Variant #0000343869 (NC_000007.13:g.114210912T>G, NC_000007.13(NM_014491.3):c.258+36151T>G (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.114210912T>G
DNA change (hg38) g.114570857T>G
Published as -
ISCN -
DB-ID FOXP2_000008
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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.258+36151T>G r.(=) p.(=)
FOXP2 NM_148898.3 ?/. - c.309T>G r.(?) p.(Asp103Glu)


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