Variant #0001043186 (NC_000019.9:g.55870782G>A, NM_000641.3:c.*6593C>T (IL11))

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.55870782G>A
DNA change (hg38) -
Published as FAM71E2(NM_001145402.2):c.1454C>T (p.(Ala485Val))
ISCN -
DB-ID COX6B2_000008
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) 0.0001 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
IL11 NM_000641.3 ?/. - c.*6593C>T r.(=) p.(=)
FAM71E2 NM_001145402.1 ?/. - c.1454C>T r.(?) p.(Ala485Val)
COX6B2 NM_144613.4 ?/. - c.-4783C>T r.(?) p.(=)


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