NM_001367773.1(ESYT2):c.2125A>G (p.Ile709Val) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Aug 3, 2022
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:: RCV004151083.1

Allele description [Variation Report for NM_001367773.1(ESYT2):c.2125A>G (p.Ile709Val)]

NM_001367773.1(ESYT2):c.2125A>G (p.Ile709Val)

Gene:

ESYT2:extended synaptotagmin 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7q36.3

Genomic location:

Preferred name:

NM_001367773.1(ESYT2):c.2125A>G (p.Ile709Val)

HGVS:

NC_000007.14:g.158741566T>C
NM_001367773.1:c.2125A>GMANE SELECT
NM_020728.3:c.2062A>G
NP_001354702.1:p.Ile709Val
NP_065779.2:p.Ile688Val
NC_000007.13:g.158534257T>C
NM_020728.2:c.2206A>G

Protein change:

I688V

Molecular consequence:

NM_001367773.1:c.2125A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_020728.3:c.2062A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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RefSeq Protein Links for Gene (Select 29057) (29)
Protein
SLC8A1 solute carrier family 8 member A1 [Homo sapiens]
SLC8A1 solute carrier family 8 member A1 [Homo sapiens]
Gene ID:6546

Gene
Gene Links for GEO Profiles (Select 89697185) (1)
Gene
Related DataSets for GEO Profiles (Select 89698122) (1)
GEO DataSets
Severe asthma: circulating CD4+ and CD8+ T-cells
Severe asthma: circulating CD4+ and CD8+ T-cells
Accession: GDS4425

GEO DataSets

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003641066	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Aug 3, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003641066

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Aug 3, 2022)

germline

clinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV003641066.2

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

Description

The c.2206A>G (p.I736V) alteration is located in exon 17 (coding exon 17) of the ESYT2 gene. This alteration results from a A to G substitution at nucleotide position 2206, causing the isoleucine (I) at amino acid position 736 to be replaced by a valine (V). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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

Last Updated: Nov 3, 2024

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