NM_000039.3(APOA1):c.662C>G (p.Thr221Ser) AND not provided

This record was updated by the submitter. Please see the current version.

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 19, 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:: RCV003098314.2

Allele description

NM_000039.3(APOA1):c.662C>G (p.Thr221Ser)

Gene:

APOA1:apolipoprotein A1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q23.3

Genomic location:

Preferred name:

NM_000039.3(APOA1):c.662C>G (p.Thr221Ser)

HGVS:

NC_000011.10:g.116835950G>C
NG_012021.1:g.6673C>G
NM_000039.3:c.662C>GMANE SELECT
NM_001318017.2:c.662C>G
NM_001318018.2:c.662C>G
NM_001318021.2:c.335C>G
NP_000030.1:p.Thr221Ser
NP_000030.1:p.Thr221Ser
NP_001304946.1:p.Thr221Ser
NP_001304947.1:p.Thr221Ser
NP_001304950.1:p.Thr112Ser
NP_001304950.1:p.Thr112Ser
LRG_767t1:c.662C>G
LRG_767:g.6673C>G
LRG_767p1:p.Thr221Ser
NC_000011.9:g.116706666G>C
NM_000039.1:c.662C>G
NM_001318021.1:c.335C>G

Protein change:

T112S

Molecular consequence:

NM_000039.3:c.662C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001318017.2:c.662C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001318018.2:c.662C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001318021.2:c.335C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

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PREDICTED: Danio rerio Yip1 domain family, member 6 (yipf6), transcript variant ...
PREDICTED: Danio rerio Yip1 domain family, member 6 (yipf6), transcript variant X1, mRNA
gi|528479271|ref|XM_005171830.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003525449	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Dec 19, 2022)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003525449

Invitae

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Dec 19, 2022)

germline

clinical testing

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

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

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 Invitae, SCV003525449.2

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

Description

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. 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 not expected to disrupt APOA1 protein function. ClinVar contains an entry for this variant (Variation ID: 1754560). This variant has not been reported in the literature in individuals affected with APOA1-related conditions. This variant is present in population databases (rs200394039, gnomAD 0.03%). This sequence change replaces threonine, which is neutral and polar, with serine, which is neutral and polar, at codon 221 of the APOA1 protein (p.Thr221Ser).

#	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 1, 2024

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