Variant #0000002740 (NC_000016.9:g.28488943T>C, CLN3(NM_000086.2):c.1211A>G)

Individual ID 00002740
Chromosome 16
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.28488943T>C
Reference Eksandh et al. 2000 Ophthalmic Genetics 21: 69-71.
DB-ID CLN3_000045
Frequency -
Average frequency (gnomAD v.2.1.1) 0.0755 View details
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     
CLN3 NM_000086.2 ./. 15 c.1211A>G r.(?) p.(His404Arg) 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     
0000002740 ? ? CLN3 1 Y Yang