NM_001256071.3(RNF213):c.11893G>A (p.Val3965Met) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 14, 2023
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:: RCV003740461.2

Allele description [Variation Report for NM_001256071.3(RNF213):c.11893G>A (p.Val3965Met)]

NM_001256071.3(RNF213):c.11893G>A (p.Val3965Met)

Genes:

RNF213-AS1:RNF213 antisense RNA 1 [Gene - HGNC]
RNF213:ring finger protein 213 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17q25.3

Genomic location:

Preferred name:

NM_001256071.3(RNF213):c.11893G>A (p.Val3965Met)

HGVS:

NC_000017.11:g.80367769G>A
NG_031980.2:g.111909G>A
NM_001256071.3:c.11893G>AMANE SELECT
NM_001410195.1:c.12040G>A
NM_020914.5:c.12040G>A
NP_001243000.2:p.Val3965Met
NP_001397124.1:p.Val4014Met
NP_065965.5:p.Val4014Met
NC_000017.10:g.78341569G>A

Protein change:

V3965M

Molecular consequence:

NM_001256071.3:c.11893G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001410195.1:c.12040G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_020914.5:c.12040G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

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intraflagellar transport protein 46 homolog isoform X1 [Homo sapiens]
intraflagellar transport protein 46 homolog isoform X1 [Homo sapiens]
gi|2462526428|ref|XP_054225354.1|

Protein
unnamed protein product [Homo sapiens]
unnamed protein product [Homo sapiens]
gi|193784112|dbj|BAG53656.1|

Protein

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004552237	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Mar 14, 2023)	germline	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

SCV004552237

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Mar 14, 2023)

germline

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV004552237.1

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

Description

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Not Available"; PolyPhen-2: "Benign"; Align-GVGD: "Not Available". The methionine amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. This variant has not been reported in the literature in individuals affected with RNF213-related conditions. This variant is present in population databases (rs761189212, gnomAD 0.006%). This sequence change replaces valine, which is neutral and non-polar, with methionine, which is neutral and non-polar, at codon 3965 of the RNF213 protein (p.Val3965Met).

#	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: Sep 29, 2024

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