NM_182548.4(LHFPL5):c.638C>A (p.Ala213Glu) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 13, 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:: RCV004019810.1

Allele description [Variation Report for NM_182548.4(LHFPL5):c.638C>A (p.Ala213Glu)]

NM_182548.4(LHFPL5):c.638C>A (p.Ala213Glu)

Gene:

LHFPL5:LHFPL tetraspan subfamily member 5 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6p21.31

Genomic location:

Preferred name:

NM_182548.4(LHFPL5):c.638C>A (p.Ala213Glu)

HGVS:

NC_000006.12:g.35814771C>A
NG_012184.2:g.14478C>A
NM_182548.4:c.638C>AMANE SELECT
NP_872354.1:p.Ala213Glu
LRG_1352t1:c.638C>A
LRG_1352p1:p.Ala213Glu
NC_000006.11:g.35782548C>A
NG_012184.1:g.14478C>A
NM_182548.3:c.638C>A

Protein change:

A213E

Links:

dbSNP: rs555379908

NCBI 1000 Genomes Browser:

rs555379908

Molecular consequence:

NM_182548.4:c.638C>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Inborn genetic diseases
Identifiers:: MeSH: D030342; MedGen: C0950123

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PHD finger protein 20-like protein 1 isoform X7 [Homo sapiens]
PHD finger protein 20-like protein 1 isoform X7 [Homo sapiens]
gi|1034660505|ref|XP_016868998.1|

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004898062	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Dec 13, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004898062

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Dec 13, 2023)

germline

clinical testing

Citation Link

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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, SCV004898062.1

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

Description

The c.638C>A (p.A213E) alteration is located in exon 2 (coding exon 2) of the LHFPL5 gene. This alteration results from a C to A substitution at nucleotide position 638, causing the alanine (A) at amino acid position 213 to be replaced by a glutamic acid (E). 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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