U.S. flag

An official website of the United States government

NM_054012.4(ASS1):c.793C>T (p.Arg265Cys) AND Citrullinemia

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Jan 22, 2024
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:
RCV001247325.14

Allele description [Variation Report for NM_054012.4(ASS1):c.793C>T (p.Arg265Cys)]

NM_054012.4(ASS1):c.793C>T (p.Arg265Cys)

Gene:
ASS1:argininosuccinate synthase 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9q34.11
Genomic location:
Preferred name:
NM_054012.4(ASS1):c.793C>T (p.Arg265Cys)
HGVS:
  • NC_000009.12:g.130480404C>T
  • NG_011542.1:g.40698C>T
  • NM_000050.4:c.793C>T
  • NM_054012.4:c.793C>TMANE SELECT
  • NP_000041.2:p.Arg265Cys
  • NP_000041.2:p.Arg265Cys
  • NP_446464.1:p.Arg265Cys
  • NC_000009.11:g.133355791C>T
  • P00966:p.Arg265Cys
Protein change:
R265C
Links:
UniProtKB: P00966#VAR_058349; dbSNP: rs148918985
NCBI 1000 Genomes Browser:
rs148918985
Molecular consequence:
  • NM_000050.4:c.793C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_054012.4:c.793C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Citrullinemia
Identifiers:
MONDO: MONDO:0015991; MedGen: C0175683; OMIM: PS215700

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001420737Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))
Pathogenic
(Jan 22, 2024)
germlineclinical testing

PubMed (5)
[See all records that cite these PMIDs]

Summary from all submissions

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

Citations

PubMed

Identification of three novel mutations in fourteen patients with citrullinemia type 1.

Kose E, Unal O, Bulbul S, Gunduz M, Häberle J, Arslan N.

Clin Biochem. 2017 Aug;50(12):686-689. doi: 10.1016/j.clinbiochem.2017.01.011. Epub 2017 Jan 27.

PubMed [citation]
PMID:
28132756

Urea cycle disorders in India: clinical course, biochemical and genetic investigations, and prenatal testing.

Bijarnia-Mahay S, Häberle J, Jalan AB, Puri RD, Kohli S, Kudalkar K, Rüfenacht V, Gupta D, Maurya D, Verma J, Shigematsu Y, Yamaguchi S, Saxena R, Verma IC.

Orphanet J Rare Dis. 2018 Oct 1;13(1):174. doi: 10.1186/s13023-018-0908-1.

PubMed [citation]
PMID:
30285816
PMCID:
PMC6167905
See all PubMed Citations (5)

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV001420737.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (5)

Description

This sequence change replaces arginine, which is basic and polar, with cysteine, which is neutral and slightly polar, at codon 265 of the ASS1 protein (p.Arg265Cys). This variant is present in population databases (rs148918985, gnomAD 0.003%). This missense change has been observed in individuals with citrullinemia type I (PMID: 28132756, 30285816). ClinVar contains an entry for this variant (Variation ID: 92373). 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 expected to disrupt ASS1 protein function with a positive predictive value of 80%. Experimental studies have shown that this missense change affects ASS1 function (PMID: 18473344). This variant disrupts the p.Arg265 amino acid residue in ASS1. Other variant(s) that disrupt this residue have been determined to be pathogenic (PMID: 12815590). This suggests that this residue is clinically significant, and that variants that disrupt this residue are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic.

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

Last Updated: Oct 26, 2024