Variant #0000287842 (NC_000001.10:g.47882221G>A, NM_012186.2:c.234G>A (FOXE3))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47882221G>A
DNA change (hg38) g.47416549G>A
Published as FOXE3(NM_012186.2):c.234G>A (p.A78=), FOXE3(NM_012186.3):c.234G>A (p.A78=)
ISCN -
DB-ID FOXE3_000033 See all 3 reported entries
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) 0.00141 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FOXE3 NM_012186.2 -/. - c.234G>A r.(?) p.(Ala78=)


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