Variant #0000002778 (NC_000015.9:g.68506628_68521840del, CLN6(NM_017882.2):c.83_297del)

Individual ID 00002778
Chromosome 15
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.68506628_68521840del
Reference Al-Muhaizea et al 2009 Pediatr Neruol 41: 74-76
DB-ID CLN6_000004
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
CLN6 NM_017882.2 ./. 2_3 c.83_297del r.spl? p.? VariO:0141 DNA deletion -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002778 ? ? CLN6 1 Y Yang