NM_001453.3(FOXC1):c.1338CGG[5] (p.Gly454_Gly456del) AND Axenfeld-Rieger syndrome type 3

Germline classification:: Likely benign (1 submission)
Last evaluated:: Jan 28, 2025
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:: RCV002061022.7

Allele description [Variation Report for NM_001453.3(FOXC1):c.1338CGG[5] (p.Gly454_Gly456del)]

NM_001453.3(FOXC1):c.1338CGG[5] (p.Gly454_Gly456del)

Gene:

FOXC1:forkhead box C1 [Gene - OMIM - HGNC]

Variant type:

Microsatellite

Cytogenetic location:

6p25.3

Genomic location:

Preferred name:

NM_001453.3(FOXC1):c.1338CGG[5] (p.Gly454_Gly456del)

HGVS:

NC_000006.12:g.1611783CGG[5]
NG_009368.1:g.6338CGG[5]
NM_001453.2:c.1353_1361del9
NM_001453.3:c.1338CGG[5]MANE SELECT
NP_001444.2:p.Gly454_Gly456del
LRG_1245t1:c.1338CGG[5]
LRG_1245:g.6338CGG[5]
LRG_1245p1:p.Gly454_Gly456del
NC_000006.11:g.1612018CGG[5]
NC_000006.11:g.1612018_1612026del
NM_001453.2:c.1353_1361delCGGCGGCGG

Links:

dbSNP: rs398123612

NCBI 1000 Genomes Browser:

rs398123612

Molecular consequence:

NM_001453.3:c.1338CGG[5] - inframe_deletion - [Sequence Ontology: SO:0001822]

Condition(s)

Name:: Axenfeld-Rieger syndrome type 3 (RIEG3)
Synonyms:: AXENFELD-RIEGER ANOMALY WITH CARDIAC DEFECTS AND/OR SENSORINEURAL HEARING LOSS
Identifiers:: MONDO: MONDO:0011233; MedGen: C2678503; Orphanet: 782; OMIM: 602482

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002378607	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Jan 28, 2025)	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

SCV002378607

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Jan 28, 2025)

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, SCV002378607.4

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

#	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 25, 2025

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