NM_130468.4(CHST14):c.1118C>T (p.Ala373Val) AND Cardiovascular phenotype

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: May 27, 2023
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:: RCV003298972.2

Allele description [Variation Report for NM_130468.4(CHST14):c.1118C>T (p.Ala373Val)]

NM_130468.4(CHST14):c.1118C>T (p.Ala373Val)

Gene:

CHST14:carbohydrate sulfotransferase 14 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

15q15.1

Genomic location:

Preferred name:

NM_130468.4(CHST14):c.1118C>T (p.Ala373Val)

HGVS:

NC_000015.10:g.40472331C>T
NG_017074.1:g.6371C>T
NM_130468.4:c.1118C>TMANE SELECT
NP_569735.1:p.Ala373Val
LRG_600t1:c.1118C>T
LRG_600:g.6371C>T
NC_000015.9:g.40764530C>T
NM_130468.3:c.1118C>T

Protein change:

A373V

Links:

dbSNP: rs756985970

NCBI 1000 Genomes Browser:

rs756985970

Molecular consequence:

NM_130468.4:c.1118C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Cardiovascular phenotype
Identifiers:: MedGen: CN230736

Recent activity

Clear Turn Off Turn On

ST3GAL3 [Pseudonaja textilis]
ST3GAL3 [Pseudonaja textilis]
Gene ID:113440699

Gene

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004000761	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (May 27, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004000761

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(May 27, 2023)

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	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV004000761.2

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

Description

The p.A373V variant (also known as c.1118C>T), located in coding exon 1 of the CHST14 gene, results from a C to T substitution at nucleotide position 1118. The alanine at codon 373 is replaced by valine, an amino acid with similar properties. This amino acid position is conserved. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, 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: May 1, 2024

ClinVar

Relating variation to medicine