Variant #0001004685 (NC_000019.9:g.38796089C>G, NM_033520.1:c.*485C>G (C19orf33))

Chromosome 19
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.38796089C>G
DNA change (hg38) -
Published as YIF1B(NM_001039672.2):c.848G>C (p.(Arg283Pro))
ISCN -
DB-ID C19orf33_000007
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C19orf33 NM_033520.1 ?/. - c.*485C>G r.(=) p.(=)
YIF1B NM_033557.3 ?/. - c.755G>C r.(?) p.(Arg252Pro)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.