NM_000260.4(MYO7A):c.4805G>A (p.Arg1602Gln) AND Usher syndrome type 1

Germline classification:: Benign (2 submissions)
Last evaluated:: Mar 6, 2018
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:: RCV000223626.14

Allele description [Variation Report for NM_000260.4(MYO7A):c.4805G>A (p.Arg1602Gln)]

NM_000260.4(MYO7A):c.4805G>A (p.Arg1602Gln)

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.4805G>A (p.Arg1602Gln)

HGVS:

NC_000011.10:g.77199771G>A
NG_009086.2:g.76526G>A
NM_000260.4:c.4805G>AMANE SELECT
NM_001127180.2:c.4691G>A
NM_001369365.1:c.4658G>A
NP_000251.3:p.Arg1602Gln
NP_000251.3:p.Arg1602Gln
NP_001120652.1:p.Arg1564Gln
NP_001356294.1:p.Arg1553Gln
LRG_1420t1:c.4805G>A
LRG_1420:g.76526G>A
LRG_1420p1:p.Arg1602Gln
NC_000011.9:g.76910816G>A
NG_009086.1:g.76507G>A
NM_000260.3:c.4805G>A
Q13402:p.Arg1602Gln
c.4805G>A

Protein change:

R1553Q

Links:

UniProtKB: Q13402#VAR_009340; dbSNP: rs139889944

NCBI 1000 Genomes Browser:

rs139889944

Molecular consequence:

NM_000260.4:c.4805G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001127180.2:c.4691G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001369365.1:c.4658G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Usher syndrome type 1 (USH1)
Synonyms:: Usher syndrome, type I, French variety; Retinitis pigmentosa and congenital deafness
Identifiers:: MONDO: MONDO:0010168; MedGen: C1568247; Orphanet: 231169; Orphanet: 886; OMIM: 276900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000268745	GeneReviews	no classification provided	not provided	germline	literature only
SCV000374398	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification Criteria 13 December 2019)	Benign (Mar 6, 2018)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000268745

GeneReviews

no classification provided

not provided

germline

literature only

SCV000374398

Illumina Laboratory Services, Illumina

criteria provided, single submitter

(ICSL Variant Classification Criteria 13 December 2019)

Benign
(Mar 6, 2018)

germline

clinical testing

Citation Link

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	literature only
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From GeneReviews, SCV000268745.2

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

From Illumina Laboratory Services, Illumina, SCV000374398.3

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

Description

This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.

#	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: Nov 10, 2024

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