NM_001164508.2(NEB):c.1544A>G (p.Gln515Arg) AND Nemaline myopathy 2

Germline classification:: Likely benign (2 submissions)
Last evaluated:: Jan 19, 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:: RCV001317075.6

Allele description [Variation Report for NM_001164508.2(NEB):c.1544A>G (p.Gln515Arg)]

NM_001164508.2(NEB):c.1544A>G (p.Gln515Arg)

Gene:

NEB:nebulin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2q23.3

Genomic location:

Preferred name:

NM_001164508.2(NEB):c.1544A>G (p.Gln515Arg)

HGVS:

NC_000002.12:g.151696662T>C
NG_009382.2:g.42826A>G
NM_001164507.2:c.1544A>G
NM_001164508.2:c.1544A>GMANE SELECT
NM_001271208.2:c.1544A>G
NM_004543.5:c.1544A>G
NP_001157979.2:p.Gln515Arg
NP_001157980.2:p.Gln515Arg
NP_001258137.2:p.Gln515Arg
NP_004534.3:p.Gln515Arg
LRG_202:g.42826A>G
NC_000002.11:g.152553176T>C
NM_004543.4:c.1544A>G

Protein change:

Q515R

Links:

dbSNP: rs368150737

NCBI 1000 Genomes Browser:

rs368150737

Molecular consequence:

NM_001164507.2:c.1544A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001164508.2:c.1544A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001271208.2:c.1544A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_004543.5:c.1544A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Nemaline myopathy 2 (NEM2)
Synonyms:: Nemaline myopathy caused by mutation in the nebulin gene; Nemaline myopathy 2, autosomal recessive
Identifiers:: MONDO: MONDO:0009725; MedGen: C1850569; OMIM: 256030

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001507720	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Jan 19, 2024)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV002077818	Natera, Inc.	no assertion criteria provided	Uncertain significance (Apr 8, 2020)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001507720

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Jan 19, 2024)

germline

clinical testing

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

SCV002077818

Natera, Inc.

no assertion criteria provided

Uncertain significance
(Apr 8, 2020)

germline

clinical testing

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, SCV001507720.3

#	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

From Natera, Inc., SCV002077818.1

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

#	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: Oct 20, 2024

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