Variant #0001030176 (NC_000011.9:g.66331605G>A, NM_003793.3:c.1334C>T (CTSF))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.66331605G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID CTSF_000043
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs142523550
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 7.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-04-02 12:17:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTSF NM_003793.3 ?/. - c.1334C>T r.(?) p.(Pro445Leu)


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