Variant #0000002573 (NC_000011.9:g.1778573A>T, CTSD(NM_001909.4):c.685T>A)

Individual ID 00002573
Chromosome 11
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.1778573A>T
Reference Steinfeld et al. 2006. Am J Hum Genet 78:988-98
DB-ID CTSD_000002
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 ./. 5 c.685T>A r.(?) p.(Phe229Ile) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002573 ? ? CTSD 1 Y Yang