NM_201384.3(PLEC):c.13383G>T (p.Leu4461=) AND multiple conditions

Germline classification:: Likely benign (1 submission)
Last evaluated:: Feb 9, 2022
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:: RCV001472435.14

Allele description [Variation Report for NM_201384.3(PLEC):c.13383G>T (p.Leu4461=)]

NM_201384.3(PLEC):c.13383G>T (p.Leu4461=)

Gene:

PLEC:plectin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

8q24.3

Genomic location:

Preferred name:

NM_201384.3(PLEC):c.13383G>T (p.Leu4461=)

HGVS:

NC_000008.11:g.143916438C>A
NG_012492.1:g.65308G>T
NM_000445.5:c.13464G>T
NM_201378.4:c.13341G>T
NM_201379.3:c.13317G>T
NM_201380.4:c.13794G>T
NM_201381.3:c.13287G>T
NM_201382.4:c.13383G>T
NM_201383.3:c.13395G>T
NM_201384.3:c.13383G>TMANE SELECT
NP_000436.2:p.Leu4488=
NP_958780.1:p.Leu4447=
NP_958781.1:p.Leu4439=
NP_958782.1:p.Leu4598=
NP_958783.1:p.Leu4429=
NP_958784.1:p.Leu4461=
NP_958785.1:p.Leu4465=
NP_958786.1:p.Leu4461=
NC_000008.10:g.144990606C>A
NM_000445.4:c.13464G>T

Links:

dbSNP: rs1586746518

NCBI 1000 Genomes Browser:

rs1586746518

Molecular consequence:

NM_000445.5:c.13464G>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_201378.4:c.13341G>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_201379.3:c.13317G>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_201380.4:c.13794G>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_201381.3:c.13287G>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_201382.4:c.13383G>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_201383.3:c.13395G>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_201384.3:c.13383G>T - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: Epidermolysis bullosa simplex 5B, with muscular dystrophy (EBS5B)
Synonyms:: EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY; Epidermolysa bullosa simplex and limb girdle muscular dystrophy; Epidermolysis bullosa simplex with muscular dystrophy
Identifiers:: MONDO: MONDO:0009181; MedGen: C2931072; Orphanet: 257; OMIM: 226670

Name:: Epidermolysis bullosa simplex, Ogna type (EBS5A)
Synonyms:: EPIDERMOLYSIS BULLOSA SIMPLEX 5A, OGNA TYPE; Pidermolysis bullosa simplex 5A, Ogna type
Identifiers:: MONDO: MONDO:0007555; MedGen: C0432317; Orphanet: 79401; OMIM: 131950

Name:: Epidermolysis bullosa simplex 5C, with pyloric atresia (EBS5C)
Synonyms:: Epidermolysis bullosa simplex with pyloric atresia; PLEC1-Related Epidermolysis Bullosa with Pyloric Atresia
Identifiers:: MONDO: MONDO:0012807; MedGen: C2677349; Orphanet: 158684; OMIM: 612138

Name:: Autosomal recessive limb-girdle muscular dystrophy type 2Q (LGMDR17)
Synonyms:: Limb-girdle muscular dystrophy, type 2Q; MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 17
Identifiers:: MONDO: MONDO:0013390; MedGen: C3150989; Orphanet: 254361; OMIM: 613723

Name:: Epidermolysis bullosa simplex with nail dystrophy (EBS5D)
Identifiers:: MONDO: MONDO:0014661; MedGen: C4225309; OMIM: 616487

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Mus musculus mitochondrial ribosomal protein S17 (Mrps17), transcript variant 2,...
Mus musculus mitochondrial ribosomal protein S17 (Mrps17), transcript variant 2, mRNA
gi|1255287574|ref|NM_001356954.1|

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001676567	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Feb 9, 2022)	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

SCV001676567

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Feb 9, 2022)

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, SCV001676567.4

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

#	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 3, 2024

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