NM_014714.4(IFT140):c.*2G>A AND not specified

Clinical significance:Likely benign (Last evaluated: Jun 18, 2015)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000348101.1

Allele description [Variation Report for NM_014714.4(IFT140):c.*2G>A]

NM_014714.4(IFT140):c.*2G>A

Gene:
IFT140:intraflagellar transport 140 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
16p13.3
Genomic location:
Preferred name:
NM_014714.4(IFT140):c.*2G>A
HGVS:
  • NC_000016.10:g.1510942C>T
  • NG_032783.1:g.106167G>A
  • NG_050910.1:g.22599C>T
  • NM_014714.4:c.*2G>AMANE SELECT
  • NC_000016.9:g.1560943C>T
  • NM_014714.3:c.*2G>A
Links:
dbSNP: rs144879630
NCBI 1000 Genomes Browser:
rs144879630
Molecular consequence:
  • NM_014714.4:c.*2G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
Observations:
1

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000332231EGL Genetic Diagnostics, Eurofins Clinical Diagnosticscriteria provided, single submitter
Likely benign
(Jun 18, 2015)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot providednot providednot providedclinical testing

Details of each submission

From EGL Genetic Diagnostics, Eurofins Clinical Diagnostics, SCV000332231.4

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

Last Updated: Dec 3, 2020

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