Variant #0000304253 (NC_000020.10:g.2638848G>A, NM_006392.3:c.1693G>A (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.2638848G>A
DNA change (hg38) g.2658202G>A
Published as NOP56(NM_006392.3):c.1693G>A (p.E565K)
ISCN -
DB-ID NOP56_000003
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) 2.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.*1051C>T - r.(=) p.(=)
NOP56 NM_006392.3 ?/. - c.1693G>A - r.(?) p.(Glu565Lys)
IDH3B NM_006899.3 ?/. - c.*549C>T - r.(=) p.(=)


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