Variant #0000002572 (NC_000011.9:g.1780799G>A, CTSD(NM_001909.4):c.299C>T)

Individual ID 00002572
Chromosome 11
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.1780799G>A
Reference Fritchie et al 2008. Acta Neuropathol 117: 201-208
DB-ID CTSD_000001
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
CTSD NM_001909.4 ./. 3 c.299C>T r.(?) p.(Ser100Phe) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002572 ? ? CTSD 1 Y Yang