Variant #0000334148 (NC_000023.10:g.50053750G>A, CCNB3(NM_033031.2):c.2581G>A)

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.50053750G>A
DNA change (hg38) g.50310750G>A
Published as CCNB3(NM_033031.2):c.2581G>A (p.(Ala861Thr))
ISCN -
DB-ID CCNB3_000018
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCNB3 NM_033031.2 ?/. - c.2581G>A r.(?) p.(Ala861Thr)