Variant #0000689863 (NC_000007.13:g.114270015A>G, NM_014491.3:c.552A>G (FOXP2))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.114270015A>G
DNA change (hg38) -
Published as FOXP2(NM_148898.3):c.627A>G (p.Q209=)
ISCN -
DB-ID FOXP2_000027
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 2020-09-15 15:50:26 +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     
FOXP2 NM_014491.3 -?/. - c.552A>G r.(?) p.(Gln184=)
FOXP2 NM_148898.3 -?/. - c.627A>G r.(?) p.(Gln209=)


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