NM_017534.6(MYH2):c.3768del (p.Thr1257fs) AND Myopathy

Germline classification:: Likely pathogenic (1 submission)
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:: RCV001260520.1

Allele description [Variation Report for NM_017534.6(MYH2):c.3768del (p.Thr1257fs)]

NM_017534.6(MYH2):c.3768del (p.Thr1257fs)

Genes:

MYH2:myosin heavy chain 2 [Gene - OMIM - HGNC]
MYHAS:myosin heavy chain gene cluster antisense RNA [Gene - HGNC]

Variant type:

Deletion

Cytogenetic location:

17p13.1

Genomic location:

Preferred name:

NM_017534.6(MYH2):c.3768del (p.Thr1257fs)

HGVS:

NC_000017.11:g.10527852del
NG_013014.1:g.26850del
NM_001100112.2:c.3768del
NM_017534.6:c.3768delMANE SELECT
NP_001093582.1:p.Thr1257fs
NP_060004.3:p.Thr1257fs
NC_000017.10:g.10431169del
NC_000017.11:g.10527851del

Protein change:

T1257fs

Links:

dbSNP: rs2073373034

NCBI 1000 Genomes Browser:

rs2073373034

Molecular consequence:

NM_001100112.2:c.3768del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_017534.6:c.3768del - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:: Myopathy
Synonyms:: Muscle disorders
Identifiers:: MONDO: MONDO:0005336; MeSH: D009135; MedGen: C0026848; Human Phenotype Ontology: HP:0003198

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001437541	Institute of Human Genetics, University of Wuerzburg	no assertion criteria provided	Likely pathogenic	unknown	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001437541

Institute of Human Genetics, University of Wuerzburg

no assertion criteria provided

Likely pathogenic

unknown

clinical testing

Help

Summary from all submissions

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

Details of each submission

From Institute of Human Genetics, University of Wuerzburg, SCV001437541.1

#	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	unknown	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Feb 7, 2023

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