Variant #0001067731 (NC_000023.10:g.70517321_70517333del, NC_000023.10(NM_007363.4):c.1028+10_1028+22del (NONO))

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.70517321_70517333del
DNA change (hg38) -
Published as -
ISCN -
DB-ID ITGB1BP2_000021
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NONO NM_007363.4 -?/. - c.1028+10_1028+22del r.(=) p.(=)
ITGB1BP2 NM_012278.1 -?/. - c.-4336_-4324del r.(?) p.(=)


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