Variant #0000277813 (NC_000020.10:g.2644201G>A, NM_006392.3:c.*5261G>A (NOP56))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2644201G>A
DNA change (hg38) g.2663555G>A
Published as IDH3B(NM_006899.5):c.228C>T (p.V76=)
ISCN -
DB-ID IDH3B_000006
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.228C>T - r.(?) p.(Val76=)
NOP56 NM_006392.3 -/. - c.*5261G>A - r.(=) p.(=)
IDH3B NM_006899.3 -/. - c.228C>T - r.(?) p.(Val76=)


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