NM_030777.4(SLC2A10):c.*29C>G AND not provided

Clinical significance:Likely benign (Last evaluated: Jun 26, 2018)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV001537025.2

Allele description [Variation Report for NM_030777.4(SLC2A10):c.*29C>G]

NM_030777.4(SLC2A10):c.*29C>G

Gene:
SLC2A10:solute carrier family 2 member 10 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
20q13.12
Genomic location:
Preferred name:
NM_030777.4(SLC2A10):c.*29C>G
HGVS:
  • NC_000020.11:g.46733863C>G
  • NG_016284.1:g.29224C>G
  • NM_030777.4:c.*29C>GMANE SELECT
  • NC_000020.10:g.45362502C>G
  • NM_030777.3:c.*29C>G
Links:
dbSNP: rs34965637
NCBI 1000 Genomes Browser:
rs34965637
Molecular consequence:
  • NM_030777.4:c.*29C>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001753849GeneDxcriteria provided, single submitter
Likely benign
(Jun 26, 2018)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From GeneDx, SCV001753849.1

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

Last Updated: Oct 8, 2021

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