Variant #0000855783 (NC_000020.10:g.2639088C>T, NM_006392.3:c.*148C>T (NOP56))

Chromosome 20
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.2639088C>T
DNA change (hg38) -
Published as IDH3B(NM_174855.3):c.1152G>A (p.*384=)
ISCN -
DB-ID IDH3B_000034
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 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
IDH3B NM_001258384.1 -?/. - c.*811G>A - r.(=) p.(=)
NOP56 NM_006392.3 -?/. - c.*148C>T - r.(=) p.(=)
IDH3B NM_006899.3 -?/. - c.*309G>A - r.(=) p.(=)


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