Variant #0000576460 (NC_000023.10:g.50089734C>T, CCNB3(NM_033031.2):c.3738C>T)

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.50089734C>T
DNA change (hg38) g.50346735C>T
Published as CCNB3(NM_033031.2):c.3738C>T (p.I1246=)
ISCN -
DB-ID CCNB3_000033
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) 9.0E-5 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.3738C>T r.(?) p.(Ile1246=)