Variant #0000692949 (NC_000020.10:g.2640761A>G, NM_006392.3:c.*1821A>G (NOP56))

Chromosome 20
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2640761A>G
DNA change (hg38) -
Published as IDH3B(NM_006899.4):c.830T>C (p.I277T)
ISCN -
DB-ID IDH3B_000024
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) 4.0E-5 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 2020-09-15 15:50:26 +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.830T>C - r.(?) p.(Ile277Thr)
NOP56 NM_006392.3 ?/. - c.*1821A>G - r.(=) p.(=)
IDH3B NM_006899.3 ?/. - c.830T>C - r.(?) p.(Ile277Thr)


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