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NM_003000.3(SDHB):c.424-14_424-9dup AND Paragangliomas 4

Germline classification:
Likely benign (1 submission)
Last evaluated:
Jun 28, 2017
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000662623.2

Allele description [Variation Report for NM_003000.3(SDHB):c.424-14_424-9dup]

NM_003000.3(SDHB):c.424-14_424-9dup

Gene:
SDHB:succinate dehydrogenase complex iron sulfur subunit B [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
1p36.13
Genomic location:
Preferred name:
NM_003000.3(SDHB):c.424-14_424-9dup
HGVS:
  • NC_000001.11:g.17027878_17027883dup
  • NG_012340.1:g.31292_31297dup
  • NM_003000.3:c.424-14_424-9dupMANE SELECT
  • LRG_316:g.31292_31297dup
  • NC_000001.10:g.17354368_17354369insAAGAGG
  • NC_000001.10:g.17354373_17354378dup
  • NM_003000.2:c.424-14_424-9dupCCTCTT
Links:
dbSNP: rs1064794554
NCBI 1000 Genomes Browser:
rs1064794554
Molecular consequence:
  • NM_003000.3:c.424-14_424-9dup - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Paragangliomas 4 (PPGL4)
Synonyms:
CAROTID BODY TUMORS AND MULTIPLE EXTRAADRENAL PHEOCHROMOCYTOMAS; Pheochromocytoma, extraadrenal and cervical paraganglioma; Paragangliomas, hereditary extraadrenal; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0007273; MedGen: C1861848; Orphanet: 29072; OMIM: 115310

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000785287Counsyl
criteria provided, single submitter

(Counsyl Autosomal Dominant Disease Classification criteria (2015))
Likely benign
(Jun 28, 2017)
unknownclinical testing

Counsyl_Autosomal_Dominant_Disease_Classification_criteria_(2015)_v1.pdf

Citation Link

Summary from all submissions

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

Details of each submission

From Counsyl, SCV000785287.2

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

Last Updated: Sep 29, 2024