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NM_001126049.2(KLLN):c.-898G>A AND Hereditary cancer-predisposing syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 18, 2013
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
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:
RCV000115555.6

Allele description [Variation Report for NM_001126049.2(KLLN):c.-898G>A]

NM_001126049.2(KLLN):c.-898G>A

Genes:
PTEN:phosphatase and tensin homolog [Gene - OMIM - HGNC]
LOC130004273:ATAC-STARR-seq lymphoblastoid silent region 2585 [Gene]
KLLN:killin, p53 regulated DNA replication inhibitor [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
10q23.31
Genomic location:
Preferred name:
NM_001126049.2(KLLN):c.-898G>A
Other names:
NM_000314.6(PTEN):c.-1084C>T
HGVS:
  • NC_000010.11:g.87863385C>T
  • NG_007466.2:g.4948C>T
  • NG_033079.1:g.5053G>A
  • NG_183718.1:g.106C>T
  • NM_000314.8:c.-1085C>TMANE SELECT
  • NM_001126049.2:c.-898G>AMANE SELECT
  • LRG_1087t1:c.-898G>A
  • LRG_311t1:c.-1084C>T
  • LRG_1087:g.5053G>A
  • LRG_311:g.4948C>T
  • NC_000010.10:g.89623142C>T
  • NM_000314.4:c.-1084C>T
  • c.-1085C>T[hg19]
Links:
dbSNP: rs538728843
NCBI 1000 Genomes Browser:
rs538728843
Molecular consequence:
  • NM_001126049.2:c.-898G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_000314.8:c.-1085C>T - upstream transcript variant - [Sequence Ontology: SO:0001986]

Condition(s)

Name:
Hereditary cancer-predisposing syndrome
Synonyms:
Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000185343Ambry Genetics
criteria provided, single submitter

(Ambry Autosomal Dominant and X-Linked criteria (9/4/14))
Uncertain significance
(Dec 18, 2013)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Ambry Genetics, SCV000185343.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 20, 2024