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NM_000362.5(TIMP3):c.234T>G (p.His78Gln) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Apr 17, 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:
RCV002030937.6

Allele description [Variation Report for NM_000362.5(TIMP3):c.234T>G (p.His78Gln)]

NM_000362.5(TIMP3):c.234T>G (p.His78Gln)

Genes:
TIMP3:TIMP metallopeptidase inhibitor 3 [Gene - OMIM - HGNC]
SYN3:synapsin III [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
22q12.3
Genomic location:
Preferred name:
NM_000362.5(TIMP3):c.234T>G (p.His78Gln)
HGVS:
  • NC_000022.11:g.32857278T>G
  • NG_009117.2:g.60574T>G
  • NG_029545.1:g.206113A>C
  • NG_029545.2:g.206103A>C
  • NM_000362.5:c.234T>GMANE SELECT
  • NM_001135774.2:c.708+7637A>C
  • NM_001369907.1:c.711+7637A>C
  • NM_001369908.1:c.711+7637A>C
  • NM_001369909.1:c.708+7637A>C
  • NM_001369910.1:c.708+7637A>C
  • NM_003490.4:c.711+7637A>CMANE SELECT
  • NM_133633.3:c.711+7637A>C
  • NP_000353.1:p.His78Gln
  • NC_000022.10:g.33253265T>G
Protein change:
H78Q
Links:
dbSNP: rs757613563
NCBI 1000 Genomes Browser:
rs757613563
Molecular consequence:
  • NM_001135774.2:c.708+7637A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001369907.1:c.711+7637A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001369908.1:c.711+7637A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001369909.1:c.708+7637A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001369910.1:c.708+7637A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_003490.4:c.711+7637A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_133633.3:c.711+7637A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_000362.5:c.234T>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV002314767Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))
Uncertain significance
(Apr 17, 2021)
germlineclinical testing

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

Summary from all submissions

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV002314767.3

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

Description

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. This variant is present in population databases (rs757613563, ExAC 0.01%). Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has not been reported in the literature in individuals with TIMP3-related conditions. This sequence change replaces histidine with glutamine at codon 78 of the TIMP3 protein (p.His78Gln). The histidine residue is moderately conserved and there is a small physicochemical difference between histidine and glutamine.

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

Last Updated: Sep 29, 2024