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NM_001370466.1(NOD2):c.2116G>A (p.Val706Met) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 20, 2019
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:
RCV001281018.1

Allele description [Variation Report for NM_001370466.1(NOD2):c.2116G>A (p.Val706Met)]

NM_001370466.1(NOD2):c.2116G>A (p.Val706Met)

Gene:
NOD2:nucleotide binding oligomerization domain containing 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
16q12.1
Genomic location:
Preferred name:
NM_001370466.1(NOD2):c.2116G>A (p.Val706Met)
HGVS:
  • NC_000016.10:g.50712108G>A
  • NG_007508.1:g.19970G>A
  • NM_001293557.2:c.2116G>A
  • NM_001370466.1:c.2116G>AMANE SELECT
  • NM_022162.3:c.2197G>A
  • NP_001280486.1:p.Val706Met
  • NP_001357395.1:p.Val706Met
  • NP_071445.1:p.Val733Met
  • LRG_177:g.19970G>A
  • NC_000016.9:g.50746019G>A
  • NR_163434.1:n.2181G>A
Protein change:
V706M
Links:
dbSNP: rs746055479
NCBI 1000 Genomes Browser:
rs746055479
Molecular consequence:
  • NM_001293557.2:c.2116G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370466.1:c.2116G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_022162.3:c.2197G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_163434.1:n.2181G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Blau syndrome (BLAUS)
Synonyms:
Synovitis granulomatous with uveitis and cranial neuropathies; Arthrocutaneouveal granulomatosis; Granulomatosis, familial, Blau type; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0008523; MedGen: C5201146; Orphanet: 90340; OMIM: 186580
Name:
Psoriatic arthritis, susceptibility to
Identifiers:
MONDO: MONDO:0100232; MedGen: C1835223; OMIM: 607507
Name:
Yao syndrome
Synonyms:
Susceptibility to Yao syndrome
Identifiers:
MONDO: MONDO:0015019; MedGen: C4310620; OMIM: 617321
Name:
Inflammatory bowel disease 1 (IBD1)
Synonyms:
Inflammatory bowel disease 1, Crohn disease; INFLAMMATORY BOWEL DISEASE (CROHN DISEASE) 1
Identifiers:
MONDO: MONDO:0009960; MedGen: CN260071; OMIM: 266600

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001468429Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Dec 20, 2019) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot 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 Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago, SCV001468429.1

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

Description

NOD2 NM_022162.2 exon 4 p.Val733Met (c.2197G>A): This variant has not been reported in the literature but is present in 0.01% (4/35436) of Latino alleles in the Genome Aggregation Database (https://gnomad.broadinstitute.org/variant/16-50746019-G-A?dataset=gnomad_r2_1). This variant amino acid Methionine (Met) is present in >40 species including mammals and is not well conserved among evolutionarily distant species; this suggests that this variant may not impact the protein. Additional computational prediction tools do not suggest an impact. In summary, data on this variant is insufficient for disease classification. Therefore, the clinical significance of this variant is uncertain.

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

Last Updated: Sep 29, 2024