Variant #0000728996 (NC_000023.10:g.49126534G>A, NM_014008.3:c.*19812G>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.49126534G>A
DNA change (hg38) -
Published as PPP1R3F(NM_033215.4):c.202G>A (p.A68T)
ISCN -
DB-ID CCDC22_000065
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 2021-02-08 18:36:18 +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.*19812G>A r.(=) p.(=)
FOXP3 NM_014009.3 -?/. - c.-5434C>T r.(?) p.(=)
PPP1R3F NM_033215.4 -?/. - c.202G>A r.(?) p.(Ala68Thr)


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