ClinVar Genomic variation as it relates to human health
NM_020975.6(RET):c.1633C>A (p.Gln545Lys)
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.1633C>A (p.Gln545Lys)
Variation ID: 1312671 Accession: VCV001312671.6
- Type and length
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single nucleotide variant, 1 bp
- Location
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Cytogenetic: 10q11.21 10: 43112209 (GRCh38) [ NCBI UCSC ] 10: 43607657 (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 Nov 6, 2021 Feb 20, 2024 Sep 26, 2023 - HGVS
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Nucleotide Protein Molecular
consequenceNM_020975.6:c.1633C>A MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_066124.1:p.Gln545Lys missense NM_000323.2:c.1633C>A NP_000314.1:p.Gln545Lys missense NM_001355216.2:c.871C>A NP_001342145.1:p.Gln291Lys missense NM_001406743.1:c.1633C>A NP_001393672.1:p.Gln545Lys missense NM_001406744.1:c.1633C>A NP_001393673.1:p.Gln545Lys missense NM_001406759.1:c.1633C>A NP_001393688.1:p.Gln545Lys missense NM_001406760.1:c.1633C>A NP_001393689.1:p.Gln545Lys missense NM_001406761.1:c.1504C>A NP_001393690.1:p.Gln502Lys missense NM_001406762.1:c.1504C>A NP_001393691.1:p.Gln502Lys missense NM_001406763.1:c.1633C>A NP_001393692.1:p.Gln545Lys missense NM_001406764.1:c.1504C>A NP_001393693.1:p.Gln502Lys missense NM_001406765.1:c.1633C>A NP_001393694.1:p.Gln545Lys missense NM_001406766.1:c.1345C>A NP_001393695.1:p.Gln449Lys missense NM_001406767.1:c.1345C>A NP_001393696.1:p.Gln449Lys missense NM_001406768.1:c.1504C>A NP_001393697.1:p.Gln502Lys missense NM_001406769.1:c.1237C>A NP_001393698.1:p.Gln413Lys missense NM_001406770.1:c.1345C>A NP_001393699.1:p.Gln449Lys missense NM_001406771.1:c.1195C>A NP_001393700.1:p.Gln399Lys missense NM_001406772.1:c.1237C>A NP_001393701.1:p.Gln413Lys missense NM_001406773.1:c.1195C>A NP_001393702.1:p.Gln399Lys missense NM_001406774.1:c.1108C>A NP_001393703.1:p.Gln370Lys missense NM_001406775.1:c.907C>A NP_001393704.1:p.Gln303Lys missense NM_001406776.1:c.907C>A NP_001393705.1:p.Gln303Lys missense NM_001406777.1:c.907C>A NP_001393706.1:p.Gln303Lys missense NM_001406778.1:c.907C>A NP_001393707.1:p.Gln303Lys missense NM_001406779.1:c.736C>A NP_001393708.1:p.Gln246Lys missense NM_001406780.1:c.736C>A NP_001393709.1:p.Gln246Lys missense NM_001406781.1:c.736C>A NP_001393710.1:p.Gln246Lys missense NM_001406782.1:c.736C>A NP_001393711.1:p.Gln246Lys missense NM_001406783.1:c.607C>A NP_001393712.1:p.Gln203Lys missense NM_001406784.1:c.643C>A NP_001393713.1:p.Gln215Lys missense NM_001406785.1:c.736C>A NP_001393714.1:p.Gln246Lys missense NM_001406786.1:c.607C>A NP_001393715.1:p.Gln203Lys missense NM_001406787.1:c.736C>A NP_001393716.1:p.Gln246Lys missense NM_001406788.1:c.448C>A NP_001393717.1:p.Gln150Lys missense NM_001406789.1:c.448C>A NP_001393718.1:p.Gln150Lys missense NM_001406790.1:c.448C>A NP_001393719.1:p.Gln150Lys missense NM_001406791.1:c.448C>A NP_001393720.1:p.Gln150Lys missense NM_001406792.1:c.184C>A NP_001393721.1:p.Gln62Lys missense NM_001406793.1:c.184C>A NP_001393722.1:p.Gln62Lys missense NM_001406794.1:c.184C>A NP_001393723.1:p.Gln62Lys missense NM_020629.2:c.1633C>A NP_065680.1:p.Gln545Lys missense NM_020630.7:c.1633C>A NP_065681.1:p.Gln545Lys missense NC_000010.11:g.43112209C>A NC_000010.10:g.43607657C>A NG_007489.1:g.40141C>A LRG_518:g.40141C>A LRG_518t1:c.1633C>A LRG_518p1:p.Gln545Lys LRG_518t2:c.1633C>A LRG_518p2:p.Gln545Lys - Protein change
- Q291K, Q545K, Q150K, Q246K, Q399K, Q413K, Q449K, Q502K, Q215K, Q370K, Q62K, Q203K, Q303K
- Other names
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- Canonical SPDI
- NC_000010.11:43112208:C: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.
Trans-Omics for Precision Medicine (TOPMed) 0.00000
- 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
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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RET | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
3446 | 3566 |
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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Uncertain significance (1) |
criteria provided, single submitter
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Jun 3, 2020 | RCV001763677.4 | |
Uncertain significance (1) |
criteria provided, single submitter
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Sep 26, 2023 | RCV003464130.1 | |
Uncertain significance (1) |
criteria provided, single submitter
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Feb 4, 2023 | RCV003645899.1 |
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
(Jun 03, 2020)
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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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GeneDx
Accession: SCV002001057.2
First in ClinVar: Nov 06, 2021 Last updated: Mar 04, 2023 |
Comment:
Not observed in large population cohorts (Lek et al., 2016); In silico analysis supports that this missense variant does not alter protein structure/function; Has not … (more)
Not observed in large population cohorts (Lek et al., 2016); In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge (less)
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Uncertain significance
(Sep 26, 2023)
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criteria provided, single submitter
Method: clinical testing
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Hirschsprung disease, susceptibility to, 1
Affected status: unknown
Allele origin:
unknown
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Baylor Genetics
Accession: SCV004208675.1
First in ClinVar: Dec 30, 2023 Last updated: Dec 30, 2023 |
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Uncertain significance
(Feb 04, 2023)
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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: SCV004434328.1
First in ClinVar: Feb 20, 2024 Last updated: Feb 20, 2024 |
Comment:
This sequence change replaces glutamine, which is neutral and polar, with lysine, which is basic and polar, at codon 545 of the RET protein (p.Gln545Lys). … (more)
This sequence change replaces glutamine, which is neutral and polar, with lysine, which is basic and polar, at codon 545 of the RET protein (p.Gln545Lys). 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: 1312671). Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Tolerated"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). 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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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
HelpThere 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 rs890269439 ...
HelpRecord last updated Feb 28, 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.