Variant #0000613509 (NC_000011.9:g.63994399G>T, NM_031471.5:c.*3435G>T (FERMT3))
| Chromosome |
11 |
| 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.63994399G>T |
| DNA change (hg38) |
g.64226927G>T |
| Published as |
NUDT22(NM_001128612.2):c.275G>T (p.(Gly92Val)) |
| ISCN |
- |
| DB-ID |
NUDT22_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) |
0.0005 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2022-09-27 17:32:42 +02:00 (CEST) |

Variant on transcripts
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