Variant #0000272858 (NC_000023.10:g.50053892C>A, CCNB3(NM_033031.2):c.2723C>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.50053892C>A
DNA change (hg38) g.50310892C>A
Published as CCNB3(NM_033031.2):c.2723C>A (p.T908N)
ISCN -
DB-ID CCNB3_000019
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_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCNB3 NM_033031.2 ?/. - c.2723C>A r.(?) p.(Thr908Asn)