Variant #0000810634 (NC_000023.10:g.70517682G>C, NC_000023.10(NM_007363.4):c.1029-4G>C (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.70517682G>C
DNA change (hg38) -
Published as NONO(NM_001145408.2):c.1029-4G>C
ISCN -
DB-ID ITGB1BP2_000011
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) 0.00023 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NONO NM_007363.4 -?/. - c.1029-4G>C r.spl? p.?
ITGB1BP2 NM_012278.1 -?/. - c.-3975G>C r.(?) p.(=)


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