Variant #0000576414 (NC_000023.10:g.49114007C>T, NM_014008.3:c.*7285C>T (CCDC22))

Chromosome X
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.49114007C>T
DNA change (hg38) g.49257550C>T
Published as FOXP3(NM_001114377.1):c.226G>A (p.(Ala76Thr))
ISCN -
DB-ID CCDC22_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) 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 2019-07-18 18:22:55 +02:00 (CEST)
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.*7285C>T r.(=) p.(=)
FOXP3 NM_014009.3 -?/. - c.331G>A r.(?) p.(Ala111Thr)


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