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NM_003001.5(SDHC):c.77+29_77+31dup AND not provided

Germline classification:
Likely benign (1 submission)
Last evaluated:
Aug 11, 2019
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:
RCV001574972.4

Allele description [Variation Report for NM_003001.5(SDHC):c.77+29_77+31dup]

NM_003001.5(SDHC):c.77+29_77+31dup

Gene:
SDHC:succinate dehydrogenase complex subunit C [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
1q23.3
Genomic location:
Preferred name:
NM_003001.5(SDHC):c.77+29_77+31dup
HGVS:
  • NC_000001.11:g.161323699_161323701dup
  • NG_012767.1:g.14324_14326dup
  • NM_001035511.3:c.77+29_77+31dup
  • NM_001035512.3:c.77+29_77+31dup
  • NM_001035513.3:c.20+9274_20+9276dup
  • NM_001278172.3:c.77+29_77+31dup
  • NM_001407115.1:c.77+29_77+31dup
  • NM_001407116.1:c.21-4697_21-4695dup
  • NM_001407117.1:c.21-4697_21-4695dup
  • NM_001407118.1:c.77+29_77+31dup
  • NM_001407119.1:c.-35+29_-35+31dup
  • NM_001407120.1:c.-153+29_-153+31dup
  • NM_001407121.1:c.21-4697_21-4695dup
  • NM_003001.5:c.77+29_77+31dupMANE SELECT
  • LRG_317:g.14324_14326dup
  • NC_000001.10:g.161293489_161293491dup
Links:
dbSNP: rs371604278
NCBI 1000 Genomes Browser:
rs371604278
Molecular consequence:
  • NM_001035511.3:c.77+29_77+31dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001035512.3:c.77+29_77+31dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001035513.3:c.20+9274_20+9276dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001278172.3:c.77+29_77+31dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407115.1:c.77+29_77+31dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407116.1:c.21-4697_21-4695dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407117.1:c.21-4697_21-4695dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407118.1:c.77+29_77+31dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407119.1:c.-35+29_-35+31dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407120.1:c.-153+29_-153+31dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407121.1:c.21-4697_21-4695dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_003001.5:c.77+29_77+31dup - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001801878GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Likely benign
(Aug 11, 2019) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From GeneDx, SCV001801878.1

#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: Dec 24, 2023