate cancer associated non-coding RNA 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
8q24.21
Genomic location:
Preferred name:
NR_109833.1(PRNCR1):n.11999A>G
HGVS:
  • NC_000008.11:g.127091872A>G
  • NC_000008.10:g.128104117A>G
  • NR_109833.1:n.11999A>G
Links:
dbSNP: rs183373024
NCBI 1000 Genomes Browser:
rs183373024
Molecular consequence:
  • NR_109833.1:n.11999A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Familial prostate cancer
Synonyms:
Hereditary prostate cancer
Identifiers:
MONDO: MONDO:0700275; MedGen: C2931456; OMIM: 176807

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001434775University of Washington Center for Mendelian Genomics, University of Washington
no assertion criteria provided
associationunknownresearch

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownyesnot providednot providednot providednot providednot providedresearch

Citations

PubMed

8q24 genetic variation and comprehensive haplotypes altering familial risk of prostate cancer.

Dupont WD, Breyer JP, Plummer WD, Chang SS, Cookson MS, Smith JA; University of Washington Center for Mendelian Genomics., Blue EE, Bamshad MJ, Smith JR.

Nat Commun. 2020 Mar 23;11(1):1523. doi: 10.1038/s41467-020-15122-1.

PubMed [citation]
PMID:
32251286
PMCID:
PMC7089954

Details of each submission

From University of Washington Center for Mendelian Genomics, University of Washington, SCV001434775.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedresearch PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 16, 2024