Variant #0000334583 (NC_000023.10:g.70517221T>G, NONO(NM_007363.4):c.944-6T>G)

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.70517221T>G
DNA change (hg38) g.71297371T>G
Published as NONO(NM_001145408.1):c.944-6T>G (p.(=))
ISCN -
DB-ID NONO_000009
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) Variant not found in online data sets
Owner VKGL-NL_Leiden
Database submission license No license selected
Created by VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NONO NM_007363.4 ?/. - c.944-6T>G r.(=) p.(=)
ITGB1BP2 NM_012278.1 ?/. - c.-4436T>G r.(?) p.(=)