NM_000260.4(MYO7A):c.2023C>T (p.Arg675Cys) AND not provided

Germline classification:: Uncertain significance (2 submissions)
Last evaluated:: Dec 6, 2018
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:: RCV001547725.5

Allele description [Variation Report for NM_000260.4(MYO7A):c.2023C>T (p.Arg675Cys)]

NM_000260.4(MYO7A):c.2023C>T (p.Arg675Cys)

Gene:

MYO7A:myosin VIIA [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q13.5

Genomic location:

Preferred name:

NM_000260.4(MYO7A):c.2023C>T (p.Arg675Cys)

HGVS:

NC_000011.10:g.77174843C>T
NG_009086.2:g.51598C>T
NM_000260.4:c.2023C>TMANE SELECT
NM_001127180.2:c.2023C>T
NM_001369365.1:c.1990C>T
NP_000251.3:p.Arg675Cys
NP_001120652.1:p.Arg675Cys
NP_001356294.1:p.Arg664Cys
LRG_1420t1:c.2023C>T
LRG_1420:g.51598C>T
LRG_1420p1:p.Arg675Cys
NC_000011.9:g.76885889C>T
NG_009086.1:g.51580C>T
NM_000260.3:c.2023C>T

Protein change:

R664C

Links:

dbSNP: rs782459520

NCBI 1000 Genomes Browser:

rs782459520

Molecular consequence:

NM_000260.4:c.2023C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001127180.2:c.2023C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001369365.1:c.1990C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001767498	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Uncertain significance (Dec 6, 2018)	germline	clinical testing	Citation Link,
SCV005190484	Breakthrough Genomics, Breakthrough Genomics	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance	germline	not provided	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001767498

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Uncertain significance
(Dec 6, 2018)

germline

clinical testing

Citation Link,

SCV005190484

Breakthrough Genomics, Breakthrough Genomics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance

germline

not provided

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	yes	not provided	not provided	not provided	not provided	not provided	clinical testing, not provided

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

Details of each submission

From GeneDx, SCV001767498.1

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

Description

Observed in association with autosomal dominant or sporadic hearing loss; no specific patient information provided (Miyagawa et al., 2013); In silico analysis, which includes protein predictors and evolutionary conservation, supports a deleterious effect; This variant is associated with the following publications: (PMID: 23967202)

#	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 Breakthrough Genomics, Breakthrough Genomics, SCV005190484.1

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

#	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: Aug 25, 2024

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