NM_001378609.3(OTOGL):c.6121+48dup AND not provided

Germline classification:: Benign (1 submission)
Last evaluated:: Aug 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:: RCV001537614.2

Allele description [Variation Report for NM_001378609.3(OTOGL):c.6121+48dup]

NM_001378609.3(OTOGL):c.6121+48dup

Gene:

OTOGL:otogelin like [Gene - OMIM - HGNC]

Variant type:

Duplication

Cytogenetic location:

12q21.31

Genomic location:

Preferred name:

NM_001378609.3(OTOGL):c.6121+48dup

HGVS:

NC_000012.12:g.80358397dup
NG_033008.1:g.153945dup
NM_001368062.3:c.5986+48dup
NM_001378609.3:c.6121+48dupMANE SELECT
NM_001378610.3:c.6121+48dup
NM_173591.7:c.6121+48dup
NC_000012.11:g.80752177dup

Links:

dbSNP: rs146138915

NCBI 1000 Genomes Browser:

rs146138915

Molecular consequence:

NM_001368062.3:c.5986+48dup - intron variant - [Sequence Ontology: SO:0001627]
NM_001378609.3:c.6121+48dup - intron variant - [Sequence Ontology: SO:0001627]
NM_001378610.3:c.6121+48dup - intron variant - [Sequence Ontology: SO:0001627]
NM_173591.7:c.6121+48dup - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001754513	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Benign (Aug 7, 2018)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001754513

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Benign
(Aug 7, 2018)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From GeneDx, SCV001754513.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Dec 24, 2023

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