NM_005249.5(FOXG1):c.219GCC[5] (p.Pro80del) AND Rett syndrome, congenital variant

Germline classification:: Likely benign (1 submission)
Last evaluated:: Oct 15, 2024
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:: RCV000874558.9

Allele description [Variation Report for NM_005249.5(FOXG1):c.219GCC[5] (p.Pro80del)]

NM_005249.5(FOXG1):c.219GCC[5] (p.Pro80del)

Gene:

FOXG1:forkhead box G1 [Gene - OMIM - HGNC]

Variant type:

Microsatellite

Cytogenetic location:

14q12

Genomic location:

Preferred name:

NM_005249.5(FOXG1):c.219GCC[5] (p.Pro80del)

HGVS:

NC_000014.9:g.28767498GCC[5]
NC_000014.9:g.28767498_28767500GCC[5]
NG_009367.1:g.5418GCC[5]
NM_005249.5:c.219GCC[5]MANE SELECT
NP_005240.3:p.Pro80del
NC_000014.8:g.29236704GCC[5]
NC_000014.8:g.29236704_29236706del
NM_005249.4:c.234_236del
NM_005249.4:c.234_236delGCC

Protein change:

P80del

Links:

dbSNP: rs786200975

NCBI 1000 Genomes Browser:

rs786200975

Molecular consequence:

NM_005249.5:c.219GCC[5] - inframe_deletion - [Sequence Ontology: SO:0001822]

Condition(s)

Name:: Rett syndrome, congenital variant
Identifiers:: MedGen: C3150705; Orphanet: 3095; OMIM: 613454

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001016749	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Oct 15, 2024)	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

SCV001016749

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Oct 15, 2024)

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, SCV001016749.6

#	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: Feb 25, 2025

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