Variant #0000287868 (NC_000023.10:g.49114183G>A, NM_014008.3:c.*7461G>A (CCDC22))

Chromosome X
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.49114183G>A
DNA change (hg38) g.49257726G>A
Published as FOXP3(NM_014009.3):c.253C>T (p.R85W)
ISCN -
DB-ID FOXP3_000009 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_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     
CCDC22 NM_014008.3 ?/. - c.*7461G>A r.(=) p.(=)
FOXP3 NM_014009.3 ?/. - c.253C>T r.(?) p.(Arg85Trp)


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