Variant #0000809635 (NC_000022.10:g.38877244G>C, NM_001098504.1:c.*4696C>G (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.38877244G>C
DNA change (hg38) -
Published as KDELR3(NM_006855.4):c.379G>C (p.E127Q)
ISCN -
DB-ID DDX17_000003
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) 7.0E-5 View details
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX17 NM_001098504.1 ?/. - c.*4696C>G r.(=) p.(=)
KDELR3 NM_006855.3 ?/. - c.379G>C r.(?) p.(Glu127Gln)


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