Variant #0000002769 (NC_000013.10:g.77575001A>G, CLN5(NM_006493.2):c.1121A>G)

Individual ID 00002769
Chromosome 13
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.77575001A>G
Reference Sleat et al. 2009. Mol Cell Pteomics 8:1708-18;Xin et al 2010 Neurology 74:565-71
DB-ID CLN5_000029
Frequency -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
CLN5 NM_006493.2 ./. 4 c.1121A>G r.(?) p.(Tyr374Cys) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002769 ? ? CLN5 1 Y Yang