Not observed in large population cohorts (Lek et al., 2016); In-silico analysis, which includes splice predictors and evolutionary conservation, is inconclusive as to whether the variant alters gene splicing. In the absence of RNA/functional studies, the actual effect of this sequence change is unknown.; In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
ClinVar Genomic variation as it relates to human health
NM_001368894.2(PAX6):c.808G>C (p.Val270Leu)
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.
Uncertain significance
1
criteria provided, single submitter
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Variant Details
- Identifiers
-
NM_001368894.2(PAX6):c.808G>C (p.Val270Leu)
Variation ID: 1305630 Accession: VCV001305630.3
- Type and length
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single nucleotide variant, 1 bp
- Location
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Cytogenetic: 11p13 11: 31793802 (GRCh38) [ NCBI UCSC ] 11: 31815350 (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 Mar 4, 2023 Jan 31, 2020 - HGVS
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... more HGVS ... less HGVSNucleotide Protein Molecular
consequenceNM_001368894.2:c.808G>C MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_001355823.1:p.Val270Leu missense NM_000280.6:c.766G>C NP_000271.1:p.Val256Leu missense NM_001127612.3:c.766G>C NP_001121084.1:p.Val256Leu missense NM_001258462.3:c.808G>C NP_001245391.1:p.Val270Leu missense NM_001258463.2:c.808G>C NP_001245392.1:p.Val270Leu missense NM_001258464.2:c.766G>C NP_001245393.1:p.Val256Leu missense NM_001258465.3:c.766G>C NP_001245394.1:p.Val256Leu missense NM_001310158.2:c.808G>C NP_001297087.1:p.Val270Leu missense NM_001310159.1:c.766G>C NP_001297088.1:p.Val256Leu missense NM_001310160.2:c.358G>C NP_001297089.1:p.Val120Leu missense NM_001310161.3:c.358G>C NP_001297090.1:p.Val120Leu missense NM_001368887.2:c.766G>C NP_001355816.1:p.Val256Leu missense NM_001368888.2:c.766G>C NP_001355817.1:p.Val256Leu missense NM_001368889.2:c.766G>C NP_001355818.1:p.Val256Leu missense NM_001368890.2:c.766G>C NP_001355819.1:p.Val256Leu missense NM_001368891.2:c.766G>C NP_001355820.1:p.Val256Leu missense NM_001368892.2:c.808G>C NP_001355821.1:p.Val270Leu missense NM_001368893.2:c.808G>C NP_001355822.1:p.Val270Leu missense NM_001368899.2:c.358G>C NP_001355828.1:p.Val120Leu missense NM_001368900.2:c.358G>C NP_001355829.1:p.Val120Leu missense NM_001368901.2:c.358G>C NP_001355830.1:p.Val120Leu missense NM_001368902.2:c.358G>C NP_001355831.1:p.Val120Leu missense NM_001368903.2:c.358G>C NP_001355832.1:p.Val120Leu missense NM_001368904.2:c.358G>C NP_001355833.1:p.Val120Leu missense NM_001368905.2:c.358G>C NP_001355834.1:p.Val120Leu missense NM_001368906.2:c.358G>C NP_001355835.1:p.Val120Leu missense NM_001368907.2:c.358G>C NP_001355836.1:p.Val120Leu missense NM_001368908.2:c.358G>C NP_001355837.1:p.Val120Leu missense NM_001368909.2:c.358G>C NP_001355838.1:p.Val120Leu missense NM_001368910.2:c.1009G>C NP_001355839.1:p.Val337Leu missense NM_001368911.2:c.811G>C NP_001355840.1:p.Val271Leu missense NM_001368912.2:c.808G>C NP_001355841.1:p.Val270Leu missense NM_001368913.2:c.808G>C NP_001355842.1:p.Val270Leu missense NM_001368914.2:c.808G>C NP_001355843.1:p.Val270Leu missense NM_001368915.2:c.766G>C NP_001355844.1:p.Val256Leu missense NM_001368916.2:c.766G>C NP_001355845.1:p.Val256Leu missense NM_001368917.2:c.766G>C NP_001355846.1:p.Val256Leu missense NM_001368918.2:c.883G>C NP_001355847.1:p.Val295Leu missense NM_001368919.2:c.883G>C NP_001355848.1:p.Val295Leu missense NM_001368920.2:c.841G>C NP_001355849.1:p.Val281Leu missense NM_001368921.2:c.607G>C NP_001355850.1:p.Val203Leu missense NM_001368922.2:c.607G>C NP_001355851.1:p.Val203Leu missense NM_001368923.2:c.607G>C NP_001355852.1:p.Val203Leu missense NM_001368924.2:c.607G>C NP_001355853.1:p.Val203Leu missense NM_001368925.2:c.607G>C NP_001355854.1:p.Val203Leu missense NM_001368926.2:c.607G>C NP_001355855.1:p.Val203Leu missense NM_001368927.2:c.607G>C NP_001355856.1:p.Val203Leu missense NM_001368928.2:c.565G>C NP_001355857.1:p.Val189Leu missense NM_001368929.2:c.358G>C NP_001355858.1:p.Val120Leu missense NM_001368930.2:c.163G>C NP_001355859.1:p.Val55Leu missense NM_001604.6:c.808G>C NP_001595.2:p.Val270Leu missense NR_160916.2:n.1147G>C non-coding transcript variant NR_160917.2:n.1152G>C non-coding transcript variant NC_000011.10:g.31793802C>G NC_000011.9:g.31815350C>G NG_008679.1:g.29160G>C LRG_720:g.29160G>C LRG_720t1:c.766G>C - Protein change
- V120L, V189L, V203L, V256L, V270L, V271L, V281L, V295L, V337L, V55L
- Other names
- -
- Canonical SPDI
- NC_000011.10:31793801:C: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.
- -
- 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. |
|||
| PAX6 | Sufficient evidence for dosage pathogenicity | Little evidence for dosage pathogenicity |
GRCh38 GRCh37 |
695 | 899 | |
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. |
|---|---|---|---|---|
| Uncertain significance (1) |
criteria provided, single submitter
|
Jan 31, 2020 | RCV001768837.3 |
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
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. |
|
|---|---|---|---|---|---|
|
Uncertain significance
(Jan 31, 2020)
|
criteria provided, single submitter
Method: clinical testing
|
Not Provided
Affected status: yes
Allele origin:
germline
|
GeneDx
Accession: SCV001993581.2
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, which includes splice predictors and evolutionary conservation, is inconclusive as to whether the … (more)
Not observed in large population cohorts (Lek et al., 2016); In-silico analysis, which includes splice predictors and evolutionary conservation, is inconclusive as to whether the variant alters gene splicing. In the absence of RNA/functional studies, the actual effect of this sequence change is unknown.; In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge (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:
Not observed in large population cohorts (Lek et al., 2016); In-silico analysis, which includes splice predictors and evolutionary conservation, is inconclusive as to whether the variant alters gene splicing. In the absence of RNA/functional studies, the actual effect of this sequence change is unknown.; In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
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 rs779126789 ...
HelpThese citations are identified by LitVar using
the rs number, so they may include citations for more than one variant
at this location. Please review the LitVar results carefully for your
variant of interest.
Record last updated Dec 25, 2023
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.