Variant #0000681576 (NC_000020.10:g.2644637_2644638insAA, NM_006392.3:c.*5697_*5698insAA (NOP56))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2644637_2644638insAA
DNA change (hg38) -
Published as IDH3B(NM_006899.4):c.50_51insTT (p.G18Sfs*10)
ISCN -
DB-ID IDH3B_000022
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
IDH3B NM_001258384.1 +?/. - c.50_51insTT - r.(?) p.(Gly18SerfsTer10)
NOP56 NM_006392.3 +?/. - c.*5697_*5698insAA - r.(=) p.(=)
IDH3B NM_006899.3 +?/. - c.50_51insTT - r.(?) p.(Gly18SerfsTer10)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.