Variant #0000304252 (NC_000023.10:g.70518595G>A, NONO(NM_007363.4):c.1210G>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.70518595G>A
DNA change (hg38) g.71298745G>A
Published as NONO(NM_001145408.1):c.1210G>A (p.A404T)
ISCN -
DB-ID NONO_000010
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00021 View details
Owner VKGL-NL_Rotterdam
Database submission license No license selected
Created by VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NONO NM_007363.4 -?/. - c.1210G>A r.(?) p.(Ala404Thr)
ITGB1BP2 NM_012278.1 -?/. - c.-3062G>A r.(?) p.(=)