Variant #0000331815 (NC_000007.13:g.114271603_114271605del, NM_014491.3:c.618_620del (FOXP2))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.114271603_114271605del
DNA change (hg38) g.114631548_114631550del
Published as FOXP2(NM_001172766.2):c.598-6_598-4del (p.?), FOXP2(NM_148898.4):c.673-3_673-1delCAG
ISCN -
DB-ID FOXP2_000003 See all 2 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 2018-01-15 20:58:59 +01:00 (CET)
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.618_620del r.(?) p.(Gln209del)
FOXP2 NM_148898.3 ?/. - c.693_695del r.(?) p.(Gln234del)


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