Variant #0000000419 (NC_000020.10:g.44523720G>A, CTSA(NM_000308.2):c.1090G>A)

Individual ID 00000196
Chromosome 20
Allele Parent #1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.44523720G>A
Reference -
DB-ID CTSA_000001
Average frequency (gnomAD v.2.1.1) 0.00026 View details
Owner Variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Variome.ir
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Clinical classification     
CTSA NM_000308.2 ./. - c.1090G>A r.(?) p.(Val364Met) likely pathogenic
CTSA NM_001167594.1 ./. - c.1039G>A r.(?) p.(Val347Met) likely pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000200 DNA SEQ-NG CTSA 2 Variome.ir