NM_138711.6(PPARG):c.420G>C (p.Lys140Asn) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 6, 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:: RCV002600253.3

Allele description [Variation Report for NM_138711.6(PPARG):c.420G>C (p.Lys140Asn)]

NM_138711.6(PPARG):c.420G>C (p.Lys140Asn)

Gene:

PPARG:peroxisome proliferator activated receptor gamma [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3p25.2

Genomic location:

Preferred name:

NM_138711.6(PPARG):c.420G>C (p.Lys140Asn)

HGVS:

NC_000003.12:g.12392643G>C
NG_011749.1:g.109794G>C
NM_001330615.4:c.420G>C
NM_001354666.3:c.420G>C
NM_001354667.3:c.420G>C
NM_001354668.2:c.510G>C
NM_001354669.2:c.-8G>C
NM_001354670.2:c.426G>C
NM_001374261.3:c.420G>C
NM_001374262.3:c.420G>C
NM_001374263.2:c.420G>C
NM_001374264.2:c.420G>C
NM_001374265.1:c.510G>C
NM_001374266.1:c.426G>C
NM_005037.7:c.420G>C
NM_015869.5:c.510G>C
NM_138711.6:c.420G>CMANE SELECT
NM_138712.5:c.420G>C
NP_001317544.2:p.Lys140Asn
NP_001341595.2:p.Lys140Asn
NP_001341596.2:p.Lys140Asn
NP_001341597.1:p.Lys170Asn
NP_001341599.1:p.Lys142Asn
NP_001361190.2:p.Lys140Asn
NP_001361191.2:p.Lys140Asn
NP_001361192.2:p.Lys140Asn
NP_001361193.2:p.Lys140Asn
NP_001361194.1:p.Lys170Asn
NP_001361195.1:p.Lys142Asn
NP_005028.5:p.Lys140Asn
NP_056953.2:p.Lys170Asn
NP_619725.3:p.Lys140Asn
NP_619726.3:p.Lys140Asn
NC_000003.11:g.12434142G>C

Protein change:

K140N

Molecular consequence:

NM_001354669.2:c.-8G>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001330615.4:c.420G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001354666.3:c.420G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001354667.3:c.420G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001354668.2:c.510G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001354670.2:c.426G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001374261.3:c.420G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001374262.3:c.420G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001374263.2:c.420G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001374264.2:c.420G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001374265.1:c.510G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001374266.1:c.426G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_005037.7:c.420G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_015869.5:c.510G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_138711.6:c.420G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_138712.5:c.420G>C - 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
SCV002945890	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Mar 6, 2022)	germline	clinical testing	PubMed (2) [See all records that cite these PMIDs] 32041611, 28492532

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002945890

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Mar 6, 2022)

germline

clinical testing

PubMed (2)
[See all records that cite these PMIDs]

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

Citations

PubMed

Six years' experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemias.

Dron JS, Wang J, McIntyre AD, Iacocca MA, Robinson JF, Ban MR, Cao H, Hegele RA.

BMC Med Genomics. 2020 Feb 10;13(1):23. doi: 10.1186/s12920-020-0669-2.

PubMed [citation]

PMID:: 32041611
PMCID:: PMC7011550

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, SCV002945890.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (2)

Description

Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). This missense change has been observed in individual(s) with dyslipidemia (PMID: 32041611). This variant is present in population databases (no rsID available, gnomAD 0.002%). This sequence change replaces lysine, which is basic and polar, with asparagine, which is neutral and polar, at codon 170 of the PPARG protein (p.Lys170Asn). 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.

#	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: Sep 29, 2024

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