ClinVar Genomic variation as it relates to human health
NM_000243.3(MEFV):c.1764G>A (p.Pro588=)
The aggregate germline classification for this variant, typically for a monogenic or Mendelian disorder as in the ACMG/AMP guidelines, or for response to a drug. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the aggregate classification.
Stars represent the aggregate review status, or the level of review supporting the aggregate germline classification for this VCV record. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status. The number of submissions which contribute to this review status is shown in parentheses.
No data submitted for somatic clinical impact
No data submitted for oncogenicity
Variant Details
- Identifiers
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NM_000243.3(MEFV):c.1764G>A (p.Pro588=)
Variation ID: 36505 Accession: VCV000036505.35
- Type and length
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single nucleotide variant, 1 bp
- Location
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Cytogenetic: 16p13.3 16: 3243888 (GRCh38) [ NCBI UCSC ] 16: 3293888 (GRCh37) [ NCBI UCSC ]
- Timeline in ClinVar
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First in ClinVar Help The date this variant first appeared in ClinVar with each type of classification.
Last submission Help The date of the most recent submission for each type of classification for this variant.
Last evaluated Help The most recent date that a submitter evaluated this variant for each type of classification.
Germline Mar 29, 2015 May 12, 2024 Feb 1, 2024 - HGVS
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Nucleotide Protein Molecular
consequenceNM_000243.3:c.1764G>A MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_000234.1:p.Pro588= synonymous NM_000243.2:c.1764A= NP_000234.1:p.Pro588= no sequence alteration NM_001198536.2:c.1306G>A NP_001185465.2:p.Gly436Arg missense NC_000016.10:g.3243888C>T NC_000016.9:g.3293888C>T NG_007871.1:g.17740= LRG_190:g.17740= LRG_190t1:c.1764= LRG_190p1:p.Pro588= - Protein change
- G436R
- Other names
- -
- Canonical SPDI
- NC_000016.10:3243887:C:T
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Functional
consequence HelpThe effect of the variant on RNA or protein function, based on experimental evidence from submitters.
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Global minor allele
frequency (GMAF) HelpThe global minor allele frequency calculated by the 1000 Genomes Project. The minor allele at this location is indicated in parentheses and may be different from the allele represented by this VCV record.
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0.35363 (T)
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Allele frequency
Help
The frequency of the allele represented by this VCV record.
1000 Genomes Project 30x 0.35056
1000 Genomes Project 0.35363
Trans-Omics for Precision Medicine (TOPMed) 0.40033
The Genome Aggregation Database (gnomAD) 0.41230
NHLBI Exome Sequencing Project (ESP) Exome Variant Server 0.42358
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation |
Variation Viewer
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Links to Variation Viewer, a genome browser to view variation data from NCBI databases. |
Related variants | ||
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HI score
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The haploinsufficiency score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team. |
TS score
Help
The triplosensitivity score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team. |
Within gene
Help
The number of variants in ClinVar that are contained within this gene, with a link to view the list of variants. |
All
Help
The number of variants in ClinVar for this gene, including smaller variants within the gene and larger CNVs that overlap or fully contain the gene. |
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MEFV | No evidence available | No evidence available |
GRCh38 GRCh37 |
949 | 1246 | |
LOC126862264 | - | - | - | GRCh38 | - | 254 |
Conditions - Germline
Condition
Help
The condition for this variant-condition (RCV) record in ClinVar. |
Classification
Help
The aggregate germline classification for this variant-condition (RCV) record in ClinVar. The number of submissions that contribute to this aggregate classification is shown in parentheses. (# of submissions) |
Review status
Help
The aggregate review status for this variant-condition (RCV) record in ClinVar. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status. |
Last evaluated
Help
The most recent date that a submitter evaluated this variant for the condition. |
Variation/condition record
Help
The RCV accession number, with most recent version number, for the variant-condition record, with a link to the RCV web page. |
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Benign (5) |
criteria provided, multiple submitters, no conflicts
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Feb 1, 2024 | RCV000030177.21 | |
Benign (4) |
criteria provided, multiple submitters, no conflicts
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Nov 12, 2023 | RCV000266471.22 | |
Benign (1) |
criteria provided, single submitter
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Jul 1, 2021 | RCV001533506.10 | |
Benign (2) |
criteria provided, single submitter
