Variant #0000334107 (NC_000023.10:g.49104722G>A, NM_014008.3:c.1163G>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.49104722G>A
DNA change (hg38) g.49248261G>A
Published as CCDC22(NM_014008.3):c.1163G>A (p.(Arg388His)), CCDC22(NM_014008.4):c.1163G>A (p.R388H)
ISCN -
DB-ID CCDC22_000021 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) 0.00133 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC22 NM_014008.3 -?/. - c.1163G>A r.(?) p.(Arg388His)
FOXP3 NM_014009.3 -?/. - c.*3073C>T r.(=) p.(=)


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