ClinVar Genomic variation as it relates to human health
NM_020975.6(RET):c.2710T>G (p.Ser904Ala)
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_020975.6(RET):c.2710T>G (p.Ser904Ala)
Variation ID: 665731 Accession: VCV000665731.12
- Type and length
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single nucleotide variant, 1 bp
- Location
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Cytogenetic: 10q11.21 10: 43120183 (GRCh38) [ NCBI UCSC ] 10: 43615631 (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 Aug 14, 2019 May 1, 2024 Feb 5, 2024 - HGVS
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Nucleotide Protein Molecular
consequenceNM_020975.6:c.2710T>G MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_066124.1:p.Ser904Ala missense NM_000323.2:c.2710T>G NP_000314.1:p.Ser904Ala missense NM_001355216.2:c.1948T>G NP_001342145.1:p.Ser650Ala missense NM_001406743.1:c.2710T>G NP_001393672.1:p.Ser904Ala missense NM_001406744.1:c.2710T>G NP_001393673.1:p.Ser904Ala missense NM_001406759.1:c.2710T>G NP_001393688.1:p.Ser904Ala missense NM_001406760.1:c.2710T>G NP_001393689.1:p.Ser904Ala missense NM_001406761.1:c.2581T>G NP_001393690.1:p.Ser861Ala missense NM_001406762.1:c.2581T>G NP_001393691.1:p.Ser861Ala missense NM_001406763.1:c.2575T>G NP_001393692.1:p.Ser859Ala missense NM_001406764.1:c.2581T>G NP_001393693.1:p.Ser861Ala missense NM_001406765.1:c.2575T>G NP_001393694.1:p.Ser859Ala missense NM_001406766.1:c.2422T>G NP_001393695.1:p.Ser808Ala missense NM_001406767.1:c.2422T>G NP_001393696.1:p.Ser808Ala missense NM_001406768.1:c.2446T>G NP_001393697.1:p.Ser816Ala missense NM_001406769.1:c.2314T>G NP_001393698.1:p.Ser772Ala missense NM_001406770.1:c.2422T>G NP_001393699.1:p.Ser808Ala missense NM_001406771.1:c.2272T>G NP_001393700.1:p.Ser758Ala missense NM_001406772.1:c.2314T>G NP_001393701.1:p.Ser772Ala missense NM_001406773.1:c.2272T>G NP_001393702.1:p.Ser758Ala missense NM_001406774.1:c.2185T>G NP_001393703.1:p.Ser729Ala missense NM_001406775.1:c.1984T>G NP_001393704.1:p.Ser662Ala missense NM_001406776.1:c.1984T>G NP_001393705.1:p.Ser662Ala missense NM_001406777.1:c.1984T>G NP_001393706.1:p.Ser662Ala missense NM_001406778.1:c.1984T>G NP_001393707.1:p.Ser662Ala missense NM_001406779.1:c.1813T>G NP_001393708.1:p.Ser605Ala missense NM_001406780.1:c.1813T>G NP_001393709.1:p.Ser605Ala missense NM_001406781.1:c.1813T>G NP_001393710.1:p.Ser605Ala missense NM_001406782.1:c.1813T>G NP_001393711.1:p.Ser605Ala missense NM_001406783.1:c.1684T>G NP_001393712.1:p.Ser562Ala missense NM_001406784.1:c.1720T>G NP_001393713.1:p.Ser574Ala missense NM_001406785.1:c.1693T>G NP_001393714.1:p.Ser565Ala missense NM_001406786.1:c.1684T>G NP_001393715.1:p.Ser562Ala missense NM_001406787.1:c.1678T>G NP_001393716.1:p.Ser560Ala missense NM_001406788.1:c.1525T>G NP_001393717.1:p.Ser509Ala missense NM_001406789.1:c.1525T>G NP_001393718.1:p.Ser509Ala missense NM_001406790.1:c.1525T>G NP_001393719.1:p.Ser509Ala missense NM_001406791.1:c.1405T>G NP_001393720.1:p.Ser469Ala missense NM_001406792.1:c.1261T>G NP_001393721.1:p.Ser421Ala missense NM_001406793.1:c.1261T>G NP_001393722.1:p.Ser421Ala missense NM_001406794.1:c.1261T>G NP_001393723.1:p.Ser421Ala missense NM_020629.2:c.2710T>G NP_065680.1:p.Ser904Ala missense NM_020630.7:c.2710T>G NP_065681.1:p.Ser904Ala missense NC_000010.11:g.43120183T>G NC_000010.10:g.43615631T>G NG_007489.1:g.48115T>G LRG_518:g.48115T>G LRG_518t1:c.2710T>G LRG_518p1:p.Ser904Ala LRG_518t2:c.2710T>G LRG_518p2:p.Ser904Ala - Protein change
- S650A, S904A, S421A, S758A, S808A, S509A, S560A, S562A, S565A, S574A, S662A, S772A, S816A, S469A, S605A, S729A, S859A, S861A
- Other names
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- Canonical SPDI
- NC_000010.11:43120182:T:G
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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.
