Variant #0001014258 (NC_000007.13:g.114066636A>G, NM_014491.3:c.70A>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.114066636A>G
DNA change (hg38) -
Published as FOXP2(NM_014491.4):c.70A>G (p.S24G)
ISCN -
DB-ID FOXP2_000042
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) 8.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 21:08:56 +01:00 (CET)
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.70A>G r.(?) p.(Ser24Gly)
FOXP2 NM_148898.3 -?/. - c.70A>G r.(?) p.(Ser24Gly)


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