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_001395207.1(SORBS2):c.2902G>A (p.Val968Ile)
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_001395207.1(SORBS2):c.2902G>A (p.Val968Ile)
Variation ID: 2223154 Accession: VCV002223154.2
- Type and length
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single nucleotide variant, 1 bp
- Location
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Cytogenetic: 4q35.1 4: 185623115 (GRCh38) [ NCBI UCSC ] 4: 186544269 (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 Feb 8, 2023 May 1, 2024 Aug 23, 2021 - HGVS
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... more HGVS ... less HGVSNucleotide Protein Molecular
consequenceNM_001395207.1:c.2902G>A MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_001382136.1:p.Val968Ile missense NM_001145670.2:c.1136-2964G>A intron variant NM_001145671.3:c.1397-2964G>A intron variant NM_001145672.2:c.1187-2964G>A intron variant NM_001145673.3:c.1676-2964G>A intron variant NM_001145674.3:c.2014G>A NP_001139146.1:p.Val672Ile missense NM_001145675.3:c.680-2964G>A intron variant NM_001270771.3:c.2602G>A NP_001257700.1:p.Val868Ile missense NM_001394245.1:c.2860G>A NP_001381174.1:p.Val954Ile missense NM_001394246.1:c.2803G>A NP_001381175.1:p.Val935Ile missense NM_001394247.1:c.2803G>A NP_001381176.1:p.Val935Ile missense NM_001394248.1:c.2734G>A NP_001381177.1:p.Val912Ile missense NM_001394249.1:c.2734G>A NP_001381178.1:p.Val912Ile missense NM_001394250.1:c.2719G>A NP_001381179.1:p.Val907Ile missense NM_001394251.1:c.2602G>A NP_001381180.1:p.Val868Ile missense NM_001394252.1:c.2602G>A NP_001381181.1:p.Val868Ile missense NM_001394253.1:c.2602G>A NP_001381182.1:p.Val868Ile missense NM_001394254.1:c.2602G>A NP_001381183.1:p.Val868Ile missense NM_001394255.1:c.2560G>A NP_001381184.1:p.Val854Ile missense NM_001394256.1:c.2560G>A NP_001381185.1:p.Val854Ile missense NM_001394257.1:c.2560G>A NP_001381186.1:p.Val854Ile missense NM_001394258.1:c.2545G>A NP_001381187.1:p.Val849Ile missense NM_001394259.1:c.2515G>A NP_001381188.1:p.Val839Ile missense NM_001394260.1:c.2515G>A NP_001381189.1:p.Val839Ile missense NM_001394261.1:c.2509G>A NP_001381190.1:p.Val837Ile missense NM_001394262.1:c.2491G>A NP_001381191.1:p.Val831Ile missense NM_001394263.1:c.2491G>A NP_001381192.1:p.Val831Ile missense NM_001394264.1:c.2416G>A NP_001381193.1:p.Val806Ile missense NM_001394265.1:c.2395G>A NP_001381194.1:p.Val799Ile missense NM_001394266.1:c.2302G>A NP_001381195.1:p.Val768Ile missense NM_001394267.1:c.2302G>A NP_001381196.1:p.Val768Ile missense NM_001394268.1:c.2302G>A NP_001381197.1:p.Val768Ile missense NM_001394270.1:c.2302G>A NP_001381199.1:p.Val768Ile missense NM_001394271.1:c.2302G>A NP_001381200.1:p.Val768Ile missense NM_001394272.1:c.2302G>A NP_001381201.1:p.Val768Ile missense NM_001394273.1:c.2275G>A NP_001381202.1:p.Val759Ile missense NM_001394274.1:c.2257G>A NP_001381203.1:p.Val753Ile missense NM_001394275.1:c.2257G>A NP_001381204.1:p.Val753Ile missense NM_001394276.1:c.2393-2964G>A intron variant NM_001394277.1:c.2059G>A NP_001381206.1:p.Val687Ile missense NM_003603.7:c.1202-2964G>A intron variant NM_021069.6:c.2302G>A NP_066547.1:p.Val768Ile missense NC_000004.12:g.185623115C>T NC_000004.11:g.186544269C>T NG_029709.1:g.338602G>A - Protein change
- V687I, V839I, V868I, V907I, V768I, V799I, V954I, V672I, V753I, V759I, V831I, V854I, V912I, V806I, V837I, V849I, V935I, V968I
- Other names
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- Canonical SPDI
- NC_000004.12:185623114:C:T
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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. |
|||
| SORBS2 | - | - |
GRCh38 GRCh37 |
92 | 235 | |
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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Aug 23, 2021 | RCV004084301.1 |
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
(Aug 23, 2021)
|
criteria provided, single submitter
Method: clinical testing
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not specified
Affected status: unknown
Allele origin:
germline
|
Ambry Genetics
Accession: SCV003551920.2
First in ClinVar: Feb 07, 2023 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 Nov 25, 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.