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Variant : CV326862 (NM_025114.3(CEP290):c.1345A>G (p.Lys449Glu)) Homo sapiens

Symbol: CV326862
Name: NM_025114.3(CEP290):c.1345A>G (p.Lys449Glu)
Condition: Bardet-Biedl syndrome [RCV000277847]|Familial aplasia of the vermis [RCV000293247]|Joubert syndrome [RCV000293247]|Leber congenital amaurosis [RCV000363136]|Meckel-Gruber syndrome [RCV000387296]|Renal dysplasia and retinal aplasia [RCV000332842]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: CEP290  
Variant Type: single nucleotide variant (SO:0001483)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: clinical testing
HGVS Name(s): NG_008417.1:g.26206A>G
NC_000012.12:g.88121011T>C
NC_000012.11:g.88514788T>C
NP_079390.3:p.Lys449Glu
NM_025114.3:c.1345A>G
NM_025114.3:c.1345A>G
NG_008417.2:g.26206A>G
Position
Human AssemblyChrPosition (strand)Source
GRCh381288,121,011 - 88,121,011CLINVAR
GRCh371288,514,788 - 88,514,788CLINVAR
Cytogenetic Map1212q21.32CLINVAR
Trait Synonyms: Agenesis of cerebellar vermis; Cerebellar vermis aplasia; CEREBELLOPARENCHYMAL DISORDER IV; DYSENCEPHALIA SPLANCHNOCYSTICA; Familial aplasia of the vermis; Leber's amaurosis; Senior-Loken syndrome
Age Of Onset: antenatal
Prevalence: 1-9 / 100 000



Disease Annotations

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11614566
Created: 2017-01-11
Species: Homo sapiens
Last Modified: 2019-10-08
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.