Variant #0000329694 (NC_000003.11:g.167183324_167183327del, NM_178824.3:c.*13341_*13344del (WDR49))

Chromosome 3
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.167183324_167183327del
DNA change (hg38) g.167465536_167465539del
Published as SERPINI2(NM_001012303.2):c.645_648del (p.(Lys216MetfsTer9))
ISCN -
DB-ID SERPINI2_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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERPINI2 NM_006217.3 ?/. - c.615_618del r.(?) p.(Lys206MetfsTer9)
WDR49 NM_178824.3 ?/. - c.*13341_*13344del r.(=) p.(=)


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