Variant #0000334142 (NC_000023.10:g.50052712G>A, CCNB3(NM_033031.2):c.1543G>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.50052712G>A
DNA change (hg38) g.50309712G>A
Published as CCNB3(NM_033031.2):c.1543G>A (p.G515R, p.(Gly515Arg))
ISCN -
DB-ID CCNB3_000012 See all 2 reported entries
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.1543G>A r.(?) p.(Gly515Arg)