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NM_032861.4(SERAC1):c.1684+91_1684+92insTTCCTTGAATGTATTATCTTATTTTATA AND not provided

Germline classification:
Likely benign (1 submission)
Last evaluated:
Jul 7, 2018
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:
RCV001580834.3

Allele description [Variation Report for NM_032861.4(SERAC1):c.1684+91_1684+92insTTCCTTGAATGTATTATCTTATTTTATA]

NM_032861.4(SERAC1):c.1684+91_1684+92insTTCCTTGAATGTATTATCTTATTTTATA

Gene:
SERAC1:serine active site containing 1 [Gene - OMIM - HGNC]
Variant type:
Insertion
Cytogenetic location:
6q25.3
Genomic location:
Preferred name:
NM_032861.4(SERAC1):c.1684+91_1684+92insTTCCTTGAATGTATTATCTTATTTTATA
HGVS:
  • NC_000006.12:g.158114716_158114717insTATAAAATAAGATAATACATTCAAGGAA
  • NG_032889.1:g.58583_58584insTATTTTATATTCCTTGAATGTATTATCT
  • NM_032861.4:c.1684+91_1684+92insTTCCTTGAATGTATTATCTTATTTTATAMANE SELECT
  • NC_000006.11:g.158535748_158535749insTATAAAATAAGATAATACATTCAAGGAA
  • NR_073096.2:n.1690_1691insTATTTTATATTCCTTGAATGTATTATCT
Links:
dbSNP: rs570922106
NCBI 1000 Genomes Browser:
rs570922106
Molecular consequence:
  • NM_032861.4:c.1684+91_1684+92insTTCCTTGAATGTATTATCTTATTTTATA - intron variant - [Sequence Ontology: SO:0001627]
  • NR_073096.2:n.1690_1691insTATTTTATATTCCTTGAATGTATTATCT - non-coding transcript variant - [Sequence Ontology: SO:0001619]

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
SCV001817891GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Likely benign
(Jul 7, 2018) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From GeneDx, SCV001817891.1

#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