NM_019098.5(CNGB3):c.2415A>C (p.Glu805Asp) AND Achromatopsia

Germline classification:: Benign (1 submission)
Last evaluated:: Jan 9, 2020
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:: RCV001276120.9

Allele description [Variation Report for NM_019098.5(CNGB3):c.2415A>C (p.Glu805Asp)]

NM_019098.5(CNGB3):c.2415A>C (p.Glu805Asp)

Gene:

CNGB3:cyclic nucleotide gated channel subunit beta 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

8q21.3

Genomic location:

Preferred name:

NM_019098.5(CNGB3):c.2415A>C (p.Glu805Asp)

HGVS:

NC_000008.11:g.86575819T>G
NG_016980.1:g.172857A>C
NM_019098.5:c.2415A>CMANE SELECT
NP_061971.3:p.Glu805Asp
NP_061971.3:p.Glu805Asp
NC_000008.10:g.87588047T>G
NM_019098.4:c.2415A>C

Protein change:

E805D

Links:

dbSNP: rs186448979

NCBI 1000 Genomes Browser:

rs186448979

Molecular consequence:

NM_019098.5:c.2415A>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Achromatopsia
Synonyms:: Rod monochromatism
Identifiers:: MONDO: MONDO:0018852; MedGen: C0152200; Human Phenotype Ontology: HP:0011516

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001461971	Natera, Inc.	no assertion criteria provided	Benign (Jan 9, 2020)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001461971

Natera, Inc.

no assertion criteria provided

Benign
(Jan 9, 2020)

germline

clinical testing

Help

Summary from all submissions

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

Details of each submission

From Natera, Inc., SCV001461971.1

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

Last Updated: Nov 3, 2024

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