Variant #0000895249 (NC_000020.10:g.2637427C>T, NM_006392.3:c.1167C>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.2637427C>T
DNA change (hg38) -
Published as NOP56(NM_006392.4):c.1167C>T (p.P389=)
ISCN -
DB-ID IDH3B_000040
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) 0.00184 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +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.*2472G>A - r.(=) p.(=)
NOP56 NM_006392.3 -?/. - c.1167C>T - r.(?) p.(Pro389=)
IDH3B NM_006899.3 -?/. - c.*1970G>A - r.(=) p.(=)


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