Variant #0000866404 (NC_000020.10:g.2644614C>T, NM_006392.3:c.*5674C>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.2644614C>T
DNA change (hg38) -
Published as IDH3B(NM_006899.4):c.74G>A (p.G25D), IDH3B(NM_006899.5):c.74G>A (p.G25D)
ISCN -
DB-ID IDH3B_000038 See all 2 reported entries
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) 0.00062 View details
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 16:01:56 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
IDH3B NM_001258384.1 -?/. - c.74G>A - r.(?) p.(Gly25Asp)
NOP56 NM_006392.3 -?/. - c.*5674C>T - r.(=) p.(=)
IDH3B NM_006899.3 -?/. - c.74G>A - r.(?) p.(Gly25Asp)


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