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NM_001854.4(COL11A1):c.4193A>C (p.Gln1398Pro) AND Inborn genetic diseases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Oct 29, 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:
RCV002553436.2

Allele description [Variation Report for NM_001854.4(COL11A1):c.4193A>C (p.Gln1398Pro)]

NM_001854.4(COL11A1):c.4193A>C (p.Gln1398Pro)

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.4193A>C (p.Gln1398Pro)
HGVS:
  • NC_000001.11:g.102898721T>G
  • NG_008033.2:g.214776A>C
  • NM_001190709.2:c.4076A>C
  • NM_001854.4:c.4193A>CMANE SELECT
  • NM_080629.3:c.4229A>C
  • NM_080630.4:c.3845A>C
  • NP_001177638.1:p.Gln1359Pro
  • NP_001845.3:p.Gln1398Pro
  • NP_542196.2:p.Gln1410Pro
  • NP_542197.3:p.Gln1282Pro
  • NC_000001.10:g.103364277T>G
  • NM_001854.3:c.4193A>C
  • NR_134980.2:n.4553A>C
Protein change:
Q1282P
Links:
dbSNP: rs775587076
NCBI 1000 Genomes Browser:
rs775587076
Molecular consequence:
  • NM_001190709.2:c.4076A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001854.4:c.4193A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_080629.3:c.4229A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_080630.4:c.3845A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NR_134980.2:n.4553A>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Inborn genetic diseases
Identifiers:
MeSH: D030342; MedGen: C0950123

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV003543292Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)
Uncertain significance
(Oct 29, 2021)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV003543292.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The c.4193A>C (p.Q1398P) alteration is located in exon 56 (coding exon 56) of the COL11A1 gene. This alteration results from a A to C substitution at nucleotide position 4193, causing the glutamine (Q) at amino acid position 1398 to be replaced by a proline (P). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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

Last Updated: Jul 23, 2024