NM_001130987.2(DYSF):c.4122C>T (p.Ser1374=) AND not specified

Germline classification:: Benign (6 submissions)
Last evaluated:: Feb 10, 2016
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV000080284.27

Allele description [Variation Report for NM_001130987.2(DYSF):c.4122C>T (p.Ser1374=)]

NM_001130987.2(DYSF):c.4122C>T (p.Ser1374=)

Gene:

DYSF:dysferlin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2p13.2

Genomic location:

Preferred name:

NM_001130987.2(DYSF):c.4122C>T (p.Ser1374=)

HGVS:

NC_000002.12:g.71611527C>T
NG_008694.1:g.162905C>T
NM_001130455.2:c.4071C>T
NM_001130976.2:c.4026C>T
NM_001130977.2:c.4026C>T
NM_001130978.2:c.4068C>T
NM_001130979.2:c.4161C>T
NM_001130980.2:c.4119C>T
NM_001130981.2:c.4119C>T
NM_001130982.2:c.4164C>T
NM_001130983.2:c.4071C>T
NM_001130984.2:c.4029C>T
NM_001130985.2:c.4122C>T
NM_001130986.2:c.4029C>T
NM_001130987.2:c.4122C>TMANE SELECT
NM_003494.4:c.4068C>T
NP_001123927.1:p.Ser1357=
NP_001124448.1:p.Ser1342=
NP_001124449.1:p.Ser1342=
NP_001124450.1:p.Ser1356=
NP_001124451.1:p.Ser1387=
NP_001124452.1:p.Ser1373=
NP_001124453.1:p.Ser1373=
NP_001124454.1:p.Ser1388=
NP_001124455.1:p.Ser1357=
NP_001124456.1:p.Ser1343=
NP_001124457.1:p.Ser1374=
NP_001124458.1:p.Ser1343=
NP_001124459.1:p.Ser1374=
NP_003485.1:p.Ser1356=
LRG_845t1:c.4068C>T
LRG_845t2:c.4122C>T
LRG_845:g.162905C>T
LRG_845p1:p.Ser1356=
LRG_845p2:p.Ser1374=
NC_000002.11:g.71838657C>T
NM_001130987.1:c.4122C>T
NM_003494.3:c.4068C>T
NP_003485.1:p.(=)
p.Ser1374Ser

Links:

dbSNP: rs2303607

NCBI 1000 Genomes Browser:

rs2303607

Molecular consequence:

NM_001130455.2:c.4071C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001130976.2:c.4026C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001130977.2:c.4026C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001130978.2:c.4068C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001130979.2:c.4161C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001130980.2:c.4119C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001130981.2:c.4119C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001130982.2:c.4164C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001130983.2:c.4071C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001130984.2:c.4029C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001130985.2:c.4122C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001130986.2:c.4029C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001130987.2:c.4122C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_003494.4:c.4068C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000112179	Eurofins Ntd Llc (ga)	criteria provided, single submitter (EGL Classification Definitions 2015)	Benign (Nov 22, 2013)	germline	clinical testing	Citation Link,
SCV000151029	Genetic Services Laboratory, University of Chicago	no assertion criteria provided	Likely benign	germline	clinical testing
SCV000309684	PreventionGenetics, part of Exact Sciences	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV000522730	GeneDx	criteria provided, single submitter (GeneDx Variant Classification (06012015))	Benign (Feb 10, 2016)	germline	clinical testing	Citation Link,
SCV000711688	Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine	criteria provided, single submitter (LMM Criteria)	Benign (Jan 13, 2015)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV002034572	Clinical Genetics, Academic Medical Center - VKGL Data-share Consensus See additional submitters Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	no assertion criteria provided	Benign	germline	clinical testing

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	not provided	2	2	not provided	not provided	not provided	clinical testing
not provided	germline	unknown	10	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

A systematic approach to assessing the clinical significance of genetic variants.

Duzkale H, Shen J, McLaughlin H, Alfares A, Kelly MA, Pugh TJ, Funke BH, Rehm HL, Lebo MS.

Clin Genet. 2013 Nov;84(5):453-63. doi: 10.1111/cge.12257.

PubMed [citation]

PMID:: 24033266
PMCID:: PMC3995020

Details of each submission

From Eurofins Ntd Llc (ga), SCV000112179.8

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	10	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		10	not provided	not provided	not provided

From Genetic Services Laboratory, University of Chicago, SCV000151029.2

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

Description

Likely benign based on allele frequency in 1000 Genomes Project or ESP global frequency and its presence in a patient with a rare or unrelated disease phenotype. NOT Sanger confirmed.

#	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 PreventionGenetics, part of Exact Sciences, SCV000309684.1

#	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 GeneDx, SCV000522730.4

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

Description

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, SCV000711688.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	2	not provided	not provided	clinical testing	PubMed (1)

Description

p.Ser1374Ser in exon 38 of DYSF: This variant is not expected to have clinical s ignificance because it does not alter an amino acid residue and is not located w ithin the splice consensus sequence. It has been identified in 2.8% (238/8600) o f European American chromosomes from a broad population by the NHLBI Exome Seque ncing Project (http://evs.gs.washington.edu/EVS; dbSNP rs2303607).

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	not provided	not provided	not provided	not provided		2	not provided	2	not provided

From Clinical Genetics, Academic Medical Center - VKGL Data-share Consensus, SCV002034572.1

#	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	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Mar 10, 2024

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