Variant #0000268617 (NC_000011.9:g.1774757G>T, NM_001909.4:c.1215C>A (CTSD))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1774757G>T
DNA change (hg38) g.1753527G>T
Published as CTSD(NM_001909.5):c.1215C>A (p.G405=)
ISCN -
DB-ID CTSD_000002 See all 2 reported entries
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) 0.01186 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFITM10 NM_001170820.3 -/. - c.-3085C>A r.(?) p.(=)
CTSD NM_001909.4 -/. - c.1215C>A r.(?) p.(Gly405=)


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