NM_000168.6(GLI3):c.3083_3084delinsTT (p.Ser1028Ile) AND not provided

Germline classification:: Benign (1 submission)
Last evaluated:: Apr 30, 2015
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:: RCV001651320.10

Allele description [Variation Report for NM_000168.6(GLI3):c.3083_3084delinsTT (p.Ser1028Ile)]

NM_000168.6(GLI3):c.3083_3084delinsTT (p.Ser1028Ile)

Gene:

GLI3:GLI family zinc finger 3 [Gene - OMIM - HGNC]

Variant type:

Indel

Cytogenetic location:

7p14.1

Genomic location:

Preferred name:

NM_000168.6(GLI3):c.3083_3084delinsTT (p.Ser1028Ile)

HGVS:

NC_000007.14:g.41965989_41965990delinsAA
NG_008434.1:g.276031_276032delinsTT
NM_000168.6:c.3083_3084delinsTTMANE SELECT
NP_000159.3:p.Ser1028Ile
NC_000007.13:g.42005587_42005588delinsAA
NM_000168.5:c.3083_3084delGCinsTT
NM_000168.5:c.3083_3084delinsTT

Protein change:

S1028I

Links:

dbSNP: rs886043721

NCBI 1000 Genomes Browser:

rs886043721

Molecular consequence:

NM_000168.6:c.3083_3084delinsTT - missense variant - [Sequence Ontology: SO:0001583]

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
SCV001870012	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Benign (Apr 30, 2015)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001870012

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Benign
(Apr 30, 2015)

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, SCV001870012.1

#	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: Nov 10, 2024

ClinVar

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