Variant #0001036713 (NC_000008.10:g.11695935C>G, NM_004462.3:c.1071C>G (FDFT1))

Chromosome 8
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.11695935C>G
DNA change (hg38) -
Published as FDFT1(NM_004462.5):c.1071C>G (p.(Ser357Arg))
ISCN -
DB-ID CTSB_000002
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00018 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
FDFT1 NM_004462.3 ?/. - c.1071C>G r.(?) p.(Ser357Arg)
CTSB NM_147780.2 ?/. - c.*6699G>C r.(=) p.(=)


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