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NM_002499.3(NEO1):c.1292-13787C>T AND Lung cancer

Clinical significance:Uncertain significance

Review status:(0/4) 0 stars out of maximum of 4 stars

no assertion criteria provided

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000099651.1

Allele description

NM_002499.3(NEO1):c.1292-13787C>T

Gene:
NEO1:neogenin 1 [Gene - OMIM]
Variant type:
single nucleotide variant
Cytogenetic location:
15q24.1
Genomic location:
Preferred name:
NM_002499.3(NEO1):c.1292-13787C>T
HGVS:
  • NC_000015.10:g.73222560C>T
  • NG_016965.1:g.175077C>T
  • NM_002499.3:c.1292-13787C>T
  • NC_000015.9:g.73514901C>T
Links:
dbSNP: rs207475590
NCBI 1000 Genomes Browser:
rs207475590
Molecular consequence:
  • NM_002499.3:c.1292-13787C>T - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Lung cancer
Synonyms:
Lung cancer, somatic
Identifiers:
MedGen: C0684249; OMIM: 211980

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000137956Leeds Institute of Molecular Medicine (LIMM)no assertion criteria providedunknownsomaticnot provided

Description

Lung squamous cell carcinoma

SCV000137956

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedsomaticnot providednot providednot providednot provided1not providedliterature only

Details of each submission

From Leeds Institute of Molecular Medicine (LIMM), SCV000137956.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providednot providednot provided

Description

Converted during submission to Uncertain significance.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1somaticnot provided1not providednot providednot providednot providednot providednot provided

Last Updated: Apr 23, 2015

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