This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
ClinVar Genomic variation as it relates to human health
NM_003567.4(BCAR3):c.1236C>G (p.Phe412Leu)
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.
Likely benign
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_003567.4(BCAR3):c.1236C>G (p.Phe412Leu)
Variation ID: 3133272 Accession: VCV003133272.1
- Type and length
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single nucleotide variant, 1 bp
- Location
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Cytogenetic: 1p22.1 1: 93582751 (GRCh38) [ NCBI UCSC ] 1: 94048308 (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 Oct 13, 2023 - HGVS
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... more HGVS ... less HGVSNucleotide Protein Molecular
consequenceNM_003567.4:c.1236C>G MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_003558.1:p.Phe412Leu missense NM_001261408.2:c.1236C>G NP_001248337.1:p.Phe412Leu missense NM_001261409.1:c.1236C>G NP_001248338.1:p.Phe412Leu missense NM_001261410.2:c.963C>G NP_001248339.1:p.Phe321Leu missense NM_001308251.1:c.264C>G NP_001295180.1:p.Phe88Leu missense NM_001412043.1:c.1236C>G NP_001398972.1:p.Phe412Leu missense NM_001412044.1:c.1236C>G NP_001398973.1:p.Phe412Leu missense NM_001412045.1:c.1236C>G NP_001398974.1:p.Phe412Leu missense NM_001412046.1:c.1236C>G NP_001398975.1:p.Phe412Leu missense NM_001412048.1:c.1236C>G NP_001398977.1:p.Phe412Leu missense NM_001412049.1:c.1236C>G NP_001398978.1:p.Phe412Leu missense NM_001412050.1:c.1236C>G NP_001398979.1:p.Phe412Leu missense NM_001412051.1:c.1236C>G NP_001398980.1:p.Phe412Leu missense NM_001412052.1:c.1236C>G NP_001398981.1:p.Phe412Leu missense NM_001412054.1:c.1305C>G NP_001398983.1:p.Phe435Leu missense NM_001412055.1:c.1311C>G NP_001398984.1:p.Phe437Leu missense NM_001412056.1:c.1365C>G NP_001398985.1:p.Phe455Leu missense NM_001412057.1:c.1107C>G NP_001398986.1:p.Phe369Leu missense NM_001412058.1:c.576C>G NP_001398987.1:p.Phe192Leu missense NM_001412059.1:c.915C>G NP_001398988.1:p.Phe305Leu missense NM_001412060.1:c.858C>G NP_001398989.1:p.Phe286Leu missense NM_001412061.1:c.858C>G NP_001398990.1:p.Phe286Leu missense NM_001412062.1:c.858C>G NP_001398991.1:p.Phe286Leu missense NM_001412064.1:c.1236C>G NP_001398993.1:p.Phe412Leu missense NM_001412065.1:c.1107C>G NP_001398994.1:p.Phe369Leu missense NM_001412066.1:c.1236C>G NP_001398995.1:p.Phe412Leu missense NM_001412067.1:c.1236C>G NP_001398996.1:p.Phe412Leu missense NM_001412072.1:c.1236C>G NP_001399001.1:p.Phe412Leu missense NM_001412073.1:c.1272C>G NP_001399002.1:p.Phe424Leu missense NM_001412074.1:c.834C>G NP_001399003.1:p.Phe278Leu missense NM_001412075.1:c.963C>G NP_001399004.1:p.Phe321Leu missense NM_001412076.1:c.900C>G NP_001399005.1:p.Phe300Leu missense NM_001412077.1:c.576C>G NP_001399006.1:p.Phe192Leu missense NR_178023.1:n.1487C>G non-coding transcript variant NR_178024.1:n.1487C>G non-coding transcript variant NC_000001.11:g.93582751G>C NC_000001.10:g.94048308G>C - Protein change
- F192L, F300L, F321L, F412L, F424L, F305L, F278L, F286L, F435L, F455L, F369L, F437L, F88L
- Other names
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- Canonical SPDI
- NC_000001.11:93582750:G: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
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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| BCAR3 | - | - |
GRCh38 GRCh37 |
73 | 87 | |
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. |
|---|---|---|---|---|
| Likely benign (1) |
criteria provided, single submitter
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Oct 13, 2023 | RCV004426165.1 |
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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Likely benign
(Oct 13, 2023)
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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: SCV004912822.1
First in ClinVar: May 01, 2024 Last updated: May 01, 2024 |
Comment:
This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of … (more)
This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. (less)
|
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 alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
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.