Variant #0000566857 (NC_000019.9:g.33793410G>A, CEBPA(NM_004364.3):c.-90C>T)

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.33793410G>A
DNA change (hg38) g.33302504G>A
Published as CEBPA(NM_001287424.1):c.16C>T (p.R6*)
ISCN -
DB-ID CEBPA_000020
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) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEBPA NM_004364.3 -?/. - c.-90C>T r.(?) p.(=)