Genomic variant #0000528912

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43152344G>A
DNA change (hg38) -
Published as CUL9(NM_015089.3):c.296G>A (p.S99N)
ISCN -
DB-ID CUL9_000005
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) Variant not found in online data sets
Owner VKGL-NL




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
SRF NM_003131.2 -?/. - c.*5416G>A likely benign r.(=) p.(=)
CUL9 NM_015089.2 -?/. - c.296G>A likely benign r.(?) p.(Ser99Asn)