NM_021815.5(SLC5A7):c.277C>A (p.Leu93Ile) AND multiple conditions

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Aug 3, 2020
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:: RCV001306683.4

Allele description [Variation Report for NM_021815.5(SLC5A7):c.277C>A (p.Leu93Ile)]

NM_021815.5(SLC5A7):c.277C>A (p.Leu93Ile)

Gene:

SLC5A7:solute carrier family 5 member 7 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2q12.3

Genomic location:

Preferred name:

NM_021815.5(SLC5A7):c.277C>A (p.Leu93Ile)

HGVS:

NC_000002.12:g.107992204C>A
NG_042267.1:g.10691C>A
NM_001305005.3:c.277C>A
NM_001305006.3:c.-39C>A
NM_001305007.3:c.-428C>A
NM_021815.5:c.277C>AMANE SELECT
NP_001291934.1:p.Leu93Ile
NP_068587.1:p.Leu93Ile
NC_000002.11:g.108608660C>A

Protein change:

L93I

Links:

dbSNP: rs1172822464

NCBI 1000 Genomes Browser:

rs1172822464

Molecular consequence:

NM_001305006.3:c.-39C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001305007.3:c.-428C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001305005.3:c.277C>A - missense variant - [Sequence Ontology: SO:0001583]
NM_021815.5:c.277C>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Neuronopathy, distal hereditary motor, type 7A
Synonyms:: HARPER-YOUNG MYOPATHY; HMN VIIA; SPINAL MUSCULAR ATROPHY, DISTAL, WITH VOCAL CORD PARALYSIS; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0008024; MedGen: C1834703; Orphanet: 139589; OMIM: 158580

Name:: Congenital myasthenic syndrome 20
Synonyms:: Myasthenic syndrome, congenital, 20, presynaptic
Identifiers:: MONDO: MONDO:0014939; MedGen: C4310694; OMIM: 617143

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001496064	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Aug 3, 2020)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001496064

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Aug 3, 2020)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group, Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV001496064.3

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

Description

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Tolerated"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals with SLC5A7-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces leucine with isoleucine at codon 93 of the SLC5A7 protein (p.Leu93Ile). The leucine residue is highly conserved and there is a small physicochemical difference between leucine and isoleucine.

#	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: Sep 29, 2024

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