NM_017775.3(TTC19):c.-73G>A AND not provided

Clinical significance:Uncertain significance (Last evaluated: Jul 2, 2015)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000328517.1

Allele description [Variation Report for NM_017775.3(TTC19):c.-73G>A]

NM_017775.3(TTC19):c.-73G>A

Gene:
TTC19:tetratricopeptide repeat domain 19 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
17p12
Genomic location:
Preferred name:
NM_017775.3(TTC19):c.-73G>A
HGVS:
  • NC_000017.11:g.15999776G>A
  • NG_029806.1:g.5397G>A
  • NM_017775.3:c.-73G>A
  • NC_000017.10:g.15903090G>A
Links:
dbSNP: rs149555498
NCBI 1000 Genomes Browser:
rs149555498
Molecular consequence:
  • NM_017775.3:c.-73G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
Observations:
1

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000332952EGL Genetic Diagnostics,Eurofins Clinical Diagnosticscriteria provided, single submitter
Uncertain significance
(Jul 2, 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, SCV000332952.4

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

Last Updated: Mar 30, 2019

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