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NM_212482.4(FN1):c.869G>A (p.Arg290His) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 21, 2023
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
Somatic classification
of clinical impact:
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:

Allele description [Variation Report for NM_212482.4(FN1):c.869G>A (p.Arg290His)]

NM_212482.4(FN1):c.869G>A (p.Arg290His)

FN1:fibronectin 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
Genomic location:
Preferred name:
NM_212482.4(FN1):c.869G>A (p.Arg290His)
  • NC_000002.12:g.215425261C>T
  • NG_012196.1:g.15808G>A
  • NM_001306129.2:c.869G>A
  • NM_001306130.2:c.869G>A
  • NM_001306131.2:c.869G>A
  • NM_001306132.2:c.869G>A
  • NM_001365517.2:c.869G>A
  • NM_001365518.2:c.869G>A
  • NM_001365519.2:c.869G>A
  • NM_001365520.2:c.869G>A
  • NM_001365521.2:c.869G>A
  • NM_001365522.2:c.869G>A
  • NM_001365523.2:c.869G>A
  • NM_001365524.2:c.869G>A
  • NM_002026.4:c.869G>A
  • NM_054034.3:c.869G>A
  • NM_212474.3:c.869G>A
  • NM_212476.3:c.869G>A
  • NM_212478.3:c.869G>A
  • NM_212482.4:c.869G>AMANE SELECT
  • NP_001293058.2:p.Arg290His
  • NP_001293059.2:p.Arg290His
  • NP_001293060.2:p.Arg290His
  • NP_001293061.2:p.Arg290His
  • NP_001352446.1:p.Arg290His
  • NP_001352447.1:p.Arg290His
  • NP_001352448.1:p.Arg290His
  • NP_001352449.1:p.Arg290His
  • NP_001352450.1:p.Arg290His
  • NP_001352451.1:p.Arg290His
  • NP_001352452.1:p.Arg290His
  • NP_001352453.1:p.Arg290His
  • NP_002017.2:p.Arg290His
  • NP_473375.2:p.Arg290His
  • NP_997639.2:p.Arg290His
  • NP_997641.2:p.Arg290His
  • NP_997643.2:p.Arg290His
  • NP_997647.2:p.Arg290His
  • NC_000002.11:g.216289984C>T
  • NM_212482.1:c.869G>A
Protein change:
dbSNP: rs150990682
NCBI 1000 Genomes Browser:
Molecular consequence:
  • NM_001306129.2:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001306130.2:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001306131.2:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001306132.2:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365517.2:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365518.2:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365519.2:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365520.2:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365521.2:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365522.2:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365523.2:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001365524.2:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_002026.4:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_054034.3:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_212474.3:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_212476.3:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_212478.3:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_212482.4:c.869G>A - missense variant - [Sequence Ontology: SO:0001583]


none provided
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))
Uncertain significance
(Mar 21, 2023)
germlineclinical testing

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

Summary from all submissions

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



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]

Details of each submission

From Invitae, SCV001511411.4

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


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 FN1 protein function. ClinVar contains an entry for this variant (Variation ID: 1020947). This variant has not been reported in the literature in individuals affected with FN1-related conditions. This variant is present in population databases (rs150990682, gnomAD 0.02%), and has an allele count higher than expected for a pathogenic variant. This sequence change replaces arginine, which is basic and polar, with histidine, which is basic and polar, at codon 290 of the FN1 protein (p.Arg290His).

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

Last Updated: May 7, 2024