NM_000268.4(NF2):c.12C>T (p.Ala4=) AND not specified

Germline classification:: Likely benign (3 submissions)
Last evaluated:: Jan 20, 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:: RCV000246364.8

Allele description [Variation Report for NM_000268.4(NF2):c.12C>T (p.Ala4=)]

NM_000268.4(NF2):c.12C>T (p.Ala4=)

Gene:

NF2:NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

22q12.2

Genomic location:

Preferred name:

NM_000268.4(NF2):c.12C>T (p.Ala4=)

HGVS:

NC_000022.11:g.29604010C>T
NG_009057.1:g.5455C>T
NM_000268.4:c.12C>TMANE SELECT
NM_016418.5:c.12C>T
NM_181825.3:c.12C>T
NM_181828.3:c.12C>T
NM_181829.3:c.12C>T
NM_181830.3:c.12C>T
NM_181831.3:c.12C>T
NM_181832.3:c.12C>T
NM_181833.3:c.12C>T
NP_000259.1:p.Ala4=
NP_000259.1:p.Ala4=
NP_057502.2:p.Ala4=
NP_861546.1:p.Ala4=
NP_861966.1:p.Ala4=
NP_861967.1:p.Ala4=
NP_861968.1:p.Ala4=
NP_861969.1:p.Ala4=
NP_861970.1:p.Ala4=
NP_861971.1:p.Ala4=
LRG_511t1:c.12C>T
LRG_511t2:c.12C>T
LRG_511:g.5455C>T
LRG_511p1:p.Ala4=
LRG_511p2:p.Ala4=
NC_000022.10:g.29999999C>T
NM_000268.3:c.12C>T
NM_000268.4:c.12C>T
NM_181832.2:c.12C>T
NR_156186.2:n.378C>T

Links:

dbSNP: rs144477078

NCBI 1000 Genomes Browser:

rs144477078

Molecular consequence:

NR_156186.2:n.378C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NM_000268.4:c.12C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_016418.5:c.12C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_181825.3:c.12C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_181828.3:c.12C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_181829.3:c.12C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_181830.3:c.12C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_181831.3:c.12C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_181832.3:c.12C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_181833.3:c.12C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000316742	PreventionGenetics, part of Exact Sciences	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely benign	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV000714119	GeneDx	criteria provided, single submitter (GeneDx Variant Classification (06012015))	Likely benign (Jan 20, 2018)	germline	clinical testing	Citation Link,
SCV003839768	Genetic Services Laboratory, University of Chicago	no assertion criteria provided	Likely benign (May 12, 2022)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000316742

PreventionGenetics, part of Exact Sciences

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely benign

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

SCV000714119

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification (06012015))

Likely benign
(Jan 20, 2018)

germline

clinical testing

Citation Link,

SCV003839768

Genetic Services Laboratory, University of Chicago

no assertion criteria provided

Likely benign
(May 12, 2022)

germline

clinical testing

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	germline	no	not provided	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

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 PreventionGenetics, part of Exact Sciences, SCV000316742.1

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

From GeneDx, SCV000714119.1

#	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 Genetic Services Laboratory, University of Chicago, SCV003839768.1

#	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	no	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

ClinVar

Relating variation to medicine