NM_173653.4(SLC9A9):c.1742T>C (p.Ile581Thr) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 26, 2017
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:: RCV000489661.1

Allele description [Variation Report for NM_173653.4(SLC9A9):c.1742T>C (p.Ile581Thr)]

NM_173653.4(SLC9A9):c.1742T>C (p.Ile581Thr)

Gene:

SLC9A9:solute carrier family 9 member A9 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3q24

Genomic location:

Preferred name:

NM_173653.4(SLC9A9):c.1742T>C (p.Ile581Thr)

HGVS:

NC_000003.12:g.143266898A>G
NG_017077.1:g.586634T>C
NG_017077.2:g.586634T>C
NM_173653.4:c.1742T>CMANE SELECT
NP_775924.1:p.Ile581Thr
NC_000003.11:g.142985740A>G
NM_173653.3:c.1742T>C

Protein change:

I581T

Links:

dbSNP: rs1085307858

NCBI 1000 Genomes Browser:

rs1085307858

Molecular consequence:

NM_173653.4:c.1742T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: CN517202

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000577516	GeneDx	criteria provided, single submitter (GeneDx Variant Classification (06012015))	Uncertain significance (Mar 26, 2017)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000577516

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification (06012015))

Uncertain significance
(Mar 26, 2017)

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, SCV000577516.4

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

Description

The I581T variant in the SLC9A9 gene has not been reported previously as a pathogenic variant, nor as a benign variant, to our knowledge. The I581T variant is not observed in large population cohorts (Lek et al., 2016; 1000 Genomes Consortium et al., 2015; Exome Variant Server). The I581T variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. This substitution occurs at a position that is conserved across species. In silico analysis is inconsistent in its predictions as to whether or not the variant is damaging to the protein structure/function. We interpret I581T as a variant of uncertain significance.

#	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: Apr 23, 2022

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