NM_001004341.2(ETV3L):c.229G>C (p.Ala77Pro) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 20, 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:: RCV004383156.1

Allele description [Variation Report for NM_001004341.2(ETV3L):c.229G>C (p.Ala77Pro)]

NM_001004341.2(ETV3L):c.229G>C (p.Ala77Pro)

Gene:

ETV3L:ETS variant transcription factor 3 like [Gene - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q23.1

Genomic location:

Preferred name:

NM_001004341.2(ETV3L):c.229G>C (p.Ala77Pro)

HGVS:

NC_000001.11:g.157099208C>G
NM_001004341.2:c.229G>CMANE SELECT
NP_001004341.1:p.Ala77Pro
NC_000001.10:g.157069000C>G

Protein change:

A77P

Molecular consequence:

NM_001004341.2:c.229G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

Recent activity

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unnamed protein product, partial [Mus musculus]
unnamed protein product, partial [Mus musculus]
gi|74209598|dbj|BAE23558.1|

Protein
Crenimugil sp. voucher M-1132 16S ribosomal RNA gene, partial sequence; mitochon...
Crenimugil sp. voucher M-1132 16S ribosomal RNA gene, partial sequence; mitochondrial
gi|2739765347|gnl|uoguelph|MULID040 6S|gb|OR859525.1|

Nucleotide
PREDICTED: Mus musculus zinc finger protein 991 (Zfp991), transcript variant X3,...
PREDICTED: Mus musculus zinc finger protein 991 (Zfp991), transcript variant X3, mRNA
gi|1907156877|ref|XM_036164319.1|

Nucleotide
PREDICTED: Mus musculus zinc finger protein 991 (Zfp991), transcript variant X15...
PREDICTED: Mus musculus zinc finger protein 991 (Zfp991), transcript variant X15, mRNA
gi|1907156901|ref|XM_036164331.1|

Nucleotide
PREDICTED: Mus musculus Scm-like with four mbt domains 2 (Sfmbt2), transcript va...
PREDICTED: Mus musculus Scm-like with four mbt domains 2 (Sfmbt2), transcript variant X2, mRNA
gi|1907140950|ref|XM_006497490.5|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004866770	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Dec 20, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004866770

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Dec 20, 2023)

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	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV004866770.1

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

Description

The c.229G>C (p.A77P) alteration is located in exon 2 (coding exon 2) of the ETV3L gene. This alteration results from a G to C substitution at nucleotide position 229, causing the alanine (A) at amino acid position 77 to be replaced by a proline (P). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	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 7, 2024

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