ClinVar Genomic variation as it relates to human health
NM_001297719.2(BMAL1):c.695T>C (p.Ile232Thr)
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_001297719.2(BMAL1):c.695T>C (p.Ile232Thr)
Variation ID: 3134458 Accession: VCV003134458.1
- Type and length
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single nucleotide variant, 1 bp
- Location
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Cytogenetic: 11p15.3 11: 13369642 (GRCh38) [ NCBI UCSC ] 11: 13391189 (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 May 1, 2024 May 1, 2024 Jan 22, 2024 - HGVS
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Nucleotide Protein Molecular
consequenceNM_001297719.2:c.695T>C MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_001284648.1:p.Ile232Thr missense NM_001030272.3:c.695T>C NP_001025443.1:p.Ile232Thr missense NM_001030273.3:c.566T>C NP_001025444.1:p.Ile189Thr missense NM_001178.6:c.695T>C NP_001169.3:p.Ile232Thr missense NM_001297722.2:c.695T>C NP_001284651.1:p.Ile232Thr missense NM_001297724.2:c.566T>C NP_001284653.1:p.Ile189Thr missense NM_001351804.1:c.695T>C NP_001338733.1:p.Ile232Thr missense NM_001351805.2:c.656T>C NP_001338734.1:p.Ile219Thr missense NM_001351806.2:c.656T>C NP_001338735.1:p.Ile219Thr missense NM_001351807.2:c.695T>C NP_001338736.1:p.Ile232Thr missense NM_001351808.2:c.566T>C NP_001338737.1:p.Ile189Thr missense NM_001351809.2:c.644T>C NP_001338738.1:p.Ile215Thr missense NM_001351810.2:c.695T>C NP_001338739.1:p.Ile232Thr missense NM_001351811.2:c.-1-55T>C intron variant NM_001351812.2:c.644T>C NP_001338741.1:p.Ile215Thr missense NM_001351813.2:c.566T>C NP_001338742.1:p.Ile189Thr missense NM_001351814.2:c.695T>C NP_001338743.1:p.Ile232Thr missense NM_001351815.2:c.695T>C NP_001338744.1:p.Ile232Thr missense NM_001351816.2:c.566T>C NP_001338745.1:p.Ile189Thr missense NM_001351817.2:c.695T>C NP_001338746.1:p.Ile232Thr missense NM_001351818.2:c.566T>C NP_001338747.1:p.Ile189Thr missense NM_001351819.2:c.695T>C NP_001338748.1:p.Ile232Thr missense NM_001351820.2:c.566T>C NP_001338749.1:p.Ile189Thr missense NM_001351821.2:c.566T>C NP_001338750.1:p.Ile189Thr missense NM_001351822.2:c.566T>C NP_001338751.1:p.Ile189Thr missense NM_001351823.2:c.566T>C NP_001338752.1:p.Ile189Thr missense NM_001351824.2:c.695T>C NP_001338753.1:p.Ile232Thr missense NR_147785.2:n.1036T>C non-coding transcript variant NR_147786.2:n.1036T>C non-coding transcript variant NR_147787.2:n.1036T>C non-coding transcript variant NR_147788.2:n.1091T>C non-coding transcript variant NR_147789.2:n.1107T>C non-coding transcript variant NR_147790.2:n.1107T>C non-coding transcript variant NR_147791.2:n.1107T>C non-coding transcript variant NC_000011.10:g.13369642T>C NC_000011.9:g.13391189T>C - Protein change
- I215T, I189T, I219T, I232T
- Other names
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- Canonical SPDI
- NC_000011.10:13369641:T:C
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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
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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 | ||
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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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BMAL1 | - | - |
GRCh38 GRCh37 |
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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
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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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Jan 22, 2024 | RCV004431811.1 |
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
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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 22, 2024)
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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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Ambry Genetics
Accession: SCV004916265.1
First in ClinVar: May 01, 2024 Last updated: May 01, 2024 |
Comment:
The c.695T>C (p.I232T) alteration is located in exon 12 (coding exon 8) of the ARNTL gene. This alteration results from a T to C substitution … (more)
The c.695T>C (p.I232T) alteration is located in exon 12 (coding exon 8) of the ARNTL gene. This alteration results from a T to C substitution at nucleotide position 695, causing the isoleucine (I) at amino acid position 232 to be replaced by a threonine (T). Based on insufficient or conflicting evidence, 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
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 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.