NM_000539.3(RHO):c.172_173delinsTA (p.Thr58Ter) AND Retinal dystrophy

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Oct 19, 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:: RCV001075164.2

Allele description [Variation Report for NM_000539.3(RHO):c.172_173delinsTA (p.Thr58Ter)]

NM_000539.3(RHO):c.172_173delinsTA (p.Thr58Ter)

Gene:

RHO:rhodopsin [Gene - OMIM - HGNC]

Variant type:

Indel

Cytogenetic location:

3q22.1

Genomic location:

Preferred name:

NM_000539.3(RHO):c.172_173delinsTA (p.Thr58Ter)

HGVS:

NC_000003.12:g.129528905_129528906delinsTA
NG_009115.1:g.5267_5268delinsTA
NM_000539.3:c.172_173delinsTAMANE SELECT
NP_000530.1:p.Thr58Ter
NC_000003.11:g.129247748_129247749delinsTA
NC_000003.11:g.129247748_129247749delinsTA

Protein change:

T58*

Links:

dbSNP: rs2084757329

NCBI 1000 Genomes Browser:

rs2084757329

Molecular consequence:

NM_000539.3:c.172_173delinsTA - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

Name:: Retinal dystrophy
Synonyms:: Inherited retinal dystrophy
Identifiers:: MONDO: MONDO:0019118; MeSH: D058499; MedGen: C0854723; Human Phenotype Ontology: HP:0000556

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001240776	Blueprint Genetics	criteria provided, single submitter (Blueprint Genetics Variant Classification Scheme)	Likely pathogenic (Oct 19, 2018)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001240776

Blueprint Genetics

criteria provided, single submitter

(Blueprint Genetics Variant Classification Scheme)

Likely pathogenic
(Oct 19, 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	clinical testing

Details of each submission

From Blueprint Genetics, SCV001240776.1

#	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: Sep 29, 2024

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