NM_001365715.1(LRCH3):c.155C>G (p.Ala52Gly) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 17, 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:: RCV004637481.1

Allele description [Variation Report for NM_001365715.1(LRCH3):c.155C>G (p.Ala52Gly)]

NM_001365715.1(LRCH3):c.155C>G (p.Ala52Gly)

Gene:

LRCH3:leucine rich repeats and calponin homology domain containing 3 [Gene - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3q29

Genomic location:

Preferred name:

NM_001365715.1(LRCH3):c.155C>G (p.Ala52Gly)

HGVS:

NC_000003.12:g.197791433C>G
NG_101629.1:g.620C>G
NG_101629.2:g.620C>G
NM_001363887.1:c.155C>G
NM_001365715.1:c.155C>GMANE SELECT
NM_001365716.1:c.155C>G
NM_001365717.1:c.155C>G
NM_001365718.1:c.155C>G
NM_001365719.2:c.155C>G
NM_032773.4:c.155C>G
NP_001350816.1:p.Ala52Gly
NP_001352644.1:p.Ala52Gly
NP_001352645.1:p.Ala52Gly
NP_001352646.1:p.Ala52Gly
NP_001352647.1:p.Ala52Gly
NP_001352648.1:p.Ala52Gly
NP_116162.1:p.Ala52Gly
NC_000003.11:g.197518304C>G
NM_032773.2:c.155C>G
NR_158582.1:n.180C>G

Protein change:

A52G

Molecular consequence:

NM_001363887.1:c.155C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001365715.1:c.155C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001365716.1:c.155C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001365717.1:c.155C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001365718.1:c.155C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001365719.2:c.155C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_032773.4:c.155C>G - missense variant - [Sequence Ontology: SO:0001583]
NR_158582.1:n.180C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

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
SCV005136799	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jun 17, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV005136799

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jun 17, 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	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV005136799.1

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

Description

The c.155C>G (p.A52G) alteration is located in exon 1 (coding exon 1) of the LRCH3 gene. This alteration results from a C to G substitution at nucleotide position 155, causing the alanine (A) at amino acid position 52 to be replaced by a glycine (G). 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: Aug 11, 2024

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