Variant #0000287867 (NC_000007.13:g.114269985_114269987del, NM_014491.3:c.522_524del (FOXP2))

Chromosome 7
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.114269985_114269987del
DNA change (hg38) g.114629930_114629932del
Published as FOXP2(NM_148898.3):c.597_599delACA (p.Q216del)
ISCN -
DB-ID FOXP2_000002
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FOXP2 NM_014491.3 -/. - c.522_524del r.(?) p.(Gln191del)
FOXP2 NM_148898.3 -/. - c.597_599del r.(?) p.(Gln216del)


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