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Variant : CV334684 (NM_025114.3(CEP290):c.-235T>G) Homo sapiens

Symbol: CV334684
Name: NM_025114.3(CEP290):c.-235T>G
Condition: Bardet-Biedl syndrome [RCV000289415]|Familial aplasia of the vermis [RCV000351356]|Joubert syndrome [RCV000351356]|Leber congenital amaurosis [RCV000397035]|Meckel-Gruber syndrome [RCV000290588]|Renal dysplasia and retinal aplasia [RCV000347916]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: CEP290  
Variant Type: single nucleotide variant (SO:0001623)
Source: CLINVAR
Molecular Consequence: 5 prime utr variant
Evidence: clinical testing
HGVS Name(s): NM_025114.3:c.-235T>G
NG_008417.1:g.5110T>G
NC_000012.12:g.88142107A>C
NC_000012.11:g.88535884A>C
Position
Human AssemblyChrPosition (strand)Source
GRCh381288,142,107 - 88,142,107CLINVAR
GRCh371288,535,884 - 88,535,884CLINVAR
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: 11615852
Created: 2017-01-11
Species: Homo sapiens
Last Modified: 2019-07-16
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.