This missense variant replaces alanine with threonine at codon 504 of the LMNA protein. Computational prediction is inconclusive regarding the impact of this variant on protein structure and function (internally defined REVEL score threshold 0.5 < inconclusive < 0.7, PMID: 27666373). To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with LMNA-related disorders in the literature. This variant has been identified in 1/249124 chromosomes in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.
ClinVar Genomic variation as it relates to human health
NM_170707.4(LMNA):c.1510G>A (p.Ala504Thr)
Germline
Classification
Help
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.
(1)
Help
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.
Uncertain significance
1
criteria provided, single submitter
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Variant Details
- Identifiers
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NM_170707.4(LMNA):c.1510G>A (p.Ala504Thr)
Variation ID: 3074640 Accession: VCV003074640.1
- Type and length
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single nucleotide variant, 1 bp
- Location
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Cytogenetic: 1q22 1: 156137134 (GRCh38) [ NCBI UCSC ] 1: 156106925 (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 Apr 20, 2024 Apr 20, 2024 Nov 20, 2023 - HGVS
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... more HGVS ... less HGVSNucleotide Protein Molecular
consequenceNM_170707.4:c.1510G>A MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_733821.1:p.Ala504Thr missense NM_005572.4:c.1510G>A MANE Plus Clinical Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_005563.1:p.Ala504Thr missense NM_001257374.3:c.1174G>A NP_001244303.1:p.Ala392Thr missense NM_001282624.2:c.1267G>A NP_001269553.1:p.Ala423Thr missense NM_001282625.2:c.1510G>A NP_001269554.1:p.Ala504Thr missense NM_001282626.2:c.1510G>A NP_001269555.1:p.Ala504Thr missense NM_001406983.1:c.1510G>A NP_001393912.1:p.Ala504Thr missense NM_001406984.1:c.1510G>A NP_001393913.1:p.Ala504Thr missense NM_001406985.1:c.1510G>A NP_001393914.1:p.Ala504Thr missense NM_001406986.1:c.1267G>A NP_001393915.1:p.Ala423Thr missense NM_001406987.1:c.1267G>A NP_001393916.1:p.Ala423Thr missense NM_001406988.1:c.1213G>A NP_001393917.1:p.Ala405Thr missense NM_001406989.1:c.1174G>A NP_001393918.1:p.Ala392Thr missense NM_001406990.1:c.952G>A NP_001393919.1:p.Ala318Thr missense NM_001406991.1:c.1510G>A NP_001393920.1:p.Ala504Thr missense NM_001406992.1:c.1510G>A NP_001393921.1:p.Ala504Thr missense NM_001406993.1:c.952G>A NP_001393922.1:p.Ala318Thr missense NM_001406994.1:c.886G>A NP_001393923.1:p.Ala296Thr missense NM_001406995.1:c.952G>A NP_001393924.1:p.Ala318Thr missense NM_001406996.1:c.952G>A NP_001393925.1:p.Ala318Thr missense NM_001406997.1:c.952G>A NP_001393926.1:p.Ala318Thr missense NM_001406998.1:c.1174G>A NP_001393927.1:p.Ala392Thr missense NM_001406999.1:c.886G>A NP_001393928.1:p.Ala296Thr missense NM_001407000.1:c.886G>A NP_001393929.1:p.Ala296Thr missense NM_001407001.1:c.886G>A NP_001393930.1:p.Ala296Thr missense NM_001407002.1:c.952G>A NP_001393931.1:p.Ala318Thr missense NM_001407003.1:c.952G>A NP_001393932.1:p.Ala318Thr missense NM_170708.4:c.1510G>A NP_733822.1:p.Ala504Thr missense NR_047544.1:n.2151G>A NR_047545.1:n.1398G>A NC_000001.11:g.156137134G>A NC_000001.10:g.156106925G>A NG_008692.2:g.59562G>A LRG_254:g.59562G>A LRG_254t1:c.1510G>A LRG_254p1:p.Ala504Thr LRG_254t2:c.1510G>A LRG_254p2:p.Ala504Thr LRG_254t3:c.1510G>A LRG_254p3:p.Ala504Thr - Protein change
- A296T, A318T, A392T, A405T, A423T, A504T
- Other names
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- Canonical SPDI
- NC_000001.11:156137133:G:A
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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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Allele frequency
Help
The frequency of the allele represented by this VCV record.
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- Links
Genes
| Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation |
Variation Viewer
Help
Links to Variation Viewer, a genome browser to view variation data from NCBI databases. |
Related variants | ||
|---|---|---|---|---|---|---|
| HI score
Help
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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| LMNA | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1847 | 2129 | |
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. |
|---|---|---|---|---|
| Uncertain significance (1) |
criteria provided, single submitter
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Nov 20, 2023 | RCV004014174.2 |
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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Uncertain Significance
(Nov 20, 2023)
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criteria provided, single submitter
Method: clinical testing
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Primary dilated cardiomyopathy
(Autosomal dominant inheritance)
Affected status: unknown
Allele origin:
germline
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All of Us Research Program, National Institutes of Health
Accession: SCV004843758.1
First in ClinVar: Apr 20, 2024 Last updated: Apr 20, 2024
Comment:
This study involves interpretation of variants in research participants for the purpose of population health screening. Participant phenotype was not available at the time of … (more)
This study involves interpretation of variants in research participants for the purpose of population health screening. Participant phenotype was not available at the time of variant classification. Additional details can be found in publication PMID: 35346344, PMCID: PMC8962531 (less)
|
Comment:
This missense variant replaces alanine with threonine at codon 504 of the LMNA protein. Computational prediction is inconclusive regarding the impact of this variant on … (more)
This missense variant replaces alanine with threonine at codon 504 of the LMNA protein. Computational prediction is inconclusive regarding the impact of this variant on protein structure and function (internally defined REVEL score threshold 0.5 < inconclusive < 0.7, PMID: 27666373). To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with LMNA-related disorders in the literature. This variant has been identified in 1/249124 chromosomes in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance. (less)
Number of individuals with the variant: 1
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Comment:
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. |
Comment:
This missense variant replaces alanine with threonine at codon 504 of the LMNA protein. Computational prediction is inconclusive regarding the impact of this variant on protein structure and function (internally defined REVEL score threshold 0.5 < inconclusive < 0.7, PMID: 27666373). To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with LMNA-related disorders in the literature. This variant has been identified in 1/249124 chromosomes in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.
Citations for germline classification of this variant
Help| There are no citations for germline classification of this variant in ClinVar. If you know of citations for this variation, please consider submitting that information to ClinVar. |
Text-mined citations for this variant ...
HelpRecord last updated May 08, 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.