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NM_020451.3(SELENON):c.1469G>A (p.Trp490Ter) AND not provided

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Apr 28, 2017
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:
RCV000591683.6

Allele description [Variation Report for NM_020451.3(SELENON):c.1469G>A (p.Trp490Ter)]

NM_020451.3(SELENON):c.1469G>A (p.Trp490Ter)

Gene:
SELENON:selenoprotein N [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1p36.11
Genomic location:
Preferred name:
NM_020451.3(SELENON):c.1469G>A (p.Trp490Ter)
Other names:
NM_020451.3(SELENON):c.1469G>A; p.Trp490Ter
HGVS:
  • NC_000001.11:g.25813962G>A
  • NG_009930.1:g.18787G>A
  • NM_020451.3:c.1469G>AMANE SELECT
  • NM_206926.2:c.1367G>A
  • NP_065184.2:p.Trp490Ter
  • NP_996809.1:p.Trp456Ter
  • LRG_857t1:c.1469G>A
  • LRG_857:g.18787G>A
  • LRG_857p1:p.Trp490Ter
  • NC_000001.10:g.26140453G>A
  • NM_020451.2:c.1469G>A
Protein change:
W456*
Links:
dbSNP: rs960468382
NCBI 1000 Genomes Browser:
rs960468382
Molecular consequence:
  • NM_020451.3:c.1469G>A - nonsense - [Sequence Ontology: SO:0001587]
  • NM_206926.2:c.1367G>A - nonsense - [Sequence Ontology: SO:0001587]
Observations:
1

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000708120Eurofins Ntd Llc (ga)
criteria provided, single submitter

(EGL Classification Definitions 2015)
Pathogenic
(Apr 28, 2017)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot providednot providednot providedclinical testing

Details of each submission

From Eurofins Ntd Llc (ga), SCV000708120.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot provided1not providednot providednot provided

Last Updated: Sep 29, 2024