Variant #0000980868 (NC_000014.8:g.29236741dup, NM_005249.4:c.256dup (FOXG1))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.29236741dup
DNA change (hg38) -
Published as FOXG1(NM_005249.5):c.256dup (p.(Gln86ProfsTer35)), FOXG1(NM_005249.5):c.256dupC (p.Q86Pfs*35)
ISCN -
DB-ID FOXG1_000020 See all 7 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
FOXG1 NM_005249.4 +/. - c.256dup r.(?) p.(Gln86ProfsTer35)


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