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Dec 1, 2023 | RCV001701571.12 |
Submissions - Germline
Classification
Help
The submitted germline classification for each SCV record. (Last evaluated) |
Review status
Help
Stars represent the review status, or the level of review supporting the submitted (SCV) record. This value is calculated by NCBI based on data from the submitter. Read our rules for calculating the review status. This column also includes a link to the submitter’s assertion criteria if provided, and the collection method. (Assertion criteria) |
Condition
Help
The condition for the classification, provided by the submitter for this submitted (SCV) record. This column also includes the affected status and allele origin of individuals observed with this variant. |
Submitter
Help
The submitting organization for this submitted (SCV) record. This column also includes the SCV accession and version number, the date this SCV first appeared in ClinVar, and the date that this SCV was last updated in ClinVar. |
More information
Help
This column includes more information supporting the classification, including citations, the comment on classification, and detailed evidence provided as observations of the variant by the submitter. |
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Benign
(Jul 05, 2018)
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criteria provided, single submitter
Method: clinical testing
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not specified
Affected status: unknown
Allele origin:
germline
|
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories
Accession: SCV000604160.2
First in ClinVar: Dec 06, 2016 Last updated: Feb 09, 2020 |
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Benign
(Jul 01, 2021)
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criteria provided, single submitter
Method: clinical testing
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Familial Mediterranean fever
Affected status: no
Allele origin:
germline
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Genome-Nilou Lab
Accession: SCV001750184.1
First in ClinVar: Jul 18, 2021 Last updated: Jul 18, 2021 |
Sex: mixed
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Benign
(Jul 01, 2021)
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criteria provided, single submitter
Method: clinical testing
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Familial Mediterranean fever, autosomal dominant
Affected status: no
Allele origin:
germline
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Genome-Nilou Lab
Accession: SCV001750183.1
First in ClinVar: Jul 18, 2021 Last updated: Jul 18, 2021 |
Sex: mixed
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Benign
(Jan 14, 2015)
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criteria provided, single submitter
Method: literature only
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Familial Mediterranean fever
(Autosomal recessive inheritance)
Affected status: unknown
Allele origin:
unknown
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Counsyl
Accession: SCV000221023.2
First in ClinVar: Mar 29, 2015 Last updated: Dec 24, 2022 |
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Benign
(Feb 01, 2024)
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criteria provided, single submitter
Method: clinical testing
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Familial Mediterranean fever
Affected status: unknown
Allele origin:
germline
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Invitae
Accession: SCV001725095.4
First in ClinVar: Jun 15, 2021 Last updated: Feb 20, 2024 |
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Benign
(Dec 01, 2023)
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criteria provided, single submitter
Method: clinical testing
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not provided
Affected status: yes
Allele origin:
germline
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CeGaT Center for Human Genetics Tuebingen
Accession: SCV004704426.3
First in ClinVar: Mar 10, 2024 Last updated: May 12, 2024 |
Comment:
MEFV: BP7, BS1, BS2
Number of individuals with the variant: 1
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Benign
(Dec 14, 2015)
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criteria provided, single submitter
Method: clinical testing
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not specified
Affected status: unknown
Allele origin:
germline
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Eurofins Ntd Llc (ga)
Accession: SCV000331609.4
First in ClinVar: Dec 06, 2016 Last updated: Dec 06, 2016 |
Number of individuals with the variant: 2
Sex: mixed
|
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benign
(Aug 18, 2011)
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criteria provided, single submitter
Method: curation, clinical testing
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Familial Mediterranean Fever
(autosomal unknown)
Affected status: unknown, yes
Allele origin:
germline
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Women's Health and Genetics/Laboratory Corporation of America, LabCorp
Accession: SCV000052837.3
First in ClinVar: Apr 04, 2013 Last updated: Apr 11, 2022 |
Comment:
Converted during submission to Benign.
