Variant #0000809636 (NC_000022.10:g.38877254C>T, NM_001098504.1:c.*4686G>A (DDX17))

Chromosome 22
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.38877254C>T
DNA change (hg38) -
Published as KDELR3(NM_006855.4):c.389C>T (p.A130V)
ISCN -
DB-ID DDX17_000004
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX17 NM_001098504.1 ?/. - c.*4686G>A r.(=) p.(=)
KDELR3 NM_006855.3 ?/. - c.389C>T r.(?) p.(Ala130Val)


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