NM_000492.3(CFTR):c.2769C>T (p.Ala923=) AND not provided

Clinical significance:Uncertain significance (Last evaluated: Apr 14, 2017)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000589671.3

Allele description [Variation Report for NM_000492.3(CFTR):c.2769C>T (p.Ala923=)]

NM_000492.3(CFTR):c.2769C>T (p.Ala923=)

Gene:
CFTR:CF transmembrane conductance regulator [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
7q31.2
Genomic location:
Preferred name:
NM_000492.3(CFTR):c.2769C>T (p.Ala923=)
HGVS:
  • NC_000007.14:g.117603643C>T
  • NG_016465.4:g.142860C>T
  • NM_000492.3:c.2769C>T
  • NP_000483.3:p.Ala923=
  • LRG_663t1:c.2769C>T
  • LRG_663:g.142860C>T
  • LRG_663p1:p.Ala923=
  • NC_000007.13:g.117243697C>T
  • NP_000483.3:p.(=)
Links:
dbSNP: rs1800108
NCBI 1000 Genomes Browser:
rs1800108
Molecular consequence:
  • NM_000492.3:c.2769C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000110856EGL Genetic Diagnostics, Eurofins Clinical Diagnosticscriteria provided, single submitter
Uncertain significance
(Apr 14, 2017)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod

Details of each submission

From EGL Genetic Diagnostics, Eurofins Clinical Diagnostics, SCV000110856.8

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided2not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot provided2not providednot providednot provided

Last Updated: Sep 6, 2021

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