Observation 1:
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Benign
(Nov 12, 2023)
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criteria provided, single submitter
Method: clinical testing
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not specified
Affected status: no
Allele origin:
germline
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Unidad de Genómica Garrahan, Hospital de Pediatría Garrahan
Accession: SCV004101992.1
First in ClinVar: Nov 20, 2023 Last updated: Nov 20, 2023 |
Comment:
This variant is classified as Benign based on local population frequency. This variant was detected in 63% of patients studied by a panel of primary … (more)
This variant is classified as Benign based on local population frequency. This variant was detected in 63% of patients studied by a panel of primary immunodeficiencies. Number of patients: 60. Only high quality variants are reported. (less)
Number of individuals with the variant: 60
Age: <18 years
Sex: mixed
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Benign
(-)
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no assertion criteria provided
Method: clinical testing
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not specified
Affected status: yes
Allele origin:
germline
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Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen
Study: VKGL Data-share Consensus
Accession: SCV001741115.3 First in ClinVar: Jul 07, 2021 Last updated: Sep 08, 2021 |
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Benign
(Nov 19, 2019)
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no assertion criteria provided
Method: clinical testing
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Familial Mediterranean fever
Affected status: unknown
Allele origin:
germline
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Natera, Inc.
Accession: SCV002087385.1
First in ClinVar: Apr 23, 2022 Last updated: Apr 23, 2022 |
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Likely benign
(-)
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no assertion criteria provided
Method: clinical testing
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not provided
Affected status: yes
Allele origin:
germline
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Genome Diagnostics Laboratory, University Medical Center Utrecht
Additional submitter:
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen
Study: VKGL Data-share Consensus
Accession: SCV001931562.1 First in ClinVar: Sep 26, 2021 Last updated: Sep 26, 2021 |
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Germline Functional Evidence
There is no functional evidence in ClinVar for this variation. If you have generated functional data for this variation, please consider submitting that data to ClinVar. |
Citations for germline classification of this variant
HelpTitle | Author | Journal | Year | Link |
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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 | Genetics in medicine : official journal of the American College of Medical Genetics | 2015 | PMID: 25741868 |
Comprehensive analysis of a large-scale screen for MEFV gene mutations: do they truly provide a "heterozygote advantage" in Turkey? | Berdeli A | Genetic testing and molecular biomarkers | 2011 | PMID: 21413889 |
Familial Mediterranean fever with a single MEFV mutation: where is the second hit? | Booty MG | Arthritis and rheumatism | 2009 | PMID: 19479870 |
MEFV mutation analysis of familial Mediterranean fever in Japan. | Tomiyama N | Clinical and experimental rheumatology | 2008 | PMID: 18328141 |
MEFV alterations and population genetics analysis in a large cohort of Greek patients with familial Mediterranean fever. | Giaglis S | Clinical genetics | 2007 | PMID: 17489852 |
The west side story: MEFV haplotype in Spanish FMF patients and controls, and evidence of high LD and a recombination "hot-spot" at the MEFV locus. | Aldea A | Human mutation | 2004 | PMID: 15024744 |
A severe autosomal-dominant periodic inflammatory disorder with renal AA amyloidosis and colchicine resistance associated to the MEFV H478Y variant in a Spanish kindred: an unusual familial Mediterranean fever phenotype or another MEFV-associated periodic inflammatory disorder? | Aldea A | American journal of medical genetics. Part A | 2004 | PMID: 14679589 |
MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implications. | Cazeneuve C | American journal of human genetics | 1999 | PMID: 10364520 |
Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population. | Aksentijevich I | American journal of human genetics | 1999 | PMID: 10090880 |
Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF). | Bernot A | Human molecular genetics | 1998 | PMID: 9668175 |
Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. The International FMF Consortium. | - | Cell | 1997 | PMID: 9288758 |
http://www.egl-eurofins.com/emvclass/emvclass.php?approved_symbol=MEFV | - | - | - | - |
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Text-mined citations for rs1231122 ...
HelpRecord last updated Jun 02, 2024
This date represents the last time this VCV record was updated. The update may be due to an update to one of the included submitted records (SCVs), or due to an update that ClinVar made to the variant such as adding HGVS expressions or a rs number. So this date may be different from the date of the “most recent submission” reported at the top of this page.