NM_001349338.3(FOXP1):c.1833G>T (p.Glu611Asp) AND not provided

Germline classification:: Likely benign (1 submission)
Last evaluated:: Oct 9, 2022
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:: RCV002842158.3

Allele description [Variation Report for NM_001349338.3(FOXP1):c.1833G>T (p.Glu611Asp)]

NM_001349338.3(FOXP1):c.1833G>T (p.Glu611Asp)

Gene:

FOXP1:forkhead box P1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3p13

Genomic location:

Preferred name:

NM_001349338.3(FOXP1):c.1833G>T (p.Glu611Asp)

HGVS:

NC_000003.12:g.70965946C>A
NG_028243.1:g.623044G>T
NM_001244808.3:c.1830G>T
NM_001244810.2:c.1881G>T
NM_001244812.3:c.1605G>T
NM_001244813.3:c.1533G>T
NM_001244814.3:c.1833G>T
NM_001244815.2:c.1533G>T
NM_001244816.2:c.1833G>T
NM_001349337.2:c.1530G>T
NM_001349338.3:c.1833G>TMANE SELECT
NM_001349340.3:c.1833G>T
NM_001349341.3:c.1830G>T
NM_001349342.3:c.1533G>T
NM_001349343.3:c.1530G>T
NM_001349344.3:c.1530G>T
NM_001370548.1:c.1530G>T
NM_032682.6:c.1833G>T
NP_001231737.1:p.Glu610Asp
NP_001231739.1:p.Glu627Asp
NP_001231741.1:p.Glu535Asp
NP_001231742.1:p.Glu511Asp
NP_001231743.1:p.Glu611Asp
NP_001231744.2:p.Glu511Asp
NP_001231745.1:p.Glu611Asp
NP_001336266.2:p.Glu510Asp
NP_001336267.1:p.Glu611Asp
NP_001336269.1:p.Glu611Asp
NP_001336270.1:p.Glu610Asp
NP_001336271.1:p.Glu511Asp
NP_001336272.1:p.Glu510Asp
NP_001336273.1:p.Glu510Asp
NP_001357477.1:p.Glu510Asp
NP_116071.2:p.Glu611Asp
NC_000003.11:g.71015097C>A
NM_032682.5:c.1833G>T
NR_146142.3:n.2349G>T
NR_146143.3:n.2346G>T

Protein change:

E510D

Molecular consequence:

NM_001244808.3:c.1830G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001244810.2:c.1881G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001244812.3:c.1605G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001244813.3:c.1533G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001244814.3:c.1833G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001244815.2:c.1533G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001244816.2:c.1833G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001349337.2:c.1530G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001349338.3:c.1833G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001349340.3:c.1833G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001349341.3:c.1830G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001349342.3:c.1533G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001349343.3:c.1530G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001349344.3:c.1530G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370548.1:c.1530G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_032682.6:c.1833G>T - missense variant - [Sequence Ontology: SO:0001583]
NR_146142.3:n.2349G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_146143.3:n.2346G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:: none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003208459	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Oct 9, 2022)	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

SCV003208459

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Oct 9, 2022)

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, SCV003208459.2

#	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: Dec 7, 2024

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