Variant #0000576419 (NC_000023.10:g.49126801C>T, NM_014008.3:c.*20079C>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.49126801C>T
DNA change (hg38) g.49270338C>T
Published as PPP1R3F(NM_033215.4):c.469C>T (p.P157S, p.(Pro157Ser))
ISCN -
DB-ID CCDC22_000047 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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC22 NM_014008.3 -?/. - c.*20079C>T r.(=) p.(=)
FOXP3 NM_014009.3 -?/. - c.-5701G>A r.(?) p.(=)
PPP1R3F NM_033215.4 -?/. - c.469C>T r.(?) p.(Pro157Ser)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.