U.S. flag

An official website of the United States government

NM_001126108.2(SLC12A3):c.1795C>T (p.Leu599Phe) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jun 29, 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:
RCV002907647.2

Allele description [Variation Report for NM_001126108.2(SLC12A3):c.1795C>T (p.Leu599Phe)]

NM_001126108.2(SLC12A3):c.1795C>T (p.Leu599Phe)

Gene:
SLC12A3:solute carrier family 12 member 3 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
16q13
Genomic location:
Preferred name:
NM_001126108.2(SLC12A3):c.1795C>T (p.Leu599Phe)
HGVS:
  • NC_000016.10:g.56884174C>T
  • NG_009386.2:g.23968C>T
  • NM_000339.2:c.1795C>T
  • NM_000339.3:c.1795C>T
  • NM_001126107.2:c.1792C>T
  • NM_001126108.2:c.1795C>TMANE SELECT
  • NM_001410896.1:c.1792C>T
  • NP_000330.3:p.Leu599Phe
  • NP_001119579.2:p.Leu598Phe
  • NP_001119580.2:p.Leu599Phe
  • NP_001397825.1:p.Leu598Phe
  • NC_000016.9:g.56918086C>T
Protein change:
L598F
Molecular consequence:
  • NM_000339.3:c.1795C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001126107.2:c.1792C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001126108.2:c.1795C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001410896.1:c.1792C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003244112Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Jun 29, 2022) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV003244112.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

This sequence change replaces leucine, which is neutral and non-polar, with phenylalanine, which is neutral and non-polar, at codon 599 of the SLC12A3 protein (p.Leu599Phe). This variant is present in population databases (rs199883951, gnomAD 0.02%). This variant has not been reported in the literature in individuals affected with SLC12A3-related conditions. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt SLC12A3 protein function. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024