Variant #0000896278 (NC_000023.10:g.49103246C>T, NM_014008.3:c.769C>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.49103246C>T
DNA change (hg38) -
Published as CCDC22(NM_014008.5):c.769C>T (p.R257C)
ISCN -
DB-ID CCDC22_000073 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) 5.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:41:49 +01:00 (CET)
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.769C>T r.(?) p.(Arg257Cys)
FOXP3 NM_014009.3 -?/. - c.*4549G>A r.(=) p.(=)


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