NM_001389712.2(GLYATL1):c.606A>G (p.Ile202Met) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 14, 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:: RCV004283354.1

Allele description [Variation Report for NM_001389712.2(GLYATL1):c.606A>G (p.Ile202Met)]

NM_001389712.2(GLYATL1):c.606A>G (p.Ile202Met)

Genes:

GLYATL1:glycine-N-acyltransferase like 1 [Gene - OMIM - HGNC]
LOC283194:uncharacterized LOC283194 [Gene]

Variant type:

single nucleotide variant

Cytogenetic location:

11q12.1

Genomic location:

Preferred name:

NM_001389712.2(GLYATL1):c.606A>G (p.Ile202Met)

HGVS:

NC_000011.10:g.58955724A>G
NM_001220494.4:c.606A>G
NM_001220496.4:c.606A>G
NM_001354699.4:c.606A>G
NM_001389711.2:c.606A>G
NM_001389712.2:c.606A>GMANE SELECT
NM_001389713.2:c.606A>G
NM_001389714.2:c.606A>G
NM_001389715.2:c.606A>G
NM_001389716.2:c.606A>G
NM_001389717.2:c.606A>G
NM_001389718.2:c.483A>G
NM_001389719.1:c.606A>G
NM_080661.6:c.699A>G
NP_001207423.1:p.Ile202Met
NP_001207425.1:p.Ile202Met
NP_001341628.1:p.Ile202Met
NP_001376640.1:p.Ile202Met
NP_001376641.1:p.Ile202Met
NP_001376642.1:p.Ile202Met
NP_001376643.1:p.Ile202Met
NP_001376644.1:p.Ile202Met
NP_001376645.1:p.Ile202Met
NP_001376646.1:p.Ile202Met
NP_001376647.1:p.Ile161Met
NP_001376648.1:p.Ile202Met
NP_542392.2:p.Ile233Met
NC_000011.9:g.58723197A>G
NM_080661.3:c.699A>G

Protein change:

I161M

Molecular consequence:

NM_001220494.4:c.606A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001220496.4:c.606A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001354699.4:c.606A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001389711.2:c.606A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001389712.2:c.606A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001389713.2:c.606A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001389714.2:c.606A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001389715.2:c.606A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001389716.2:c.606A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001389717.2:c.606A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001389718.2:c.483A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001389719.1:c.606A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_080661.6:c.699A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003909972	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Mar 14, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003909972

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Mar 14, 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, SCV003909972.2

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

Description

The c.699A>G (p.I233M) alteration is located in exon 7 (coding exon 7) of the GLYATL1 gene. This alteration results from a A to G substitution at nucleotide position 699, causing the isoleucine (I) at amino acid position 233 to be replaced by a methionine (M). 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: Nov 24, 2024

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