NM_003494.3(DYSF):c.1642delG (p.Glu548Lysfs) AND not provided

replaced

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Sep 5, 2012
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

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:: RCV000080240.3

Allele description

NM_003494.3(DYSF):c.1642delG (p.Glu548Lysfs)

Gene:

DYSF:dysferlin [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

2p13.2

Genomic location:

Preferred name:

NM_003494.3(DYSF):c.1642delG (p.Glu548Lysfs)

HGVS:

NC_000002.12:g.71551610delG
NG_008694.1:g.102988delG
NM_001130987.1:c.1696delG
NM_003494.3:c.1642delG
NP_001124459.1:p.Glu566Lysfs
NP_003485.1:p.Glu548Lysfs
NC_000002.11:g.71778740delG

Links:

dbSNP: rs398123772

NCBI 1000 Genomes Browser:

rs398123772

Molecular consequence:

NM_003494.3:c.1642delG - frameshift variant - [Sequence Ontology: SO:0001589]

Observations:

Condition(s)

Identifiers:: MedGen: CN517202

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000112135	EGL Genetic Diagnostics,Eurofins Clinical Diagnostics	no assertion criteria provided	Pathogenic (Sep 5, 2012)	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

SCV000112135

EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

no assertion criteria provided

Pathogenic
(Sep 5, 2012)

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	1	not provided	not provided	350	not provided	clinical testing

Citations

PubMed

Free the data: one laboratory's approach to knowledge-based genomic variant classification and preparation for EMR integration of genomic data.

Bean LJ, Tinker SW, da Silva C, Hegde MR.

Hum Mutat. 2013 Sep;34(9):1183-8. doi: 10.1002/humu.22364. Epub 2013 Aug 5.

PubMed [citation]

PMID:: 23757202

Details of each submission

From EGL Genetic Diagnostics,Eurofins Clinical Diagnostics, SCV000112135.3

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	1	not provided	not provided	clinical testing (GTR000502388)	PubMed (1)
2	not provided	0	not provided	not provided	clinical testing (GTR000502549)	PubMed (1)
3	not provided	0	not provided	not provided	clinical testing	PubMed (1)
4	not provided	0	not provided	not provided	clinical testing	PubMed (1)
5	not provided	0	not provided	not provided	clinical testing	PubMed (1)
6	not provided	0	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	146	not provided	not provided	(GTR000502388)	1	not provided	not provided	not provided
2	germline	unknown	84	not provided	not provided	(GTR000502549)	0	not provided	not provided	not provided
3	germline	unknown	2	not provided	not provided		0	not provided	not provided	not provided
4	germline	unknown	not provided	not provided	not provided		0	not provided	not provided	not provided
5	germline	unknown	105	not provided	not provided		0	not provided	not provided	not provided
6	germline	unknown	13	not provided	not provided		0	not provided	not provided	not provided

Last Updated: Feb 13, 2018

ClinVar

Relating variation to medicine