Variant #0000568552 (NC_000019.9:g.56160776C>T, NM_007279.2:c.-5695C>T (U2AF2))

Chromosome 19
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.56160776C>T
DNA change (hg38) g.55649410C>T
Published as CCDC106(NM_013301.2):c.139C>T (p.(Pro47Ser))
ISCN -
DB-ID CCDC106_000002
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) 0.00065 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
U2AF2 NM_007279.2 -?/. - c.-5695C>T r.(?) p.(=)
CCDC106 NM_013301.2 -?/. - c.139C>T r.(?) p.(Pro47Ser)
ZNF581 NM_016535.3 -?/. - c.*4245C>T r.(=) p.(=)


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