ClinVar Genomic variation as it relates to human health
NM_001368894.2(PAX6):c.1211del (p.Gly404fs)
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_001368894.2(PAX6):c.1211del (p.Gly404fs)
Variation ID: 800476 Accession: VCV000800476.2
- Type and length
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Deletion, 1 bp
- Location
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Cytogenetic: 11p13 11: 31790724 (GRCh38) [ NCBI UCSC ] 11: 31812272 (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 Dec 23, 2019 Dec 23, 2019 Aug 15, 2019 - HGVS
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Nucleotide Protein Molecular
consequenceNM_001368894.2:c.1211del MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_001355823.1:p.Gly404fs frameshift NM_000280.6:c.1169del NP_000271.1:p.Gly390fs frameshift NM_001127612.3:c.1169del NP_001121084.1:p.Gly390fs frameshift NM_001258462.3:c.1211del NP_001245391.1:p.Gly404fs frameshift NM_001258463.2:c.1211del NP_001245392.1:p.Gly404fs frameshift NM_001258464.2:c.1169del NP_001245393.1:p.Gly390fs frameshift NM_001258465.3:c.1169del NP_001245394.1:p.Gly390fs frameshift NM_001310158.2:c.1211del NP_001297087.1:p.Gly404fs frameshift NM_001310160.2:c.761del NP_001297089.1:p.Gly254fs frameshift NM_001310161.3:c.761del NP_001297090.1:p.Gly254fs frameshift NM_001368887.2:c.1169del NP_001355816.1:p.Gly390fs frameshift NM_001368888.2:c.1169del NP_001355817.1:p.Gly390fs frameshift NM_001368889.2:c.1169del NP_001355818.1:p.Gly390fs frameshift NM_001368890.2:c.1169del NP_001355819.1:p.Gly390fs frameshift NM_001368891.2:c.1169del NP_001355820.1:p.Gly390fs frameshift NM_001368892.2:c.1211del NP_001355821.1:p.Gly404fs frameshift NM_001368893.2:c.1211del NP_001355822.1:p.Gly404fs frameshift NM_001368899.2:c.761del NP_001355828.1:p.Gly254fs frameshift NM_001368900.2:c.761del NP_001355829.1:p.Gly254fs frameshift NM_001368901.2:c.761del NP_001355830.1:p.Gly254fs frameshift NM_001368902.2:c.761del NP_001355831.1:p.Gly254fs frameshift NM_001368903.2:c.761del NP_001355832.1:p.Gly254fs frameshift NM_001368904.2:c.761del NP_001355833.1:p.Gly254fs frameshift NM_001368905.2:c.761del NP_001355834.1:p.Gly254fs frameshift NM_001368906.2:c.761del NP_001355835.1:p.Gly254fs frameshift NM_001368907.2:c.761del NP_001355836.1:p.Gly254fs frameshift NM_001368908.2:c.761del NP_001355837.1:p.Gly254fs frameshift NM_001368909.2:c.761del NP_001355838.1:p.Gly254fs frameshift NM_001368910.2:c.1412del NP_001355839.1:p.Gly471fs frameshift NM_001368911.2:c.1078-705del intron variant NM_001368912.2:c.1075-705del intron variant NM_001368913.2:c.1075-705del intron variant NM_001368914.2:c.1075-705del intron variant NM_001368915.2:c.1033-705del intron variant NM_001368916.2:c.1033-705del intron variant NM_001368917.2:c.1033-705del intron variant NM_001368918.2:c.1286del NP_001355847.1:p.Gly429fs frameshift NM_001368919.2:c.1286del NP_001355848.1:p.Gly429fs frameshift NM_001368920.2:c.1244del NP_001355849.1:p.Gly415fs frameshift NM_001368921.2:c.874-705del intron variant NM_001368922.2:c.1010del NP_001355851.1:p.Gly337fs frameshift NM_001368923.2:c.1010del NP_001355852.1:p.Gly337fs frameshift NM_001368924.2:c.1010del NP_001355853.1:p.Gly337fs frameshift NM_001368925.2:c.1010del NP_001355854.1:p.Gly337fs frameshift NM_001368926.2:c.1010del NP_001355855.1:p.Gly337fs frameshift NM_001368927.2:c.1010del NP_001355856.1:p.Gly337fs frameshift NM_001368928.2:c.968del NP_001355857.1:p.Gly323fs frameshift NM_001368929.2:c.625-705del intron variant NM_001368930.2:c.566del NP_001355859.1:p.Gly189fs frameshift NM_001604.6:c.1211del NP_001595.2:p.Gly404fs frameshift NR_160917.2:n.1555del non-coding transcript variant NC_000011.10:g.31790726del NC_000011.9:g.31812274del NG_008679.1:g.32238del LRG_720:g.32238del LRG_720t1:c.1169del - Protein change
- G471fs, G189fs, G254fs, G323fs, G337fs, G390fs, G404fs, G415fs, G429fs
- Other names
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- Canonical SPDI
- NC_000011.10:31790723:CCC:CC
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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
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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
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The triplosensitivity score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team. |
Within gene
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The number of variants in ClinVar that are contained within this gene, with a link to view the list of variants. |
All
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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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PAX6 | Sufficient evidence for dosage pathogenicity | Little evidence for dosage pathogenicity |
GRCh38 GRCh37 |
668 | 870 |
Conditions - Germline
Condition
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The condition for this variant-condition (RCV) record in ClinVar. |
Classification
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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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Pathogenic (1) |
criteria provided, single submitter
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Aug 15, 2019 | RCV000984462.2 |
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
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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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Pathogenic
(Aug 15, 2019)
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criteria provided, single submitter
Method: clinical testing
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Aniridia 1
(Autosomal dominant inheritance)
Affected status: yes
Allele origin:
de novo
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Wessex Regional Genetics Laboratory, Salisbury District Hospital
Accession: SCV001055821.1
First in ClinVar: Dec 23, 2019 Last updated: Dec 23, 2019 |
Observation 1:
Number of individuals with the variant: 1
Observation 2:
Number of individuals with the variant: 1
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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 rs1592367444 ...
HelpRecord last updated Apr 06, 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.