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Variant : CV334659 (NM_025114.3(CEP290):c.-38G>C) Homo sapiens

Symbol: CV334659
Name: NM_025114.3(CEP290):c.-38G>C
Condition: Bardet-Biedl syndrome [RCV000366586]|Familial aplasia of the vermis [RCV000388544]|Joubert syndrome [RCV000388544]|Leber congenital amaurosis [RCV000269659]|Meckel-Gruber syndrome [RCV000326938]|Renal dysplasia and retinal aplasia [RCV000277677]
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: 5 prime utr variant
Evidence: clinical testing
HGVS Name(s): NG_008417.1:g.5307G>C
NC_000012.12:g.88141910C>G
NC_000012.11:g.88535687C>G
NG_021187.1:g.4615C>G
NG_008417.2:g.5307G>C
NM_025114.3:c.-38G>C
Position
Human AssemblyChrPosition (strand)Source
GRCh381288,141,910 - 88,141,910CLINVAR
GRCh371288,535,687 - 88,535,687CLINVAR
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: 11646196
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.