NM_003000.3(SDHB):c.527A>G (p.Glu176Gly) AND Hereditary cancer-predisposing syndrome

Clinical significance:Uncertain significance (Last evaluated: Nov 9, 2018)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV001023850.1

Allele description [Variation Report for NM_003000.3(SDHB):c.527A>G (p.Glu176Gly)]

NM_003000.3(SDHB):c.527A>G (p.Glu176Gly)

Gene:
SDHB:succinate dehydrogenase complex iron sulfur subunit B [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1p36.13
Genomic location:
Preferred name:
NM_003000.3(SDHB):c.527A>G (p.Glu176Gly)
HGVS:
  • NC_000001.11:g.17027762T>C
  • NG_012340.1:g.31409A>G
  • NM_003000.2:c.527A>G
  • NM_003000.3:c.527A>GMANE SELECT
  • NP_002991.2:p.Glu176Gly
  • NP_002991.2:p.Glu176Gly
  • LRG_316t1:c.527A>G
  • LRG_316:g.31409A>G
  • LRG_316p1:p.Glu176Gly
  • NC_000001.10:g.17354257T>C
  • NC_000001.10:g.17354257T>C
Protein change:
E176G
Links:
dbSNP: rs201082445
NCBI 1000 Genomes Browser:
rs201082445
Molecular consequence:
  • NM_003000.2:c.527A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_003000.3:c.527A>G - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Name:
Hereditary cancer-predisposing syndrome
Synonyms:
Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015356; MedGen: C0027672

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001185782Ambry Geneticscriteria provided, single submitter
Uncertain significance
(Nov 9, 2018)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot provided1not providedclinical testing

Details of each submission

From Ambry Genetics, SCV001185782.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided

Description

The p.E176G variant (also known as c.527A>G), located in coding exon 5 of the SDHB gene, results from an A to G substitution at nucleotide position 527. The glutamic acid at codon 176 is replaced by glycine, an amino acid with similar properties. This amino acid position is poorly conserved in available vertebrate species. In addition, the in silico prediction for this alteration is inconclusive. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknown1not providednot provided1not providednot providednot provided

Last Updated: Oct 25, 2021

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