Variant #0000569286 (NC_000020.10:g.2644357C>T, NM_006392.3:c.*5417C>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.2644357C>T |
DNA change (hg38) |
g.2663711C>T |
Published as |
IDH3B(NM_006899.4):c.165G>A (p.P55=) |
ISCN |
- |
DB-ID |
IDH3B_000018 |
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) |
0.00015 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2020-07-16 14:39:47 +02:00 (CEST) |

Variant on transcripts
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