Variant #0000528914 (NC_000006.11:g.43154017C>G, CUL9(NM_015089.2):c.1075C>G)

Chromosome 6
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.43154017C>G
DNA change (hg38) g.43186279C>G
Published as CUL9(NM_015089.2):c.1075C>G (p.(Gln359Glu))
ISCN -
DB-ID CUL9_000007
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) 0.00638 View details
Owner VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SRF NM_003131.2 -?/. - c.*7089C>G r.(=) p.(=)
CUL9 NM_015089.2 -?/. - c.1075C>G r.(?) p.(Gln359Glu)