NM_001130144.3(LTBP3):c.3482A>G (p.Asp1161Gly) AND Brachyolmia-amelogenesis imperfecta syndrome

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 3, 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:: RCV003755726.3

Allele description [Variation Report for NM_001130144.3(LTBP3):c.3482A>G (p.Asp1161Gly)]

NM_001130144.3(LTBP3):c.3482A>G (p.Asp1161Gly)

Gene:

LTBP3:latent transforming growth factor beta binding protein 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q13.1

Genomic location:

Preferred name:

NM_001130144.3(LTBP3):c.3482A>G (p.Asp1161Gly)

HGVS:

NC_000011.10:g.65539785T>C
NG_016437.1:g.23444A>G
NG_047172.1:g.19721T>C
NG_185472.1:g.17T>C
NM_001130144.3:c.3482A>GMANE SELECT
NM_001164266.1:c.2990A>G
NM_021070.4:c.3341A>G
NP_001123616.1:p.Asp1161Gly
NP_001157738.1:p.Asp997Gly
NP_066548.2:p.Asp1114Gly
NC_000011.9:g.65307256T>C

Protein change:

D1114G

Links:

dbSNP: rs2496116464

NCBI 1000 Genomes Browser:

rs2496116464

Molecular consequence:

NM_001130144.3:c.3482A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001164266.1:c.2990A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_021070.4:c.3341A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Brachyolmia-amelogenesis imperfecta syndrome
Synonyms:: PLATYSPONDYLY WITH AMELOGENESIS IMPERFECTA; Tooth agenesis, selective, 6; Dental anomalies and short stature
Identifiers:: MONDO: MONDO:0011018; MedGen: C1832594; Orphanet: 2899; OMIM: 601216

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004500381	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Mar 3, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004500381

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Mar 3, 2023)

germline

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical 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, SCV004500381.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

Description

This variant is not present in population databases (gnomAD no frequency). 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. An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be disruptive. This variant has not been reported in the literature in individuals affected with LTBP3-related conditions. This sequence change replaces aspartic acid, which is acidic and polar, with glycine, which is neutral and non-polar, at codon 1161 of the LTBP3 protein (p.Asp1161Gly).

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: May 16, 2025

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