Variant #0000276884 (NC_000009.11:g.100616728_100616733del, NM_004473.3:c.532_537del (FOXE1))

Chromosome 9
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.100616728_100616733del
DNA change (hg38) g.97854446_97854451del
Published as FOXE1(NM_004473.3):c.505_510del (p.(Ala172_Ala173del)), FOXE1(NM_004473.3):c.532_537delGCCGCC (p.A178_A179del), FOXE1(NM_004473.4):c.532_537delGCCG...
ISCN -
DB-ID FOXE1_000004 See all 4 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FOXE1 NM_004473.3 -/. - c.532_537del r.(?) p.(Ala178_Ala179del)


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