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NM_001243133.2(NLRP3):c.779G>C (p.Arg260Pro) AND Familial cold autoinflammatory syndrome 1

Germline classification:
not provided (1 submission)
Review status:
no classification provided
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:
RCV000084230.2

Allele description [Variation Report for NM_001243133.2(NLRP3):c.779G>C (p.Arg260Pro)]

NM_001243133.2(NLRP3):c.779G>C (p.Arg260Pro)

Gene:
NLRP3:NLR family pyrin domain containing 3 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1q44
Genomic location:
Preferred name:
NM_001243133.2(NLRP3):c.779G>C (p.Arg260Pro)
HGVS:
  • NC_000001.11:g.247424228G>C
  • NG_007509.2:g.13056G>C
  • NM_001079821.3:c.779G>C
  • NM_001127461.3:c.779G>C
  • NM_001127462.3:c.779G>C
  • NM_001243133.2:c.779G>CMANE SELECT
  • NM_004895.5:c.785G>C
  • NM_183395.3:c.779G>C
  • NP_001073289.1:p.Arg262Pro
  • NP_001073289.2:p.Arg260Pro
  • NP_001120933.2:p.Arg260Pro
  • NP_001120934.2:p.Arg260Pro
  • NP_001230062.1:p.Arg260Pro
  • NP_001230062.1:p.Arg260Pro
  • NP_004886.3:p.Arg262Pro
  • NP_004886.3:p.Arg262Pro
  • NP_899632.2:p.Arg260Pro
  • LRG_197t1:c.785G>C
  • LRG_197:g.13056G>C
  • LRG_197p1:p.Arg262Pro
  • NC_000001.10:g.247587530G>C
  • NM_001079821.2:c.785G>C
  • NM_001243133.1:c.779G>C
  • NM_004895.4:c.785G>C
Protein change:
R260P
Links:
dbSNP: rs180177442
NCBI 1000 Genomes Browser:
rs180177442
Molecular consequence:
  • NM_001079821.3:c.779G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001127461.3:c.779G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001127462.3:c.779G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001243133.2:c.779G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_004895.5:c.785G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_183395.3:c.779G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Familial cold autoinflammatory syndrome 1 (FCAS1)
Synonyms:
CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 1; Familial cold inflammatory syndrome 1
Identifiers:
MONDO: MONDO:0007349; MedGen: C4551895; Orphanet: 47045; OMIM: 120100

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000116366Unité médicale des maladies autoinflammatoires, CHRU Montpellier
no classification provided
not providedunknownnot provided

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providednot providednot providednot providednot providednot provided1not providedliterature only

Details of each submission

From Unité médicale des maladies autoinflammatoires, CHRU Montpellier, SCV000116366.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providednot providednot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownnot provided1not providednot providednot providednot providednot providednot provided

Last Updated: Jun 23, 2024