Variant #0000568538 (NC_000019.9:g.55870844_55870873del, NM_000641.3:c.*6532_*6561del (IL11))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.55870844_55870873del
DNA change (hg38) g.55359476_55359505del
Published as FAM71E2(NM_001145402.1):c.1393_1422del (p.(Val465_Ala474del))
ISCN -
DB-ID COX6B2_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
IL11 NM_000641.3 -?/. - c.*6532_*6561del r.(=) p.(=)
FAM71E2 NM_001145402.1 -?/. - c.1393_1422del r.(?) p.(Val465_Ala474del)
COX6B2 NM_144613.4 -?/. - c.-4844_-4815del r.(?) p.(=)


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