Variant #0000984846 (NC_000023.10:g.70523738G>A, NM_007363.4:c.*3812G>A (NONO))

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.70523738G>A
DNA change (hg38) -
Published as ITGB1BP2(NM_012278.4):c.616G>A (p.G206S)
ISCN -
DB-ID ITGB1BP2_000017
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 2024-04-19 20:27:30 +02:00 (CEST)
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.*3812G>A r.(=) p.(=)
ITGB1BP2 NM_012278.1 ?/. - c.616G>A r.(?) p.(Gly206Ser)


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