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NM_000093.5(COL5A1):c.2695G>A (p.Gly899Ser) AND Familial thoracic aortic aneurysm and aortic dissection

Germline classification:
Likely benign (1 submission)
Last evaluated:
May 31, 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:
RCV002314633.9

Allele description [Variation Report for NM_000093.5(COL5A1):c.2695G>A (p.Gly899Ser)]

NM_000093.5(COL5A1):c.2695G>A (p.Gly899Ser)

Gene:
COL5A1:collagen type V alpha 1 chain [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9q34.3
Genomic location:
Preferred name:
NM_000093.5(COL5A1):c.2695G>A (p.Gly899Ser)
Other names:
p.G899S:GGC>AGC
HGVS:
  • NC_000009.12:g.134789203G>A
  • NG_008030.1:g.152398G>A
  • NM_000093.5:c.2695G>AMANE SELECT
  • NM_001278074.1:c.2695G>A
  • NP_000084.3:p.Gly899Ser
  • NP_000084.3:p.Gly899Ser
  • NP_001265003.1:p.Gly899Ser
  • LRG_737t1:c.2695G>A
  • LRG_737t2:c.2695G>A
  • LRG_737:g.152398G>A
  • LRG_737p1:p.Gly899Ser
  • LRG_737p2:p.Gly899Ser
  • NC_000009.11:g.137681049G>A
  • NM_000093.3:c.2695G>A
  • NM_000093.4:c.2695G>A
Protein change:
G899S
Links:
dbSNP: rs149964491
NCBI 1000 Genomes Browser:
rs149964491
Molecular consequence:
  • NM_000093.5:c.2695G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001278074.1:c.2695G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Familial thoracic aortic aneurysm and aortic dissection (TAAD)
Synonyms:
Thoracic aortic aneurysm and aortic dissection; Thoracic aortic aneurysms and dissections
Identifiers:
MONDO: MONDO:0019625; MedGen: C4707243; Orphanet: 91387; OMIM: PS607086

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000738409Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(May 31, 2018) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV000738409.5

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

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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

Last Updated: Nov 24, 2024