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NM_004370.6(COL12A1):c.741T>G (p.Ile247Met) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 12, 2023
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:
RCV000697672.8

Allele description [Variation Report for NM_004370.6(COL12A1):c.741T>G (p.Ile247Met)]

NM_004370.6(COL12A1):c.741T>G (p.Ile247Met)

Gene:
COL12A1:collagen type XII alpha 1 chain [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
6q13
Genomic location:
Preferred name:
NM_004370.6(COL12A1):c.741T>G (p.Ile247Met)
HGVS:
  • NC_000006.12:g.75189299A>C
  • NG_042181.1:g.21609T>G
  • NM_004370.6:c.741T>GMANE SELECT
  • NM_080645.3:c.73+13421T>G
  • NP_004361.3:p.Ile247Met
  • NC_000006.11:g.75899015A>C
  • NM_004370.5:c.741T>G
Protein change:
I247M
Links:
dbSNP: rs371124522
NCBI 1000 Genomes Browser:
rs371124522
Molecular consequence:
  • NM_080645.3:c.73+13421T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_004370.6:c.741T>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Ullrich congenital muscular dystrophy 2 (UCMD2)
Identifiers:
MONDO: MONDO:0014654; MedGen: C4225314; Orphanet: 75840; OMIM: 616470
Name:
Bethlem myopathy 2 (BTHLM2)
Identifiers:
MONDO: MONDO:0034022; MedGen: C4225313; Orphanet: 610; OMIM: 616471

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000826297Invitae
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))
Uncertain significance
(Dec 12, 2023)
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):240-242.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Invitae, SCV000826297.6

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

Description

This sequence change replaces isoleucine, which is neutral and non-polar, with methionine, which is neutral and non-polar, at codon 247 of the COL12A1 protein (p.Ile247Met). The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This variant has not been reported in the literature in individuals affected with COL12A1-related conditions. ClinVar contains an entry for this variant (Variation ID: 575452). 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) has been performed at Invitae for this missense variant, however the output from this modeling did not meet the statistical confidence thresholds required to predict the impact of this variant on COL12A1 protein function. 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.

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

Last Updated: Mar 5, 2024