NM_016729.3(FOLR1):c.474G>C (p.Lys158Asn) AND Cerebral folate transport deficiency

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Nov 13, 2021
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:: RCV001890953.4

Allele description [Variation Report for NM_016729.3(FOLR1):c.474G>C (p.Lys158Asn)]

NM_016729.3(FOLR1):c.474G>C (p.Lys158Asn)

Gene:

FOLR1:folate receptor alpha [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q13.4

Genomic location:

Preferred name:

NM_016729.3(FOLR1):c.474G>C (p.Lys158Asn)

HGVS:

NC_000011.10:g.72195728G>C
NG_015863.1:g.11171G>C
NM_000802.3:c.474G>C
NM_016724.3:c.474G>C
NM_016725.3:c.474G>C
NM_016729.3:c.474G>CMANE SELECT
NP_000793.1:p.Lys158Asn
NP_057936.1:p.Lys158Asn
NP_057937.1:p.Lys158Asn
NP_057941.1:p.Lys158Asn
NC_000011.9:g.71906772G>C

Protein change:

K158N

Links:

dbSNP: rs750638602

NCBI 1000 Genomes Browser:

rs750638602

Molecular consequence:

NM_000802.3:c.474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_016724.3:c.474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_016725.3:c.474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_016729.3:c.474G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Cerebral folate transport deficiency
Synonyms:: Neurodegeneration due to cerebral folate transport deficiency; Cerebral folate deficiency syndrome; FOLATE RECEPTOR DEFICIENCY; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0013110; MedGen: C2751584; Orphanet: 217382; OMIM: 613068

Recent activity

Clear Turn Off Turn On

Chain B, Histone H4
Chain B, Histone H4
gi|2700920799|pdb|8V7L|B

Protein

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
SCV002164902	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Nov 13, 2021)	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

SCV002164902

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Nov 13, 2021)

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 Labcorp Genetics (formerly Invitae), Labcorp, SCV002164902.3

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

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: "Benign"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals affected with FOLR1-related conditions. This variant is present in population databases (rs750638602, gnomAD 0.0009%). This sequence change replaces lysine, which is basic and polar, with asparagine, which is neutral and polar, at codon 158 of the FOLR1 protein (p.Lys158Asn). 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

ClinVar

Relating variation to medicine