Trans-Omics for Precision Medicine (TOPMed) 0.00002
- 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 | ||
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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
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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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RET | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
3522 | 3642 |
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
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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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Uncertain significance (2) |
criteria provided, multiple submitters, no conflicts
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Feb 5, 2024 | RCV000824078.9 | |
Uncertain significance (1) |
criteria provided, single submitter
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Jan 3, 2022 | RCV002478933.1 | |
Uncertain significance (1) |
criteria provided, single submitter
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Jun 12, 2023 | RCV002427074.3 |
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
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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
(Jan 03, 2022)
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criteria provided, single submitter
Method: clinical testing
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Hirschsprung disease, susceptibility to, 1
Familial medullary thyroid carcinoma MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB Pheochromocytoma MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA
Affected status: unknown
Allele origin:
unknown
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Fulgent Genetics, Fulgent Genetics
Accession: SCV002782298.1
First in ClinVar: Dec 31, 2022 Last updated: Dec 31, 2022 |
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Uncertain significance
(Jan 22, 2024)
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criteria provided, single submitter
Method: clinical testing
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Multiple endocrine neoplasia, type 2
Affected status: unknown
Allele origin:
germline
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Invitae
Accession: SCV000964960.6
First in ClinVar: Aug 14, 2019 Last updated: Feb 20, 2024 |
Comment:
This sequence change replaces serine, which is neutral and polar, with alanine, which is neutral and non-polar, at codon 904 of the RET protein (p.Ser904Ala). … (more)
This sequence change replaces serine, which is neutral and polar, with alanine, which is neutral and non-polar, at codon 904 of the RET protein (p.Ser904Ala). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with RET-related conditions. ClinVar contains an entry for this variant (Variation ID: 665731). An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be disruptive. 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. (less)
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Uncertain Significance
(Feb 05, 2024)
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criteria provided, single submitter
Method: clinical testing
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Multiple endocrine neoplasia, type 2
(Autosomal dominant inheritance)
Affected status: unknown
Allele origin:
germline
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All of Us Research Program, National Institutes of Health
Accession: SCV004815283.1
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)
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Comment:
This missense variant replaces serine with alanine at codon 904 of the RET protein. Computational prediction is inconclusive regarding the impact of this variant on … (more)
This missense variant replaces serine with alanine at codon 904 of the RET 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 RET-related disorders in the literature. This variant has not been identified in the general population by the Genome Aggregation Database (gnomAD). A different variant affecting the same codon, c.2711C>T (p.Ser904Phe), is considered to be pathogenic (ClinVar Variation ID: 36304), suggesting that Ser at this position is important for protein function. 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: 3
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Uncertain significance
(Jun 12, 2023)
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criteria provided, single submitter
Method: clinical testing
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Hereditary cancer-predisposing syndrome
Affected status: unknown
Allele origin:
germline
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Ambry Genetics
Accession: SCV002741401.3
First in ClinVar: Nov 29, 2022 Last updated: May 01, 2024 |
Comment:
The p.S904A variant (also known as c.2710T>G), located in coding exon 15 of the RET gene, results from a T to G substitution at nucleotide … (more)
The p.S904A variant (also known as c.2710T>G), located in coding exon 15 of the RET gene, results from a T to G substitution at nucleotide position 2710. The serine at codon 904 is replaced by alanine, an amino acid with similar properties. Other alterations at codon 904 have been detected in MEN 2B and medullary thyroid cancer families; however the pathogenicity of these alterations remains unclear (Elisei R et al, J. Clin. Endocrinol. Metab. 2007 Dec; 92(12):4725-9. Menko FH et al, J. Clin. Endocrinol. Metab. 2002 Jan; 87(1):393-7). This amino acid position is highly conserved in available vertebrate species. In addition, the in silico prediction for this alteration is inconclusive. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear. (less)
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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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Predicting phenotypic severity of uncertain gene variants in the RET proto-oncogene. | Crockett DK | PloS one | 2011 | PMID: 21479187 |
RET genetic screening in patients with medullary thyroid cancer and their relatives: experience with 807 individuals at one center. | Elisei R | The Journal of clinical endocrinology and metabolism | 2007 | PMID: 17895320 |
Atypical MEN type 2B associated with two germline RET mutations on the same allele not involving codon 918. | Menko FH | The Journal of clinical endocrinology and metabolism | 2002 | PMID: 11788682 |
Text-mined citations for rs1588877711 ...
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.