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NM_001384479.1(AGT):c.1097G>T (p.Arg366Leu) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jul 22, 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:
RCV001967789.4

Allele description [Variation Report for NM_001384479.1(AGT):c.1097G>T (p.Arg366Leu)]

NM_001384479.1(AGT):c.1097G>T (p.Arg366Leu)

Gene:
AGT:angiotensinogen [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1q42.2
Genomic location:
Preferred name:
NM_001384479.1(AGT):c.1097G>T (p.Arg366Leu)
HGVS:
  • NC_000001.11:g.230705933C>A
  • NG_008836.2:g.13658G>T
  • NM_001382817.3:c.1097G>T
  • NM_001384479.1:c.1097G>TMANE SELECT
  • NP_001369746.2:p.Arg366Leu
  • NP_001371408.1:p.Arg366Leu
  • NC_000001.10:g.230841679C>A
Protein change:
R366L
Links:
dbSNP: rs74315283
NCBI 1000 Genomes Browser:
rs74315283
Molecular consequence:
  • NM_001382817.3:c.1097G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001384479.1:c.1097G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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    Assertion and evidence details

    Help
    Submission AccessionSubmitterReview Status
    (Assertion method)    		Clinical Significance
    (Last evaluated)    		OriginMethodCitations
    SCV002217740Labcorp Genetics (formerly Invitae), Labcorp
    criteria provided, single submitter

    (Invitae Variant Classification Sherloc (09022015))    		Uncertain significance
    (Jul 22, 2021)     		germlineclinical testing

    PubMed (3)
    [See all records that cite these PMIDs]

    Help

    Summary from all submissions

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

    Citations

    PubMed

    Aberrant 5' splice sites in human disease genes: mutation pattern, nucleotide structure and comparison of computational tools that predict their utilization.

    Buratti E, Chivers M, Královicová J, Romano M, Baralle M, Krainer AR, Vorechovsky I.

    Nucleic Acids Res. 2007;35(13):4250-63. Epub 2007 Jun 18.

    PubMed [citation]
    PMID:
    17576681
    PMCID:
    PMC1934990

    Statistical features of human exons and their flanking regions.

    Zhang MQ.

    Hum Mol Genet. 1998 May;7(5):919-32.

    PubMed [citation]
    PMID:
    9536098
    See all PubMed Citations (3)

    Details of each submission

    From Labcorp Genetics (formerly Invitae), Labcorp, SCV002217740.3

    #EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
    1not providednot providednot providednot providedclinical testing PubMed (3)

    Description

    This sequence change replaces arginine with leucine at codon 375 of the AGT protein (p.Arg375Leu). The arginine residue is highly conserved and there is a moderate physicochemical difference between arginine and leucine. This variant also falls at the last nucleotide of exon 3, which is part of the consensus splice site for this exon. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with AGT-related conditions. 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: "Possibly Damaging"; Align-GVGD: "Class C0"). Variants that disrupt the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. 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