Variant #0001056829 (NC_000020.10:g.2637755G>A, NM_006392.3:c.1310G>A (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.2637755G>A
DNA change (hg38) -
Published as NOP56(NM_006392.4):c.1310G>A (p.(Arg437Lys))
ISCN -
DB-ID IDH3B_000047
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) 7.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
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.*2144C>T - r.(=) p.(=)
NOP56 NM_006392.3 -?/. - c.1310G>A - r.(?) p.(Arg437Lys)
IDH3B NM_006899.3 -?/. - c.*1642C>T - r.(=) p.(=)


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