NM_001130987.2(DYSF):c.4129G>A (p.Val1377Ile) AND Qualitative or quantitative defects of dysferlin

Germline classification:: Likely benign (1 submission)
Last evaluated:: Jun 14, 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:: RCV002775735.3

Allele description [Variation Report for NM_001130987.2(DYSF):c.4129G>A (p.Val1377Ile)]

NM_001130987.2(DYSF):c.4129G>A (p.Val1377Ile)

Gene:

DYSF:dysferlin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2p13.2

Genomic location:

Preferred name:

NM_001130987.2(DYSF):c.4129G>A (p.Val1377Ile)

HGVS:

NC_000002.12:g.71611534G>A
NG_008694.1:g.162912G>A
NM_001130455.2:c.4078G>A
NM_001130976.2:c.4033G>A
NM_001130977.2:c.4033G>A
NM_001130978.2:c.4075G>A
NM_001130979.2:c.4168G>A
NM_001130980.2:c.4126G>A
NM_001130981.2:c.4126G>A
NM_001130982.2:c.4171G>A
NM_001130983.2:c.4078G>A
NM_001130984.2:c.4036G>A
NM_001130985.2:c.4129G>A
NM_001130986.2:c.4036G>A
NM_001130987.2:c.4129G>AMANE SELECT
NM_003494.4:c.4075G>A
NP_001123927.1:p.Val1360Ile
NP_001124448.1:p.Val1345Ile
NP_001124449.1:p.Val1345Ile
NP_001124450.1:p.Val1359Ile
NP_001124451.1:p.Val1390Ile
NP_001124452.1:p.Val1376Ile
NP_001124453.1:p.Val1376Ile
NP_001124454.1:p.Val1391Ile
NP_001124455.1:p.Val1360Ile
NP_001124456.1:p.Val1346Ile
NP_001124457.1:p.Val1377Ile
NP_001124458.1:p.Val1346Ile
NP_001124459.1:p.Val1377Ile
NP_003485.1:p.Val1359Ile
LRG_845t1:c.4075G>A
LRG_845t2:c.4129G>A
LRG_845:g.162912G>A
LRG_845p1:p.Val1359Ile
LRG_845p2:p.Val1377Ile
NC_000002.11:g.71838664G>A

Protein change:

V1345I

Molecular consequence:

NM_001130455.2:c.4078G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001130976.2:c.4033G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001130977.2:c.4033G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001130978.2:c.4075G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001130979.2:c.4168G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001130980.2:c.4126G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001130981.2:c.4126G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001130982.2:c.4171G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001130983.2:c.4078G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001130984.2:c.4036G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001130985.2:c.4129G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001130986.2:c.4036G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001130987.2:c.4129G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_003494.4:c.4075G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Qualitative or quantitative defects of dysferlin
Synonyms:: Dysferlinopathy
Identifiers:: MONDO: MONDO:0016145; MedGen: C2931687

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003024942	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Jun 14, 2023)	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

SCV003024942

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Jun 14, 2023)

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, SCV003024942.2

#	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: Sep 29, 2024

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