NM_005619.5(RTN2):c.792C>A (p.Phe264Leu) AND not specified

Germline classification:: Benign (2 submissions)
Last evaluated:: Jan 21, 2021
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:: RCV000445188.3

Allele description [Variation Report for NM_005619.5(RTN2):c.792C>A (p.Phe264Leu)]

NM_005619.5(RTN2):c.792C>A (p.Phe264Leu)

Gene:

RTN2:reticulon 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.32

Genomic location:

Preferred name:

NM_005619.5(RTN2):c.792C>A (p.Phe264Leu)

HGVS:

NC_000019.10:g.45494188G>T
NG_032157.1:g.7866C>A
NM_005619.5:c.792C>AMANE SELECT
NM_206900.3:c.792C>A
NP_005610.1:p.Phe264Leu
NP_996783.1:p.Phe264Leu
NC_000019.9:g.45997446G>T
NM_005619.3:c.792C>A
NM_005619.4:c.792C>A

Protein change:

F264L

Links:

dbSNP: rs61745812

NCBI 1000 Genomes Browser:

rs61745812

Molecular consequence:

NM_005619.5:c.792C>A - missense variant - [Sequence Ontology: SO:0001583]
NM_206900.3:c.792C>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000519912	GeneDx	criteria provided, single submitter (GeneDx Variant Classification (06012015))	Benign (Jan 15, 2017)	germline	clinical testing	Citation Link,
SCV000614895	Athena Diagnostics	criteria provided, single submitter (Athena Diagnostics criteria)	Benign (Jan 21, 2021)	unknown	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000519912

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification (06012015))

Benign
(Jan 15, 2017)

germline

clinical testing

Citation Link,

SCV000614895

Athena Diagnostics

criteria provided, single submitter

(Athena Diagnostics criteria)

Benign
(Jan 21, 2021)

unknown

clinical testing

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	unknown	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

A Standardized DNA Variant Scoring System for Pathogenicity Assessments in Mendelian Disorders.

Karbassi I, Maston GA, Love A, DiVincenzo C, Braastad CD, Elzinga CD, Bright AR, Previte D, Zhang K, Rowland CM, McCarthy M, Lapierre JL, Dubois F, Medeiros KA, Batish SD, Jones J, Liaquat K, Hoffman CA, Jaremko M, Wang Z, Sun W, Buller-Burckle A, et al.

Hum Mutat. 2016 Jan;37(1):127-34. doi: 10.1002/humu.22918. Epub 2015 Oct 29.

PubMed [citation]

PMID:: 26467025
PMCID:: PMC4737317

Details of each submission

From GeneDx, SCV000519912.4

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

Description

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

#	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 Athena Diagnostics, SCV000614895.2

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

#	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: Sep 29, 2024

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