Variant #0000576461 (NC_000023.10:g.50089805G>A, CCNB3(NM_033031.2):c.3809G>A)

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50089805G>A
DNA change (hg38) g.50346806G>A
Published as CCNB3(NM_033031.2):c.3809G>A (p.(Arg1270Lys))
ISCN -
DB-ID CCNB3_000023 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 -
Methylation -
Average frequency (large NGS studies) 0.00341 View details
Owner VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCNB3 NM_033031.2 -?/. - c.3809G>A r.(?) p.(Arg1270Lys)