Variant #0000530444 (NC_000007.13:g.114298286C>T, NM_014491.3:c.1432C>T (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.114298286C>T
DNA change (hg38) g.114658231C>T
Published as FOXP2(NM_148898.3):c.1507C>T (p.R503*)
ISCN -
DB-ID FOXP2_000022
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-23 13:31:51 +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.1432C>T r.(?) p.(Arg478Ter)
FOXP2 NM_148898.3 +/. - c.1507C>T r.(?) p.(Arg503Ter)


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