Variant #0000530441 (NC_000007.13:g.114282473del, NM_014491.3:c.784del (FOXP2))

Chromosome 7
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.114282473del
DNA change (hg38) g.114642418del
Published as FOXP2(NM_148898.4):c.859delA (p.S287Vfs*12)
ISCN -
DB-ID FOXP2_000019
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FOXP2 NM_014491.3 +/. - c.784del r.(?) p.(Ser262ValfsTer12)
FOXP2 NM_148898.3 +/. - c.859del r.(?) p.(Ser287ValfsTer12)


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