Variant #0000856675 (NC_000023.10:g.49113891G>A, NM_014008.3:c.*7169G>A (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.49113891G>A
DNA change (hg38) -
Published as FOXP3(NM_014009.3):c.447C>T (p.L149=)
ISCN -
DB-ID CCDC22_000071
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 2022-05-09 15:47:41 +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     
CCDC22 NM_014008.3 -?/. - c.*7169G>A r.(=) p.(=)
FOXP3 NM_014009.3 -?/. - c.447C>T r.(?) p.(Leu149=)


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