Variant #0000272856 (NC_000023.10:g.50052532T>C, CCNB3(NM_033031.2):c.1363T>C)

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.50052532T>C
DNA change (hg38) g.50309532T>C
Published as CCNB3(NM_033031.2):c.1363T>C (p.S455P)
ISCN -
DB-ID CCNB3_000010
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.1363T>C r.(?) p.(Ser455Pro)