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NM_003560.4(PLA2G6):c.2222G>A (p.Arg741Gln) AND multiple conditions

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Dec 7, 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:
RCV002496284.1

Allele description [Variation Report for NM_003560.4(PLA2G6):c.2222G>A (p.Arg741Gln)]

NM_003560.4(PLA2G6):c.2222G>A (p.Arg741Gln)

Gene:
PLA2G6:phospholipase A2 group VI [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
22q13.1
Genomic location:
Preferred name:
NM_003560.4(PLA2G6):c.2222G>A (p.Arg741Gln)
HGVS:
  • NC_000022.11:g.38112558C>T
  • NG_007094.3:g.107221G>A
  • NG_033059.2:g.3112G>A
  • NM_001004426.3:c.2060G>A
  • NM_001199562.3:c.2060G>A
  • NM_001349864.2:c.2222G>A
  • NM_001349865.2:c.2060G>A
  • NM_001349866.2:c.2060G>A
  • NM_001349867.2:c.1688G>A
  • NM_001349868.2:c.1544G>A
  • NM_001349869.2:c.1526G>A
  • NM_003560.4:c.2222G>AMANE SELECT
  • NP_001004426.1:p.Arg687Gln
  • NP_001186491.1:p.Arg687Gln
  • NP_001336793.1:p.Arg741Gln
  • NP_001336794.1:p.Arg687Gln
  • NP_001336795.1:p.Arg687Gln
  • NP_001336796.1:p.Arg563Gln
  • NP_001336797.1:p.Arg515Gln
  • NP_001336798.1:p.Arg509Gln
  • NP_003551.2:p.Arg741Gln
  • LRG_1015t1:c.2222G>A
  • LRG_1015:g.107221G>A
  • LRG_1015p1:p.Arg741Gln
  • NC_000022.10:g.38508565C>T
  • NG_007094.2:g.98133G>A
  • NM_003560.2:c.2222G>A
  • NM_003560.3:c.2222G>A
  • O60733:p.Arg741Gln
Protein change:
R509Q; Arg741Gln
Links:
UniProtKB: O60733#VAR_062530; OMIM: 603604.0009; dbSNP: rs121908686
NCBI 1000 Genomes Browser:
rs121908686
Molecular consequence:
  • NM_001004426.3:c.2060G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001199562.3:c.2060G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001349864.2:c.2222G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001349865.2:c.2060G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001349866.2:c.2060G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001349867.2:c.1688G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001349868.2:c.1544G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001349869.2:c.1526G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_003560.4:c.2222G>A - missense variant - [Sequence Ontology: SO:0001583]
Functional consequence:
Unknown function

Condition(s)

Name:
Infantile neuroaxonal dystrophy (NBIA2A)
Synonyms:
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A; Seitelberger disease; Infantile neuroaxonal dystrophy 1
Identifiers:
MONDO: MONDO:0024457; MedGen: C0270724; Orphanet: 35069; OMIM: 256600
Name:
Neurodegeneration with brain iron accumulation 2B
Synonyms:
NEUROAXONAL DYSTROPHY, ATYPICAL; NEURODEGENERATION WITH BRAIN IRON ACCUMULATION, PLA2G6-RELATED; aNAD; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0012444; MedGen: C1857747; Orphanet: 35069; OMIM: 610217
Name:
Autosomal recessive Parkinson disease 14
Synonyms:
DYSTONIA-PARKINSONISM, ADULT-ONSET; Parkinson disease 14
Identifiers:
MONDO: MONDO:0013060; MedGen: C2751842; Orphanet: 199351; OMIM: 612953

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002805551Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Pathogenic
(Dec 7, 2021) 		unknownclinical testing

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

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Fulgent Genetics, Fulgent Genetics, SCV002805551.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Apr 6, 2024