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NM_001854.4(COL11A1):c.2916+3A>G AND Connective tissue disorder

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jun 1, 2018
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:
RCV000680460.2

Allele description [Variation Report for NM_001854.4(COL11A1):c.2916+3A>G]

NM_001854.4(COL11A1):c.2916+3A>G

Gene:
COL11A1:collagen type XI alpha 1 chain [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1p21.1
Genomic location:
Preferred name:
NM_001854.4(COL11A1):c.2916+3A>G
HGVS:
  • NC_000001.11:g.102965484T>C
  • NG_008033.2:g.148013A>G
  • NM_001190709.2:c.2799+3A>G
  • NM_001854.4:c.2916+3A>GMANE SELECT
  • NM_080629.3:c.2952+3A>G
  • NM_080630.4:c.2568+3A>G
  • NC_000001.10:g.103431040T>C
  • NC_000001.10:g.103431040T>C
  • NM_001854.3:c.2916+3A>G
Links:
dbSNP: rs200515572
NCBI 1000 Genomes Browser:
rs200515572
Molecular consequence:
  • NM_001190709.2:c.2799+3A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001854.4:c.2916+3A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_080629.3:c.2952+3A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_080630.4:c.2568+3A>G - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Connective tissue disorder
Synonyms:
Connective tissue disease
Identifiers:
MONDO: MONDO:0003900; MedGen: C0009782

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000807835Center for Human Genetics, Inc, Center for Human Genetics, Inc
criteria provided, single submitter

(ACMG Guidelines, 2015)
Uncertain significance
(Jun 1, 2018)
germlineclinical testing

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot 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 Human Genetics, Inc, Center for Human Genetics, Inc, SCV000807835.1

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

Last Updated: Jul 15, 2024