Variant #0000576456 (NC_000023.10:g.50053275C>T, CCNB3(NM_033031.2):c.2106C>T)

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50053275C>T
DNA change (hg38) g.50310275C>T
Published as CCNB3(NM_033031.2):c.2106C>T (p.A702=)
ISCN -
DB-ID CCNB3_000030
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) 0.00028 View details
Owner VKGL-NL_AMC
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCNB3 NM_033031.2 -/. - c.2106C>T r.(?) p.(Ala702=)