NM_001426.4(EN1):c.618_647del (p.Val209_Ala218del) AND not provided

Germline classification:: Likely benign (1 submission)
Last evaluated:: Jan 1, 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:: RCV003886026.8

Allele description [Variation Report for NM_001426.4(EN1):c.618_647del (p.Val209_Ala218del)]

NM_001426.4(EN1):c.618_647del (p.Val209_Ala218del)

Gene:

EN1:engrailed homeobox 1 [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

2q14.2

Genomic location:

Preferred name:

NM_001426.4(EN1):c.618_647del (p.Val209_Ala218del)

HGVS:

NC_000002.12:g.118846541_118846570del
NG_007123.1:g.6634_6663del
NM_001426.4:c.618_647delMANE SELECT
NP_001417.3:p.Val209_Ala218del
NC_000002.11:g.119604117_119604146del

Molecular consequence:

NM_001426.4:c.618_647del - inframe_deletion - [Sequence Ontology: SO:0001822]

Observations:

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

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ras-related protein Rab-24 isoform 2 [Mus musculus]
ras-related protein Rab-24 isoform 2 [Mus musculus]
gi|2711571225|ref|NP_001416026.1|

Protein
ras-related protein Rab-24 isoform 1 [Mus musculus]
ras-related protein Rab-24 isoform 1 [Mus musculus]
gi|6679591|ref|NP_033026.1|

Protein

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004699487	CeGaT Center for Human Genetics Tuebingen	criteria provided, single submitter (CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)	Likely benign (Jan 1, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004699487

CeGaT Center for Human Genetics Tuebingen

criteria provided, single submitter

(CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)

Likely benign
(Jan 1, 2024)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	1	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From CeGaT Center for Human Genetics Tuebingen, SCV004699487.8

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

Description

EN1: BS2

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

Last Updated: Oct 20, 2024

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Relating variation to medicine